Anyone take Humira (Adalimumab)?

[alixmillsvox]

Yesterday my rheumatologist has finally decided to give me something other than anti-inflammatories and anti-depressants for my list of symptoms which he has decided are due to either Ankylosing Spondylitis, Psoriatic Arthritis (Palindromic Rheumatism was mentioned too) or possibly all of the above, with a side order of Fibromyalgia. Just wondering if anyone here has taken Humira (Adalimumab) as I've read about it and am freaking out a bit! I know that whichever condition I may have that is actually causing inflammation could potentially put me in a wheelchair by fusing my joints together, so that needs to be addressed, but the side effects sound awful and I'm eager to hear from anyone who has experience of this drug (good AND bad). I've got to go back in about 2 weeks to start treatment (after they took about a pint of blood yesterday) and want all the info before I do! TIA Alix xx

[Magpiemoles]

Both my sons have taken this injection for 18 months.  They have had little side effects and their severe Crohn’s disease appears to be stable. They think of it as a wonder drug. My nephew uses it for RA is doing very well. All three have just graduated from university. All drugs have many potential side effects which you have to be made aware off. You won’t get them all and I believe the benefits far outweigh the risks. You will be monitored as to your response anyway. Good luck

[alixmillsvox]

Thankyou so much for replying! That is really encouraging!! I have finally got my appointment to start treatment on 20th august (theres a waiting list I wasn't aware of when I wrote my original post!). I remain hopeful that it'll help without too many side effects. I'm ready to get my life back! Thanks again x