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Thanks, she was diagnosed at 23 and is now 37 I believe, she's a miracle. Had 2

strokes within a week of each other about a month ago which has affected her

speech, but she doesn't give up on life, she lives everyday to the fullest.

My " aunt " (mother of this girl) as I said sent in the same paperwork each time,

didn't use an atty, and the doctor at the U of M also used the same letter, only

changing the date. Unfortunately, it takes time, even when someone doesn't have

time. Again, the govt is screwed up, all they worry about is their expensive

parties and yachts and vacations, most don't give a damn about someone who is

sick or suffering till it happens to them or someone real close to them, then

most concentrate on that and still forget about the rest of us out here.

And you are right, the govt just figures we're so sick and tired of it all we

will drop the case... most that are faking would, which is again why we have to

fight so damn hard, even those with terminal problems... the govt looks at the

documents and says nope, they'll get better, no need to help them. When they

finally do approve it they don't give you enough to live on if you're her age

(23) b/c she had been in college and had very little work exp, or like me who

did have work exp but at 32 when this happened I still didn't have a lot of

credits, but thankfully enough to get some monthly income. I could go on and on

about how crappy the govt takes care of disabled people, you have to be homeless

then you're still out of luck.

Connie

Re: Disability

> Connie'

> Thank's for the information. The government just

> figure's you will finally give-up if they hassle you

> enough.I hope your friend is doing okay? I also have a

> real good friend who's son just found out not long

> ago that he has terminal cancer,they put in for

> dissability and they told him it would take 30 to 120

> day's and the man is terminal and has no insurance and

> income.They are fighting to get it sooner.

> Thank's

>

--

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Thanks Marti,

I live in Wisconsin. First things first though. Have

got to apply for disability. My husband doesn't

acknowledge or believe the pain and because he has

never heard of PA believes that I just don't want to

work. I am still quite capable of design work most of

the time but am concerned about the near future. PA

has a tendency to progress rapidly unlike the

government and it may take quite a while to get

approved. Without insurance I would have to go without

treatment and that just isn't an option. It's good to

know that I can still work part-time because jobs will

still be coming in and I don't want to have to turn

them down.

Once I am on disability I'll be able to connect to

other related sources I'm sure. This whole think is

such a long process.

Thanks for answering

Mickey

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---n't

> acknowledge or believe the pain and because he has

> never heard of PA believes that I just don't want to

> work.

Hi Mickey,

Will your husband read some of our posts? Will he read info on PA?

You said a mouthful in one short sentence-PA progresses rapidly while

the government does not. Do you have a supportive Doc for disability?

That really helps to get it. Also maybe your husband would listen to

the Doc.

I wish you good luck!

Marti

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--Hi Mickey,

That denial can be a hard one. One of my good friends confronted me

and said Can you honestly say your arthritis is getting worse or do

you just think it is (x-rays,etc show it is getting worse but NObody

likes to hear that) I have a good friend with RA, fibro and

bipolar. She has to stay completely away from many of our meds or

she goes into a manic phase-esp the prednisone does that to her.

Good Luck at the Doc!

Marti

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Marti,

I don't understand why a friend or spouse would

question it. Do they have little respect for you to

think you are making it up for attention or sympathy?

That is truly an insult.

Good news, after my third dose of MTX I actually sat

on the floor CROSS LEGGED and played with my

grandbaby. First time in a year and a half. Did too

much through the day though because I felt better and

paid dearly for it by supper time. Oh well, it was fun

to move around. I have to be careful not to go nuts on

days I feel better. I've never been one to sit around

because I have ADHD and it's like being in a straight

jacket when I can't walk.

Mickey

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-Hi Mickey,

Don't know why people are the way they are. Sometimes I think it is

just too painful for them to deal with the truth. My friend thinks

there might be some guilt involved,esp with family. She says if they

admit how sick we are then they feel responsible for helping. I

think some people like to think these illnesses would never happen to

them. They find a reason to blame the sick person for their illness

so they can continue thinking they are safe from it all.

Glad to hear the good news about the MTX, I hear you on trying not

to overdo it on the good days too!

Marti

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Hi Mickey,

It sounds like your husband has had a tough life. I didn't realize

that people might fear death from our illnesses until a young friend

blurted it out one day. I was surprised but took the opportunity to

explain that we don't die we just live a harder life. It really

relieved her mind. Sorry your husband has gotten so distant. Hope

things turn around soon.

Best Wishes,

Marti

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Welcome back, Marge! Sounds like a fun trip. I'm so happy to hear that

you had a good time.

Sorry about your insurance trouble. I hope it's nothing.

Good luck on the 8th with your interview!

[ ] disability

> Hi all, I'm home from my 10 days in New Jersey....great time with a

stop over in the Poconos. My interview for disability will be August

8th...I'm trying to have all my documentation in order...they said it

will probably be 5 months until I hear the results re approval or

not...since I have a small amount in my savings account, I will not be

eligible for short term assistance...I have to call my insurance

company, for some reason they denied my last visit to the rheummy (after

paying for 3 years of visits). I hope it doesn;t have anything to do

with my switching to cobra...shouldn't...but...can't figure out why it

would be different....any suggestions anyone has for me would be

appreciated related to the interview...my best friend is going with me

and I have 2 letters from past co-workers documenting change in my

ability to carry out everyday work tasks....will must close hands aren't

working too well and I am back spacing to correct constantly...it is 1

a.m. and i hope to get some sleep in the near future....warm milk

time....hope you are well...missed you over the alst 10 days...but the

fishing was grfeat...had to put away my fly rod...cou.ldn't cast it..oh

well one more thing for uncle arthur.....marge

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> I know many people who were denied disability the

first attempt and had to see attorneys. <

Yeah...I had heard that from a lot of people so I expected it...no surprise

there!

> As far as housekeeping, I hear what you are saying. <

But she said I was not to do ANYTHING that caused pain...so what am I supposed

to do? Everything hurts from a mild ache to terrible spasms. It is not my nature

to just sit around. WC got me on video doing housework and my benefits were

stopped. Will disability send someone out to spy on me also? I go bowling with

my friends...I look funny as I don't bend or twist, but I have fun...even though

I know I will pay for it later.

So does life completely stop for those on disability?

I am also attempting to become self-employed with dog evaluations & training,

and photography...later opening up a boarding kennel...how will that affect

things?

I just can't see me giving up on life.

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> I have to really pace myself with cleaning. <

That is what I have been doing...no major cleaning at all, just a little each

day.

But the lawyer said to do nothing that causes pain. I just don't see how that is

possible. I have already gained 50 hateful pounds from not being as active as I

used to be, and that is while being on a low fat & sugar diet! It is going to

kill me to put on more weight.

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I've always heard it takes an attorney to help anyone get

their SS disability. For those of you on SSD, how much

did you have to end up paying to an attorney for help to

get it?

joe

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> Well Joe Ihad a company called Allsup Inc. they were excellent Joe. They

have a 95% success rate. They do everything for you...

Carol -

Hang onto that for now. I'm doing research on the revision surgery and

hope that I might get some relief via that route. If I do, I will still be

able

to stay at my job. Thanks for being willing to check.

joe

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> For those of you on SSD, how much did you have to end up paying to an attorney

for help to get it?

I'm not on it yet, but my lawyer is taking 25% with a $5400 max cap from my

first check...when and if I get it.

Vivian H.

Vivian H.

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There is a limit $4,000.00 or 25%, but not over $4,000.00 Michigan's rate. Chris

Re: Re: Disability

> For those of you on SSD, how much did you have to end up paying to an

attorney for help to get it?

I'm not on it yet, but my lawyer is taking 25% with a $5400 max cap from my

first check...when and if I get it.

Vivian H.

Vivian H.

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In a message dated 10/30/2003 5:07:17 AM Pacific Standard Time, mellowcargo2003@... writes:

I received a "partially favorable decision" from SSA. The appeals judge ruled in my favor for getting disability going back to Aug. 2001. However SSA will take 60 days to evaluate that decision then either approve, deny or require more information from me. The waiting game goes on..............Bob

i need some help..i am working p/t..barely making it...where do i start?? help please...ssi?? disability??

Peace, Sielicki

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Hi . Go to theSocial Security office and get some information. There are two types of disability, depending on your financial status, family etc. The supplemental depends on financial hardship, etc. while the other part depends on your past earnings and how much you've paid in.

www.ssa.gov/disability/

www.nosscr.org/faqind.html

The first link is to the government site and the second is a "frequently asked questions" site that may be helpful. You can apply on your own and then if turned down see an attorney or get an attorney right off the bat. The initial decision doesn't take too long, but should it go against you the appeal can drag out for a long time. The attorneys are bound by law that they can only charge 25% of whatever your initial payment from ssi is. You can easily find attorneys who work on the basis that you only pay if you win. Do your homework and get doctors to write letters on your behalf, etc. should you decide to try to go apply on your own behalf. Good luck. -dz-

i need some help..i am working p/t..barely making it...where do i start?? help please...ssi?? disability?? Peace, Sielicki

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Dear Al:

I was 33 years old when I was diagnosed and became disabled I also had

a broken back. However, I went in with no lawyer, I have 3 bachelors and a

masters and speak two languages, that was also stacked against me. I took all

the prescription medication that I am supposed to take a day at the allotted

time (I am on valium for anti anxiety, Oxycontin for pain, neorontin, predisone,

MTX etc.......and I could barely speak. The judge asked if this is what I was

like on a regular day and I said yes. I got my check 3 months later. I don't

know what meds you are on but the problem or what type of job you did or do

that matters.

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Ally,

I went on SS disability when I was 30. I was approved right away and didn't

have to go before a judge so I can't offer you any first hand experience.

Here are some articles that may help:

RHEUMATOID ARTHRITIS & Disability

http://www.ssdisability.net/arthritis.html

Preparing for a Disability Hearing

http://www.lawhelp.org/program/766/RTF1.cfm?pagename=Preparing%20for%20a%20D

isability%20Hearing

Preparing For Your Day In Court

http://arthritis.about.com/library/weekly/aa111898.htm

Good luck,

a

> Hello Everyone,

>

> Sorry it has been so long since I have posted. Please know that I

> always read your posts and I think about this group all of the time

> sometimes I'm just a little quiet. My disability hearing is

> scheduled for Monday and I need advice. I am so nervous. I have a

> lot stacked against me as I am 26 yrs old (no judge wants to label

> someone this young disabled--according to my attorney) and my blood

> tests do not show a positive RF. Is there anything that can and

> should be said during the hearing. I really don't feel very prepared

> for it....my attorney hasn't told me a lot about what to expect. Any

> advice would be greatly appreciated.

>

> Thanks-Ally

>

>

>

>

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Good luck, Ally!

I can't give you any advice from personal experience, but I see that

others are trying to help guide you.

Do keep in mind that a significant percentage of people with RA are

never RF-positive (up to 30%, depending on the source of the

information).

Please let us know how it goes.

[ ] Disability

> Hello Everyone,

>

> Sorry it has been so long since I have posted. Please know that I

> always read your posts and I think about this group all of the time

> sometimes I'm just a little quiet. My disability hearing is

> scheduled for Monday and I need advice. I am so nervous. I have a

> lot stacked against me as I am 26 yrs old (no judge wants to label

> someone this young disabled--according to my attorney) and my blood

> tests do not show a positive RF. Is there anything that can and

> should be said during the hearing. I really don't feel very prepared

> for it....my attorney hasn't told me a lot about what to expect. Any

> advice would be greatly appreciated.

>

> Thanks-Ally

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In a message dated 12/5/2003 3:41:27 AM Pacific Standard Time, szeis_1@... writes:

I just received a notice that I am going to get SSDI starting next month. Also qualified

effective Jan 2002 so I will get retro amount minus lawyer fees.

Also went to see doctor. She ordered lab work to see where I am with viral load, etc.

Next Tuesday will be my 48th shot but she wants me to continue until we get lab

results. So far being 3b I was on tx 24 wks, off for 3 mos, and now 48 wks. Bob

where did you go first???

Peace, Sielicki

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,

I applied for SSDI. I was approved for SSI. I was told SSDI was like

insurance premiums.

I have worked since I was 16 years old and had disability taken out.

But, SSDI goes by the last 10 years. I was in college 4 of those years and

working for the state after that.

The state didn't take SSDI out.

So, I was approved for SSI of only $790 a month. I am thankful for that, but

do not understand how all of this works.

I do not receive Medicare, but the state's insurance of MediCAl.

There is even a difference between straight MediCAl and ? MediCal I am

finding out.

I did find out I have straight MediCal whatever that means.

This is just my experience. I hope it helps.

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In a message dated 1/9/04 2:21:59 PM Pacific Standard Time,

j.sloane@... writes:

But it will be higher than for someone who has never worked -- that

amount is about 550 per month last time I checked it out.

So, I am getting the same as someone who never worked. Ouch. California adds

to this amount...I am not sure why. But that is why I am receiving $790 a

month. I know that if I moved to another state, I would be receiving the $500

and

something a month.

It also took me about 2 years before I was approved. I had an attorney. I was

denied the first time. I sent an email to a public figure and received a

phone call shortly after that from my doc saying he received the paper work.

Things moved fast after that.

I'd be ok on this amount if I didn't have the medical installment debts and

tax installment debts I am paying.

I also applied for low income housing and was approved for it. I am thankful

for that.

Mostly, I just want to get well and get back to work.

Kate

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Your message has been edited.

Please read the file entitled " Cleaning " Instructions found at

/files/ for more information.

Lyme Aid Owner

==========

It depends on how much you have put into the system from what I understand.

[ ] Disability

Can anyone tell me how the state, and/or govenment desides how much

we get for disabilty? And, also how Medicare works. I have managed

to work through my Lyme for the last 16 years, however as sick as I

have been recently, I may have to go on disabilty before it is all

said and done. Any input will be greatly appreciated.

thanks,

:)

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, There's a group regarding disability online Disinissues, I

think it's called that you can join on regarding disability and

insurance issues.

I can tell you that your disability amount will be determined by how

much you have earned in your working life and how much you have paid

into the system. You can get a report from Social Security that will

tell you what that amount will be. It's not a fortune that's for sure!

But it will be higher than for someone who has never worked -- that

amount is about 550 per month last time I checked it out.

It's a long process, especially with something like Lyme Disease. It

took me about 18 months the third time I tried, and had to use a

lawyer. Then, once you are on disability you have to wait for Medicare

to kick in.

If you are too sick to work, I would not delay in applying, as it

takes a while. But do check out the resources I mentioned above.

There's a lot to learn about the application process.

Good Luck to you,

Blessings,

> Can anyone tell me how the state, and/or govenment desides how much

> we get for disabilty? And, also how Medicare works. I have managed

> to work through my Lyme for the last 16 years, however as sick as I

> have been recently, I may have to go on disabilty before it is all

> said and done. Any input will be greatly appreciated.

>

> thanks,

> :)

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Your message has been edited.

Please read the file entitled " Cleaning " Instructions found at

/files/ for more information.

Lyme Aid Owner

==========

I don't know what state you live in, but you can also go to the Medicaid website

and then go to the state you live in on the Medicaid website and that will give

you info also.

You can do the same thing for your Medicare.

I am not an LD patient, but my best friend has LD (25 years) and I'm her

caregiver, support, etc. and have been with her through every battle she has

fought over the years.

The best advice I can give you to help your disability process is to ask

friends or relatives to write a " To Whom It May Concern " letter. In the letter

have them describe - from their point of view - how you look, act, what you can

and can't do physically, mentally, emotionally...anything. Have them be totally

honest about how you used to be and the changes they notice now. This letter

doesn't need to be fancy or in any specific format. It can be handwritten and

can be as short or as long as the person wants. The more letters you have, the

better.

My friend and I live in Ohio. She applied for Social Security Disability

without a lawyer and was successful on the first attempt...which is unheard of

in Ohio as the first and usually the second attempt is automatically declined.

She had several letters from friends and relatives to support her request.

Also, record keeping is vital. Document everything, never give out a piece of

paper unless you make a copy of it for yourself.

If you have not done so, begin to keep a copy of all of your medical records,

any test results, lab results, etc.

It is not unusual (in our experience) for someone to ask for something that

was months prior...so document and copy everything.

Also, you could contact your county Social Services for information.

Don't let the process overwhelm you. It can be done...patience and

documentation are key.

Hugs,

Sandy

[ ] Re: Disability

, There's a group regarding disability online Disinissues, I

think it's called that you can join on regarding disability and

insurance issues.

I can tell you that your disability amount will be determined by how

much you have earned in your working life and how much you have paid

into the system. You can get a report from Social Security that will

tell you what that amount will be. It's not a fortune that's for sure!

But it will be higher than for someone who has never worked -- that

amount is about 550 per month last time I checked it out.

It's a long process, especially with something like Lyme Disease. It

took me about 18 months the third time I tried, and had to use a

lawyer. Then, once you are on disability you have to wait for Medicare

to kick in.

If you are too sick to work, I would not delay in applying, as it

takes a while. But do check out the resources I mentioned above.

There's a lot to learn about the application process.

Good Luck to you,

Blessings,

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