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I probably didn't look hard enough. But I didn't see anything.

Can you direct me to a specific research.

Thinking back to when I was a child, I don't remember being held

back a year was so detrimental.

From: sList

[mailto:sList ] On Behalf Of Hawk

Sent: Saturday, June 05, 2010 11:02 PM

To: sList

Subject: Re: Retention and parent conferences

Did you look at the link I provided? It is a great resource

on retenetion http://www.wrightslaw.com/info/retain.index.htm

There are viewpoints and

research from National

Association of School Psychologists, Harvard Civil Rights Projectm California

School Psychologist, US Dept of Education, Uiversity of Wisconsin and the

American Federation of Teachers. ALL say that retention does NOT work and is a

detriment to children.

Gabi and others,

Let me ask everyone here : If

I was your kid's ( grandkid's, nephew, friend etc) teacher, what would you

ask me? What would you say to me?

In my previous postings maybe a

year ago or more, I said several times that one can expect several of

the list members here to be nurses, doctors, laywers, teachers,

principals, ESE specialists, OTs, behavior specialists, counselors, cluster

teachers and also at the same time be parents, grand parents, aunts, uncles,

godparents, siblings and friends of kids with autism. This is

possible, right? It is also possible to have one gen ed kid and one with

autism, right? So, it is OK to compare a cluster to a gen ed room,

and see the difference. Do we like what we see? Are gen ed teachers held to a

higher standard? Are cluster teachers less accountable? What is my role as a

parent, grand parent, aunt, uncle or advocate? What can I do now to make things

better for my kid. What is within my power, and when am I banging my head

against the wall? What can I change being outside the school system?

Many of us became attracted

to our profession and chose a career that is related to ASD because

autism had come into our lives. Some grew up with autism. One of the list

members here has an older sister with autism. She just did not know it as a

kid. She thought that everybody's older sisters were like her sister. It is

very possible to work for an organization that provides services for children

with ASD and be happy. I have done this for many, many years now. It has

enriched my life, made me a better person and helped me in absolutely all aspects

of my personal and professional life. I have met, and continue to meet,

the most interesting, beautiful and caring people because of my

involvement with ASD. Many of them read these postings every day :)

I meet people every day

who don't know much about autism. I advocate for spectrum kids day and night,

at work, at airports, in restaurants and in bars.

This list is uplifting because it

provides me with great opporunities to change things. I am finally

e-mailing Christ, and I have a better understanding of what the

issues really are. Often times, it really takes a village or a county.

When I said that I accept private

e-mails with fake names, it was because I respect people's need for

privacy and because it prevents gossip. Some may be more

vulnerable than others because they hold certain positions in our

community. Members who are " rich and famous " or

well-known often times do not want to expose themselves or their families.

They still have questions and need help. This is why I said that it

is not about who is who in the community. My posting was about

the kids and their progress at school.

So, what are the big issues?

What is it that retention cannot help? Let's talk about the

strategies and why they are not working? Lots of educators and coaches are

reading this. Let's talk about it. How do we get to the bottom of this? How can

we help each other?

Information is empowering and can

change the way we do things. When we change the way we do things, things will

change.

Thanks for all feedback privately

and here. It is highly appreciated.

Liz

To: " sList "

<sList >

Sent: Sat, June 5, 2010 1:05:59 PM

Subject: Re: Retention and parent conferences

Hello Liz,

Do you work in the school system?

Or is a well-informed parent of a child with disability?

I don't care who is who in the

community, I'm just wondering since you offered to inform, where your knowledge

comes from.

Thank you

And I don't have a lot of time now,

but to retain a student is, in many cases, the easy way out of a bigger

problem. Another year of the same strategies that didn't work the first time is

a waste of time for the student.

Sent from my iPhone

On Jun 5, 2010, at 9:51 AM, Lizzie Berg <floridalizzie@ yahoo.com>

wrote:

I recently met a parent who is in

stunned because her kid;s teacher suggested retention next year. Here is what I

think:

The students have the right to stay

in elementary school from K through 5, which is 6 years, right? ESE kids have

the right to stay another 2 years before they have to, by law, move

to middle school. Most cluster students do not meet promotion

criteria because they are below grade level academically. General education

(gen.ed.) students who do not have a disability and who do not receive services

at school will not be promoted if they do not meet criteria. This is not up for

debate, the teachers and the parents do not have an option here. The

students need to be retained. Typically this is done in kindergarten or first

grade. It is also commonly done in third grade for various reasons. Gen ed

students who are retained are often evaluated to see if their is a more serious

underlying problem here. Some children in kindergarten are simply immature and

they catch up soon. Others have a learning disability and need more intense

instruction.

The goal is that by the time the

students leave the elementary school, they should hopefully be able to perform

academically at fifth grade level. They should be able to read and write like a

fifth grader.

Cluster students and other

ESE kids have the right to be retained two years in elementary school. It

is your teacher's responsibility to explain this to you, and in

my opinion, they should be held responible for giving you a copy of

the promotion criteria.

I cannot understand why parents of

cluster students are in a hurry to get them out of elementary school and into

middle? Why???

You can ask them to retain your

child any school year. If you are not sure what to do,

retain again in 5th grade.

If nobody at your school has

suggested retention, there is something very wrong with your school. It is in

our county;s and community's interest that all students receive the maximum

learning gains possible while they are in elementary school.

All parents should by now have

finished their spring teacher-parent conference. This conference should focus

on 2 things: academic and social progress, and promotion versus retention. The

conference form that you get a copy of should say somethng like this "

Retention discusses, the parents would like ______, and therefore X will

be in so and so grade next school year " . If you want him to be promoted

the conference form should say something like this: " retention discussed,

and the parents want X to be promoted due to good cause " .

Cood Cause: ESE

kids (and others) cannot be retained more than 2 years.

Therfore they will be promoted no matter what. The promotion crteria will be

waved, and the child is promoted due to something that is called " Good

Cause " . If you retain him in kindergarten for a year, he has to move to

first grade next year. You can retain him again in first year, but after that

he has to move up no matter what.

If you have not been invited for a

spring conference, there is something very wrong with your school,. This is a

red flag. You should by now have the copy of your conference form in your hand

or you should have it filed in your big binder.

The teacher has to have a minimum

of 2 conferences with you each year. This is state law. In my opinion, you

should request no less than 4 conferences, one for each marking period. You

receive the progress report and report card ina yellow envelope eah marking

period, right? There is a line outside the on the envelop that you need to

sign, and next to it is a question that you should answer: " Do you want a

conference " I can't imagine why you would say no right then. Why?

And if you don't get they paricular envelope, I strongly suggest that you

request your conference right then!!!

When I read about all the nonsense

that takes place in our schools, I want to cry. One way to fix this

is by empowering and encouraging the kids' families. The best ammunition so to

say, is to be more informed about the educational system. It is great to know a

lot about the law, but it is equally important to know how things work in real

life. Families and friends of ASD kids who take this seriously need to get

their " a-- in the class " . Four conferences a year is a

must. Let's start this next year.

If you have specific questions related to

your school that I may be able to help you with, just e-mail me privately. Make

up a fake name if that helps. This is about the kids and

their education, not who is who in the community.

Liz

From: Karp <denisekarpmyacc (DOT) net>

To: <deniseslist@ yahoogroups. com>

Sent: Thu, June 3, 2010 8:45:26 PM

Subject: FDDC: $60 Million in Grants Available

From: Florida Developmental Disabilities Council [mailto:vandab@ fddc.org]

Sent: Thursday, June 03, 2010 4:17 PM

To: denisekarpmyacc (DOT) net

Subject: $60 Million in Grants Available

Error! Filename not

specified.

FOR IMMEDIATE

RELEASE

Contact: HHS Press Office

Thursday, June 3,

2010

Announcement from the

Florida Developmental Disabilities Council

For more information, please contact

HHS Press Office *

HHS announces availability of $60 million in

Affordable Care Act Grants

to help people navigate their health and long-term care options

HHS Secretary Kathleen

Sebelius announced the availability of $60 million in Affordable Care Act

grants to states and communities to help individuals and their caregivers

better understand and navigate their health and long-term care

options.

Through this opportunity made possible by the Affordable Care Act HHS'

Administration on Aging (AoA) and the Centers for Medicare & Medicaid

Services (CMS) will work collaboratively to award funds for an integrated

approach that focuses on the unique needs of seniors, disabled Americans

and their caregivers as they seek health care and long-term care.

" The Affordable Care Act seeks to lower health care costs, improve

the quality of health care and perhaps most importantly give people more

control over their own care. These new grants, authorized under the new

law, will help seniors, individuals with disabilities and their families

get better quality care and more control. We've also streamlined the process

for states and people who rely on these funds, " said Secretary

Sebelius.

" We know how difficult it can be for caregivers and patients to try

and deal with a sudden illness or chronic disease while at the same time

trying to navigate through a complex health care system to figure out

where you can get help. These new funds that we have bundled together

will help promote better opportunities for coordination of health and

long-term supports, " said Sebelius.

The purpose of this new grant program authorized by the Affordable Care

Act is to create streamlined, coordinated statewide systems of

information, counseling, and access that will help people find

consumer-friendly answers they seek to meet their health and long-term

care needs. AoA and CMS will administer the funding through

separate announcements, but will coordinate implementation and monitoring

through a single process.

Some specific areas of focus will include assisting individuals who are

under-served and hard to reach with information about their Medicare and

Medicaid benefits, helping older adults and individuals with disabilities

live at home or in settings of their choosing with the right supports,

assisting people transition from hospital or nursing home stays back into

the community, and strengthening linkages between the medical and social

service systems.

" When it comes to long-term health care, each patient has a unique

mix of complex medical and social needs that must be considered when

seeking care, " said Marilyn Tavenner, acting CMS administrator.

" Our health care system can offer many options to meeting those

needs from traditional nursing home care to home and community-based

services. Making patients and their families aware of these options

will help them make inherently difficult decisions about long-term

care. This integrated program will help families make informed

choices and make sure patients have more control over their own

care. "

AoA and CMS have provided grants to states for several years to develop

person-centered systems of information, counseling and access to make it

easier for individuals to learn about and access their health and

long-term services and support options. This grant program through the

Affordable Care Act strengthens and enhances the ability of states to

truly integrate the medical and social services care models.

" AoA's national network of community-based organizations has long

served as the central place for individuals and families seeking

information and help to address health and long term care

challenges. This collaborative opportunity between AoA and CMS will

further strengthen the network's capacity to help people in a more

coordinated and comprehensive way in the communities where they

live, " said Kathy Greenlee, assistant secretary for aging.

Funds will be available to states, area agencies on aging (aaa's),

State Health Insurance Assistance Programs (SHIPs) and Aging and

Disability Resource Centers (ADRCs). Through the grant

program, states and local aging and disability programs will receive

funds to:

*provide outreach and assistance to

Medicare beneficiaries on their Medicare

benefits including prevention;

*use additional funds

through a competitive process to

provide Options Counseling on health and long-term care

through ADRCs;

*use additional funds through a

competitive process to strengthen the ADRCs role

in Money follows the Person program and support state Medicaid agencies

as

they transition individuals from nursing homes to community-based care;

and

*coordinate and continue to embed

tested Care Transition models that integrate

the medical and social service systems to help older individuals and

those with

disabilities remain in their own homes and communities after a

hospital,

rehabilitation or skilled nursing facility visit.

" CMS and AoA share a long-standing goal of expanding access to

community-based care for the elderly and individuals with

disabilities. The Affordable Care Act provides significant

resources for state Medicaid agencies and providers to balance the

nation's long-term care systems and assure that individuals have a choice

of where and how they receive their services, " said Mann,

director of CMS's Center for Medicaid, CHIP, and Survey and

Certification.

The announcement combines funding opportunities from several provisions

in the Affordable Care Act signed into law by President Obama on March

23, 2010,including the Role of Public Programs (Title II, Sections 2403 -

Money Follows the Person and 2405 - Funding for Aging and Disability

Resource Centers) and Improving the Quality and Efficiency of Health Care

(Title III. Section 3306 - Funding for Outreach and Assistance for

Low-Income Programs).

These grants also complement President Obama's " Year of Community

Living Initiative, " which focuses on better serving those

individuals with disabilities who need ongoing services and support

programs in the community such as those provided by AoA, CMS and other

HHS agencies.

The deadline for applications is: Monday, July 30, 2010. Grants

will be awarded in September 2010. For more information about this

grant opportunity, please visit http://www.aoa. gov/AoARoot/ Grants/Funding/ index.aspx

or www.grants.gov.

To learn more about the Affordable Care Act, please visit

www.healthreform. gov. Note: All HHS press releases,

fact sheets and other press materials are available at http://www.hhs. gov/news.

Forward email

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Guest guest

I probably didn't look hard enough. But I didn't see anything.

Can you direct me to a specific research.

Thinking back to when I was a child, I don't remember being held

back a year was so detrimental.

From: sList

[mailto:sList ] On Behalf Of Hawk

Sent: Saturday, June 05, 2010 11:02 PM

To: sList

Subject: Re: Retention and parent conferences

Did you look at the link I provided? It is a great resource

on retenetion http://www.wrightslaw.com/info/retain.index.htm

There are viewpoints and

research from National

Association of School Psychologists, Harvard Civil Rights Projectm California

School Psychologist, US Dept of Education, Uiversity of Wisconsin and the

American Federation of Teachers. ALL say that retention does NOT work and is a

detriment to children.

Gabi and others,

Let me ask everyone here : If

I was your kid's ( grandkid's, nephew, friend etc) teacher, what would you

ask me? What would you say to me?

In my previous postings maybe a

year ago or more, I said several times that one can expect several of

the list members here to be nurses, doctors, laywers, teachers,

principals, ESE specialists, OTs, behavior specialists, counselors, cluster

teachers and also at the same time be parents, grand parents, aunts, uncles,

godparents, siblings and friends of kids with autism. This is

possible, right? It is also possible to have one gen ed kid and one with

autism, right? So, it is OK to compare a cluster to a gen ed room,

and see the difference. Do we like what we see? Are gen ed teachers held to a

higher standard? Are cluster teachers less accountable? What is my role as a

parent, grand parent, aunt, uncle or advocate? What can I do now to make things

better for my kid. What is within my power, and when am I banging my head

against the wall? What can I change being outside the school system?

Many of us became attracted

to our profession and chose a career that is related to ASD because

autism had come into our lives. Some grew up with autism. One of the list

members here has an older sister with autism. She just did not know it as a

kid. She thought that everybody's older sisters were like her sister. It is

very possible to work for an organization that provides services for children

with ASD and be happy. I have done this for many, many years now. It has

enriched my life, made me a better person and helped me in absolutely all aspects

of my personal and professional life. I have met, and continue to meet,

the most interesting, beautiful and caring people because of my

involvement with ASD. Many of them read these postings every day :)

I meet people every day

who don't know much about autism. I advocate for spectrum kids day and night,

at work, at airports, in restaurants and in bars.

This list is uplifting because it

provides me with great opporunities to change things. I am finally

e-mailing Christ, and I have a better understanding of what the

issues really are. Often times, it really takes a village or a county.

When I said that I accept private

e-mails with fake names, it was because I respect people's need for

privacy and because it prevents gossip. Some may be more

vulnerable than others because they hold certain positions in our

community. Members who are " rich and famous " or

well-known often times do not want to expose themselves or their families.

They still have questions and need help. This is why I said that it

is not about who is who in the community. My posting was about

the kids and their progress at school.

So, what are the big issues?

What is it that retention cannot help? Let's talk about the

strategies and why they are not working? Lots of educators and coaches are

reading this. Let's talk about it. How do we get to the bottom of this? How can

we help each other?

Information is empowering and can

change the way we do things. When we change the way we do things, things will

change.

Thanks for all feedback privately

and here. It is highly appreciated.

Liz

To: " sList "

<sList >

Sent: Sat, June 5, 2010 1:05:59 PM

Subject: Re: Retention and parent conferences

Hello Liz,

Do you work in the school system?

Or is a well-informed parent of a child with disability?

I don't care who is who in the

community, I'm just wondering since you offered to inform, where your knowledge

comes from.

Thank you

And I don't have a lot of time now,

but to retain a student is, in many cases, the easy way out of a bigger

problem. Another year of the same strategies that didn't work the first time is

a waste of time for the student.

Sent from my iPhone

On Jun 5, 2010, at 9:51 AM, Lizzie Berg <floridalizzie@ yahoo.com>

wrote:

I recently met a parent who is in

stunned because her kid;s teacher suggested retention next year. Here is what I

think:

The students have the right to stay

in elementary school from K through 5, which is 6 years, right? ESE kids have

the right to stay another 2 years before they have to, by law, move

to middle school. Most cluster students do not meet promotion

criteria because they are below grade level academically. General education

(gen.ed.) students who do not have a disability and who do not receive services

at school will not be promoted if they do not meet criteria. This is not up for

debate, the teachers and the parents do not have an option here. The

students need to be retained. Typically this is done in kindergarten or first

grade. It is also commonly done in third grade for various reasons. Gen ed

students who are retained are often evaluated to see if their is a more serious

underlying problem here. Some children in kindergarten are simply immature and

they catch up soon. Others have a learning disability and need more intense

instruction.

The goal is that by the time the

students leave the elementary school, they should hopefully be able to perform

academically at fifth grade level. They should be able to read and write like a

fifth grader.

Cluster students and other

ESE kids have the right to be retained two years in elementary school. It

is your teacher's responsibility to explain this to you, and in

my opinion, they should be held responible for giving you a copy of

the promotion criteria.

I cannot understand why parents of

cluster students are in a hurry to get them out of elementary school and into

middle? Why???

You can ask them to retain your

child any school year. If you are not sure what to do,

retain again in 5th grade.

If nobody at your school has

suggested retention, there is something very wrong with your school. It is in

our county;s and community's interest that all students receive the maximum

learning gains possible while they are in elementary school.

All parents should by now have

finished their spring teacher-parent conference. This conference should focus

on 2 things: academic and social progress, and promotion versus retention. The

conference form that you get a copy of should say somethng like this "

Retention discusses, the parents would like ______, and therefore X will

be in so and so grade next school year " . If you want him to be promoted

the conference form should say something like this: " retention discussed,

and the parents want X to be promoted due to good cause " .

Cood Cause: ESE

kids (and others) cannot be retained more than 2 years.

Therfore they will be promoted no matter what. The promotion crteria will be

waved, and the child is promoted due to something that is called " Good

Cause " . If you retain him in kindergarten for a year, he has to move to

first grade next year. You can retain him again in first year, but after that

he has to move up no matter what.

If you have not been invited for a

spring conference, there is something very wrong with your school,. This is a

red flag. You should by now have the copy of your conference form in your hand

or you should have it filed in your big binder.

The teacher has to have a minimum

of 2 conferences with you each year. This is state law. In my opinion, you

should request no less than 4 conferences, one for each marking period. You

receive the progress report and report card ina yellow envelope eah marking

period, right? There is a line outside the on the envelop that you need to

sign, and next to it is a question that you should answer: " Do you want a

conference " I can't imagine why you would say no right then. Why?

And if you don't get they paricular envelope, I strongly suggest that you

request your conference right then!!!

When I read about all the nonsense

that takes place in our schools, I want to cry. One way to fix this

is by empowering and encouraging the kids' families. The best ammunition so to

say, is to be more informed about the educational system. It is great to know a

lot about the law, but it is equally important to know how things work in real

life. Families and friends of ASD kids who take this seriously need to get

their " a-- in the class " . Four conferences a year is a

must. Let's start this next year.

If you have specific questions related to

your school that I may be able to help you with, just e-mail me privately. Make

up a fake name if that helps. This is about the kids and

their education, not who is who in the community.

Liz

From: Karp <denisekarpmyacc (DOT) net>

To: <deniseslist@ yahoogroups. com>

Sent: Thu, June 3, 2010 8:45:26 PM

Subject: FDDC: $60 Million in Grants Available

From: Florida Developmental Disabilities Council [mailto:vandab@ fddc.org]

Sent: Thursday, June 03, 2010 4:17 PM

To: denisekarpmyacc (DOT) net

Subject: $60 Million in Grants Available

Error! Filename not

specified.

FOR IMMEDIATE

RELEASE

Contact: HHS Press Office

Thursday, June 3,

2010

Announcement from the

Florida Developmental Disabilities Council

For more information, please contact

HHS Press Office *

HHS announces availability of $60 million in

Affordable Care Act Grants

to help people navigate their health and long-term care options

HHS Secretary Kathleen

Sebelius announced the availability of $60 million in Affordable Care Act

grants to states and communities to help individuals and their caregivers

better understand and navigate their health and long-term care

options.

Through this opportunity made possible by the Affordable Care Act HHS'

Administration on Aging (AoA) and the Centers for Medicare & Medicaid

Services (CMS) will work collaboratively to award funds for an integrated

approach that focuses on the unique needs of seniors, disabled Americans

and their caregivers as they seek health care and long-term care.

" The Affordable Care Act seeks to lower health care costs, improve

the quality of health care and perhaps most importantly give people more

control over their own care. These new grants, authorized under the new

law, will help seniors, individuals with disabilities and their families

get better quality care and more control. We've also streamlined the process

for states and people who rely on these funds, " said Secretary

Sebelius.

" We know how difficult it can be for caregivers and patients to try

and deal with a sudden illness or chronic disease while at the same time

trying to navigate through a complex health care system to figure out

where you can get help. These new funds that we have bundled together

will help promote better opportunities for coordination of health and

long-term supports, " said Sebelius.

The purpose of this new grant program authorized by the Affordable Care

Act is to create streamlined, coordinated statewide systems of

information, counseling, and access that will help people find

consumer-friendly answers they seek to meet their health and long-term

care needs. AoA and CMS will administer the funding through

separate announcements, but will coordinate implementation and monitoring

through a single process.

Some specific areas of focus will include assisting individuals who are

under-served and hard to reach with information about their Medicare and

Medicaid benefits, helping older adults and individuals with disabilities

live at home or in settings of their choosing with the right supports,

assisting people transition from hospital or nursing home stays back into

the community, and strengthening linkages between the medical and social

service systems.

" When it comes to long-term health care, each patient has a unique

mix of complex medical and social needs that must be considered when

seeking care, " said Marilyn Tavenner, acting CMS administrator.

" Our health care system can offer many options to meeting those

needs from traditional nursing home care to home and community-based

services. Making patients and their families aware of these options

will help them make inherently difficult decisions about long-term

care. This integrated program will help families make informed

choices and make sure patients have more control over their own

care. "

AoA and CMS have provided grants to states for several years to develop

person-centered systems of information, counseling and access to make it

easier for individuals to learn about and access their health and

long-term services and support options. This grant program through the

Affordable Care Act strengthens and enhances the ability of states to

truly integrate the medical and social services care models.

" AoA's national network of community-based organizations has long

served as the central place for individuals and families seeking

information and help to address health and long term care

challenges. This collaborative opportunity between AoA and CMS will

further strengthen the network's capacity to help people in a more

coordinated and comprehensive way in the communities where they

live, " said Kathy Greenlee, assistant secretary for aging.

Funds will be available to states, area agencies on aging (aaa's),

State Health Insurance Assistance Programs (SHIPs) and Aging and

Disability Resource Centers (ADRCs). Through the grant

program, states and local aging and disability programs will receive

funds to:

*provide outreach and assistance to

Medicare beneficiaries on their Medicare

benefits including prevention;

*use additional funds

through a competitive process to

provide Options Counseling on health and long-term care

through ADRCs;

*use additional funds through a

competitive process to strengthen the ADRCs role

in Money follows the Person program and support state Medicaid agencies

as

they transition individuals from nursing homes to community-based care;

and

*coordinate and continue to embed

tested Care Transition models that integrate

the medical and social service systems to help older individuals and

those with

disabilities remain in their own homes and communities after a

hospital,

rehabilitation or skilled nursing facility visit.

" CMS and AoA share a long-standing goal of expanding access to

community-based care for the elderly and individuals with

disabilities. The Affordable Care Act provides significant

resources for state Medicaid agencies and providers to balance the

nation's long-term care systems and assure that individuals have a choice

of where and how they receive their services, " said Mann,

director of CMS's Center for Medicaid, CHIP, and Survey and

Certification.

The announcement combines funding opportunities from several provisions

in the Affordable Care Act signed into law by President Obama on March

23, 2010,including the Role of Public Programs (Title II, Sections 2403 -

Money Follows the Person and 2405 - Funding for Aging and Disability

Resource Centers) and Improving the Quality and Efficiency of Health Care

(Title III. Section 3306 - Funding for Outreach and Assistance for

Low-Income Programs).

These grants also complement President Obama's " Year of Community

Living Initiative, " which focuses on better serving those

individuals with disabilities who need ongoing services and support

programs in the community such as those provided by AoA, CMS and other

HHS agencies.

The deadline for applications is: Monday, July 30, 2010. Grants

will be awarded in September 2010. For more information about this

grant opportunity, please visit http://www.aoa. gov/AoARoot/ Grants/Funding/ index.aspx

or www.grants.gov.

To learn more about the Affordable Care Act, please visit

www.healthreform. gov. Note: All HHS press releases,

fact sheets and other press materials are available at http://www.hhs. gov/news.

Forward email

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org.

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Florida

Developmental Disabilities Council | 124 Marriott Drive | Suite 203 |

Tallahassee | FL | 32301

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Guest guest

I probably didn't look hard enough. But I didn't see anything.

Can you direct me to a specific research.

Thinking back to when I was a child, I don't remember being held

back a year was so detrimental.

From: sList

[mailto:sList ] On Behalf Of Hawk

Sent: Saturday, June 05, 2010 11:02 PM

To: sList

Subject: Re: Retention and parent conferences

Did you look at the link I provided? It is a great resource

on retenetion http://www.wrightslaw.com/info/retain.index.htm

There are viewpoints and

research from National

Association of School Psychologists, Harvard Civil Rights Projectm California

School Psychologist, US Dept of Education, Uiversity of Wisconsin and the

American Federation of Teachers. ALL say that retention does NOT work and is a

detriment to children.

Gabi and others,

Let me ask everyone here : If

I was your kid's ( grandkid's, nephew, friend etc) teacher, what would you

ask me? What would you say to me?

In my previous postings maybe a

year ago or more, I said several times that one can expect several of

the list members here to be nurses, doctors, laywers, teachers,

principals, ESE specialists, OTs, behavior specialists, counselors, cluster

teachers and also at the same time be parents, grand parents, aunts, uncles,

godparents, siblings and friends of kids with autism. This is

possible, right? It is also possible to have one gen ed kid and one with

autism, right? So, it is OK to compare a cluster to a gen ed room,

and see the difference. Do we like what we see? Are gen ed teachers held to a

higher standard? Are cluster teachers less accountable? What is my role as a

parent, grand parent, aunt, uncle or advocate? What can I do now to make things

better for my kid. What is within my power, and when am I banging my head

against the wall? What can I change being outside the school system?

Many of us became attracted

to our profession and chose a career that is related to ASD because

autism had come into our lives. Some grew up with autism. One of the list

members here has an older sister with autism. She just did not know it as a

kid. She thought that everybody's older sisters were like her sister. It is

very possible to work for an organization that provides services for children

with ASD and be happy. I have done this for many, many years now. It has

enriched my life, made me a better person and helped me in absolutely all aspects

of my personal and professional life. I have met, and continue to meet,

the most interesting, beautiful and caring people because of my

involvement with ASD. Many of them read these postings every day :)

I meet people every day

who don't know much about autism. I advocate for spectrum kids day and night,

at work, at airports, in restaurants and in bars.

This list is uplifting because it

provides me with great opporunities to change things. I am finally

e-mailing Christ, and I have a better understanding of what the

issues really are. Often times, it really takes a village or a county.

When I said that I accept private

e-mails with fake names, it was because I respect people's need for

privacy and because it prevents gossip. Some may be more

vulnerable than others because they hold certain positions in our

community. Members who are " rich and famous " or

well-known often times do not want to expose themselves or their families.

They still have questions and need help. This is why I said that it

is not about who is who in the community. My posting was about

the kids and their progress at school.

So, what are the big issues?

What is it that retention cannot help? Let's talk about the

strategies and why they are not working? Lots of educators and coaches are

reading this. Let's talk about it. How do we get to the bottom of this? How can

we help each other?

Information is empowering and can

change the way we do things. When we change the way we do things, things will

change.

Thanks for all feedback privately

and here. It is highly appreciated.

Liz

To: " sList "

<sList >

Sent: Sat, June 5, 2010 1:05:59 PM

Subject: Re: Retention and parent conferences

Hello Liz,

Do you work in the school system?

Or is a well-informed parent of a child with disability?

I don't care who is who in the

community, I'm just wondering since you offered to inform, where your knowledge

comes from.

Thank you

And I don't have a lot of time now,

but to retain a student is, in many cases, the easy way out of a bigger

problem. Another year of the same strategies that didn't work the first time is

a waste of time for the student.

Sent from my iPhone

On Jun 5, 2010, at 9:51 AM, Lizzie Berg <floridalizzie@ yahoo.com>

wrote:

I recently met a parent who is in

stunned because her kid;s teacher suggested retention next year. Here is what I

think:

The students have the right to stay

in elementary school from K through 5, which is 6 years, right? ESE kids have

the right to stay another 2 years before they have to, by law, move

to middle school. Most cluster students do not meet promotion

criteria because they are below grade level academically. General education

(gen.ed.) students who do not have a disability and who do not receive services

at school will not be promoted if they do not meet criteria. This is not up for

debate, the teachers and the parents do not have an option here. The

students need to be retained. Typically this is done in kindergarten or first

grade. It is also commonly done in third grade for various reasons. Gen ed

students who are retained are often evaluated to see if their is a more serious

underlying problem here. Some children in kindergarten are simply immature and

they catch up soon. Others have a learning disability and need more intense

instruction.

The goal is that by the time the

students leave the elementary school, they should hopefully be able to perform

academically at fifth grade level. They should be able to read and write like a

fifth grader.

Cluster students and other

ESE kids have the right to be retained two years in elementary school. It

is your teacher's responsibility to explain this to you, and in

my opinion, they should be held responible for giving you a copy of

the promotion criteria.

I cannot understand why parents of

cluster students are in a hurry to get them out of elementary school and into

middle? Why???

You can ask them to retain your

child any school year. If you are not sure what to do,

retain again in 5th grade.

If nobody at your school has

suggested retention, there is something very wrong with your school. It is in

our county;s and community's interest that all students receive the maximum

learning gains possible while they are in elementary school.

All parents should by now have

finished their spring teacher-parent conference. This conference should focus

on 2 things: academic and social progress, and promotion versus retention. The

conference form that you get a copy of should say somethng like this "

Retention discusses, the parents would like ______, and therefore X will

be in so and so grade next school year " . If you want him to be promoted

the conference form should say something like this: " retention discussed,

and the parents want X to be promoted due to good cause " .

Cood Cause: ESE

kids (and others) cannot be retained more than 2 years.

Therfore they will be promoted no matter what. The promotion crteria will be

waved, and the child is promoted due to something that is called " Good

Cause " . If you retain him in kindergarten for a year, he has to move to

first grade next year. You can retain him again in first year, but after that

he has to move up no matter what.

If you have not been invited for a

spring conference, there is something very wrong with your school,. This is a

red flag. You should by now have the copy of your conference form in your hand

or you should have it filed in your big binder.

The teacher has to have a minimum

of 2 conferences with you each year. This is state law. In my opinion, you

should request no less than 4 conferences, one for each marking period. You

receive the progress report and report card ina yellow envelope eah marking

period, right? There is a line outside the on the envelop that you need to

sign, and next to it is a question that you should answer: " Do you want a

conference " I can't imagine why you would say no right then. Why?

And if you don't get they paricular envelope, I strongly suggest that you

request your conference right then!!!

When I read about all the nonsense

that takes place in our schools, I want to cry. One way to fix this

is by empowering and encouraging the kids' families. The best ammunition so to

say, is to be more informed about the educational system. It is great to know a

lot about the law, but it is equally important to know how things work in real

life. Families and friends of ASD kids who take this seriously need to get

their " a-- in the class " . Four conferences a year is a

must. Let's start this next year.

If you have specific questions related to

your school that I may be able to help you with, just e-mail me privately. Make

up a fake name if that helps. This is about the kids and

their education, not who is who in the community.

Liz

From: Karp <denisekarpmyacc (DOT) net>

To: <deniseslist@ yahoogroups. com>

Sent: Thu, June 3, 2010 8:45:26 PM

Subject: FDDC: $60 Million in Grants Available

From: Florida Developmental Disabilities Council [mailto:vandab@ fddc.org]

Sent: Thursday, June 03, 2010 4:17 PM

To: denisekarpmyacc (DOT) net

Subject: $60 Million in Grants Available

Error! Filename not

specified.

FOR IMMEDIATE

RELEASE

Contact: HHS Press Office

Thursday, June 3,

2010

Announcement from the

Florida Developmental Disabilities Council

For more information, please contact

HHS Press Office *

HHS announces availability of $60 million in

Affordable Care Act Grants

to help people navigate their health and long-term care options

HHS Secretary Kathleen

Sebelius announced the availability of $60 million in Affordable Care Act

grants to states and communities to help individuals and their caregivers

better understand and navigate their health and long-term care

options.

Through this opportunity made possible by the Affordable Care Act HHS'

Administration on Aging (AoA) and the Centers for Medicare & Medicaid

Services (CMS) will work collaboratively to award funds for an integrated

approach that focuses on the unique needs of seniors, disabled Americans

and their caregivers as they seek health care and long-term care.

" The Affordable Care Act seeks to lower health care costs, improve

the quality of health care and perhaps most importantly give people more

control over their own care. These new grants, authorized under the new

law, will help seniors, individuals with disabilities and their families

get better quality care and more control. We've also streamlined the process

for states and people who rely on these funds, " said Secretary

Sebelius.

" We know how difficult it can be for caregivers and patients to try

and deal with a sudden illness or chronic disease while at the same time

trying to navigate through a complex health care system to figure out

where you can get help. These new funds that we have bundled together

will help promote better opportunities for coordination of health and

long-term supports, " said Sebelius.

The purpose of this new grant program authorized by the Affordable Care

Act is to create streamlined, coordinated statewide systems of

information, counseling, and access that will help people find

consumer-friendly answers they seek to meet their health and long-term

care needs. AoA and CMS will administer the funding through

separate announcements, but will coordinate implementation and monitoring

through a single process.

Some specific areas of focus will include assisting individuals who are

under-served and hard to reach with information about their Medicare and

Medicaid benefits, helping older adults and individuals with disabilities

live at home or in settings of their choosing with the right supports,

assisting people transition from hospital or nursing home stays back into

the community, and strengthening linkages between the medical and social

service systems.

" When it comes to long-term health care, each patient has a unique

mix of complex medical and social needs that must be considered when

seeking care, " said Marilyn Tavenner, acting CMS administrator.

" Our health care system can offer many options to meeting those

needs from traditional nursing home care to home and community-based

services. Making patients and their families aware of these options

will help them make inherently difficult decisions about long-term

care. This integrated program will help families make informed

choices and make sure patients have more control over their own

care. "

AoA and CMS have provided grants to states for several years to develop

person-centered systems of information, counseling and access to make it

easier for individuals to learn about and access their health and

long-term services and support options. This grant program through the

Affordable Care Act strengthens and enhances the ability of states to

truly integrate the medical and social services care models.

" AoA's national network of community-based organizations has long

served as the central place for individuals and families seeking

information and help to address health and long term care

challenges. This collaborative opportunity between AoA and CMS will

further strengthen the network's capacity to help people in a more

coordinated and comprehensive way in the communities where they

live, " said Kathy Greenlee, assistant secretary for aging.

Funds will be available to states, area agencies on aging (aaa's),

State Health Insurance Assistance Programs (SHIPs) and Aging and

Disability Resource Centers (ADRCs). Through the grant

program, states and local aging and disability programs will receive

funds to:

*provide outreach and assistance to

Medicare beneficiaries on their Medicare

benefits including prevention;

*use additional funds

through a competitive process to

provide Options Counseling on health and long-term care

through ADRCs;

*use additional funds through a

competitive process to strengthen the ADRCs role

in Money follows the Person program and support state Medicaid agencies

as

they transition individuals from nursing homes to community-based care;

and

*coordinate and continue to embed

tested Care Transition models that integrate

the medical and social service systems to help older individuals and

those with

disabilities remain in their own homes and communities after a

hospital,

rehabilitation or skilled nursing facility visit.

" CMS and AoA share a long-standing goal of expanding access to

community-based care for the elderly and individuals with

disabilities. The Affordable Care Act provides significant

resources for state Medicaid agencies and providers to balance the

nation's long-term care systems and assure that individuals have a choice

of where and how they receive their services, " said Mann,

director of CMS's Center for Medicaid, CHIP, and Survey and

Certification.

The announcement combines funding opportunities from several provisions

in the Affordable Care Act signed into law by President Obama on March

23, 2010,including the Role of Public Programs (Title II, Sections 2403 -

Money Follows the Person and 2405 - Funding for Aging and Disability

Resource Centers) and Improving the Quality and Efficiency of Health Care

(Title III. Section 3306 - Funding for Outreach and Assistance for

Low-Income Programs).

These grants also complement President Obama's " Year of Community

Living Initiative, " which focuses on better serving those

individuals with disabilities who need ongoing services and support

programs in the community such as those provided by AoA, CMS and other

HHS agencies.

The deadline for applications is: Monday, July 30, 2010. Grants

will be awarded in September 2010. For more information about this

grant opportunity, please visit http://www.aoa. gov/AoARoot/ Grants/Funding/ index.aspx

or www.grants.gov.

To learn more about the Affordable Care Act, please visit

www.healthreform. gov. Note: All HHS press releases,

fact sheets and other press materials are available at http://www.hhs. gov/news.

Forward email

Error!

Filename not specified.

This email was sent to

denisekarpmyacc (DOT) net by vandabfddc (DOT)

org.

Update Profile/Email Address | Instant removal with SafeUnsubscribeâ„¢ | Privacy Policy.

Email

Marketing by

Error!

Filename not specified.

Florida

Developmental Disabilities Council | 124 Marriott Drive | Suite 203 |

Tallahassee | FL | 32301

Error! Filename not specified.

--

AutismOnTheGo.com

Link to comment
Share on other sites

Guest guest

, I don't mean to be rude but the " r " I am

interested in is research and not resource. You can find a resource for almost

anything.

From:

sList [mailto:sList ] On Behalf

Of Hawk

Sent: Saturday, June 05, 2010 11:02 PM

To: sList

Subject: Re: Retention and parent conferences

Did you look at the link I provided? It is a great resource

on retenetion http://www.wrightslaw.com/info/retain.index.htm

There are viewpoints and

research from National

Association of School Psychologists, Harvard Civil Rights Projectm California

School Psychologist, US Dept of Education, Uiversity of Wisconsin and the

American Federation of Teachers. ALL say that retention does NOT work and is a

detriment to children.

Gabi and others,

Let me ask everyone here : If

I was your kid's ( grandkid's, nephew, friend etc) teacher, what would you

ask me? What would you say to me?

In my previous postings maybe a

year ago or more, I said several times that one can expect several of

the list members here to be nurses, doctors, laywers, teachers,

principals, ESE specialists, OTs, behavior specialists, counselors, cluster

teachers and also at the same time be parents, grand parents, aunts, uncles,

godparents, siblings and friends of kids with autism. This is possible,

right? It is also possible to have one gen ed kid and one with autism,

right? So, it is OK to compare a cluster to a gen ed room, and see

the difference. Do we like what we see? Are gen ed teachers held to a higher

standard? Are cluster teachers less accountable? What is my role as a parent,

grand parent, aunt, uncle or advocate? What can I do now to make things better

for my kid. What is within my power, and when am I banging my head against the

wall? What can I change being outside the school system?

Many of us became attracted

to our profession and chose a career that is related to ASD because

autism had come into our lives. Some grew up with autism. One of the list

members here has an older sister with autism. She just did not know it as a

kid. She thought that everybody's older sisters were like her sister. It is

very possible to work for an organization that provides services for children

with ASD and be happy. I have done this for many, many years now. It has

enriched my life, made me a better person and helped me in absolutely all

aspects of my personal and professional life. I have met, and continue to

meet, the most interesting, beautiful and caring people because of my

involvement with ASD. Many of them read these postings every day :)

I meet people every day

who don't know much about autism. I advocate for spectrum kids day and night,

at work, at airports, in restaurants and in bars.

This list is uplifting because it

provides me with great opporunities to change things. I am finally e-mailing

Christ, and I have a better understanding of what the issues really

are. Often times, it really takes a village or a county.

When I said that I accept private

e-mails with fake names, it was because I respect people's need for

privacy and because it prevents gossip. Some may be more

vulnerable than others because they hold certain positions in our

community. Members who are " rich and famous " or

well-known often times do not want to expose themselves or their families.

They still have questions and need help. This is why I said that it

is not about who is who in the community. My posting was about

the kids and their progress at school.

So, what are the big issues?

What is it that retention cannot help? Let's talk about the

strategies and why they are not working? Lots of educators and coaches are

reading this. Let's talk about it. How do we get to the bottom of this? How can

we help each other?

Information is empowering and can

change the way we do things. When we change the way we do things, things will

change.

Thanks for all feedback privately

and here. It is highly appreciated.

Liz

To: " sList "

<sList >

Sent: Sat, June 5, 2010 1:05:59 PM

Subject: Re: Retention and parent conferences

Hello Liz,

Do you work in the school system?

Or is a well-informed parent of a child with disability?

I don't care who is who in the

community, I'm just wondering since you offered to inform, where your knowledge

comes from.

Thank you

And I don't have a lot of time now,

but to retain a student is, in many cases, the easy way out of a bigger

problem. Another year of the same strategies that didn't work the first time is

a waste of time for the student.

Sent from my iPhone

On Jun 5, 2010, at 9:51 AM, Lizzie Berg <floridalizzie@ yahoo.com>

wrote:

I recently met a parent who is in

stunned because her kid;s teacher suggested retention next year. Here is what I

think:

The students have the right to stay

in elementary school from K through 5, which is 6 years, right? ESE kids have

the right to stay another 2 years before they have to, by law, move

to middle school. Most cluster students do not meet promotion

criteria because they are below grade level academically. General education

(gen.ed.) students who do not have a disability and who do not receive services

at school will not be promoted if they do not meet criteria. This is not up for

debate, the teachers and the parents do not have an option here. The

students need to be retained. Typically this is done in kindergarten or first

grade. It is also commonly done in third grade for various reasons. Gen ed

students who are retained are often evaluated to see if their is a more serious

underlying problem here. Some children in kindergarten are simply immature and

they catch up soon. Others have a learning disability and need more intense

instruction.

The goal is that by the time the

students leave the elementary school, they should hopefully be able to perform

academically at fifth grade level. They should be able to read and write like a

fifth grader.

Cluster students and other

ESE kids have the right to be retained two years in elementary school. It

is your teacher's responsibility to explain this to you, and in

my opinion, they should be held responible for giving you a copy of

the promotion criteria.

I cannot understand why parents of

cluster students are in a hurry to get them out of elementary school and into

middle? Why???

You can ask them to retain your

child any school year. If you are not sure what to do,

retain again in 5th grade.

If nobody at your school has

suggested retention, there is something very wrong with your school. It is in

our county;s and community's interest that all students receive the maximum

learning gains possible while they are in elementary school.

All parents should by now have

finished their spring teacher-parent conference. This conference should focus

on 2 things: academic and social progress, and promotion versus retention. The

conference form that you get a copy of should say somethng like this " Retention

discusses, the parents would like ______, and therefore X will be in so

and so grade next school year " . If you want him to be promoted the

conference form should say something like this: " retention discussed, and

the parents want X to be promoted due to good cause " .

Cood Cause: ESE

kids (and others) cannot be retained more than 2 years.

Therfore they will be promoted no matter what. The promotion crteria will be

waved, and the child is promoted due to something that is called " Good

Cause " . If you retain him in kindergarten for a year, he has to move to

first grade next year. You can retain him again in first year, but after that

he has to move up no matter what.

If you have not been invited for a

spring conference, there is something very wrong with your school,. This is a

red flag. You should by now have the copy of your conference form in your hand

or you should have it filed in your big binder.

The teacher has to have a minimum

of 2 conferences with you each year. This is state law. In my opinion, you

should request no less than 4 conferences, one for each marking period. You

receive the progress report and report card ina yellow envelope eah marking

period, right? There is a line outside the on the envelop that you need to

sign, and next to it is a question that you should answer: " Do you want a

conference " I can't imagine why you would say no right then. Why?

And if you don't get they paricular envelope, I strongly suggest that you

request your conference right then!!!

When I read about all the nonsense

that takes place in our schools, I want to cry. One way to fix this

is by empowering and encouraging the kids' families. The best ammunition so to

say, is to be more informed about the educational system. It is great to know a

lot about the law, but it is equally important to know how things work in real

life. Families and friends of ASD kids who take this seriously need to get

their " a-- in the class " . Four conferences a year is a

must. Let's start this next year.

If you have specific questions

related to your school that I may be able to help you with, just e-mail me

privately. Make up a fake name if that helps. This is about the kids and

their education, not who is who in the community.

Liz

From: Karp <denisekarpmyacc (DOT) net>

To: <deniseslist@ yahoogroups. com>

Sent: Thu, June 3, 2010 8:45:26 PM

Subject: FDDC: $60 Million in Grants Available

From: Florida Developmental Disabilities Council [mailto:vandab@ fddc.org]

Sent: Thursday, June 03, 2010 4:17 PM

To: denisekarpmyacc (DOT) net

Subject: $60 Million in Grants Available

Error! Filename not

specified.

FOR IMMEDIATE

RELEASE

Contact: HHS Press Office

Thursday, June 3,

2010

Announcement from the

Florida Developmental Disabilities Council

For more information, please contact

HHS Press Office *

HHS announces availability of $60 million in

Affordable Care Act Grants

to help people navigate their health and long-term care options

HHS Secretary Kathleen

Sebelius announced the availability of $60 million in Affordable Care Act

grants to states and communities to help individuals and their caregivers

better understand and navigate their health and long-term care

options.

Through this opportunity made possible by the Affordable Care Act HHS'

Administration on Aging (AoA) and the Centers for Medicare & Medicaid

Services (CMS) will work collaboratively to award funds for an integrated

approach that focuses on the unique needs of seniors, disabled Americans

and their caregivers as they seek health care and long-term care.

" The Affordable Care Act seeks to lower health care costs, improve

the quality of health care and perhaps most importantly give people more

control over their own care. These new grants, authorized under the new

law, will help seniors, individuals with disabilities and their families

get better quality care and more control. We've also streamlined the

process for states and people who rely on these funds, " said

Secretary Sebelius.

" We know how difficult it can be for caregivers and patients to try

and deal with a sudden illness or chronic disease while at the same time

trying to navigate through a complex health care system to figure out

where you can get help. These new funds that we have bundled together

will help promote better opportunities for coordination of health and

long-term supports, " said Sebelius.

The purpose of this new grant program authorized by the Affordable Care

Act is to create streamlined, coordinated statewide systems of information,

counseling, and access that will help people find consumer-friendly

answers they seek to meet their health and long-term care needs.

AoA and CMS will administer the funding through separate announcements,

but will coordinate implementation and monitoring through a single

process.

Some specific areas of focus will include assisting individuals who are

under-served and hard to reach with information about their Medicare and

Medicaid benefits, helping older adults and individuals with disabilities

live at home or in settings of their choosing with the right supports,

assisting people transition from hospital or nursing home stays back into

the community, and strengthening linkages between the medical and social

service systems.

" When it comes to long-term health care, each patient has a unique

mix of complex medical and social needs that must be considered when

seeking care, " said Marilyn Tavenner, acting CMS administrator.

" Our health care system can offer many options to meeting those

needs from traditional nursing home care to home and community-based

services. Making patients and their families aware of these options

will help them make inherently difficult decisions about long-term

care. This integrated program will help families make informed

choices and make sure patients have more control over their own

care. "

AoA and CMS have provided grants to states for several years to develop

person-centered systems of information, counseling and access to make it

easier for individuals to learn about and access their health and

long-term services and support options. This grant program through the

Affordable Care Act strengthens and enhances the ability of states to

truly integrate the medical and social services care models.

" AoA's national network of community-based organizations has long

served as the central place for individuals and families seeking

information and help to address health and long term care

challenges. This collaborative opportunity between AoA and CMS will

further strengthen the network's capacity to help people in a more

coordinated and comprehensive way in the communities where they

live, " said Kathy Greenlee, assistant secretary for aging.

Funds will be available to states, area agencies on aging (aaa's),

State Health Insurance Assistance Programs (SHIPs) and Aging and

Disability Resource Centers (ADRCs). Through the grant

program, states and local aging and disability programs will receive

funds to:

*provide outreach and assistance to

Medicare beneficiaries on their Medicare

benefits including prevention;

*use additional funds

through a competitive process to

provide Options Counseling on health and long-term care

through ADRCs;

*use additional funds through a

competitive process to strengthen the ADRCs role

in Money follows the Person program and support state Medicaid agencies

as

they transition individuals from nursing homes to community-based care;

and

*coordinate and continue to embed

tested Care Transition models that integrate

the medical and social service systems to help older individuals and

those with

disabilities remain in their own homes and communities after a

hospital,

rehabilitation or skilled nursing facility visit.

" CMS and AoA share a long-standing goal of expanding access to

community-based care for the elderly and individuals with

disabilities. The Affordable Care Act provides significant

resources for state Medicaid agencies and providers to balance the

nation's long-term care systems and assure that individuals have a choice

of where and how they receive their services, " said Mann,

director of CMS's Center for Medicaid, CHIP, and Survey and

Certification.

The announcement combines funding opportunities from several provisions

in the Affordable Care Act signed into law by President Obama on March

23, 2010,including the Role of Public Programs (Title II, Sections 2403 -

Money Follows the Person and 2405 - Funding for Aging and Disability

Resource Centers) and Improving the Quality and Efficiency of Health Care

(Title III. Section 3306 - Funding for Outreach and Assistance for

Low-Income Programs).

These grants also complement President Obama's " Year of Community

Living Initiative, " which focuses on better serving those

individuals with disabilities who need ongoing services and support

programs in the community such as those provided by AoA, CMS and other

HHS

agencies.

The deadline for applications is: Monday, July 30, 2010. Grants

will be awarded in September 2010. For more information about this

grant opportunity, please visit http://www.aoa. gov/AoARoot/ Grants/Funding/ index.aspx

or www.grants.gov.

To learn more about the Affordable Care Act, please visit

www.healthreform. gov. Note: All HHS press releases,

fact sheets and other press materials are available at http://www.hhs. gov/news.

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Tallahassee | FL | 32301

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Guest guest

I held my son back ...he did a K class in his preschool and then I had him do K in public school. It was the best thing I could have done! He has Aspergers, totally mainstreamed and is now going into HS this fall.

-- $60 Million in Grants Available

Error! Filename not specified.

FOR IMMEDIATE RELEASE Contact: HHS Press OfficeThursday, June 3, 2010

Announcement from the

Florida Developmental Disabilities Council

For more information, please contact

HHS Press Office *

HHS announces availability of $60 million in Affordable Care Act Grantsto help people navigate their health and long-term care options

HHS Secretary Kathleen Sebelius announced the availability of $60 million in Affordable Care Act grants to states and communities to help individuals and their caregivers better understand and navigate their health and long-term care options. Through this opportunity made possible by the Affordable Care Act HHS' Administration on Aging (AoA) and the Centers for Medicare & Medicaid Services (CMS) will work collaboratively to award funds for an integrated approach that focuses on the unique needs of seniors, disabled Americans and their caregivers as they seek health care and long-term care. "The Affordable Care Act seeks to lower health care costs, improve the quality of health care and perhaps most importantly give people more control over their own care. These new grants, authorized under the new law, will help seniors, individuals with disabilities and their families get better quality care and more control. We've also streamlined the process for states and people who rely on these funds," said Secretary Sebelius. "We know how difficult it can be for caregivers and patients to try and deal with a sudden illness or chronic disease while at the same time trying to navigate through a complex health care system to figure out where you can get help. These new funds that we have bundled together will help promote better opportunities for coordination of health and long-term supports," said Sebelius. The purpose of this new grant program authorized by the Affordable Care Act is to create streamlined, coordinated statewide systems of information, counseling, and access that will help people find consumer-friendly answers they seek to meet their health and long-term care needs. AoA and CMS will administer the funding through separate announcements, but will coordinate implementation and monitoring through a single process. Some specific areas of focus will include assisting individuals who are under-served and hard to reach with information about their Medicare and Medicaid benefits, helping older adults and individuals with disabilities live at home or in settings of their choosing with the right supports, assisting people transition from hospital or nursing home stays back into the community, and strengthening linkages between the medical and social service systems. "When it comes to long-term health care, each patient has a unique mix of complex medical and social needs that must be considered when seeking care," said Marilyn Tavenner, acting CMS administrator. "Our health care system can offer many options to meeting those needs from traditional nursing home care to home and community-based services. Making patients and their families aware of these options will help them make inherently difficult decisions about long-term care. This integrated program will help families make informed choices and make sure patients have more control over their own care." AoA and CMS have provided grants to states for several years to develop person-centered systems of information, counseling and access to make it easier for individuals to learn about and access their health and long-term services and support options. This grant program through the Affordable Care Act strengthens and enhances the ability of states to truly integrate the medical and social services care models. "AoA's national network of community-based organizations has long served as the central place for individuals and families seeking information and help to address health and long term care challenges. This collaborative opportunity between AoA and CMS will further strengthen the network's capacity to help people in a more coordinated and comprehensive way in the communities where they live," said Kathy Greenlee, assistant secretary for aging. Funds will be available to states, area agencies on aging (aaa's), State Health Insurance Assistance Programs (SHIPs) and Aging and Disability Resource Centers (ADRCs). Through the grant program, states and local aging and disability programs will receive funds to: *provide outreach and assistance to Medicare beneficiaries on their Medicare

benefits including prevention; *use additional funds through a competitive process to

provide Options Counseling on health and long-term care through ADRCs; *use additional funds through a competitive process to strengthen the ADRCs role

in Money follows the Person program and support state Medicaid agencies as

they transition individuals from nursing homes to community-based care; and *coordinate and continue to embed tested Care Transition models that integrate

the medical and social service systems to help older individuals and those with

disabilities remain in their own homes and communities after a hospital,

rehabilitation or skilled nursing facility visit. "CMS and AoA share a long-standing goal of expanding access to community-based care for the elderly and individuals with disabilities. The Affordable Care Act provides significant resources for state Medicaid agencies and providers to balance the nation's long-term care systems and assure that individuals have a choice of where and how they receive their services," said Mann, director of CMS's Center for Medicaid, CHIP, and Survey and Certification. The announcement combines funding opportunities from several provisions in the Affordable Care Act signed into law by President Obama on March 23, 2010,including the Role of Public Programs (Title II, Sections 2403 - Money Follows the Person and 2405 - Funding for Aging and Disability Resource Centers) and Improving the Quality and Efficiency of Health Care (Title III. Section 3306 - Funding for Outreach and Assistance for Low-Income Programs). These grants also complement President Obama's "Year of Community Living Initiative," which focuses on better serving those individuals with disabilities who need ongoing services and support programs in the community such as those provided by AoA, CMS and other HHS agencies. The deadline for applications is: Monday, July 30, 2010. Grants will be awarded in September 2010. For more information about this grant opportunity, please visit http://www.aoa. gov/AoARoot/ Grants/Funding/ index.aspx or www.grants.gov. To learn more about the Affordable Care Act, please visit www.healthreform. gov. Note: All HHS press releases, fact sheets and other press materials are available at http://www.hhs. gov/news.

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Guest guest

I held my son back ...he did a K class in his preschool and then I had him do K in public school. It was the best thing I could have done! He has Aspergers, totally mainstreamed and is now going into HS this fall.

-- $60 Million in Grants Available

Error! Filename not specified.

FOR IMMEDIATE RELEASE Contact: HHS Press OfficeThursday, June 3, 2010

Announcement from the

Florida Developmental Disabilities Council

For more information, please contact

HHS Press Office *

HHS announces availability of $60 million in Affordable Care Act Grantsto help people navigate their health and long-term care options

HHS Secretary Kathleen Sebelius announced the availability of $60 million in Affordable Care Act grants to states and communities to help individuals and their caregivers better understand and navigate their health and long-term care options. Through this opportunity made possible by the Affordable Care Act HHS' Administration on Aging (AoA) and the Centers for Medicare & Medicaid Services (CMS) will work collaboratively to award funds for an integrated approach that focuses on the unique needs of seniors, disabled Americans and their caregivers as they seek health care and long-term care. "The Affordable Care Act seeks to lower health care costs, improve the quality of health care and perhaps most importantly give people more control over their own care. These new grants, authorized under the new law, will help seniors, individuals with disabilities and their families get better quality care and more control. We've also streamlined the process for states and people who rely on these funds," said Secretary Sebelius. "We know how difficult it can be for caregivers and patients to try and deal with a sudden illness or chronic disease while at the same time trying to navigate through a complex health care system to figure out where you can get help. These new funds that we have bundled together will help promote better opportunities for coordination of health and long-term supports," said Sebelius. The purpose of this new grant program authorized by the Affordable Care Act is to create streamlined, coordinated statewide systems of information, counseling, and access that will help people find consumer-friendly answers they seek to meet their health and long-term care needs. AoA and CMS will administer the funding through separate announcements, but will coordinate implementation and monitoring through a single process. Some specific areas of focus will include assisting individuals who are under-served and hard to reach with information about their Medicare and Medicaid benefits, helping older adults and individuals with disabilities live at home or in settings of their choosing with the right supports, assisting people transition from hospital or nursing home stays back into the community, and strengthening linkages between the medical and social service systems. "When it comes to long-term health care, each patient has a unique mix of complex medical and social needs that must be considered when seeking care," said Marilyn Tavenner, acting CMS administrator. "Our health care system can offer many options to meeting those needs from traditional nursing home care to home and community-based services. Making patients and their families aware of these options will help them make inherently difficult decisions about long-term care. This integrated program will help families make informed choices and make sure patients have more control over their own care." AoA and CMS have provided grants to states for several years to develop person-centered systems of information, counseling and access to make it easier for individuals to learn about and access their health and long-term services and support options. This grant program through the Affordable Care Act strengthens and enhances the ability of states to truly integrate the medical and social services care models. "AoA's national network of community-based organizations has long served as the central place for individuals and families seeking information and help to address health and long term care challenges. This collaborative opportunity between AoA and CMS will further strengthen the network's capacity to help people in a more coordinated and comprehensive way in the communities where they live," said Kathy Greenlee, assistant secretary for aging. Funds will be available to states, area agencies on aging (aaa's), State Health Insurance Assistance Programs (SHIPs) and Aging and Disability Resource Centers (ADRCs). Through the grant program, states and local aging and disability programs will receive funds to: *provide outreach and assistance to Medicare beneficiaries on their Medicare

benefits including prevention; *use additional funds through a competitive process to

provide Options Counseling on health and long-term care through ADRCs; *use additional funds through a competitive process to strengthen the ADRCs role

in Money follows the Person program and support state Medicaid agencies as

they transition individuals from nursing homes to community-based care; and *coordinate and continue to embed tested Care Transition models that integrate

the medical and social service systems to help older individuals and those with

disabilities remain in their own homes and communities after a hospital,

rehabilitation or skilled nursing facility visit. "CMS and AoA share a long-standing goal of expanding access to community-based care for the elderly and individuals with disabilities. The Affordable Care Act provides significant resources for state Medicaid agencies and providers to balance the nation's long-term care systems and assure that individuals have a choice of where and how they receive their services," said Mann, director of CMS's Center for Medicaid, CHIP, and Survey and Certification. The announcement combines funding opportunities from several provisions in the Affordable Care Act signed into law by President Obama on March 23, 2010,including the Role of Public Programs (Title II, Sections 2403 - Money Follows the Person and 2405 - Funding for Aging and Disability Resource Centers) and Improving the Quality and Efficiency of Health Care (Title III. Section 3306 - Funding for Outreach and Assistance for Low-Income Programs). These grants also complement President Obama's "Year of Community Living Initiative," which focuses on better serving those individuals with disabilities who need ongoing services and support programs in the community such as those provided by AoA, CMS and other HHS agencies. The deadline for applications is: Monday, July 30, 2010. Grants will be awarded in September 2010. For more information about this grant opportunity, please visit http://www.aoa. gov/AoARoot/ Grants/Funding/ index.aspx or www.grants.gov. To learn more about the Affordable Care Act, please visit www.healthreform. gov. Note: All HHS press releases, fact sheets and other press materials are available at http://www.hhs. gov/news.

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I held my son back ...he did a K class in his preschool and then I had him do K in public school. It was the best thing I could have done! He has Aspergers, totally mainstreamed and is now going into HS this fall.

-- $60 Million in Grants Available

Error! Filename not specified.

FOR IMMEDIATE RELEASE Contact: HHS Press OfficeThursday, June 3, 2010

Announcement from the

Florida Developmental Disabilities Council

For more information, please contact

HHS Press Office *

HHS announces availability of $60 million in Affordable Care Act Grantsto help people navigate their health and long-term care options

HHS Secretary Kathleen Sebelius announced the availability of $60 million in Affordable Care Act grants to states and communities to help individuals and their caregivers better understand and navigate their health and long-term care options. Through this opportunity made possible by the Affordable Care Act HHS' Administration on Aging (AoA) and the Centers for Medicare & Medicaid Services (CMS) will work collaboratively to award funds for an integrated approach that focuses on the unique needs of seniors, disabled Americans and their caregivers as they seek health care and long-term care. "The Affordable Care Act seeks to lower health care costs, improve the quality of health care and perhaps most importantly give people more control over their own care. These new grants, authorized under the new law, will help seniors, individuals with disabilities and their families get better quality care and more control. We've also streamlined the process for states and people who rely on these funds," said Secretary Sebelius. "We know how difficult it can be for caregivers and patients to try and deal with a sudden illness or chronic disease while at the same time trying to navigate through a complex health care system to figure out where you can get help. These new funds that we have bundled together will help promote better opportunities for coordination of health and long-term supports," said Sebelius. The purpose of this new grant program authorized by the Affordable Care Act is to create streamlined, coordinated statewide systems of information, counseling, and access that will help people find consumer-friendly answers they seek to meet their health and long-term care needs. AoA and CMS will administer the funding through separate announcements, but will coordinate implementation and monitoring through a single process. Some specific areas of focus will include assisting individuals who are under-served and hard to reach with information about their Medicare and Medicaid benefits, helping older adults and individuals with disabilities live at home or in settings of their choosing with the right supports, assisting people transition from hospital or nursing home stays back into the community, and strengthening linkages between the medical and social service systems. "When it comes to long-term health care, each patient has a unique mix of complex medical and social needs that must be considered when seeking care," said Marilyn Tavenner, acting CMS administrator. "Our health care system can offer many options to meeting those needs from traditional nursing home care to home and community-based services. Making patients and their families aware of these options will help them make inherently difficult decisions about long-term care. This integrated program will help families make informed choices and make sure patients have more control over their own care." AoA and CMS have provided grants to states for several years to develop person-centered systems of information, counseling and access to make it easier for individuals to learn about and access their health and long-term services and support options. This grant program through the Affordable Care Act strengthens and enhances the ability of states to truly integrate the medical and social services care models. "AoA's national network of community-based organizations has long served as the central place for individuals and families seeking information and help to address health and long term care challenges. This collaborative opportunity between AoA and CMS will further strengthen the network's capacity to help people in a more coordinated and comprehensive way in the communities where they live," said Kathy Greenlee, assistant secretary for aging. Funds will be available to states, area agencies on aging (aaa's), State Health Insurance Assistance Programs (SHIPs) and Aging and Disability Resource Centers (ADRCs). Through the grant program, states and local aging and disability programs will receive funds to: *provide outreach and assistance to Medicare beneficiaries on their Medicare

benefits including prevention; *use additional funds through a competitive process to

provide Options Counseling on health and long-term care through ADRCs; *use additional funds through a competitive process to strengthen the ADRCs role

in Money follows the Person program and support state Medicaid agencies as

they transition individuals from nursing homes to community-based care; and *coordinate and continue to embed tested Care Transition models that integrate

the medical and social service systems to help older individuals and those with

disabilities remain in their own homes and communities after a hospital,

rehabilitation or skilled nursing facility visit. "CMS and AoA share a long-standing goal of expanding access to community-based care for the elderly and individuals with disabilities. The Affordable Care Act provides significant resources for state Medicaid agencies and providers to balance the nation's long-term care systems and assure that individuals have a choice of where and how they receive their services," said Mann, director of CMS's Center for Medicaid, CHIP, and Survey and Certification. The announcement combines funding opportunities from several provisions in the Affordable Care Act signed into law by President Obama on March 23, 2010,including the Role of Public Programs (Title II, Sections 2403 - Money Follows the Person and 2405 - Funding for Aging and Disability Resource Centers) and Improving the Quality and Efficiency of Health Care (Title III. Section 3306 - Funding for Outreach and Assistance for Low-Income Programs). These grants also complement President Obama's "Year of Community Living Initiative," which focuses on better serving those individuals with disabilities who need ongoing services and support programs in the community such as those provided by AoA, CMS and other HHS agencies. The deadline for applications is: Monday, July 30, 2010. Grants will be awarded in September 2010. For more information about this grant opportunity, please visit http://www.aoa. gov/AoARoot/ Grants/Funding/ index.aspx or www.grants.gov. To learn more about the Affordable Care Act, please visit www.healthreform. gov. Note: All HHS press releases, fact sheets and other press materials are available at http://www.hhs. gov/news.

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I think we should all know by know by now that nothing in life is black or white.As far as being held back it depends on the specific situation. The age, the personality, the exceptionality, all of the circumstances involved play a part in the outcome for the child. What works for one child may not work for the other. There can not be a rigid set if rules to govern what is best for our children.I must express though, that I find it very hard toexcept that being held back would be more tramatic for a child than the loss of a parent. This sounds like a very unbalanced comparison. BuschSent from my iPhone

I probably didn't look hard enough. But I didn't see anything.

Can you direct me to a specific research.

Thinking back to when I was a child, I don't remember being held

back a year was so detrimental.

From: sList

[mailto:sList ] On Behalf Of Hawk

Sent: Saturday, June 05, 2010 11:02 PM

To: sList

Subject: Re: Retention and parent conferences

Did you look at the link I provided? It is a great resource

on retenetion http://www.wrightslaw.com/info/retain.index.htm

There are viewpoints and

research from National

Association of School Psychologists, Harvard Civil Rights Projectm California

School Psychologist, US Dept of Education, Uiversity of Wisconsin and the

American Federation of Teachers. ALL say that retention does NOT work and is a

detriment to children.

On searxat, Jun 5, 2010 at 9:23 PM, Lizzie Berg <floridalizzie> wrote:

Gabi and others,

Let me ask everyone here : If

I was your kid's ( grandkid's, nephew, friend etc) teacher, what would you

ask me? What would you say to me?

In my previous postings maybe a

year ago or more, I said several times that one can expect several of

the list members here to be nurses, doctors, laywers, teachers,

principals, ESE specialists, OTs, behavior specialists, counselors, cluster

teachers and also at the same time be parents, grand parents, aunts, uncles,

godparents, siblings and friends of kids with autism. This is

possible, right? It is also possible to have one gen ed kid and one with

autism, right? So, it is OK to compare a cluster to a gen ed room,

and see the difference. Do we like what we see? Are gen ed teachers held to a

higher standard? Are cluster teachers less accountable? What is my role as a

parent, grand parent, aunt, uncle or advocate? What can I do now to make things

better for my kid. What is within my power, and when am I banging my head

against the wall? What can I change being outside the school system?

Many of us became attracted

to our profession and chose a career that is related to ASD because

autism had come into our lives. Some grew up with autism. One of the list

members here has an older sister with autism. She just did not know it as a

kid. She thought that everybody's older sisters were like her sister. It is

very possible to work for an organization that provides services for children

with ASD and be happy. I have done this for many, many years now. It has

enriched my life, made me a better person and helped me in absolutely all aspects

of my personal and professional life. I have met, and continue to meet,

the most interesting, beautiful and caring people because of my

involvement with ASD. Many of them read these postings every day :)

I meet people every day

who don't know much about autism. I advocate for spectrum kids day and night,

at work, at airports, in restaurants and in bars.

This list is uplifting because it

provides me with great opporunities to change things. I am finally

e-mailing Christ, and I have a better understanding of what the

issues really are. Often times, it really takes a village or a county.

When I said that I accept private

e-mails with fake names, it was because I respect people's need for

privacy and because it prevents gossip. Some may be more

vulnerable than others because they hold certain positions in our

community. Members who are "rich and famous" or

well-known often times do not want to expose themselves or their families.

They still have questions and need help. This is why I said that it

is not about who is who in the community. My posting was about

the kids and their progress at school.

So, what are the big issues?

What is it that retention cannot help? Let's talk about the

strategies and why they are not working? Lots of educators and coaches are

reading this. Let's talk about it. How do we get to the bottom of this? How can

we help each other?

Information is empowering and can

change the way we do things. When we change the way we do things, things will

change.

Thanks for all feedback privately

and here. It is highly appreciated.

Liz

From: Gabi <bijcom>

To: "sList "

<sList >

Sent: Sat, June 5, 2010 1:05:59 PM

Subject: Re: Retention and parent conferences

Hello Liz,

Do you work in the school system?

Or is a well-informed parent of a child with disability?

I don't care who is who in the

community, I'm just wondering since you offered to inform, where your knowledge

comes from.

Thank you

And I don't have a lot of time now,

but to retain a student is, in many cases, the easy way out of a bigger

problem. Another year of the same strategies that didn't work the first time is

a waste of time for the student.

Sent from my iPhone

On Jun 5, 2010, at 9:51 AM, Lizzie Berg <floridalizzie@ yahoo.com>

wrote:

I recently met a parent who is in

stunned because her kid;s teacher suggested retention next year. Here is what I

think:

The students have the right to stay

in elementary school from K through 5, which is 6 years, right? ESE kids have

the right to stay another 2 years before they have to, by law, move

to middle school. Most cluster students do not meet promotion

criteria because they are below grade level academically. General education

(gen.ed.) students who do not have a disability and who do not receive services

at school will not be promoted if they do not meet criteria. This is not up for

debate, the teachers and the parents do not have an option here. The

students need to be retained. Typically this is done in kindergarten or first

grade. It is also commonly done in third grade for various reasons. Gen ed

students who are retained are often evaluated to see if their is a more serious

underlying problem here. Some children in kindergarten are simply immature and

they catch up soon. Others have a learning disability and need more intense

instruction.

The goal is that by the time the

students leave the elementary school, they should hopefully be able to perform

academically at fifth grade level. They should be able to read and write like a

fifth grader.

Cluster students and other

ESE kids have the right to be retained two years in elementary school. It

is your teacher's responsibility to explain this to you, and in

my opinion, they should be held responible for giving you a copy of

the promotion criteria.

I cannot understand why parents of

cluster students are in a hurry to get them out of elementary school and into

middle? Why???

You can ask them to retain your

child any school year. If you are not sure what to do,

retain again in 5th grade.

If nobody at your school has

suggested retention, there is something very wrong with your school. It is in

our county;s and community's interest that all students receive the maximum

learning gains possible while they are in elementary school.

All parents should by now have

finished their spring teacher-parent conference. This conference should focus

on 2 things: academic and social progress, and promotion versus retention. The

conference form that you get a copy of should say somethng like this"

Retention discusses, the parents would like ______, and therefore X will

be in so and so grade next school year". If you want him to be promoted

the conference form should say something like this: "retention discussed,

and the parents want X to be promoted due to good cause".

Cood Cause: ESE

kids (and others) cannot be retained more than 2 years.

Therfore they will be promoted no matter what. The promotion crteria will be

waved, and the child is promoted due to something that is called "Good

Cause". If you retain him in kindergarten for a year, he has to move to

first grade next year. You can retain him again in first year, but after that

he has to move up no matter what.

If you have not been invited for a

spring conference, there is something very wrong with your school,. This is a

red flag. You should by now have the copy of your conference form in your hand

or you should have it filed in your big binder.

The teacher has to have a minimum

of 2 conferences with you each year. This is state law. In my opinion, you

should request no less than 4 conferences, one for each marking period. You

receive the progress report and report card ina yellow envelope eah marking

period, right? There is a line outside the on the envelop that you need to

sign, and next to it is a question that you should answer: "Do you want a

conference" I can't imagine why you would say no right then. Why?

And if you don't get they paricular envelope, I strongly suggest that you

request your conference right then!!!

When I read about all the nonsense

that takes place in our schools, I want to cry. One way to fix this

is by empowering and encouraging the kids' families. The best ammunition so to

say, is to be more informed about the educational system. It is great to know a

lot about the law, but it is equally important to know how things work in real

life. Families and friends of ASD kids who take this seriously need to get

their "a-- in the class". Four conferences a year is a

must. Let's start this next year.

If you have specific questions related to

your school that I may be able to help you with, just e-mail me privately. Make

up a fake name if that helps. This is about the kids and

their education, not who is who in the community.

Liz

From: Karp <denisekarpmyacc (DOT) net>

To: <deniseslist@ yahoogroups. com>

Sent: Thu, June 3, 2010 8:45:26 PM

Subject: FDDC: $60 Million in Grants Available

From: Florida Developmental Disabilities Council [mailto:vandab@ fddc.org]

Sent: Thursday, June 03, 2010 4:17 PM

To: denisekarpmyacc (DOT) net

Subject: $60 Million in Grants Available

Error! Filename not

specified.

FOR IMMEDIATE

RELEASE

Contact: HHS Press Office

Thursday, June 3,

2010

Announcement from the

Florida Developmental Disabilities Council

For more information, please contact

HHS Press Office *

HHS announces availability of $60 million in

Affordable Care Act Grants

to help people navigate their health and long-term care options

HHS Secretary Kathleen

Sebelius announced the availability of $60 million in Affordable Care Act

grants to states and communities to help individuals and their caregivers

better understand and navigate their health and long-term care

options.

Through this opportunity made possible by the Affordable Care Act HHS'

Administration on Aging (AoA) and the Centers for Medicare & Medicaid

Services (CMS) will work collaboratively to award funds for an integrated

approach that focuses on the unique needs of seniors, disabled Americans

and their caregivers as they seek health care and long-term care.

"The Affordable Care Act seeks to lower health care costs, improve

the quality of health care and perhaps most importantly give people more

control over their own care. These new grants, authorized under the new

law, will help seniors, individuals with disabilities and their families

get better quality care and more control. We've also streamlined the process

for states and people who rely on these funds," said Secretary

Sebelius.

"We know how difficult it can be for caregivers and patients to try

and deal with a sudden illness or chronic disease while at the same time

trying to navigate through a complex health care system to figure out

where you can get help. These new funds that we have bundled together

will help promote better opportunities for coordination of health and

long-term supports," said Sebelius.

The purpose of this new grant program authorized by the Affordable Care

Act is to create streamlined, coordinated statewide systems of

information, counseling, and access that will help people find

consumer-friendly answers they seek to meet their health and long-term

care needs. AoA and CMS will administer the funding through

separate announcements, but will coordinate implementation and monitoring

through a single process.

Some specific areas of focus will include assisting individuals who are

under-served and hard to reach with information about their Medicare and

Medicaid benefits, helping older adults and individuals with disabilities

live at home or in settings of their choosing with the right supports,

assisting people transition from hospital or nursing home stays back into

the community, and strengthening linkages between the medical and social

service systems.

"When it comes to long-term health care, each patient has a unique

mix of complex medical and social needs that must be considered when

seeking care," said Marilyn Tavenner, acting CMS administrator.

"Our health care system can offer many options to meeting those

needs from traditional nursing home care to home and community-based

services. Making patients and their families aware of these options

will help them make inherently difficult decisions about long-term

care. This integrated program will help families make informed

choices and make sure patients have more control over their own

care."

AoA and CMS have provided grants to states for several years to develop

person-centered systems of information, counseling and access to make it

easier for individuals to learn about and access their health and

long-term services and support options. This grant program through the

Affordable Care Act strengthens and enhances the ability of states to

truly integrate the medical and social services care models.

"AoA's national network of community-based organizations has long

served as the central place for individuals and families seeking

information and help to address health and long term care

challenges. This collaborative opportunity between AoA and CMS will

further strengthen the network's capacity to help people in a more

coordinated and comprehensive way in the communities where they

live," said Kathy Greenlee, assistant secretary for aging.

Funds will be available to states, area agencies on aging (aaa's),

State Health Insurance Assistance Programs (SHIPs) and Aging and

Disability Resource Centers (ADRCs). Through the grant

program, states and local aging and disability programs will receive

funds to:

*provide outreach and assistance to

Medicare beneficiaries on their Medicare

benefits including prevention;

*use additional funds

through a competitive process to

provide Options Counseling on health and long-term care

through ADRCs;

*use additional funds through a

competitive process to strengthen the ADRCs role

in Money follows the Person program and support state Medicaid agencies

as

they transition individuals from nursing homes to community-based care;

and

*coordinate and continue to embed

tested Care Transition models that integrate

the medical and social service systems to help older individuals and

those with

disabilities remain in their own homes and communities after a

hospital,

rehabilitation or skilled nursing facility visit.

"CMS and AoA share a long-standing goal of expanding access to

community-based care for the elderly and individuals with

disabilities. The Affordable Care Act provides significant

resources for state Medicaid agencies and providers to balance the

nation's long-term care systems and assure that individuals have a choice

of where and how they receive their services," said Mann,

director of CMS's Center for Medicaid, CHIP, and Survey and

Certification.

The announcement combines funding opportunities from several provisions

in the Affordable Care Act signed into law by President Obama on March

23, 2010,including the Role of Public Programs (Title II, Sections 2403 -

Money Follows the Person and 2405 - Funding for Aging and Disability

Resource Centers) and Improving the Quality and Efficiency of Health Care

(Title III. Section 3306 - Funding for Outreach and Assistance for

Low-Income Programs).

These grants also complement President Obama's "Year of Community

Living Initiative," which focuses on better serving those

individuals with disabilities who need ongoing services and support

programs in the community such as those provided by AoA, CMS and other

HHS agencies.

The deadline for applications is: Monday, July 30, 2010. Grants

will be awarded in September 2010. For more information about this

grant opportunity, please visit http://www.aoa. gov/AoARoot/ Grants/Funding/ index.aspx

or www.grants.gov.

To learn more about the Affordable Care Act, please visit

www.healthreform. gov. Note: All HHS press releases,

fact sheets and other press materials are available at http://www.hhs. gov/news.

Forward email

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Developmental Disabilities Council | 124 Marriott Drive | Suite 203 |

Tallahassee | FL | 32301

Error! Filename not specified.

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Guest guest

I think we should all know by know by now that nothing in life is black or white.As far as being held back it depends on the specific situation. The age, the personality, the exceptionality, all of the circumstances involved play a part in the outcome for the child. What works for one child may not work for the other. There can not be a rigid set if rules to govern what is best for our children.I must express though, that I find it very hard toexcept that being held back would be more tramatic for a child than the loss of a parent. This sounds like a very unbalanced comparison. BuschSent from my iPhone

I probably didn't look hard enough. But I didn't see anything.

Can you direct me to a specific research.

Thinking back to when I was a child, I don't remember being held

back a year was so detrimental.

From: sList

[mailto:sList ] On Behalf Of Hawk

Sent: Saturday, June 05, 2010 11:02 PM

To: sList

Subject: Re: Retention and parent conferences

Did you look at the link I provided? It is a great resource

on retenetion http://www.wrightslaw.com/info/retain.index.htm

There are viewpoints and

research from National

Association of School Psychologists, Harvard Civil Rights Projectm California

School Psychologist, US Dept of Education, Uiversity of Wisconsin and the

American Federation of Teachers. ALL say that retention does NOT work and is a

detriment to children.

On searxat, Jun 5, 2010 at 9:23 PM, Lizzie Berg <floridalizzie> wrote:

Gabi and others,

Let me ask everyone here : If

I was your kid's ( grandkid's, nephew, friend etc) teacher, what would you

ask me? What would you say to me?

In my previous postings maybe a

year ago or more, I said several times that one can expect several of

the list members here to be nurses, doctors, laywers, teachers,

principals, ESE specialists, OTs, behavior specialists, counselors, cluster

teachers and also at the same time be parents, grand parents, aunts, uncles,

godparents, siblings and friends of kids with autism. This is

possible, right? It is also possible to have one gen ed kid and one with

autism, right? So, it is OK to compare a cluster to a gen ed room,

and see the difference. Do we like what we see? Are gen ed teachers held to a

higher standard? Are cluster teachers less accountable? What is my role as a

parent, grand parent, aunt, uncle or advocate? What can I do now to make things

better for my kid. What is within my power, and when am I banging my head

against the wall? What can I change being outside the school system?

Many of us became attracted

to our profession and chose a career that is related to ASD because

autism had come into our lives. Some grew up with autism. One of the list

members here has an older sister with autism. She just did not know it as a

kid. She thought that everybody's older sisters were like her sister. It is

very possible to work for an organization that provides services for children

with ASD and be happy. I have done this for many, many years now. It has

enriched my life, made me a better person and helped me in absolutely all aspects

of my personal and professional life. I have met, and continue to meet,

the most interesting, beautiful and caring people because of my

involvement with ASD. Many of them read these postings every day :)

I meet people every day

who don't know much about autism. I advocate for spectrum kids day and night,

at work, at airports, in restaurants and in bars.

This list is uplifting because it

provides me with great opporunities to change things. I am finally

e-mailing Christ, and I have a better understanding of what the

issues really are. Often times, it really takes a village or a county.

When I said that I accept private

e-mails with fake names, it was because I respect people's need for

privacy and because it prevents gossip. Some may be more

vulnerable than others because they hold certain positions in our

community. Members who are "rich and famous" or

well-known often times do not want to expose themselves or their families.

They still have questions and need help. This is why I said that it

is not about who is who in the community. My posting was about

the kids and their progress at school.

So, what are the big issues?

What is it that retention cannot help? Let's talk about the

strategies and why they are not working? Lots of educators and coaches are

reading this. Let's talk about it. How do we get to the bottom of this? How can

we help each other?

Information is empowering and can

change the way we do things. When we change the way we do things, things will

change.

Thanks for all feedback privately

and here. It is highly appreciated.

Liz

From: Gabi <bijcom>

To: "sList "

<sList >

Sent: Sat, June 5, 2010 1:05:59 PM

Subject: Re: Retention and parent conferences

Hello Liz,

Do you work in the school system?

Or is a well-informed parent of a child with disability?

I don't care who is who in the

community, I'm just wondering since you offered to inform, where your knowledge

comes from.

Thank you

And I don't have a lot of time now,

but to retain a student is, in many cases, the easy way out of a bigger

problem. Another year of the same strategies that didn't work the first time is

a waste of time for the student.

Sent from my iPhone

On Jun 5, 2010, at 9:51 AM, Lizzie Berg <floridalizzie@ yahoo.com>

wrote:

I recently met a parent who is in

stunned because her kid;s teacher suggested retention next year. Here is what I

think:

The students have the right to stay

in elementary school from K through 5, which is 6 years, right? ESE kids have

the right to stay another 2 years before they have to, by law, move

to middle school. Most cluster students do not meet promotion

criteria because they are below grade level academically. General education

(gen.ed.) students who do not have a disability and who do not receive services

at school will not be promoted if they do not meet criteria. This is not up for

debate, the teachers and the parents do not have an option here. The

students need to be retained. Typically this is done in kindergarten or first

grade. It is also commonly done in third grade for various reasons. Gen ed

students who are retained are often evaluated to see if their is a more serious

underlying problem here. Some children in kindergarten are simply immature and

they catch up soon. Others have a learning disability and need more intense

instruction.

The goal is that by the time the

students leave the elementary school, they should hopefully be able to perform

academically at fifth grade level. They should be able to read and write like a

fifth grader.

Cluster students and other

ESE kids have the right to be retained two years in elementary school. It

is your teacher's responsibility to explain this to you, and in

my opinion, they should be held responible for giving you a copy of

the promotion criteria.

I cannot understand why parents of

cluster students are in a hurry to get them out of elementary school and into

middle? Why???

You can ask them to retain your

child any school year. If you are not sure what to do,

retain again in 5th grade.

If nobody at your school has

suggested retention, there is something very wrong with your school. It is in

our county;s and community's interest that all students receive the maximum

learning gains possible while they are in elementary school.

All parents should by now have

finished their spring teacher-parent conference. This conference should focus

on 2 things: academic and social progress, and promotion versus retention. The

conference form that you get a copy of should say somethng like this"

Retention discusses, the parents would like ______, and therefore X will

be in so and so grade next school year". If you want him to be promoted

the conference form should say something like this: "retention discussed,

and the parents want X to be promoted due to good cause".

Cood Cause: ESE

kids (and others) cannot be retained more than 2 years.

Therfore they will be promoted no matter what. The promotion crteria will be

waved, and the child is promoted due to something that is called "Good

Cause". If you retain him in kindergarten for a year, he has to move to

first grade next year. You can retain him again in first year, but after that

he has to move up no matter what.

If you have not been invited for a

spring conference, there is something very wrong with your school,. This is a

red flag. You should by now have the copy of your conference form in your hand

or you should have it filed in your big binder.

The teacher has to have a minimum

of 2 conferences with you each year. This is state law. In my opinion, you

should request no less than 4 conferences, one for each marking period. You

receive the progress report and report card ina yellow envelope eah marking

period, right? There is a line outside the on the envelop that you need to

sign, and next to it is a question that you should answer: "Do you want a

conference" I can't imagine why you would say no right then. Why?

And if you don't get they paricular envelope, I strongly suggest that you

request your conference right then!!!

When I read about all the nonsense

that takes place in our schools, I want to cry. One way to fix this

is by empowering and encouraging the kids' families. The best ammunition so to

say, is to be more informed about the educational system. It is great to know a

lot about the law, but it is equally important to know how things work in real

life. Families and friends of ASD kids who take this seriously need to get

their "a-- in the class". Four conferences a year is a

must. Let's start this next year.

If you have specific questions related to

your school that I may be able to help you with, just e-mail me privately. Make

up a fake name if that helps. This is about the kids and

their education, not who is who in the community.

Liz

From: Karp <denisekarpmyacc (DOT) net>

To: <deniseslist@ yahoogroups. com>

Sent: Thu, June 3, 2010 8:45:26 PM

Subject: FDDC: $60 Million in Grants Available

From: Florida Developmental Disabilities Council [mailto:vandab@ fddc.org]

Sent: Thursday, June 03, 2010 4:17 PM

To: denisekarpmyacc (DOT) net

Subject: $60 Million in Grants Available

Error! Filename not

specified.

FOR IMMEDIATE

RELEASE

Contact: HHS Press Office

Thursday, June 3,

2010

Announcement from the

Florida Developmental Disabilities Council

For more information, please contact

HHS Press Office *

HHS announces availability of $60 million in

Affordable Care Act Grants

to help people navigate their health and long-term care options

HHS Secretary Kathleen

Sebelius announced the availability of $60 million in Affordable Care Act

grants to states and communities to help individuals and their caregivers

better understand and navigate their health and long-term care

options.

Through this opportunity made possible by the Affordable Care Act HHS'

Administration on Aging (AoA) and the Centers for Medicare & Medicaid

Services (CMS) will work collaboratively to award funds for an integrated

approach that focuses on the unique needs of seniors, disabled Americans

and their caregivers as they seek health care and long-term care.

"The Affordable Care Act seeks to lower health care costs, improve

the quality of health care and perhaps most importantly give people more

control over their own care. These new grants, authorized under the new

law, will help seniors, individuals with disabilities and their families

get better quality care and more control. We've also streamlined the process

for states and people who rely on these funds," said Secretary

Sebelius.

"We know how difficult it can be for caregivers and patients to try

and deal with a sudden illness or chronic disease while at the same time

trying to navigate through a complex health care system to figure out

where you can get help. These new funds that we have bundled together

will help promote better opportunities for coordination of health and

long-term supports," said Sebelius.

The purpose of this new grant program authorized by the Affordable Care

Act is to create streamlined, coordinated statewide systems of

information, counseling, and access that will help people find

consumer-friendly answers they seek to meet their health and long-term

care needs. AoA and CMS will administer the funding through

separate announcements, but will coordinate implementation and monitoring

through a single process.

Some specific areas of focus will include assisting individuals who are

under-served and hard to reach with information about their Medicare and

Medicaid benefits, helping older adults and individuals with disabilities

live at home or in settings of their choosing with the right supports,

assisting people transition from hospital or nursing home stays back into

the community, and strengthening linkages between the medical and social

service systems.

"When it comes to long-term health care, each patient has a unique

mix of complex medical and social needs that must be considered when

seeking care," said Marilyn Tavenner, acting CMS administrator.

"Our health care system can offer many options to meeting those

needs from traditional nursing home care to home and community-based

services. Making patients and their families aware of these options

will help them make inherently difficult decisions about long-term

care. This integrated program will help families make informed

choices and make sure patients have more control over their own

care."

AoA and CMS have provided grants to states for several years to develop

person-centered systems of information, counseling and access to make it

easier for individuals to learn about and access their health and

long-term services and support options. This grant program through the

Affordable Care Act strengthens and enhances the ability of states to

truly integrate the medical and social services care models.

"AoA's national network of community-based organizations has long

served as the central place for individuals and families seeking

information and help to address health and long term care

challenges. This collaborative opportunity between AoA and CMS will

further strengthen the network's capacity to help people in a more

coordinated and comprehensive way in the communities where they

live," said Kathy Greenlee, assistant secretary for aging.

Funds will be available to states, area agencies on aging (aaa's),

State Health Insurance Assistance Programs (SHIPs) and Aging and

Disability Resource Centers (ADRCs). Through the grant

program, states and local aging and disability programs will receive

funds to:

*provide outreach and assistance to

Medicare beneficiaries on their Medicare

benefits including prevention;

*use additional funds

through a competitive process to

provide Options Counseling on health and long-term care

through ADRCs;

*use additional funds through a

competitive process to strengthen the ADRCs role

in Money follows the Person program and support state Medicaid agencies

as

they transition individuals from nursing homes to community-based care;

and

*coordinate and continue to embed

tested Care Transition models that integrate

the medical and social service systems to help older individuals and

those with

disabilities remain in their own homes and communities after a

hospital,

rehabilitation or skilled nursing facility visit.

"CMS and AoA share a long-standing goal of expanding access to

community-based care for the elderly and individuals with

disabilities. The Affordable Care Act provides significant

resources for state Medicaid agencies and providers to balance the

nation's long-term care systems and assure that individuals have a choice

of where and how they receive their services," said Mann,

director of CMS's Center for Medicaid, CHIP, and Survey and

Certification.

The announcement combines funding opportunities from several provisions

in the Affordable Care Act signed into law by President Obama on March

23, 2010,including the Role of Public Programs (Title II, Sections 2403 -

Money Follows the Person and 2405 - Funding for Aging and Disability

Resource Centers) and Improving the Quality and Efficiency of Health Care

(Title III. Section 3306 - Funding for Outreach and Assistance for

Low-Income Programs).

These grants also complement President Obama's "Year of Community

Living Initiative," which focuses on better serving those

individuals with disabilities who need ongoing services and support

programs in the community such as those provided by AoA, CMS and other

HHS agencies.

The deadline for applications is: Monday, July 30, 2010. Grants

will be awarded in September 2010. For more information about this

grant opportunity, please visit http://www.aoa. gov/AoARoot/ Grants/Funding/ index.aspx

or www.grants.gov.

To learn more about the Affordable Care Act, please visit

www.healthreform. gov. Note: All HHS press releases,

fact sheets and other press materials are available at http://www.hhs. gov/news.

Forward email

Error!

Filename not specified.

This email was sent to

denisekarpmyacc (DOT) net by vandabfddc (DOT)

org.

Update Profile/Email Address | Instant removal with SafeUnsubscribeâ„¢ | Privacy Policy.

Email

Marketing by

Error!

Filename not specified.

Florida

Developmental Disabilities Council | 124 Marriott Drive | Suite 203 |

Tallahassee | FL | 32301

Error! Filename not specified.

--

AutismOnTheGo.com

Link to comment
Share on other sites

Guest guest

I think we should all know by know by now that nothing in life is black or white.As far as being held back it depends on the specific situation. The age, the personality, the exceptionality, all of the circumstances involved play a part in the outcome for the child. What works for one child may not work for the other. There can not be a rigid set if rules to govern what is best for our children.I must express though, that I find it very hard toexcept that being held back would be more tramatic for a child than the loss of a parent. This sounds like a very unbalanced comparison. BuschSent from my iPhone

I probably didn't look hard enough. But I didn't see anything.

Can you direct me to a specific research.

Thinking back to when I was a child, I don't remember being held

back a year was so detrimental.

From: sList

[mailto:sList ] On Behalf Of Hawk

Sent: Saturday, June 05, 2010 11:02 PM

To: sList

Subject: Re: Retention and parent conferences

Did you look at the link I provided? It is a great resource

on retenetion http://www.wrightslaw.com/info/retain.index.htm

There are viewpoints and

research from National

Association of School Psychologists, Harvard Civil Rights Projectm California

School Psychologist, US Dept of Education, Uiversity of Wisconsin and the

American Federation of Teachers. ALL say that retention does NOT work and is a

detriment to children.

On searxat, Jun 5, 2010 at 9:23 PM, Lizzie Berg <floridalizzie> wrote:

Gabi and others,

Let me ask everyone here : If

I was your kid's ( grandkid's, nephew, friend etc) teacher, what would you

ask me? What would you say to me?

In my previous postings maybe a

year ago or more, I said several times that one can expect several of

the list members here to be nurses, doctors, laywers, teachers,

principals, ESE specialists, OTs, behavior specialists, counselors, cluster

teachers and also at the same time be parents, grand parents, aunts, uncles,

godparents, siblings and friends of kids with autism. This is

possible, right? It is also possible to have one gen ed kid and one with

autism, right? So, it is OK to compare a cluster to a gen ed room,

and see the difference. Do we like what we see? Are gen ed teachers held to a

higher standard? Are cluster teachers less accountable? What is my role as a

parent, grand parent, aunt, uncle or advocate? What can I do now to make things

better for my kid. What is within my power, and when am I banging my head

against the wall? What can I change being outside the school system?

Many of us became attracted

to our profession and chose a career that is related to ASD because

autism had come into our lives. Some grew up with autism. One of the list

members here has an older sister with autism. She just did not know it as a

kid. She thought that everybody's older sisters were like her sister. It is

very possible to work for an organization that provides services for children

with ASD and be happy. I have done this for many, many years now. It has

enriched my life, made me a better person and helped me in absolutely all aspects

of my personal and professional life. I have met, and continue to meet,

the most interesting, beautiful and caring people because of my

involvement with ASD. Many of them read these postings every day :)

I meet people every day

who don't know much about autism. I advocate for spectrum kids day and night,

at work, at airports, in restaurants and in bars.

This list is uplifting because it

provides me with great opporunities to change things. I am finally

e-mailing Christ, and I have a better understanding of what the

issues really are. Often times, it really takes a village or a county.

When I said that I accept private

e-mails with fake names, it was because I respect people's need for

privacy and because it prevents gossip. Some may be more

vulnerable than others because they hold certain positions in our

community. Members who are "rich and famous" or

well-known often times do not want to expose themselves or their families.

They still have questions and need help. This is why I said that it

is not about who is who in the community. My posting was about

the kids and their progress at school.

So, what are the big issues?

What is it that retention cannot help? Let's talk about the

strategies and why they are not working? Lots of educators and coaches are

reading this. Let's talk about it. How do we get to the bottom of this? How can

we help each other?

Information is empowering and can

change the way we do things. When we change the way we do things, things will

change.

Thanks for all feedback privately

and here. It is highly appreciated.

Liz

From: Gabi <bijcom>

To: "sList "

<sList >

Sent: Sat, June 5, 2010 1:05:59 PM

Subject: Re: Retention and parent conferences

Hello Liz,

Do you work in the school system?

Or is a well-informed parent of a child with disability?

I don't care who is who in the

community, I'm just wondering since you offered to inform, where your knowledge

comes from.

Thank you

And I don't have a lot of time now,

but to retain a student is, in many cases, the easy way out of a bigger

problem. Another year of the same strategies that didn't work the first time is

a waste of time for the student.

Sent from my iPhone

On Jun 5, 2010, at 9:51 AM, Lizzie Berg <floridalizzie@ yahoo.com>

wrote:

I recently met a parent who is in

stunned because her kid;s teacher suggested retention next year. Here is what I

think:

The students have the right to stay

in elementary school from K through 5, which is 6 years, right? ESE kids have

the right to stay another 2 years before they have to, by law, move

to middle school. Most cluster students do not meet promotion

criteria because they are below grade level academically. General education

(gen.ed.) students who do not have a disability and who do not receive services

at school will not be promoted if they do not meet criteria. This is not up for

debate, the teachers and the parents do not have an option here. The

students need to be retained. Typically this is done in kindergarten or first

grade. It is also commonly done in third grade for various reasons. Gen ed

students who are retained are often evaluated to see if their is a more serious

underlying problem here. Some children in kindergarten are simply immature and

they catch up soon. Others have a learning disability and need more intense

instruction.

The goal is that by the time the

students leave the elementary school, they should hopefully be able to perform

academically at fifth grade level. They should be able to read and write like a

fifth grader.

Cluster students and other

ESE kids have the right to be retained two years in elementary school. It

is your teacher's responsibility to explain this to you, and in

my opinion, they should be held responible for giving you a copy of

the promotion criteria.

I cannot understand why parents of

cluster students are in a hurry to get them out of elementary school and into

middle? Why???

You can ask them to retain your

child any school year. If you are not sure what to do,

retain again in 5th grade.

If nobody at your school has

suggested retention, there is something very wrong with your school. It is in

our county;s and community's interest that all students receive the maximum

learning gains possible while they are in elementary school.

All parents should by now have

finished their spring teacher-parent conference. This conference should focus

on 2 things: academic and social progress, and promotion versus retention. The

conference form that you get a copy of should say somethng like this"

Retention discusses, the parents would like ______, and therefore X will

be in so and so grade next school year". If you want him to be promoted

the conference form should say something like this: "retention discussed,

and the parents want X to be promoted due to good cause".

Cood Cause: ESE

kids (and others) cannot be retained more than 2 years.

Therfore they will be promoted no matter what. The promotion crteria will be

waved, and the child is promoted due to something that is called "Good

Cause". If you retain him in kindergarten for a year, he has to move to

first grade next year. You can retain him again in first year, but after that

he has to move up no matter what.

If you have not been invited for a

spring conference, there is something very wrong with your school,. This is a

red flag. You should by now have the copy of your conference form in your hand

or you should have it filed in your big binder.

The teacher has to have a minimum

of 2 conferences with you each year. This is state law. In my opinion, you

should request no less than 4 conferences, one for each marking period. You

receive the progress report and report card ina yellow envelope eah marking

period, right? There is a line outside the on the envelop that you need to

sign, and next to it is a question that you should answer: "Do you want a

conference" I can't imagine why you would say no right then. Why?

And if you don't get they paricular envelope, I strongly suggest that you

request your conference right then!!!

When I read about all the nonsense

that takes place in our schools, I want to cry. One way to fix this

is by empowering and encouraging the kids' families. The best ammunition so to

say, is to be more informed about the educational system. It is great to know a

lot about the law, but it is equally important to know how things work in real

life. Families and friends of ASD kids who take this seriously need to get

their "a-- in the class". Four conferences a year is a

must. Let's start this next year.

If you have specific questions related to

your school that I may be able to help you with, just e-mail me privately. Make

up a fake name if that helps. This is about the kids and

their education, not who is who in the community.

Liz

From: Karp <denisekarpmyacc (DOT) net>

To: <deniseslist@ yahoogroups. com>

Sent: Thu, June 3, 2010 8:45:26 PM

Subject: FDDC: $60 Million in Grants Available

From: Florida Developmental Disabilities Council [mailto:vandab@ fddc.org]

Sent: Thursday, June 03, 2010 4:17 PM

To: denisekarpmyacc (DOT) net

Subject: $60 Million in Grants Available

Error! Filename not

specified.

FOR IMMEDIATE

RELEASE

Contact: HHS Press Office

Thursday, June 3,

2010

Announcement from the

Florida Developmental Disabilities Council

For more information, please contact

HHS Press Office *

HHS announces availability of $60 million in

Affordable Care Act Grants

to help people navigate their health and long-term care options

HHS Secretary Kathleen

Sebelius announced the availability of $60 million in Affordable Care Act

grants to states and communities to help individuals and their caregivers

better understand and navigate their health and long-term care

options.

Through this opportunity made possible by the Affordable Care Act HHS'

Administration on Aging (AoA) and the Centers for Medicare & Medicaid

Services (CMS) will work collaboratively to award funds for an integrated

approach that focuses on the unique needs of seniors, disabled Americans

and their caregivers as they seek health care and long-term care.

"The Affordable Care Act seeks to lower health care costs, improve

the quality of health care and perhaps most importantly give people more

control over their own care. These new grants, authorized under the new

law, will help seniors, individuals with disabilities and their families

get better quality care and more control. We've also streamlined the process

for states and people who rely on these funds," said Secretary

Sebelius.

"We know how difficult it can be for caregivers and patients to try

and deal with a sudden illness or chronic disease while at the same time

trying to navigate through a complex health care system to figure out

where you can get help. These new funds that we have bundled together

will help promote better opportunities for coordination of health and

long-term supports," said Sebelius.

The purpose of this new grant program authorized by the Affordable Care

Act is to create streamlined, coordinated statewide systems of

information, counseling, and access that will help people find

consumer-friendly answers they seek to meet their health and long-term

care needs. AoA and CMS will administer the funding through

separate announcements, but will coordinate implementation and monitoring

through a single process.

Some specific areas of focus will include assisting individuals who are

under-served and hard to reach with information about their Medicare and

Medicaid benefits, helping older adults and individuals with disabilities

live at home or in settings of their choosing with the right supports,

assisting people transition from hospital or nursing home stays back into

the community, and strengthening linkages between the medical and social

service systems.

"When it comes to long-term health care, each patient has a unique

mix of complex medical and social needs that must be considered when

seeking care," said Marilyn Tavenner, acting CMS administrator.

"Our health care system can offer many options to meeting those

needs from traditional nursing home care to home and community-based

services. Making patients and their families aware of these options

will help them make inherently difficult decisions about long-term

care. This integrated program will help families make informed

choices and make sure patients have more control over their own

care."

AoA and CMS have provided grants to states for several years to develop

person-centered systems of information, counseling and access to make it

easier for individuals to learn about and access their health and

long-term services and support options. This grant program through the

Affordable Care Act strengthens and enhances the ability of states to

truly integrate the medical and social services care models.

"AoA's national network of community-based organizations has long

served as the central place for individuals and families seeking

information and help to address health and long term care

challenges. This collaborative opportunity between AoA and CMS will

further strengthen the network's capacity to help people in a more

coordinated and comprehensive way in the communities where they

live," said Kathy Greenlee, assistant secretary for aging.

Funds will be available to states, area agencies on aging (aaa's),

State Health Insurance Assistance Programs (SHIPs) and Aging and

Disability Resource Centers (ADRCs). Through the grant

program, states and local aging and disability programs will receive

funds to:

*provide outreach and assistance to

Medicare beneficiaries on their Medicare

benefits including prevention;

*use additional funds

through a competitive process to

provide Options Counseling on health and long-term care

through ADRCs;

*use additional funds through a

competitive process to strengthen the ADRCs role

in Money follows the Person program and support state Medicaid agencies

as

they transition individuals from nursing homes to community-based care;

and

*coordinate and continue to embed

tested Care Transition models that integrate

the medical and social service systems to help older individuals and

those with

disabilities remain in their own homes and communities after a

hospital,

rehabilitation or skilled nursing facility visit.

"CMS and AoA share a long-standing goal of expanding access to

community-based care for the elderly and individuals with

disabilities. The Affordable Care Act provides significant

resources for state Medicaid agencies and providers to balance the

nation's long-term care systems and assure that individuals have a choice

of where and how they receive their services," said Mann,

director of CMS's Center for Medicaid, CHIP, and Survey and

Certification.

The announcement combines funding opportunities from several provisions

in the Affordable Care Act signed into law by President Obama on March

23, 2010,including the Role of Public Programs (Title II, Sections 2403 -

Money Follows the Person and 2405 - Funding for Aging and Disability

Resource Centers) and Improving the Quality and Efficiency of Health Care

(Title III. Section 3306 - Funding for Outreach and Assistance for

Low-Income Programs).

These grants also complement President Obama's "Year of Community

Living Initiative," which focuses on better serving those

individuals with disabilities who need ongoing services and support

programs in the community such as those provided by AoA, CMS and other

HHS agencies.

The deadline for applications is: Monday, July 30, 2010. Grants

will be awarded in September 2010. For more information about this

grant opportunity, please visit http://www.aoa. gov/AoARoot/ Grants/Funding/ index.aspx

or www.grants.gov.

To learn more about the Affordable Care Act, please visit

www.healthreform. gov. Note: All HHS press releases,

fact sheets and other press materials are available at http://www.hhs. gov/news.

Forward email

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