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Hi Regena,

I just received mine yesterday.

Shay

Michigan

-- [ ] stimulus payment

hello everyone. my name is regena. i'm have mrh(multicentric

reticulohistiocytosis) and extremely rare form of RA. i was recently

approved for ssdi in january '09 after a 3 year fight. i was wondering if

anyone has recieved their stimulus payment?

regena

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My mother received hers I believe. I think she said she got it last week.

>

>

> hello everyone. my name is regena. i'm have mrh(multicentric

reticulohistiocytosis) and extremely rare form of RA. i was recently approved

for ssdi in january '09 after a 3 year fight. i was wondering if anyone has

recieved their stimulus payment?

>

> regena

>

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Betty and I got ours a couple of weeks ago. Direct deposit was first in

line, then the mailed-out's after as time allowed. By the middle of June,

everybody should have received theirs.

Dennis in eastexas

On Fri, May 22, 2009 at 9:36 PM, franticteacher <franticteacher@...>wrote:

>

>

> My mother received hers I believe. I think she said she got it last week.

>

>

>

>

> >

> >

> > hello everyone. my name is regena. i'm have mrh(multicentric

> reticulohistiocytosis) and extremely rare form of RA. i was recently

> approved for ssdi in january '09 after a 3 year fight. i was wondering if

> anyone has recieved their stimulus payment?

> >

> > regena

> >

>

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Hi Regina!  3 relatives of mine already received their Stimulus checks in past

one to 2 weeks.  Best wishes and I wish you Better health and sorry to hear of

your rare type of

R A.  What were your Symptoms?  Did you and do You --have lots of Pain with that

type of R A.   I've had R A several years but i don't know which type.  I  had

severe Pain, etc. several yrs. ago but in past few years I've not had much pain,

fortunately and all i take for

my R A  is two, 200 mg. of non-prescription  Ibuprofen, daily; but i know my

Luck can change at any moment.  It is somewhat worse recently (the swelling in

some of my fingers).  I  WAS  diagnosed with R.A. bout 6  or 7 years ago.  I did

see a Rheumatoligist

(spelling).  I took MTX in small doses for 7 weeks and quit seeing the

Rheumatoligist, due

to different reasons (one reason:  there seemed to be Chance that I had

Pulmonary Fibrosis and I didn't think I could take some of the meds for R.A. -

IF i did have PF.   I

won't get into all that right now.                 Wishing you a pain-free

day!         Judy

From: flybutter <flybutter22@...>

Subject: [ ] stimulus payment

Date: Friday, May 22, 2009, 8:02 PM

hello everyone. my name is regena. i'm have mrh(multicentric reticulohistiocytos

is) and extremely rare form of RA. i was recently approved for ssdi in january

'09 after a 3 year fight. i was wondering if anyone has recieved their stimulus

payment?

regena

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Hi Judy!! thanks for the reply. i was diagnosed about 5 years ago with chronic

RA when i noticed my hands,wrists,fingers and knees were consistently swollen

and i had full body itching. no matter what i did or what meds i took the

swelling never went down. then i develop this rather large nodules on my

fingers, elbows, face and neck.

 

 the rheumatologist i was seeing was not concerned, said they were rheumatoid

nodules and prescribed MTX and prednisone. well my symptoms weren't going away.

i'd go back to the doctor and he's just upping the meds. the MTX was makng me

sick unable to function worse than i already was. so i decided to stop seeing

him and stopped the meds altogether.

 

 for about 4 months all i was taking was alo vera to help with the itching. at

this point i was stooped over unable to walk in constant pain and itching all

over everyday. finally ,my mom sent me to an internist who immediatley put me on

prednisone and referred to another rhuemy.

 

 well i was skeptical of course. but this doctor was sent to me by god. he took

one look at my hands, my knees,my ankles and knew i didn't have chronic RA. he

actually had to pull out the medical books and send me to the university of

north carolina chapel hill before i could get a proper diagnosis. after all that

i was diagnosed with MRH and although there is no set in stone treatment since

this is so rare we have been trying different things. it's a relief to know i'm

not crazy and my symptoms and pain are real. having a good doctor makes all the

difference. thanks for listening

 

pain free days

regena

From: flybutter <flybutter22>

Subject: [ ] stimulus payment

@gro ups.com

Date: Friday, May 22, 2009, 8:02 PM

hello everyone. my name is regena. i'm have mrh(multicentric reticulohistiocytos

is) and extremely rare form of RA. i was recently approved for ssdi in january

'09 after a 3 year fight. i was wondering if anyone has recieved their stimulus

payment?

regena

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We haven't received a stimulus payment. Is everyone elligible for it?

Debbie L

>

>

> hello everyone. my name is regena. i'm have mrh(multicentric

reticulohistiocytosis) and extremely rare form of RA. i was recently approved

for ssdi in january '09 after a 3 year fight. i was wondering if anyone has

recieved their stimulus payment?

>

> regena

>

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