testing question

[Guest guest]

No, it is not unreasonable. In the past, when has been tested by school

psychologists who don't spend time in the classroom with her, I have strongly

requested the psychologist spend classroom time with , working one on one

with her in various activities, so she could become accustomed to this person.

I also specified mid morning evaluations, after snack, and on Monday, Tuesday or

Wednesday, because when was younger, those were her best school days.

Thursdays and Fridays she began to wear down.

Your request is valid, in my eyes.

Sharon H.

Mom to , (15, DS) and , (11)

South Carolina

" Be kinder than necessary, for everyone you meet is fighting some kind of

battle. "

Testing question

If my son does not cooperate with a therapist who is trying to evaluate him,

is it fair of the therapist to NOT re-attempt the testing? Her report just

states that he was " uncooperative " . She didn't come back on another day to try

again. He apparantly just had one chance to be evaluated by a therapist who he

has only seen 3 times (10 minutes each time) since August. He doesn't really

know her, and for Isaac, he has to build some level of relationship with a

person before he'll work for them. To me this seems unfair. I don't actually

think the therapist likes my son either, and he may sense that and therefore not

cooperate. He was just silly and goofy during her attempt and couldn't make any

progress.

I feel like he should be entitled to another attempt by someone else.......is

that unreasonable??

Jill

Mom to 8 year old Isaac (DS)

[Guest guest]

Ditto, you want the evaluation to represent what your son can do, not

how well he takes tests. If the person administering the eval cannot do

it successfully, it's not your son's fault. We have had two noteworthy

evals in 's history.

The first is the negative example. Preschool assessment team as we were

transitioning to the school district from Early Intervention. They took

her to another part of the room, behind some partitions. She was 2 1/2,

and had never seen this woman before in her life. I was told I had to

stay where I was, I could not accompany her (though I could hear

everything was was really right there, didn't know it.) The

woman basically barked commands at her like " put in " (trying to get her

to put an object into a shape sorter or something like that), " hold

crayon " (to see if she could draw), etc.). It was awful, and I didn't

know what to do. Luckily, had obviously checked out, and just

sat there playing with a toy, ignoring the woman's commands. The report

made her sound like a bump on a log with no skills and I read them the

riot act about it afterwards, but the reality was, the woman didn't

really care if she assessed her abilities, she just wanted to show she

couldn't do these things so that she would qualify for services (almost

exactly her words.)

The second was the best ever. Last year, we allowed the school

psychologist who frequently observes , participates in IEP

meetings, and is a great member of our team, to perform IQ testing on

. She did the testing in the morning each day, in short

segments. If seemed to be losing interest, she had a small

bag of Skittles there to remind her of the reward she would get for

trying her best and answering all the questions. She did not test her

every day, so that didn't get too bored of testing. She

allowed her to get up and walk around the room to take breaks when

necessary, and was kind throughout. It was truly important for her to

get the most accurate date she could on , and she did her best

to make sure the test reflected what was capable of on that

exam. We discussed all these strategies at a team meeting prior to the

testing, and everyone felt that this would work well and it did.

We've had everything in between as well, but now that we've seen a good

assessment, we will never settle for anything less :-) Good luck, and I

hope you get a good therapist in there to evaluate your son.

, mom to (11), (9 DS), and Sammy (7)

Sharon wrote:

> No, it is not unreasonable. In the past, when has been tested by

> school psychologists who don't spend time in the classroom with her, I

> have strongly requested the psychologist spend classroom time with

> , working one on one with her in various activities, so she could

> become accustomed to this person. I also specified mid morning

> evaluations, after snack, and on Monday, Tuesday or Wednesday, because

> when was younger, those were her best school days. Thursdays and

> Fridays she began to wear down.

> Your request is valid, in my eyes.

>

> Sharon H.

> Mom to , (15, DS) and , (11)

> South Carolina

>

> " Be kinder than necessary, for everyone you meet is fighting some kind

> of battle. "

>

> Testing question

>

> If my son does not cooperate with a therapist who is trying to

> evaluate him, is it fair of the therapist to NOT re-attempt the

> testing? Her report just states that he was " uncooperative " . She

> didn't come back on another day to try again. He apparantly just had

> one chance to be evaluated by a therapist who he has only seen 3 times

> (10 minutes each time) since August. He doesn't really know her, and

> for Isaac, he has to build some level of relationship with a person

> before he'll work for them. To me this seems unfair. I don't actually

> think the therapist likes my son either, and he may sense that and

> therefore not cooperate. He was just silly and goofy during her

> attempt and couldn't make any progress.

>

> I feel like he should be entitled to another attempt by someone

> else.......is that unreasonable??

>

> Jill

> Mom to 8 year old Isaac (DS)

>

>

[Guest guest]

I was thinking of going to a Neuro. I will stand strong & not get an MRI.  I

would fry from it.

Are there alternative tests for MS?

Kathy

[Guest guest]

Hi,

One therapist told me:

Some Italian internist Dr. found out by accident (by looking into the scans of

his wife and later comparing these with MS-patients) and many MS-patients seem

to have a problem with the blood flow between head and rest of body, so the

veins in the neck (V. Jugularis) should be at least opened for 0.8 centimeter,

They can check that with a Doppler/sound test...

The test is supposed to be harmless, although that may not be completely true,

it's probably like 100 times safer than MRI,

I'm not saying that this test is proof for MS, one Doctor I spoke on this he

confirmed it may be useful to have a test done like this if you have

MS-symptoms, but he said so far they're still investigating link MS and problems

at the V. Jugularis...

gr,

.

>

>

>

> I was thinking of going to a Neuro. I will stand strong & not get an MRI.  I

would fry from it.

>

> Are there alternative tests for MS?

>

>

> Kathy

>

>

>

>

>

[Guest guest]

Hi, ,

 

I was mis-dxed with MS for 2 years (in 1980s).  After I had MRIs (early 1990s),

the specialist concluded I did not have actual MS.  I did show abnormalties on

brain scans, but he concluded, from the preponderance of symptoms I was having

(MS-like symptoms in all quadrants of my body), that it was not MS.  I also

have the problem with the V. Jugularis veins, but mine comes and goes.  (When I

have it, however, it could sometimes be causing stroke/ seizures; I

recognise a tightened feeling in my neck after many years of it coming and

going, and I do notice this is when I am at higher risk for having strokes/

seizures and especially migraine-type episodes.)

 

I mention all of this because it appears *to me* (I have not read this

anywhere) that the clogging of the V. Jugularis is caused directly by calcium

efflux.  And I assume this is why it " comes and goes " for me.  If this is

true, it could mean we have commonalities with MS, but not necessarily that

we all have MS.  It is already known, I believe, that MS is an ion channel

disease.  (I may be wrong about this being a proven conclusion, however, I

know it has been suspected for many years by Dr. Alessio Fasano, and others, and

studies were at least undertaken to check for that.)  If MS is, however, a

channelopathy (as is celiac disease), it would mean people with MS, celiac

disease, and, likely, ES all have commonalities, but not necessarily the same

exact disease. 

 

The reason this is important is, people with MS can have a steady down-hill road

to debilitation and incapacitation.  One who believes they have MS can easily

become trapped into thinking there is no hope and this is their fate.  However,

consider me: I was nearly completely bed-bound for 13 years, barely able to live

a normal life for most of my life before that, and here I am; I now hike and

bike and work nearly as well as a normal person.  True, my health is not

100%, but I am nothing like I used to be.  If you keep looking into MS, be sure

that you do not fall into a fatalistic attitude on the way.  Your attitude is

all you have; docs don't have the answers, science doesn't have all the

answers.  YOU have the possibility to find what works for you.  Believe that,

and never let go of that.

 

Good luck, ,

Diane

From: <@...>

Subject: Re: testing question

Date: Friday, July 1, 2011, 8:05 PM

 

Hi,

One therapist told me:

Some Italian internist Dr. found out by accident (by looking into the scans of

his wife and later comparing these with MS-patients) and many MS-patients seem

to have a problem with the blood flow between head and rest of body, so the

veins in the neck (V. Jugularis) should be at least opened for 0.8 centimeter,

They can check that with a Doppler/sound test...

The test is supposed to be harmless, although that may not be completely true,

it's probably like 100 times safer than MRI,

I'm not saying that this test is proof for MS, one Doctor I spoke on this he

confirmed it may be useful to have a test done like this if you have

MS-symptoms, but he said so far they're still investigating link MS and problems

at the V. Jugularis...

gr,

.

>

>

>

> I was thinking of going to a Neuro. I will stand strong & not get an MRI.  I

would fry from it.

>

> Are there alternative tests for MS?

>

>

> Kathy

>

>

>

>

>

[Guest guest]

There is no reason ahving a fatalistic attitude with MS.

Many people have resolved these problems with Rife frequency therapy.

I quote here from the *The Rife Handbook* by nenah Sylver:

*****************************

With all autoimmune disorders, the body’s

immune cells attack the person’s own tissues. Autoimmune

disorders are often due to the presence of tiny Mycoplasma—

so-called “stealth pathogensâ€â€”whose lack of a cell wall allow

them to invade our cells and assume some of the properties

of our own tissue. O ur immune cells sense something hiding

in our cells, and attack them.

If the Mycoplasma invade the central nervous system, the

disease is Multiple Sclerosis (although MS can also have a

non-autoimmune origin). I f the Mycoplasma invade our joints,

the disease is rheumatoid arthritis. If the body attacks foreign

proteins that it mistakes for its own tissues, resulting in a

severe inflammatory response that could be anywhere, the

disease is Lupus erythematosus.

*****************************

I have no proof, but I believe that the chemtrails contain Mycoplasma's, which

is a breeding ground for a lot of diseases.

The only disadvantage of a Rife frequency therapy is, that it consumes a lot of

time.

Greetings,

Claessens

member Verband Baubiologie

www.milieuziektes.nl

www.milieuziektes.be

www.hetbitje.nl

checked by Norton

Re: testing question

Date: Friday, July 1, 2011, 8:05 PM

Hi,

One therapist told me:

Some Italian internist Dr. found out by accident (by looking into the scans of

his wife and later comparing these with MS-patients) and many MS-patients seem

to have a problem with the blood flow between head and rest of body, so the

veins in the neck (V. Jugularis) should be at least opened for 0.8 centimeter,

They can check that with a Doppler/sound test...

The test is supposed to be harmless, although that may not be completely true,

it's probably like 100 times safer than MRI,

I'm not saying that this test is proof for MS, one Doctor I spoke on this he

confirmed it may be useful to have a test done like this if you have

MS-symptoms, but he said so far they're still investigating link MS and problems

at the V. Jugularis...

gr,

.

>

>

>

> I was thinking of going to a Neuro. I will stand strong & not get an MRI. I

would fry from it.

>

> Are there alternative tests for MS?

>

>

> Kathy

>

>

>

>

>

[Guest guest]

& all,

I'm so glad you shared on Rife machines. I started w a Rife practioner in the

spring. I made amazing gains. He said I had hypersensitivity. no other dx. yet.

Went twice a week. Haven't gone in a month & feel terrible. I need to go back.

My electro senstity has increased, from a new cell tower. 

I''d like info on the  ES CD. Diane, I''m glad you've improved so much. I " d

like to talk.

Kathy

From: charles <charles@...>

Subject: Re: Re: testing question

Date: Saturday, July 2, 2011, 10:22 AM

 

There is no reason ahving a fatalistic attitude with MS.

Many people have resolved these problems with Rife frequency therapy.

I quote here from the *The Rife Handbook* by nenah Sylver:

*****************************

With all autoimmune disorders, the body’s

immune cells attack the person’s own tissues. Autoimmune

disorders are often due to the presence of tiny Mycoplasma—

so-called “stealth pathogensâ€â€”whose lack of a cell wall allow

them to invade our cells and assume some of the properties

of our own tissue. O ur immune cells sense something hiding

in our cells, and attack them.

If the Mycoplasma invade the central nervous system, the

disease is Multiple Sclerosis (although MS can also have a

non-autoimmune origin). I f the Mycoplasma invade our joints,

the disease is rheumatoid arthritis. If the body attacks foreign

proteins that it mistakes for its own tissues, resulting in a

severe inflammatory response that could be anywhere, the

disease is Lupus erythematosus.

*****************************

I have no proof, but I believe that the chemtrails contain Mycoplasma's, which

is a breeding ground for a lot of diseases.

The only disadvantage of a Rife frequency therapy is, that it consumes a lot of

time.

Greetings,

Claessens

member Verband Baubiologie

www.milieuziektes.nl

www.milieuziektes.be

www.hetbitje.nl

checked by Norton

[Guest guest]

All,

To those who have not experienced a Rife.

I forgot to share the story, my  practitioner shared.

 He had a patient w lung cancer. Mainstream attempted surgery, opened her & told

her they could not do anything.

She went to him & bought her own Rife. She healed.

Kathy

-

[Guest guest]

Hello Kathy,

if you look at the internet, you may find quite a lot of Rife machines.

See: http://www.milieuziektes.nl/Pagina161.html

A very nice handsome machine, and not so expensive is the F-Scan Compact.

It has 350 standard preprogrammed programs, and 10 memory banks for each 50

frequencies.

It is very effective with two handelectrodes.

I can recommend it.

In the USA it is available by dr. Loyd.

See: http://www.royalrife.com

Greetings,

Claessens

member Verband Baubiologie

www.milieuziektes.nl

www.milieuziektes.be

www.hetbitje.nl

checked by Norton

Re: Re: testing question

All,

To those who have not experienced a Rife.

I forgot to share the story, my practitioner shared.

He had a patient w lung cancer. Mainstream attempted surgery, opened her &

told her they could not do anything.

She went to him & bought her own Rife. She healed.

Kathy

-

[Guest guest]

Hi, Kathy,

 

I don't have an " ES CD " , Sweetie.  I was writing about similarities in ES, CD

(celiac disease), and MS.  Sorry to have confused you by my abbreviations. 

 

If you want to discuss more on this subject, please contact me privately,

thanks.

 

Diane

From: KathyB <calicocat477@...>

Subject: Re: Re: testing question

Date: Saturday, July 2, 2011, 8:37 PM

 

& all,

I'm so glad you shared on Rife machines. I started w a Rife practioner in the

spring. I made amazing gains. He said I had hypersensitivity. no other dx. yet.

Went twice a week. Haven't gone in a month & feel terrible. I need to go back.

My electro senstity has increased, from a new cell tower. 

I''d like info on the  ES CD. Diane, I''m glad you've improved so much. I " d

like to talk.

Kathy

From: charles <charles@...>

Subject: Re: Re: testing question

Date: Saturday, July 2, 2011, 10:22 AM

 

There is no reason ahving a fatalistic attitude with MS.

Many people have resolved these problems with Rife frequency therapy.

I quote here from the *The Rife Handbook* by nenah Sylver:

*****************************

With all autoimmune disorders, the body’s

immune cells attack the person’s own tissues. Autoimmune

disorders are often due to the presence of tiny Mycoplasma—

so-called “stealth pathogensâ€â€”whose lack of a cell wall allow

them to invade our cells and assume some of the properties

of our own tissue. O ur immune cells sense something hiding

in our cells, and attack them.

If the Mycoplasma invade the central nervous system, the

disease is Multiple Sclerosis (although MS can also have a

non-autoimmune origin). I f the Mycoplasma invade our joints,

the disease is rheumatoid arthritis. If the body attacks foreign

proteins that it mistakes for its own tissues, resulting in a

severe inflammatory response that could be anywhere, the

disease is Lupus erythematosus.

*****************************

I have no proof, but I believe that the chemtrails contain Mycoplasma's, which

is a breeding ground for a lot of diseases.

The only disadvantage of a Rife frequency therapy is, that it consumes a lot of

time.

Greetings,

Claessens

member Verband Baubiologie

www.milieuziektes.nl

www.milieuziektes.be

www.hetbitje.nl

checked by Norton

[Guest guest]

I did once send an *ES-CD* to Marc .

Greetings,

Claessens

member Verband Baubiologie

www.milieuziektes.nl

www.milieuziektes.be

www.hetbitje.nl

checked by Norton

Re: Re: testing question

Date: Saturday, July 2, 2011, 10:22 AM

There is no reason ahving a fatalistic attitude with MS.

Many people have resolved these problems with Rife frequency therapy.

I quote here from the *The Rife Handbook* by nenah Sylver:

*****************************

With all autoimmune disorders, the body’s

immune cells attack the person’s own tissues. Autoimmune

disorders are often due to the presence of tiny Mycoplasma—

so-called “stealth pathogensâ€â€”whose lack of a cell wall allow

them to invade our cells and assume some of the properties

of our own tissue. O ur immune cells sense something hiding

in our cells, and attack them.

If the Mycoplasma invade the central nervous system, the

disease is Multiple Sclerosis (although MS can also have a

non-autoimmune origin). I f the Mycoplasma invade our joints,

the disease is rheumatoid arthritis. If the body attacks foreign

proteins that it mistakes for its own tissues, resulting in a

severe inflammatory response that could be anywhere, the

disease is Lupus erythematosus.

*****************************

I have no proof, but I believe that the chemtrails contain Mycoplasma's, which

is a breeding ground for a lot of diseases.

The only disadvantage of a Rife frequency therapy is, that it consumes a lot

of time.

Greetings,

Claessens

member Verband Baubiologie

www.milieuziektes.nl

www.milieuziektes.be

www.hetbitje.nl

checked by Norton

[Guest guest]

> I did once send an *ES-CD* to Marc .

Yes indeed! Perhaps I should post MP3's for people to download?

Marc

[Guest guest]

Evie wrote:

> I don't have an " ES CD " ,

I have been working on an ES or more precisely, " EMR Electrosmog " DVD

since March, but am only now getting it to the point of announcing it.

Those on this group might be interested, especially if you don't have

broadband to see the videos of research and presentations about this

subject.

http://seahorseCorral.org/emrdvd.html

I made this to help spread the message to friends here that couldn't

understand my problem.

I'm interested in hearing comments or suggestions.

[Guest guest]

this looks intruiging, love the pad, could you put a paypal payment

on your site

puk

In a message dated 06/07/2011 03:44:09 GMT Daylight Time,

sandreas41@... writes:

Evie wrote:

> I don't have an " ES CD " ,

I have been working on an ES or more precisely, " EMR Electrosmog " DVD

since March, but am only now getting it to the point of announcing it.

Those on this group might be interested, especially if you don't have

broadband to see the videos of research and presentations about this

subject.

_http://seahorseCorral.org/emrdvd.html_

(http://seahorsecorral.org/emrdvd.html)

I made this to help spread the message to friends here that couldn't

understand my problem.

I'm interested in hearing comments or suggestions.

[Guest guest]

Some years ago, iI have assembled a CD with the most importat issues, studies

and reports.

But the news comes so fast, that it is impossible to maintain everything.

Therefore, I place important stuff on the website, in a kind of blog.

That can be updated every minute.

Greetings,

Claessens

member Verband Baubiologie

www.milieuziektes.nl

www.milieuziektes.be

www.hetbitje.nl

checked by Norton

Re: Re: testing question

this looks intruiging, love the pad, could you put a paypal payment

on your site

puk

In a message dated 06/07/2011 03:44:09 GMT Daylight Time,

sandreas41@... writes:

Evie wrote:

> I don't have an " ES CD " ,

I have been working on an ES or more precisely, " EMR Electrosmog " DVD

since March, but am only now getting it to the point of announcing it.

Those on this group might be interested, especially if you don't have

broadband to see the videos of research and presentations about this

subject.

_http://seahorseCorral.org/emrdvd.html_

(http://seahorsecorral.org/emrdvd.html)

I made this to help spread the message to friends here that couldn't

understand my problem.

I'm interested in hearing comments or suggestions.