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Hi,

My name is Sandy and I have had RA for over 7 years now, and have now

been also diagnosed with FM. Oh joy! Anyhow, my Dr. prescribed

Humira injections for me starting Thursday...that is the day I will

learn how to give my self the injections. Let me tell you...SCARED

can't begin to describe how I feel about this whole thing. I hate

needles!!! Please, please, someone help me out here and give me the

411 on the drug itself, does it help, and how bad is it giving

yourself a shot every week? I am freaked!!!

Thanks

Sandy

>

> Is there any reason why your doctor has not tried the TNF blocking

drugs, i.e.

> Enbrel or Humira? IMO they work better than anything you are

currently on.

>

>

>

>

> >

> > My name is Holly and I am new to the group. I have lupus and

> > rheumatoid arthritis. My RA is kicking my butt. I started on

> > prednisone, plaquenil, safasalazin, and volteren 4 months ago,

and in

> > that time my sed rate tripled. The medicine did not work. My

doctor

> > told me that there is a 90% chance that I will be in a wheelchair

by

> > my 27th birthday next December. She wants me to try a

experimental

> > drug called MRA that is supposed to be better than methotrexate.

Has

> > anyone tried this, or even heard about it. I have 2 weeks to

make my

> > decision, and I am really scared, but feel like I have no other

> > choices as my inflamation is just getting worse. Any thoughts?

> > Thanks, Holly

> >

>

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