Jump to content
RemedySpot.com

Disability?

Rate this topic


Guest guest

Recommended Posts

I'm pretty new to all of this, but if it is preventing

you from being able to work I believe you can. I'm

really trying to figure out where I found that

information and as soon as I do I will pass it on.

=====

(^) (^) (^) \(/,,,, ,\( /,,, ,\(/,,,,

BETHANNE

AIH 9/01

30 pred/50 imuran

__________________________________________________

Link to comment
Share on other sites

Yes! My disability was approved for AIH. I have to be reapproved every 6

months.

My doctor encouraged me to apply for disability and I struggled with

thinking of myself as " disabled " . I finally came to terms with it when I

thought of myself having an " inability " to work just now.

Sue (Oregon)

[ ] Disability?

Can you get disability with having AIH?

Link to comment
Share on other sites

you can get disability with any condition thatmakes you unable to

work.............short term disability....almost anything. (usually a state

funded program) SSD- social security disability....you have to be out of work

more than 6 months. you can only start collecting at 6 months. You can file

as soon sa you know. My docs told me work would be imposible (long

term...polite way od saying almost never) I applied then , was turned down

once, gave it to a disability lawyerand by the time he was through I reieved

a nice size check with the back months paid to. SSD pays from the time you

file, so it pays not to wait.

I sure hope this is clear, cause it's one ot those mornings that the brain

farts are having a ball!

Judie

Link to comment
Share on other sites

  • 2 years later...

i had insurance when my rheumi helped me get disability. i was denied the

first round, but approved as soon as i aquired an atty that only collects if

they

win for you. it only took me six mos. i was 42. check with the state or

county clinic. they might have a long wait time. good luck kathy in il

Link to comment
Share on other sites

When I was trying to get disability, I went to an attorney that specializes

in that field. At the end of my interview, I asked her, " What can you do for

me that I can't do for myself? " She said that she knew what papers to fill

out when I'm denied. I already knew that, so I left her to rip off the next

poor uninformed. As far as I know, there's nothing a lawyer can do that you

can't do for yourself, but they still get a large portion of your badly

needed money for doing essentially nothing!

The basic steps are:

Apply for disability- If you're not dying within a year, you're denied in

most cases.

Apply for reconsideration- At this point they actually look at your

appliction and medical info.

Apply for a judicial decision- This is your only time to really convince

them on a personal level.

If these steps don't work, you start over again....

Dennis

Re: [ ] disability?

>

> i had insurance when my rheumi helped me get disability. i was denied the

> first round, but approved as soon as i aquired an atty that only collects

> if they

> win for you. it only took me six mos. i was 42. check with the state or

> county clinic. they might have a long wait time. good luck kathy in il

>

Link to comment
Share on other sites

I've been on Social Security Disability since 1991, and it took 2 years to

get it. The process has changed since then. All we had at the judicial

appeal were a federal judge, his assistant, and me, my wife, and daughter.

Now, as I understand it, there is a judge, an employment specialist, and a

physical therapist (I think). They do have all bases covered, and you'll

have to have your doctor's favor on your side. It takes persistance. The

only thing that saved us was that we built our house out of our pockets and

didn't have a mortgage.

As for medical care, it depends on your assets and income. If you can prove

you're living below the poverty level, you can be taken care of by using

state medicade while waiting for medicare. If you need to see a doctor, go

to the emergency room. A doctor (of some kind) will examine you free through

the indigent care program, but you still have to pay for all prescriptions.

That's what I know it to be, your mileage may vary.

Dennis

[ ] disability?

>

>

>

> Is anyone in here on disability? Since I don't have insurance at the

> moment, I can't afford to go to a rheumatologist and get on

> medication. So, I'm getting by on ibuprofen which may not even be

> helping much, but I'm afraid to stop taking it to find out! There is

> no way I could hold a job right now...I have so much pain and some

> days can hardly walk! I was just wondering if there is any help out

> there for people in my situation...and how difficult is it to get on

> disability?

>

>

>

>

>

>

>

>

>

>

Link to comment
Share on other sites

Im not quite sure what all of the circumstances of you situation are.

But, I can definately relate to getting sick with RA at a time i

didnt have healthcare insurance, which now makes me medically

unisurable.

I saught out medical care at a teaching hospital. Almost any

institution that trains medical doctors has a " residents clinic.

Usually, they will only charge you a percentage of the cost,

depending on your income. They may aslo have " sample " drugs to help

decrease the cost. The quality of care I have gotten has been

exceptional.

One of the first things they told me to do was to apply for SS

Disability. You can do all of it online, if your comfortable with

that, I think it is www.socialsecurity.gov ,

All that said, I submitted my application and was turned down 4

months later. I was told by many people you dont have to hire a

lawyer to file an appeal, but the chances of winning the appeal are

better with a lawyer. It took me a year and a half to finally get an

appeals hearing, then 120 days to get the judges descision. I got a

favorable decision and it is retroactive back to Feb of 2002, so

Medicare should also be in effect for me. However, I have not seen or

heard anything from SS yet, and its another 100 days after the apeals

decision.

So nearly three years into this im still waiting. But, now that I

have gotten the motivation to type tonihgt, I think the next letter

will be to my senator. I hope at least a little bit of this helps

Larry

SUPPORT , " " <Havenwood86@c...> wrote:

>

>

> Is anyone in here on disability? Since I don't have insurance at the

> moment, I can't afford to go to a rheumatologist and get on

> medication. So, I'm getting by on ibuprofen which may not even be

> helping much, but I'm afraid to stop taking it to find out! There is

> no way I could hold a job right now...I have so much pain and some

> days can hardly walk! I was just wondering if there is any help out

> there for people in my situation...and how difficult is it to get on

> disability?

Link to comment
Share on other sites

Can you get on Medicaid? That would give you the medicine or money needed

for RXs.

and for Doctor bills. Meanwhile submit to social security disability, that

takes a while.

Good luck.

Colletti

Link to comment
Share on other sites

Age makes a difference, too. I was close to 50 and got it first time. I was told

if two or

more weight bearing joints (bilaterally) are affected it's easier and your

vocation. I was

a nurse so it was deemed unsafe for me to work anymore. Though I really couldn't

work anymore I almost felt guilty because I knew so many people that had to

appeal

(and usually got it then). Most people will tell you to plan on getting turned

down the

first time.

JaninIowa

> When I was trying to get disability, I went to an attorney that specializes

> in that field. At the end of my interview, I asked her, " What can you do for

> me that I can't do for myself? " She said that she knew what papers to fill

> out when I'm denied. I already knew that, so I left her to rip off the next

> poor uninformed. As far as I know, there's nothing a lawyer can do that you

> can't do for yourself, but they still get a large portion of your badly

> needed money for doing essentially nothing!

>

> The basic steps are:

> Apply for disability- If you're not dying within a year, you're denied in

> most cases.

> Apply for reconsideration- At this point they actually look at your

> appliction and medical info.

> Apply for a judicial decision- This is your only time to really convince

> them on a personal level.

> If these steps don't work, you start over again....

>

> Dennis

>

> Re: [ ] disability?

>

>

> >

> > i had insurance when my rheumi helped me get disability. i was denied the

> > first round, but approved as soon as i aquired an atty that only collects

> > if they

> > win for you. it only took me six mos. i was 42. check with the state or

> > county clinic. they might have a long wait time. good luck kathy in il

> >

Link to comment
Share on other sites

Thanks Jan and everyone who replied to my question about disability! I

am in the process of filling out the forms now...keeping my fingers

crossed!

> > When I was trying to get disability, I went to an attorney that

specializes

> > in that field. At the end of my interview, I asked her, " What can

you do for

> > me that I can't do for myself? " She said that she knew what papers

to fill

> > out when I'm denied. I already knew that, so I left her to rip off

the next

> > poor uninformed. As far as I know, there's nothing a lawyer can do

that you

> > can't do for yourself, but they still get a large portion of your

badly

> > needed money for doing essentially nothing!

> >

> > The basic steps are:

> > Apply for disability- If you're not dying within a year, you're

denied in

> > most cases.

> > Apply for reconsideration- At this point they actually look at your

> > appliction and medical info.

> > Apply for a judicial decision- This is your only time to really

convince

> > them on a personal level.

> > If these steps don't work, you start over again....

> >

> > Dennis

> >

> > Re: [ ] disability?

> >

> >

> > >

> > > i had insurance when my rheumi helped me get disability. i was

denied the

> > > first round, but approved as soon as i aquired an atty that only

collects

> > > if they

> > > win for you. it only took me six mos. i was 42. check with the

state or

> > > county clinic. they might have a long wait time. good luck kathy

in il

> > >

Link to comment
Share on other sites

Good luck ! I am 41 years old, and I am on disability. I

applied, and received it the first time, but it took a year. You

just have to have faith, and don't give up. Big hugs, and prayers, T

> > > When I was trying to get disability, I went to an attorney that

> specializes

> > > in that field. At the end of my interview, I asked her, " What

can

> you do for

> > > me that I can't do for myself? " She said that she knew what

papers

> to fill

> > > out when I'm denied. I already knew that, so I left her to rip

off

> the next

> > > poor uninformed. As far as I know, there's nothing a lawyer can

do

> that you

> > > can't do for yourself, but they still get a large portion of

your

> badly

> > > needed money for doing essentially nothing!

> > >

> > > The basic steps are:

> > > Apply for disability- If you're not dying within a year, you're

> denied in

> > > most cases.

> > > Apply for reconsideration- At this point they actually look at

your

> > > appliction and medical info.

> > > Apply for a judicial decision- This is your only time to really

> convince

> > > them on a personal level.

> > > If these steps don't work, you start over again....

> > >

> > > Dennis

> > >

> > > Re: [ ] disability?

> > >

> > >

> > > >

> > > > i had insurance when my rheumi helped me get disability. i was

> denied the

> > > > first round, but approved as soon as i aquired an atty that

only

> collects

> > > > if they

> > > > win for you. it only took me six mos. i was 42. check with the

> state or

> > > > county clinic. they might have a long wait time. good luck

kathy

> in il

> > > >

Link to comment
Share on other sites

  • 5 years later...

Just wondering if anyone here is on or has applied for social security

disability? I haven't been able to work for over a year, let alone function in

daily activities. I have applied for disability, but everyone I have talked to

says I will get denied no matter what the first time. I truly need it right now,

and was wondering if anyone has any tips or is on it?

Thank you

Bridget

Link to comment
Share on other sites

My best tip: Get a lawyer who specializes in this stuff. Don't even mess around

trying to do it on your own.

Everybody I've ever heard talk about this, on this list and others through the

years, validates this conclusion. The people who got lawyers went through the

process calmly, with very little hassle, and (after the requisite number of

appeals) got everything coming to them in the end. The ones who didn't found

themselves running around trying to take care of endless details, were

shamelessly jerked around the by system, never felt entirely aware of what was

going on, and often didn't get all of what they deserved when it finally got

resolved.

Another tip: the people who were successful in the past were usually the ones

who didn't drag Lyme into it at all (since chronic Lyme is such an iffy

diagnosis from the " official " POV). The main thing is to document your specific

symptoms disabilities: you can't think, you're always tired, etc. etc. Doesn't

matter what causes these problems; what does matter is that you can prove that

you have them.

Let your doctors (both LLMD and GP) know on your next visit that you're building

an SSD case. They can start the process of noting your disabilities in your file

(they know how to do this), so you'll have the documentation on hand when the

lawyer asks for it.

Sara

On Dec 31, 2009, at 11:55 25AM, bridget wrote:

> Just wondering if anyone here is on or has applied for social security

disability? I haven't been able to work for over a year, let alone function in

daily activities. I have applied for disability, but everyone I have talked to

says I will get denied no matter what the first time. I truly need it right now,

and was wondering if anyone has any tips or is on it?

> Thank you

> Bridget

>

>

>

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

>

> Lyme Disease News continually updated from thousands of sources around the

> net: http://www.topix.net/health/lyme-disease

>

> MedWorm: The latest items on: Lyme Disease

> http://tinyurl.com/23dgy8

>

Link to comment
Share on other sites

Thank you Sara!

Bridget

>

> > Just wondering if anyone here is on or has applied for social security

disability? I haven't been able to work for over a year, let alone function in

daily activities. I have applied for disability, but everyone I have talked to

says I will get denied no matter what the first time. I truly need it right now,

and was wondering if anyone has any tips or is on it?

> > Thank you

> > Bridget

> >

> >

> >

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

> >

> > Lyme Disease News continually updated from thousands of sources around the

> > net: http://www.topix.net/health/lyme-disease

> >

> > MedWorm: The latest items on: Lyme Disease

> > http://tinyurl.com/23dgy8

> >

Link to comment
Share on other sites

  • 10 months later...

My husband has had numberous surgery for ctoma and has lost most of his hearing in his right ear. We haven't applied for disability through SSI because we've been told he wouldn't qualify. He presently is on long term disability from the side effects of a fistula in his ear. This is rare but it does happen. He had vertigo extremely bad and wasn't able to drive. He now has vertigo but since his last surgery, he is able to drive. He will never be able to return to his old job but we are hoping he may be retrained for a job that this won't interfere with. (not sure what that is presently)

I would love to hear how others are coping with the after effects of ctoma and fistula.

From: jlowe684 <jblakey684@...>cholesteatoma Sent: Sat, November 27, 2010 10:02:30 PMSubject: Disability?

Hi all. I have suffered from ctoma my whole life. It went undiagnosed for the first 10 years, the doctors just treated recurring ear infections, until I had a CT scan and they found it. I have since had 6 surgeries on it, my last one was on 11/10/10. Everytime I explain my situation to someone, one of the first questions they ask is "Why aren't you on disability for that?" It's not really something I've ever put a lot of thought into, and lately I've been thinking more about it. I just wanted to find out if anyone else out there gets disability benefits from this disease. I don't want to try to cheat the system and get something I shouldn't get, so if I don't qualify for it, then that's ok. But I know I've suffered a lot, and according to my doctor, I'm probably going to suffer a lot more, and it's never going to go away.

Link to comment
Share on other sites

Hi, I am in the same boat. My C-Toma went misdiagnosed for 12 years. I had it

removed back in 2005 but I still get a lot of pain most days in my right ear and

some days in my left ear as well. My C-Toma was in my right ear, my hearing in

that ear is at 40% and my right ear was 60% last time I had it tested. I get

dizzy a lot sometimes too and have been trying to get on disability since 2007.

I used to work for Sprint as a Customer Service Rep., but I cannot do that

anymore because the headphones hurt my ears really bad after just an hour of

using them. I have had to call in sick like crazy because of the pain I get

which at times is so bad that I just take aspirin or ibprofin and try to go back

to bed. If I get water in my right ear then it makes it hurt bad too and gets

me dizzy as well. Changes in the weather seem to make it bad too it is just

crazy. I have seen a judge and had a lawyer to help try and was denied for SSI

now I appealed it and everyone even my doctor says I should be on disability. I

cannot do the things I used to do. Having this is nowhere near right and the

judges just don't think ear trouble is a disability. I will tell you now that

even though I wouldn't wish this on even my worst enemy, but I would still like

them to be able to understand what some of us go through afterwards, not

anywhere near all, but some. I have been told by my doctor that nothing is

wrong with my right ear from the looks of it and the ent's cannot see anything

wrong yet the pain is still there, so my doctor believes it is probably nerve

damage. This all started for me when I was 13 or 14 when my stepdad poured

boiling peroxide into my right ear. Good luck if you try to get on disability

with this, I for one am going to keep trying. Oh yeah I cannot even use

eardrops because those get me dizzy too :( Try to take care and Happy Holidays.

Skaggs aka BOWLINGNINJA

>

> My husband has had numberous surgery for ctoma and has lost most of his

hearing

> in his right ear.  We haven't applied for disability through SSI because

we've

> been told he wouldn't qualify.  He presently is on long term disability from

the

> side effects of a fistula in his ear.  This is rare but it does happen.  He

had

> vertigo extremely bad and wasn't able to drive.  He now has vertigo but

since

> his last surgery, he is able to drive.  He will never be able to return to

his

> old job but we are hoping he may be retrained for a job that this won't

> interfere with.  (not sure what that is presently) 

>

>

> I would love to hear how others are coping with the after effects of ctoma and

> fistula. 

>

>

>

>

>

> ________________________________

> From: jlowe684 <jblakey684@...>

> cholesteatoma

> Sent: Sat, November 27, 2010 10:02:30 PM

> Subject: Disability?

>

>  

> Hi all. I have suffered from ctoma my whole life. It went undiagnosed for the

> first 10 years, the doctors just treated recurring ear infections, until I had

a

> CT scan and they found it. I have since had 6 surgeries on it, my last one was

> on 11/10/10. Everytime I explain my situation to someone, one of the first

> questions they ask is " Why aren't you on disability for that? " It's not really

> something I've ever put a lot of thought into, and lately I've been thinking

> more about it. I just wanted to find out if anyone else out there gets

> disability benefits from this disease. I don't want to try to cheat the system

> and get something I shouldn't get, so if I don't qualify for it, then that's

ok.

> But I know I've suffered a lot, and according to my doctor, I'm probably going

> to suffer a lot more, and it's never going to go away.

>

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...