Jump to content
RemedySpot.com

help??

Rate this topic


Guest guest

Recommended Posts

I just looked at mine and my brother's shot records (for 1967 and 1970)

and we, too, had MMR all separate. The weird thing is that there's a

rubella record for me, but not for my brother. I wonder if they only

gave it to girls back then?? Not giving them in combos also make me

think that that's why we didn't have (at least as many) of the immediate

and severe reactions as we do now. (Though I know alot of us suffer from

other long term effects, and DTP was given in combos then)

I am actually amazed that I'm as healthy as I am, because according to

my records I was given DTP at 2, 3 and 4 months of age, instead 2, 4

and 6 months, like my brother. And he's the one that suffered from ear

infections, croup cugh, etc. I was, and always have been, pretty

healthy.

Link to comment
Share on other sites

http://www.whale.to/Vaccines/hepatitis.html

http://www.whale.to/Vaccines/autism.html

Help??

>From: Reiss <lisa@...>

>

>I am hoping that either Rick Rollens or Ray Gallup will get this....if

>any one else has info. please forward it.

>

>I am as many of you know activly working on getting a philosophical

>exemption passed for the State of Connecticut. I attended the 8/3

>hearing in Washington. I have heard the numerous rates of increase

>regarding Autism and the strong link to the MMR vaccine. I have a Sen.

>who is interested but I need to explain this properly....Any help would

>be appreciated.

>

>Here is my question....

>What makes people think it is the MMR vaccine? Do the autism rates

>correspond with this vaccine? I remember seeing on my shot record and

>my husband's that we both got Measles, Mumps and Rubella....but it was

>separate I think....11 years ago, is that when they combined them all

>into one vaccine? or was MMR as a one vaccine given previously to 11

>years ago?

>

>ANY info would be appreciated especially with sources.

>Thanks a ton...

>

>

>--

>@...

>***************************************************************

>We Must Have The Freedom To Choose & Respect Everyone's Choice

>***************************************************************

>Any information obtained here is not to be construed as medical

>OR legal advice. The decision to vaccinate and how you

>implement that decision is yours and yours alone.

>

>---------------------------

Link to comment
Share on other sites

,

I'm not the autism expert you need. But I'm mailing to you a floppy

containing the posts on autism that I've collected. Some good info is on

there.

On Tue, 17 Aug 1999 13:11:17 -0400 Reiss <lisa@...> writes:

>From: Reiss <lisa@...>

>

>I am hoping that either Rick Rollens or Ray Gallup will get this....if

>any one else has info. please forward it.

>

>I am as many of you know activly working on getting a philosophical

>exemption passed for the State of Connecticut. I attended the 8/3

>hearing in Washington. I have heard the numerous rates of increase

>regarding Autism and the strong link to the MMR vaccine. I have a

>Sen.

>who is interested but I need to explain this properly....Any help

>would

>be appreciated.

>

>Here is my question....

>What makes people think it is the MMR vaccine? Do the autism rates

>correspond with this vaccine? I remember seeing on my shot record and

>my husband's that we both got Measles, Mumps and Rubella....but it was

>separate I think....11 years ago, is that when they combined them all

>into one vaccine? or was MMR as a one vaccine given previously to 11

>years ago?

>

>ANY info would be appreciated especially with sources.

>Thanks a ton...

>

>

>--

>@...

>***************************************************************

>We Must Have The Freedom To Choose & Respect Everyone's Choice

>***************************************************************

>Any information obtained here is not to be construed as medical

>OR legal advice. The decision to vaccinate and how you

>implement that decision is yours and yours alone.

>

>---------------------------

Link to comment
Share on other sites

  • 3 years later...

Hi,

You really need to contact your local school system

and see if you can get him re - evaluated. He should

definitely be communicating more verbally by now.

--- nursebetty_2002 <bethseanrobson@...>

wrote:

> i have a three year old...he does not really

> speak...he attempt words

> about 10. none of them two sylabuls. He does a good

> job

> communicating his needs with sign and yes/no

> questions(we ask the

> questions) When he was younger he was given the

> label of hyptonia and

> he he meet all of his milestones late. We and are

> doing the thearpy

> thing BUT we have never recieved a conclusive

> diagonsis of any sort

> if any one has any ideas Please let me know

Link to comment
Share on other sites

I would strongly recommend an evaluation by the EI in your area. Also quite

helpful in case they screw up and say he is developing better than he actually

is (it happened to me) I'd also get a full evaluation from a children's

hospital. Use that to prove the EI's results are incorrect and obtain the

services he needs from the district and hopefully privately if it is possible

for you. I'd get right on it too before the holidays get underway and people

are harder to reach.

Tammy

[ ] help??

i have a three year old...he does not really speak...he attempt words

about 10. none of them two sylabuls. He does a good job

communicating his needs with sign and yes/no questions(we ask the

questions) When he was younger he was given the label of hyptonia and

he he meet all of his milestones late. We and are doing the thearpy

thing BUT we have never recieved a conclusive diagonsis of any sort

if any one has any ideas Please let me know

Link to comment
Share on other sites

Yes, he sounds just like my daughter. She is dyspraxic. She is 5 now and

doing much better. She still has a hard time doing some things, but she is

making progress and she tries hard. Her vocab has grown drastically, since

beginning the use of EFA's. My suggestion is to take him to a pediatric

neurologist who is familiar with apraxia and apraxia related issues.

Thank you,

Sheila

>From: " nursebetty_2002 " <bethseanrobson@...>

>Reply-

>

>Subject: [ ] help??

>Date: Wed, 25 Sep 2002 18:09:16 -0000

>

>i have a three year old...he does not really speak...he attempt words

>about 10. none of them two sylabuls. He does a good job

>communicating his needs with sign and yes/no questions(we ask the

>questions) When he was younger he was given the label of hyptonia and

>he he meet all of his milestones late. We and are doing the thearpy

>thing BUT we have never recieved a conclusive diagonsis of any sort

>if any one has any ideas Please let me know

_________________________________________________________________

Join the world’s largest e-mail service with MSN Hotmail.

http://www.hotmail.com

Link to comment
Share on other sites

Hi and welcome!

I agree with the otheers who posted. IF your son has been in speech

theerapy for some time and not making any progress you may not have a

good match. Try and find an SLP familiar with apraxia who can make an

accurate diagnosis. DO not let anyone tell you he is too young. Oral

apraxia can be diagnosed as young as 18 months.

A developmental pediatrician and/or a child study team at a

children's Hospital may be a route to take. These independent

evaluations will be a help when the school district evaluates in case

there are any discrepancies.

Please feel free to write with questions as we all know how scary it

is in those early days.

denise

Mom to 4.3, low tone, verbal apraxia and my little sweety and

2.7 a typical terrible 2 who is big brother's biggerst fan!

> i have a three year old...he does not really speak...he attempt

words

> about 10. none of them two sylabuls. He does a good job

> communicating his needs with sign and yes/no questions(we ask the

> questions) When he was younger he was given the label of hyptonia

and

> he he meet all of his milestones late. We and are doing the

thearpy

> thing BUT we have never recieved a conclusive diagonsis of any sort

> if any one has any ideas Please let me know

Link to comment
Share on other sites

  • 5 years later...

I had my appointment today and I was told that my results showed no

detection of the BCR/ABL translocation. Does this mean that I have

reached the second stage of remission??? I mean- is this correct!!!

Thanks a bunch!

corina

Link to comment
Share on other sites

Join the conversation

You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.

Guest
Reply to this topic...

×   Pasted as rich text.   Paste as plain text instead

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.

Loading...
×
×
  • Create New...