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Apraxia and SSI

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I was wondering if anyone has applied for SSI Disability for Speech Apraxia to

help pay for the therapy etc. If you were successful or unsuccessful please

share your experience with this.

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Hi - I live in Massachusetts and I am in the processing of applying for

MassHealth. I haven't received the final decision yet but will post back

once I do which should be within the next 30 days. We were rejected based

on income but are being reviewed now based on my son's disability. I

starting down this path to help pay for a AAC device. We shall see.

From:

[mailto: ] On Behalf Of mommywork11

Sent: Tuesday, March 01, 2011 11:01 AM

Subject: [ ] Apraxia and SSI

I was wondering if anyone has applied for SSI Disability for Speech Apraxia

to help pay for the therapy etc. If you were successful or unsuccessful

please share your experience with this.

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We applied and met the income requirements, but were denied. We appealed and

were again denied....my son seems to fit the criteria, but I'm done fighting

it....I don't feel like going to court over it, which would be the next step.

Best of luck, I have heard that some children with apraxia DO get it!

-Brittany

>

> I was wondering if anyone has applied for SSI Disability for Speech Apraxia to

help pay for the therapy etc. If you were successful or unsuccessful please

share your experience with this.

>

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We were approved for SSI in January.  My son has Apraxia and we had no

problem.  Did you maybe not have the support of doctors therapist that were in

agreement that he had a disability?  I also made sure that on the questionnaire

that I filled out I wrote that without appropriate therapy his speech will be

affected long term and that I did not have the money to pay for appropriate

therapy for him.  I also noted his problems eating and possible sensory

problems.  The only thing that held up his being approved was the income. 

When I finally saw the papers they had an incorrect amount in our savings

account.  I took bank statements to my local office and he was approved in 2

weeks now we are waiting on back pay from the time that we applied.  Did you

apply online or at your local office, I have heard that when you do it online it

gets " lost " a lot.

From: Brit <spinachbreath@...>

Subject: [ ] Re: Apraxia and SSI

Date: Tuesday, March 1, 2011, 5:30 PM

We applied and met the income requirements, but were denied. We appealed and

were again denied....my son seems to fit the criteria, but I'm done fighting

it....I don't feel like going to court over it, which would be the next step.

Best of luck, I have heard that some children with apraxia DO get it!

-Brittany

>

> I was wondering if anyone has applied for SSI Disability for Speech Apraxia to

help pay for the therapy etc. If you were successful or unsuccessful please

share your experience with this.

>

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Guest guest

> >

> > I was wondering if anyone has applied for SSI Disability for Speech Apraxia

to help pay for the therapy etc. If you were successful or unsuccessful please

share your experience with this.

> >

>My daughter is apraxic also. Are there other diagnoses that your child has

recieved? If the child has other disorders(my daughter is also autistic,ADHD,and

behavioral issues),that would help. If you need lawyer help, there are pro-bono

ssi lawyers that will help.(they get paid if you do)

Dawn

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Hmmmm..there are some good stories! Maybe I should re-visit the idea!

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Guest guest

We were very thorough on his questionnaires and all the drs/therapists were in

agreement that he had apraxia. He did their SS evals and those drs. didn't give

him a diagnosis, but his scores were super low, supporting our statements. I

applied in office and appealed in office as well. I also detailed his sensory

and ADHD issues (which ADHD in itself is said to be a possible way to receive

SSI). I know that a lot of it is on who actually reads your info, which is why I

appealed it with high hopes and explained his issues verrrrry thoroughly so that

if the person reading didn't know anything about speech/sensory/apraxia issues,

they could still get the whole picture. I'm not sure why we didn't get it (aside

from their silly statement that even though it appears that he does have some

delays, they seem age appropriate...huh?! I've never heard of an average 3 year

old not being able to communicate), but I have heard that it's not THAT easy to

get, so I'm really happy to hear that some of you HAVE gotten it! I only wish

that WE could be one of those stories...we can't afford additional therapy from

what the school is providing right now and the NV/fish oil takes a lot out of

our money as well (we are a single income family of 5). My husband has a job

interview for a higher paying job next week (not that his now is bad, we just

have so many expenses!), so please keep us in your prayers!!

Thanks,

Brittany

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to help pay for the therapy etc. If you were successful or unsuccessful please

share your experience with this.

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Guest guest

I'm sorry that you had so much trouble.  Are you able to apply again?  maybe

someone else will be assigned to your case? I feel your pain, we are also a

family of 5 on 1 income. I was terribly upset when we had to stop seeing his

private therapist  because we couldn't afford it.  She was the one who was

helping him.  We managed to see her for just over 3 months using our tax refund

from last year to pay for it and stopped when I didn't have money left to buy

food.  There has been progress since but not at nearly the rate he was

progressing with her.

Another thing that i did was kind of talk up my doctors and therapists at every

visit about hoping he would get SSD.  Or therapist through school district

seemed to be against it and said " do you really think it's necessary "   I told

her that the reason why we are in early intervention is because the earlier my

son gets help the better he will do through out his life.  If he gets SSD he

can receive more therapy including during the summer and that is detrimental to

his improvement.  I could see her attitude change after that.  My pediatrician

also told me that she would do/give me anything she could to help me help my

son.  I made sure that everyone was on my side before SS sent out their forms

to my doctors and therapists.  Maybe you did that as well, I am just trying to

think of everything that I did to my son get approved. 

If you do get him approved you could also try to get back pay to the 1st time

you applied.

Did you question them about how he could be age appropriate and have delays?

-I just remembered that I wrote a lot about how it affects our home life because

he screams for hours everyday from frustration because we don't know what he

wants or needs.

From: Brit <spinachbreath@...>

Subject: [ ] Re: Apraxia and SSI

Date: Wednesday, March 2, 2011, 8:49 AM

We were very thorough on his questionnaires and all the drs/therapists

were in agreement that he had apraxia. He did their SS evals and those drs.

didn't give him a diagnosis, but his scores were super low, supporting our

statements. I applied in office and appealed in office as well. I also detailed

his sensory and ADHD issues (which ADHD in itself is said to be a possible way

to receive SSI). I know that a lot of it is on who actually reads your info,

which is why I appealed it with high hopes and explained his issues verrrrry

thoroughly so that if the person reading didn't know anything about

speech/sensory/apraxia issues, they could still get the whole picture. I'm not

sure why we didn't get it (aside from their silly statement that even though it

appears that he does have some delays, they seem age appropriate...huh?! I've

never heard of an average 3 year old not being able to communicate), but I have

heard that it's not THAT easy to get, so

I'm really happy to hear that some of you HAVE gotten it! I only wish that WE

could be one of those stories...we can't afford additional therapy from what the

school is providing right now and the NV/fish oil takes a lot out of our money

as well (we are a single income family of 5). My husband has a job interview for

a higher paying job next week (not that his now is bad, we just have so many

expenses!), so please keep us in your prayers!!

Thanks,

Brittany

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to help pay for the therapy etc. If you were successful or unsuccessful please

share your experience with this.

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Guest guest

Janel,

Thanks for the advice :-) Not much time to respond right now, but I wanted you

to know I saw your message.

Unfortunately, we DID do all of that...I spent countless hours filling out

paperwork and going back over it and reading other people's stories online about

what they did to get SSI. We did appeal once already and the next appeal would

be going to court, which I am not up for. I had talked to all of his therapists

and doctors and everyone was on board and several even wrote me extra letters to

send in with my appeal....our ST even wrote a very detailed letter that outlined

their first decision and explained why everything they said meant that he really

did have a disability....still obviously didn't help....grrrrr! I spent so much

time on it and he IS affected every day! Anyway, end rant. I am glad to see that

others have been able to get it.

-Brittany

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Guest guest

Sounds like you did everything right.  It's not right that some get approved

and others don't.  Try again and maybe other people will review your

case...hopefully!

From: Brit <spinachbreath@...>

Subject: [ ] Re: Apraxia and SSI

Date: Thursday, March 3, 2011, 7:50 AM

 

Janel,

Thanks for the advice :-) Not much time to respond right now, but I wanted you

to know I saw your message.

Unfortunately, we DID do all of that...I spent countless hours filling out

paperwork and going back over it and reading other people's stories online about

what they did to get SSI. We did appeal once already and the next appeal would

be going to court, which I am not up for. I had talked to all of his therapists

and doctors and everyone was on board and several even wrote me extra letters to

send in with my appeal....our ST even wrote a very detailed letter that outlined

their first decision and explained why everything they said meant that he really

did have a disability....still obviously didn't help....grrrrr! I spent so much

time on it and he IS affected every day! Anyway, end rant. I am glad to see that

others have been able to get it.

-Brittany

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