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, I had the same problem with SSD but hired a lawyer who

specialized in such cases. Once a judge reviewed my records and my

own reasons for asking for disability, he changed his mind before we

even appeared before him. I've been on SSD for one year now.

I was a college professor, driving for over one hour one way before

daylight and could not feel the gas pedal or brakes beneath my feet.

Plus, I was almost falling asleep while driving. My head tended to

fall forward and I had to " prop " my head a lot, not looking

professional at all. I sat most of the time because I could not stand

for very long, or I would tend to lose my balance. I had to move from

building to building across campus, making it a slow and tiresome

process while subject to tripping and falling on the broken & uneven

sidewalks. All this information (of course I was checked out by

independent examiners and phychologists to see if this were true) with

my medical records helped me win my case.

I also have a problem that no one else I know of with CMT seems to

have--I have a lot of memory loss. I'm having problems typing,

spelling, remembering names, etc. No, I do not have Alzheimer's.

Keep trying, .

Joe

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In response to everyone trying or who has gotten disability, I'm finally in

the process of writing a letter to " Whom It May Concern " and since I'm

having trouble with my family records since my parents died while I was

still a teenager, I remembered a picture taken when I was about 8 or so with

my parents and my father had a cane. I remember him being a handsome man,

but did wonder why he couldn't do alot of things other dads did. I'm going

to enclose a copy of this with my letter. Point being, anything I can

remember from when I was growing up I assume would help with their decision

whether or not I'm worthy, in their eyes, for disability. It's been almost

exactly a year now since I went to the ER with no feeling in my hand

thinking I had a stroke, then a long depression period, but I know I have to

get my butt in gear and get this done. I'm starting to lose my balance more

at work and blame it on the mats on the floor, but that's not it.

I guess the more you give them from the get go, the better off. My biggest

worry is how to explain how I can work, it's only about 25 hrs a week, even

though I know it's getting harder, then have someone question me about

something they don't understand. Like being between a rock and a hard

place.

Good luck everyone.

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Thanks Jim,

I think I'm intimidated by people when they look at me and think " How can she be

in pain, she looks normal to me? " ..I need to stand up for myself. My

neurologist has me down as 100% disabled right after she took the 3 hr. nerve

test last year. I would think that's good enough. Thanks again.

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,

Don't give up, keep applying. I am sure you will eventually be approved. And

once you are your first check will be from the 7th month of the lst

application. It can be very discouraging. Make sure you make a copy of

everything you

fill out. They check those papers over and against each other. That way you

got the same answers to all their questions that they ask 50 differant ways.

Also did you look over and list any of those items that I had sent a while

back of things I have trouble with. If you printed it off, go over that list

again next time you fill out more paper work. It will help. I know, I've been

there.

Elaine

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,

Tthis is a struggle for many with disabilities. It's like the people who get

yelled at who use handicapped spaces and look perfectly okay, but would get too

exhausted from a variety of diseases if they parked in regular spots. I work

with people with severe mental illnesses.

Although many " appear " mentally ill, many more have no outward appearing

disabilities and face many questions from even family as to how they qualify for

help.

And yes, your neurologist's certifying you as 100% disabled will help

immensely. The hard part is getting her to complete the forms Social

Security and others will send her thoroughly and getting her office

staff to send in records quickly.

Again, good luck.

Jim

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Geez ,

I don't know if its in the files. I just looked here on my computer and it's

not in mine, I dont know why but its not. It was sent I believe with a heading

of " things I have problems with " .

Elaine

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Hi ,

It took me 4 years before I finaly recived my SSD the first hearing the judge

didn't even want to look at the info my lawyer got on CMT plus I was 32 at the

time but at the second hearing the judge was more

interested in my CMT and she took the info from my lawyer and I won. But I also

hurt my back at work so I was on workers comp but with WC you only have to prove

you can't do the same job you were doing SSD you have to prove you can't work at

all they even go by how educated you are if you went to collage and have a

degree they take that into consideration. I was a comstruction worker and I

droped out of school in the 9th grade so they take all that into consideration.

Good luck and don't give up I don't know how long you have been fighting but

after you win it's well worth it take it from me after 4 years of fighting to

get it.

Tommy

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Get employment records where employer states he was or is carring you and that

because of your disease you did 50% less production than co-workers with same

job. Also list all drugs you take, dosage and amount of misery without them.

Call local and national ss #'s and explain disease, make folder and get to

everyone in SSA including director. After I did this I was approved in less than

30 days. Get to know SSA workers and tell all your prediciment. One told me I

was the first to get 100% disability for teeth problems. EDUCATE THEM!!!!

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:

I sent you some ideas on how to get approved for disability. I was approved 30

days after my 1st application. My file was also sent to a review group,like an

IRS audit, and they changed my actual disability

date to 3 months earlier. I still had to wait 5 months for my first check of

$1446.00 per month but over the next 2 months. I got 3 extra checks besides my

regular monthy check.

I filed as soon as my employer had to let me go and he followed the rules that

stated that I was not to see the letter. Even though I made $32,000.00 a year

the letter had to say I only gave value of less than,I think, $8200.00 per yr at

that time. (2000).

Also I did not do any correspondence by e-mail, I sent every thing in large

padded envelopes marked, OFFICIAL BUSINESS OPEN IMMEDIATELY, stamped in red with

a stamp I went by my old office and borrowed.

I went and saw and called my caseworker so much that I finally got the tel# of

the person who was on the commitee that actually made the decision about my

fate.

I called her so much and flirted and told her how awed I was with her great

responsibility and explained all about my disease, the falling,

unfelt injuries, the pain, the humiliation of not being what I

was befpre, the drugs etc.

She got to think of me as a person and finally told me that I was approved even

though she was not allowed to give out that info

also that I was picked for review. She was in Austin, TX. and the

review was in Baltimore. I sat here in San Angelo, TX for two months

worried sick until I got the official letter.

MY advice is be thorough, charming, persistent and pray alot.JC did more at a

better price than any lawyer can. I wish I could teach you TEXAS respect, charm,

manners and old boy dumb,(really), with but you get the message. GOOD LUCK AND

GOD'S SPEED.

Blanek

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  • 5 months later...

With the experience I had with SSI and didn't go on the basis of my CMT, it is

very discouraging. Besides all the information you can find with this group, I

would suggest you emphasize HSMN (aka CMT) to them and SPELL it out. Hereditary

Sensor and Motor Neuropathy, meaning it is a slow progession of the nervous

system dying. SSDI has a thing that you must be on your deathbed to receive it.

Good Luck in the days ahead.

Debbie

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  • 4 months later...

Depending on what state you live in and what you do, it is very difficult to

prove discrimination. The state I live in is a " Right to Work " state, meaning

that it is very non-union, and all employers have the right to fire you for

anything they wish. I got fired once because i stayed at work for 22 straight

hours, even tho ther e was no one else there when any of the shifts changed, and

the state labor board refused to help me. As far as SSD, that is federal, tho

the separate states have Disability determination boards that regulate and

decide who is disabled. RA is on the list of diseases that qualify you as

disabled. My cousin got the first time she applied because she has RA, and she

was only about 20 then. I suggest finding a lawyer who gets paid on a

contingency basis- no-win/no fee. Social Security puts a cap on how much they

get paid to help you get your benefits. Also, if your lawyer isn't no-win, no

fee, being a government case, they are not allowed to charge you more than

25% of the settlement. I believe the SSA office in your area has a list of

lawyers. It is usually at least 6 mos before you hear anything at all about your

case after you file, because they are always so backed up. I have been fighting

for it for 2 years now, and just had my hearing in Dec., then the judge decided

I needed another eye exam. It will be another month or more before I have a

decision, but the way I understand it, most of the people who go to hearing get

their benefits. So start with the phone book.

Sorry such a long post. Good Luck!!

Jane

So Shy <so_shy234@...> wrote:

I was hoping that maybe someone might be able to offer some advice to

me. I have just applied for social security disability. I had been

working part time for the last couple of years and prior to that full

time for the same company for several years. Since my diagnosis of RA

almost 2 1/2 years ago I was constantly being treated horribly by my

boss and my co-workers. I finally couldn't take it anymore and I

walked off my job last September. I've spoken to numerous lawyers who

have said there isn't anything I can do because I have no proof that it

had anything to do with my disability. Needless to say, I started

looking for another job but soon realized that I have so many

limitations that it'd be difficult to find anything that would be

willing to accomodate me. I have days that I can't use this hand or

the other. Sometimes I have difficulty talking, other days walking,

not to mention being tired, having to take naps, and if I get an

infection being taken off my meds(enbrel & methotrexate)then having to

start over again. It's not all the time but it is at least once a week.

I've talked to my doctor about social security and he says I may have

difficulty getting it cause I'm so young....I'm 36.

Can anyone give me some advice what to do? I'd appreciate any

suggestions.

Sincerely,

o and missed some work due to dealing with side effects of medication

and lack of mobility. It was shortly after being diagnosed and having

limitations that my position was cut to part time....coincidence, can't

say that it was. I tolerated quite a bit from my employer for the next

couple of years and last may I was hospitalized for a week because of

extreme pain in my hip and the inability to walk. September last year I

was taken off of all my arthritis medication because of an infr

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All I can say is good luck am finally near the end of this mess myself and it

has taken three years. They said I was too young and I was 46.

My best suggestion is , realize this will take awhile, and get a lawyer who

specializes in SS/ My will work with no money up front and 25 percent of

settlement/

I use binder and binder in New York. in WI

So Shy <so_shy234@...> wrote:

I was hoping that maybe someone might be able to offer some advice to

me. I have just applied for social security disability. I had been

working part time for the last couple of years and prior to that full

time for the same company for several years. Since my diagnosis of RA

almost 2 1/2 years ago I was constantly being treated horribly by my

boss and my co-workers. I finally couldn't take it anymore and I

walked off my job last September. I've spoken to numerous lawyers who

have said there isn't anything I can do because I have no proof that it

had anything to do with my disability. Needless to say, I started

looking for another job but soon realized that I have so many

limitations that it'd be difficult to find anything that would be

willing to accomodate me. I have days that I can't use this hand or

the other. Sometimes I have difficulty talking, other days walking,

not to mention being tired, having to take naps, and if I get an

infection being taken off my meds(enbrel & methotrexate)then having to

start over again. It's not all the time but it is at least once a week.

I've talked to my doctor about social security and he says I may have

difficulty getting it cause I'm so young....I'm 36.

Can anyone give me some advice what to do? I'd appreciate any

suggestions.

Sincerely,

o and missed some work due to dealing with side effects of medication

and lack of mobility. It was shortly after being diagnosed and having

limitations that my position was cut to part time....coincidence, can't

say that it was. I tolerated quite a bit from my employer for the next

couple of years and last may I was hospitalized for a week because of

extreme pain in my hip and the inability to walk. September last year I

was taken off of all my arthritis medication because of an infr

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I was 30 years old when I applied for SSDI and I got it on the first try. I

included letters from all my doctors, shrinks, meds I have been on, ANY

hospitalizations and I also included letters from friends. My worker had a

theory... Whose ever file was the fattest that day got approved. I don't know

if

this helps any but that's my scoop.

*Soft Hugs*

Stina

Fibromyalgia Awareness

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hi... I myself filed for ss disability a few yrs back.... I was basically forced

to do it because of social services... see i was working part time but not

enough hours for them... i was getting food stamps cause of kids, and had

medical which i can get no matter what... they are cutting programs so bad that

they made me go thru all the paper work for it... even knowing i made just a lil

too much... worse thing i ever went thru.... and MY JOB..... im so lucky cause

they totally understand and work with me for whatever the day brings me.... You

cant find jobs like that out there... so i am very lucky but dont understand how

they dont give the benifits to those who .... gee..... need it real bad!!!! I

was told when my hours got under a few to go back and then they would help me

cause i made 60 to much...That was a long 8 months goin thru that hassle... and

when i lose the job i have, i will have no choice , i will have to have a

lawyer... sucks but dont see another way around it....

when ya cant do it, ya cant do it.... period

---------------------------------

Bring words and photos together (easily) with

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, your doctor has a lot to do with your getting SSD. The one you are using

right now sounds like the type you don't want. The important thing for you is to

know yu aren't employable, that you cannot sell yourself as a worker, and have a

doctor that will back you on it. SSD rules change by area of the country and the

mood of the latest government. Usually, if your ailment is not life-threatening,

they disallow your application just so you might give up and save the taxpayers

some money. It will take time and a bit of work on your part. Above all, keep a

daily record of your abilities/disabilities each day, from not being able to

walk to not opening a jar or feed yurself, etc... Document everything you can

for the record, it'll come in handy. You should be able to get statements from

yur part-time employers about how it affects your work for them, that will help.

Furthermore, don't just give up and call it hopeless. That's what the Feds are

looking for, a way to keep you off the rolls. It can be tough but hang in there

and don't give up.

Dennis- BTDT

[ ] Social Security Disability

I was hoping that maybe someone might be able to offer some advice to

me. I have just applied for social security disability. I had been

working part time for the last couple of years and prior to that full

time for the same company for several years. Since my diagnosis of RA

almost 2 1/2 years ago I was constantly being treated horribly by my

boss and my co-workers. I finally couldn't take it anymore and I

walked off my job last September. I've spoken to numerous lawyers who

have said there isn't anything I can do because I have no proof that it

had anything to do with my disability. Needless to say, I started

looking for another job but soon realized that I have so many

limitations that it'd be difficult to find anything that would be

willing to accomodate me. I have days that I can't use this hand or

the other. Sometimes I have difficulty talking, other days walking,

not to mention being tired, having to take naps, and if I get an

infection being taken off my meds(enbrel & methotrexate)then having to

start over again. It's not all the time but it is at least once a week.

I've talked to my doctor about social security and he says I may have

difficulty getting it cause I'm so young....I'm 36.

Can anyone give me some advice what to do? I'd appreciate any

suggestions.

Sincerely,

o and missed some work due to dealing with side effects of medication

and lack of mobility. It was shortly after being diagnosed and having

limitations that my position was cut to part time....coincidence, can't

say that it was. I tolerated quite a bit from my employer for the next

couple of years and last may I was hospitalized for a week because of

extreme pain in my hip and the inability to walk. September last year I

was taken off of all my arthritis medication because of an infr

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>

> I was hoping that maybe someone might be able to offer some advice

to

> me. I have just applied for social security disability. I had

been

> working part time for the last couple of years and prior to that

full

> time for the same company for several years. Since my diagnosis of

RA

> almost 2 1/2 years ago I was constantly being treated horribly by

my

> boss and my co-workers. I finally couldn't take it anymore and I

> walked off my job last September. I've spoken to numerous lawyers

who

> have said there isn't anything I can do because I have no proof

that it

> had anything to do with my disability. Needless to say, I started

> looking for another job but soon realized that I have so many

> limitations that it'd be difficult to find anything that would be

> willing to accomodate me. I have days that I can't use this hand

or

> the other. Sometimes I have difficulty talking, other days

walking,

> not to mention being tired, having to take naps, and if I get an

> infection being taken off my meds(enbrel & methotrexate)then having

to

> start over again. It's not all the time but it is at least once a

week.

>

> I've talked to my doctor about social security and he says I may

have

> difficulty getting it cause I'm so young....I'm 36.

>

> Can anyone give me some advice what to do? I'd appreciate any

> suggestions.

>

> Sincerely,

>

>

>

>

>

> o and missed some work due to dealing with side effects of

medication

> and lack of mobility. It was shortly after being diagnosed and

having

> limitations that my position was cut to part time....coincidence,

can't

> say that it was. I tolerated quite a bit from my employer for the

next

> couple of years and last may I was hospitalized for a week because

of

> extreme pain in my hip and the inability to walk. September last

year I

> was taken off of all my arthritis medication because of an infr

>

Hi ---I am in a very similar situation. I have only been

able to work part-time for the past four years not only due to pain/

med. side-effects; but also the ever present fatigue. I recently have

had increasing neck and shoulder pain; had an MRI that showed alot of

damage in my cervical spine. I am a Physical Therapist, so the

constant exercise, up & down from the mat, and esp. lifting has

really done me in. Now I just can't lift the kids out of wheelchairs

anymore. I hated to leave my job. My rheumy said he would support me--

-now that I have read his notes I'm really scared. I have spoken

about my difficulty working every visit--he made no mention of that.

One visit where he injected a nodule on my foot because I was

limping, unable to wear shoes, and very limited--no note at all!! Now

that I have quit my job, have no income( my husband died 8 years

ago), I am just really afraid he won't make a strong case for me. His

only mention was a hand written note out of sequence that I almost

missed saying " Phone call from patient, wants disability---will

support. "

I am using Allsup, Inc. to help me---all they do is SS disabilty

cases. This is very scary and depressing---my whole future depends

on a decision by an overworked person who doesn't know me . An awful

situation to be in. Any questions let me know. Louise

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In a message dated 1/30/2006 3:12:50 PM Central Standard Time,

so_shy234@... writes:

Can anyone give me some advice what to do? I'd appreciate any

suggestions.

Keep reapplying if you are turned down. be a pest if need be. iwas thinking

of applying myself, but decided not to. Being only 27 and not worked in te

last 3 yrs, i know they will turn me down in an instant. Besides that, i still

would like to go out and work. Like someone said, its hard finding a job

that will accomodate people like us... but i will still search. Cant do much

till my daughter starts some kind of schooling.

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, there's something I had a hard time understanding in all this, but I

finally got it. Before I get to that, your age doesn't have much to do with

getting on SSD. If you have a legitimate complaint, you should apply for SSD.

Having not worked for 3 years, you haven't accumulated enough to have a large

check from Social Security. However, this is what I finally understood, you can

still work part time as long as you don't earn more than $7xx per month. Apply

for SSD!

When I applied in 1991, I was also drawing unemployment. Thank goodness it was

renewed every 6 months during that time or I would have been up a creek. The 2

systems didn't talk to each other like they do now, so it would be harder to get

both at the same time.

Whatever you decide to do, I hope it goes well for you, So_Shy.

Dennis

Re: [ ] Social Security Disability

In a message dated 1/30/2006 3:12:50 PM Central Standard Time,

so_shy234@... writes:

Can anyone give me some advice what to do? I'd appreciate any

suggestions.

Keep reapplying if you are turned down. be a pest if need be. iwas thinking

of applying myself, but decided not to. Being only 27 and not worked in te

last 3 yrs, i know they will turn me down in an instant. Besides that, i

still

would like to go out and work. Like someone said, its hard finding a job

that will accomodate people like us... but i will still search. Cant do much

till my daughter starts some kind of schooling.

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In a message dated 1/31/2006 12:01:05 PM Central Standard Time,

betnden@... writes:

, there's something I had a hard time understanding in all this, but I

finally got it. Before I get to that, your age doesn't have much to do with

getting on SSD. If you have a legitimate complaint, you should apply for SSD.

Thank You Dennis. I will definately think about applying for SSD.

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Actually, age does have a lot to do with it. You have to fight harder a lot of

the time if you are younger when you apply. I have been trying to get SSD for

over three years, and am just now waiting for word of the judge's decision in my

case. Every case is different, but if you have documented Seropositive Ra, it is

on the list of things they will pay disability for, so should not be too much of

a problem, except waiting on them to get off their thumbs and look at the file.

That can take upp to 18 months. Its pretty ridiculous. I have had to wait so

long that Dr's have actually found new problems and some of my conditions have

worsened a lot, because I can't get any type of medical care where I live,

because the state won't give me Medicaid unless I get a government check or have

a chronic condition that they will treat at the Health Department.

As far as working goes, you CANNOT work at all and get disability. If you can

work more than 10 hours a week, they won't grant your claim. I found that out

the hard way. (The first Year) So be prepared that getting SSD is going to be a

long, arduous process, which will probably bankrupt you financially. We lost our

house, and now live with my in-laws, and I am over 40,000 dollars in debt for

medical bills. I say this from my personal experience. I don't know your whole

story, but as long as your RA shows up in blood tests, you will most likely get

it the first time you apply. If it does not, and your condition (s) won't blind

you, you are going to have one hell of a rough time. By all means, go for it, I

just wanted to tell you some of the stuff no one warned me about. And I still

don't know if I will recieve my benefits. So Good Luck

Jane

N2kids@... wrote:

In a message dated 1/31/2006 12:01:05 PM Central Standard Time,

betnden@... writes:

, there's something I had a hard time understanding in all this, but I

finally got it. Before I get to that, your age doesn't have much to do with

getting on SSD. If you have a legitimate complaint, you should apply for SSD.

Thank You Dennis. I will definately think about applying for SSD.

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AMEN!!!!!

I also have been waiting almost three years for SS, just before Christmas I

was told my case has finally been assigned to a judge. Also my conditions have

worsened.

If it were not for the support of my sister and parents I would be living in a

homeless shelter, I am Abie to see most of my doctors through a medical grant at

our local hospital and my parents help pay for rheumy appointments. As for drugs

if I can't get it through a drug assistance program I do without, It is not a

easy journey in WI

Bargeman <mtbargeman30@...> wrote:

Actually, age does have a lot to do with it. You have to fight harder a lot of

the time if you are younger when you apply. I have been trying to get SSD for

over three years, and am just now waiting for word of the judge's decision in my

case. Every case is different, but if you have documented Seropositive Ra, it is

on the list of things they will pay disability for, so should not be too much of

a problem, except waiting on them to get off their thumbs and look at the file.

That can take upp to 18 months. Its pretty ridiculous. I have had to wait so

long that Dr's have actually found new problems and some of my conditions have

worsened a lot, because I can't get any type of medical care where I live,

because the state won't give me Medicaid unless I get a government check or have

a chronic condition that they will treat at the Health Department.

As far as working goes, you CANNOT work at all and get disability. If you can

work more than 10 hours a week, they won't grant your claim. I found that out

the hard way. (The first Year) So be prepared that getting SSD is going to be a

long, arduous process, which will probably bankrupt you financially. We lost our

house, and now live with my in-laws, and I am over 40,000 dollars in debt for

medical bills. I say this from my personal experience. I don't know your whole

story, but as long as your RA shows up in blood tests, you will most likely get

it the first time you apply. If it does not, and your condition (s) won't blind

you, you are going to have one hell of a rough time. By all means, go for it, I

just wanted to tell you some of the stuff no one warned me about. And I still

don't know if I will recieve my benefits. So Good Luck

Jane

N2kids@... wrote:

In a message dated 1/31/2006 12:01:05 PM Central Standard Time,

betnden@... writes:

, there's something I had a hard time understanding in all this, but I

finally got it. Before I get to that, your age doesn't have much to do with

getting on SSD. If you have a legitimate complaint, you should apply for SSD.

Thank You Dennis. I will definately think about applying for SSD.

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  • 11 months later...

I know a lot of you have been able to continue working your job.

However, for those unable to continue employment, is there anyone that

has been approved for SS disability? I would apprciate if you would

email me as I have some questions.

Thank You

Barbara

barbdig@...

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Barbara,

You have my sympathy. I am exactly like you! I feel like a carbon

copy! I get tired just going through the grocery store, and feel

like a walking zombie! I am always over bundled with multiple

layers of clothers and ALWAYS cold and shivering! CAN'T GET WARM.

Fatigued, sore, nausea and edema. My bloodwork looks good on paper,

but I am a mess with the side effects.

Although I worked for many years before having my children, I was a

stay at home Mom when I was dx'd with CML. Basically, I can't get

any benefits.

I would like to get a part time job, but with my up and down life

dealing with side effects, there is no way at this point that I

could hold onto a job.

I feel like I am trapped and have no benefit options. I feel

disabled, and all of my friends/family feel that I am too, but I

have no leg to stand on as far as getting Disability. Something is

really wrong with our system.

Sincerely, Lynn

>

> Well, guess that's what I get for not telling my doctor about all

of my side

> effects. I knew, from reading and the list, what the side effects

were and

> just tolerated them without complaining too much to the doctor I

can just go

> to the grocery store will and have to come home and take a nap.

That's in

> addition to what happens with every bite that goes into my body,

the fact

> that I spend most of the winter wrapped in 3 layers of clothing

because I

> can't get warm. How in the world could I handle an 8+ hour job.

If I were

> an employer, I wouldn't want someone that has to be close to the

restroom,

> take naps frequently, have problems concentrating or remembering

things and

> never knew when they would feel like coming to work. I had been

doing taxes

> for the past 6 years. Can you imagine the germs I get sitting in

that

> everyday, not to mention, worrying if I was going to remember all

the right

> things to include in the tax return.

>

> I wonder what it is the lawyers do to convince the SS Board that

people are

> unable to work?

>

> It was obvious from the response of my application they knew

nothing about

> CML. They didn't even know what it was because they said, " you

said you are

> disabled because of leukemia, cnl, joint pain, nausea and

weakness. The

> treatment you have been receiving has brought this condition under

> control.(it has?) Although you may experience discomfort,

evidence shows

> you are able to move about and perform your normal daily

activities. "

>

> Oh well, maybe I need to do a little more research. I guess I

didn't give

> them enough information to understand my limitations.

>

> Thanks for listening.

>

>

>

>

>

> Barbara

>

> _____

>

> From: [mailto: ] On Behalf

Of

> lunaemica@...

> Sent: Tuesday, February 06, 2007 10:06 AM

>

> Subject: Re: [ ] Social Security Disability

>

>

>

> I am currently working 2 days @ 8 hours each instead of full time

because of

> the side-effects I'm experiencing. I hate not being able to work

full time

> and I especially hate not being able to be a fully involved, fully

energized

> Mom and wife like I had been. I am, however, alive and for that I

am so

> thankful for Gleevec eventhough it causes me such discomfort and

fatigue. My

> new doctor as well as my old oncologist agree that my side-effects

from

> Gleevec are debilitating enough that I should not and can not go

back to

> work full time. I have been on this work schedule since diagnosis

in 10/05.

> I have tried a few times to add a few hours or a day here and

there but I

> find that any more hours than those I'm working cause my side-

effects to

> worsen and leave me so wiped out I literally can't even move.

> My long term disability company is begining to be difficult about

things;

> saying stuff like, 'we have thousands of patients with CML who are

all fine

> to work' and 'as far as we are concerned your cancer is cured'. I

forsee

> that I may have an uphill battle ahead of me to help them to

understand that

> some patients on Gleevec have moderate to extreme side-effects

that cause

> them not to be able to function as they would normally. I have not

had to

> approach SS Disability yet and hope that I will not as I've heard

that is a

> long uphill battle and that you HAVE To have a lawyer to win.

> Hang in there and I hope you are able to get your disability.

Please keep us

> updated.

> Thanks,

>

>

> [ ] Social Security Disability

>

> I know a lot of you have been able to continue working your job.

> However, for those unable to continue employment, is there anyone

that

> has been approved for SS disability? I would apprciate if you

would

> email me as I have some questions.

> Thank You

>

> Barbara

> barbdig (DOT) com

>

>

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  • 4 years later...
Guest guest

They deny most of the time. When they denied me I called my

Congressman's office and asked for a ombudsman. I got my first

disability check two weeks later.

Marla

On 3/4/2011 8:47 PM, Vivian Cone wrote:

>

> Heidi

>

> From all that has come through today from others on line it looks like

> everyone goes through similar situations. The on-line application was easy

> and the gentleman that I met at the social security office was very polite

> but the doctor they send you too I am convinced more than ever gets

> paid to

> deny all applicants. Be prepared for this, I was not prepared for the

> letdown. The doctor did not even examined me...he was genuine quack!

>

> Now I am going to start looking for an attorney that deals with this - to

> see what happens.

>

> Hang in there and God bless - Vivian in CA

>

>

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Guest guest

Vivian,

Thank you! Everyone here on this site is so kind and it really helps especially

when I'm feeling out of sorts all the time. I appreciate all the information

given here and especially for keeping us all up to date. I know God is

only giving me what I can handle and there is a light at the end of the tunnel.

Everything happens for a reason, I just haven't figured out what it is yet?? God

bless everyone!

Heidi in Denver

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