As anyone taking stealra had any side effects from it I have been taken off humria and ment to start stealra in a few wks
I have been on Humira for about 8 months. At the start it worked well, but for the past 2 months I have had flare ups. Has anyone else had the problem of a biologic that has stopped working? If so, what do you think caused it?
I'm seeing my Derm this week. I hope I can get some answers.
I am 55 years old from Auckland, NZ . Recently I have been prescribe above medicine by my skin specialist for psoriasis. . Twice daily of 125mg dose. I am only 4 days into it.( 8 doses all together so far)
The affected areas are my back of scalp , chest and both the ankles
Earlier I was on acitretin,for few months but it didn't suited me
After reading the side effects I am bit concern how it is going to affect internally.
Any members taking this medicine has any problems.
Any highlights… read more
Wondering if anyone else has had the experience of being diagnosed by one rumatologist with psoratic arthriatis and got started on methotrexate at only 7.5mg a week, when next seen 4 months later by a different doctor at the hospital he decided that it wasn't arthritis but fibromalgia and he stopped all my meds including pain killers and has referred me to psychiatric team as he says the pain is all in my head
Right mow I just want to curl up and die, I hardly sleep for the pain, have to use a… read more
I have had psoriasis and psoriatic arthritis since I was a teen. I have been on so many meds..none last long. They seem to work and then my body attacks them so they are unable to work
Enbrel- didn't do much
Humira- worked like a charm totally clear for almost a year. Then I had a reaction my whole body turned red and swelled up it took the doctors months to clear that mess up
Remicade- is made from rat pee...not a joke...it made my arms and legs feel like pins and needles...it… read more
heard probiotics is good bacteria that helps digestion and might help the immune system...
For the last year I have been on a range of treatments for my psoriasis. Starting with phototherapy, then methotrexate and currently ciclosporin. Nothing has really worked. Starting biologics soon. I am suffering from extreme tiredness and a lot of headaches. Does anyone else suffer from this and can offer any help?