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My name is Miriam and I have been lurking on this last for the last

few months. I have found the information I have been reading to be

very insightful and helpful.

I am 37 with 7 children and was disagnosed with RA about 1 years ago

but have suffered with pain since I was 12. I got passed around to

Dr's who said they didn't find anything wrong and I had given up.

Late last year I couldn't take the pain anymore and it was from head

to toe with extreme exhaustion and my company doctor sent me to a

rhematologist who promised to get to the bottom of the problem, after

all these years! I tried things like Vioxx, Celebrex, Cochicine and

who knows what else and the pain kept getting worse. I am now on MTX

and Enbreal and Vioxx. I am not in the extreme pain I had been in

but I still am in pain constantly. I can barely walk due to the

damage to the metatarsal joints in my feet, I can barely write

because my hands are so sore and everything in between hurts also.

My 16 year old daughter was recently diagnosed with JRA after 4 years

of being in pain, my not liking the doctors I took her to until I

finally took her to my own rheumy. Based on when my problems

started, I probably have JRA and not RA. I am not sure if it makes a

difference or what the real differences are between them, except when

you got diagnosed.

I work full time and am really struggling. I haven't been staying a

full 8 hours because I just can't make it. Are medications ever

supposed to make me feel " normal " again or is this as good as it

gets? Should I hope or expect for more relief? I am not in the mind

numbing pain I was in prior to my current meds and recently came off

prednisone (gained 30 pounds)but I am having a hard time imagining

that this is as good as its going to get.

Sorry for the length, and thanks for all the great info I have

already gathered.

Miriam

Cleveland, OH

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Orthotics can be a big help for sore feet. You end up wearing ugly

shoes or running shoes for life (my opinion) but they are a great

help. I am very uncomfortable walking without them but practically

normal with them, as long as I'm not too tired.

If you don't or can't get them then you need a shoe with lots of room

for your toes - you could consider something as simple as an extra

insole to help make the shoe fot your foot better. At one point I

was cutting off the toe portion of the insoles because as your toes

shift on you they can rub very painfully.

I also use wool socks (preferably with a padded sole - you have to

look but they exist). The wool gives you a little more cushioning

and believe me every little bit counts when your cartilege is gone.

Annette

> My name is Miriam and I have been lurking on this last for the last

> few months. I have found the information I have been reading to be

> very insightful and helpful.

>

> I am 37 with 7 children and was disagnosed with RA about 1 years

ago

> but have suffered with pain since I was 12. I got passed around to

> Dr's who said they didn't find anything wrong and I had given up.

> Late last year I couldn't take the pain anymore and it was from

head

> to toe with extreme exhaustion and my company doctor sent me to a

> rhematologist who promised to get to the bottom of the problem,

after

> all these years! I tried things like Vioxx, Celebrex, Cochicine

and

> who knows what else and the pain kept getting worse. I am now on

MTX

> and Enbreal and Vioxx. I am not in the extreme pain I had been in

> but I still am in pain constantly. I can barely walk due to the

> damage to the metatarsal joints in my feet, I can barely write

> because my hands are so sore and everything in between hurts also.

>

> My 16 year old daughter was recently diagnosed with JRA after 4

years

> of being in pain, my not liking the doctors I took her to until I

> finally took her to my own rheumy. Based on when my problems

> started, I probably have JRA and not RA. I am not sure if it makes

a

> difference or what the real differences are between them, except

when

> you got diagnosed.

>

> I work full time and am really struggling. I haven't been staying

a

> full 8 hours because I just can't make it. Are medications ever

> supposed to make me feel " normal " again or is this as good as it

> gets? Should I hope or expect for more relief? I am not in the

mind

> numbing pain I was in prior to my current meds and recently came

off

> prednisone (gained 30 pounds)but I am having a hard time imagining

> that this is as good as its going to get.

>

> Sorry for the length, and thanks for all the great info I have

> already gathered.

>

> Miriam

> Cleveland, OH

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Share on other sites

Orthotics can be a big help for sore feet. You end up wearing ugly

shoes or running shoes for life (my opinion) but they are a great

help. I am very uncomfortable walking without them but practically

normal with them, as long as I'm not too tired.

If you don't or can't get them then you need a shoe with lots of room

for your toes - you could consider something as simple as an extra

insole to help make the shoe fot your foot better. At one point I

was cutting off the toe portion of the insoles because as your toes

shift on you they can rub very painfully.

I also use wool socks (preferably with a padded sole - you have to

look but they exist). The wool gives you a little more cushioning

and believe me every little bit counts when your cartilege is gone.

Annette

> My name is Miriam and I have been lurking on this last for the last

> few months. I have found the information I have been reading to be

> very insightful and helpful.

>

> I am 37 with 7 children and was disagnosed with RA about 1 years

ago

> but have suffered with pain since I was 12. I got passed around to

> Dr's who said they didn't find anything wrong and I had given up.

> Late last year I couldn't take the pain anymore and it was from

head

> to toe with extreme exhaustion and my company doctor sent me to a

> rhematologist who promised to get to the bottom of the problem,

after

> all these years! I tried things like Vioxx, Celebrex, Cochicine

and

> who knows what else and the pain kept getting worse. I am now on

MTX

> and Enbreal and Vioxx. I am not in the extreme pain I had been in

> but I still am in pain constantly. I can barely walk due to the

> damage to the metatarsal joints in my feet, I can barely write

> because my hands are so sore and everything in between hurts also.

>

> My 16 year old daughter was recently diagnosed with JRA after 4

years

> of being in pain, my not liking the doctors I took her to until I

> finally took her to my own rheumy. Based on when my problems

> started, I probably have JRA and not RA. I am not sure if it makes

a

> difference or what the real differences are between them, except

when

> you got diagnosed.

>

> I work full time and am really struggling. I haven't been staying

a

> full 8 hours because I just can't make it. Are medications ever

> supposed to make me feel " normal " again or is this as good as it

> gets? Should I hope or expect for more relief? I am not in the

mind

> numbing pain I was in prior to my current meds and recently came

off

> prednisone (gained 30 pounds)but I am having a hard time imagining

> that this is as good as its going to get.

>

> Sorry for the length, and thanks for all the great info I have

> already gathered.

>

> Miriam

> Cleveland, OH

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