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hi all..well for those of you that know me, I just wanted to give

everyone update. As you know, my wife has had RA for the past 12

months. Shes 29 and started taking remicade in March. The Remicade

was helping a lot with a combination with Methotrexate and Folic

Acid. She received her last infusion in Oct and at that time, she

went in a week early because she was hurting and they also increased

the dossage from 3mg/k to 5mg/k. 2 weeks after the infusion, she

was still hurting and it looks like her body is building antibodies

against the Remicade. Also, 3-4 months ago, she started getting

rashes the size of a quarter on her back, behind the ears and now on

the side of her face and chest. they said it was drug induced LUPUS

and that all the other autoimmune drugs would cause the same rash.

We have found that it's being caused my the Remicade and theres only

like 8 cases of this reported and when its reported, they report it

in dermatology reports not rheumtology reports.

Now its back to the drawing boards because shes on increased amount

of methotrexate, folic acid, and steriods - prendisone (20mg per day)

If anyone has any ideas or thoughts, please let me know..i dont want

her to take the 20mg of prendisone beacuse of the long term

effects. Also, any ideas on other treatments would help. I've

heard a lot about the food book, but cant get my wife to belive in

it because she never hurts after eating any particular food. Any

other alternative treatments..acupuncture..etc.

Thanks

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