Remicade Experiences

[Guest guest]

I was diagnosed with RA in May 09 and started Methotrexate (now up to 8/wk). In

Sept I started Humira injections which did absolutely nothing for me. I am

supposed to start Remicade infusions next week. Can anyone who's been on

Remicade let me know what it's really been like for you? What kind of side

affects do you have and how long do they last? Reading the official technical

info is like reading horror stories and I know most of the time that doesn't

happen. A few " real life " stories would be really comforting about now. Thanks.

from California

[Guest guest]

Hi ,

    Welcome to the group. I was diagnosed with RA in November 1999. I started

Remicade in March 2000 and have been on it ever since, without any side effects.

Take care,

Steph in VA

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Things Done

[Guest guest]

In a message dated 4/13/2010 3:43:13 P.M. Central Daylight Time,

mark@... writes:

> My mom was diagnosed with RA about 3 months ago. She has been on several

medications which are not helping in any way. She is 72 and is in alot of

pain. I believe with the next visit she will inquire about the possibility

of Remicade Infusions. I would sincerely appreciate anyone that has

experienced a similar experience to let us know how the injections went and

what

to expect. She is otherwise healthy. Thanks much.!!!

I'm 65 and have been on Remicade for about a year. I feel a little tired

after my infusion, but don't really have any side effects and it's helping

with my RA.

dd