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I was a member here a long time ago and left the group because I didn't have the

time to participate much. Lately, I have nothing but time...

I have had PsA for the last ten years which has been managed fairly well on MTX.

For the last two months I have had a really nasty flare up and the MTX is no

longer enough. My hands and feet are so bad that I can barely use them at times

and my shoulders, hips and spine (SI) are not much better. I am waiting for

approval to start Humira. I'm just wondering what other people's experience

with this has been, particularly how long they had to wait before any effect was

noticed. So far, I've been off work for the last two months and was told by my

rheumy that it could be two to three more months. I'm desperate to get on with

my life and it's starting to get unbearable living like this. I also have

diabetes and fibromyalgia and both have worsened with this flare up.

I'm looking for some light at the end of this long, dark tunnel...

" WordPower99 " <heather.watson@...>

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