Humira for psoriatic arthritis
Common Questions and Answers about Humira for psoriatic arthritis
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I used to take a drug for psoriatic arthritis that can induce MS or MS-like symptoms in rare cases. I had tingling and numbness on the left side of my face, extending down through my left arm. I also had burning sensations in my fingertips, and buzzing in my fingertips, along with recurrent uveitis. I was MRIed twice. The first time I had 1 lesion, and the second (one month later) there were 3 more lesions. I was taken off the drug and I didn't have any symptoms.
I'm 33 and have psoriatic arthritis and was recently started on Humira. Within a day of starting I had pain in my fingers, toes, shines and forearms (none of which I had before). Has anyone else experienced new joint pain after starting Humira?
I'm 33 and have psoriatic arthritis and was recently started on Humira. Within a day of starting I had pain in my fingers, toes, shines and forearms (none of which I had before). Has anyone else experienced new joint pain after starting Humira?
regulators have approved the drug for rheumatoid arthritis, psoriatic arthritis and ankylosing spondylitis, a painful, progressive form of spinal arthritis. All three forms of arthritis are chronic disorders in which the immune system attacks joints, causing stiffness, pain and restricted motion.
The drug is injected under the skin once a month. It is made to be used alongside drugs that suppress the immune system.
ve had some experience with Humira. I was off and on it for 6 months for Psoriatic Arthritis. Sometimes cold and flu like symptoms could be a side effect. My primary care would always ask me when I would show up for what I knew was a sinus infection if I've had my Humira shot when I was on it.
The one thing I have learned about dealing with these strong drugs is to always go to your doctor first because they make treating normal illnesses more difficult.
It's too bad that you have that phobia. It has given my sister a new life. Without it she could not function. I saw how bad she was for years before being treated with it. Is it possible to work with a psychologist to help you overcome the phobia? Truly it makes the difference if my sister can work or even care for herself. I know that the medication is very expensive and even with insurance it is costly. The drug company is good about helping with part of the expense.
About 6 months ago he was diagnosed with Psoriatic arthritis after having his hands and body start crippling his abailities in daily living, and began taking Humira as treatment. Recently he has decided that we can no longer be intimate and we need to separate. He is terrified of getting the herpes infection and believes if he does it will be considerably worse for him and he won't be able to continue the Humira and thus end up crippled.
He concluded that the relief (although moderate) provided by the NSAIDs was further evidence for Reactive Arthritis and that I should try Humira. I have been on Humira for about 6 weeks with no effect. If anything, pain has gotten worse (though worsening should probably be attributed to discontinuation of NSAIDs).
There is also a small patch on my legs which is ignoring what ever I trow at it. But yes, Humira saved me as well as psoriatic arthritis that was developing too. I have had no complications with infections and I am so grateful. This disease is surely genetic with environmental predisposition and hope we finally nail it down for good.
I just got my first shot of Humira for my suspected psoriatic arthritus yesterday (i realize this is in RA, but there's no other section), and I had a quesiton. For those of you that take it or have knowledge about it, I know that it lowers your white blood count. People in my house are sick quite a bit during the year, so other than screenings (which I obviously will be getting), how do I protect myself? Supplements? Immune-boosting foods?
She saw the rhuematologist who said it was Psoriatic Arthritis and prescribed naprxen whic did not help then feldene which helped a little and now she will start taking methotrexate injections every week.
My daughter is going through severe depression and is unable to attend school on somedays due to severe fatigue. She is on the 504 Plan and is in all honors classes but is so tired. She wants to work part-time for extra money like her friends but is so tired all the time.
All other testing was negative so she said I had psoriatic arthritis and put me on humira. Even though I had all the classic symptoms of an autoimmune condition. After 7 months and steady decline in health I took myself off and told her something else was going on I was way to sick for this to be arthritis..I do have spondyloarthritis and osteoarthritis which I've had 5 surgeries on back neck and SI joint. I had 3 other Doctors tell me to find a new rheumy so I did.
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!
The Humira was for Psoriatic Arthritis but I am no longer taking this. Where exactly do you find a Genetic Specialist what kind of Doctor is this, never heard of this.
I had all sorts of blood work done. yes they did check the thyroid, etc. all came back fine. However I just found out i'm a diabetic and now am on medication and not incilin
I wonder if closing the hole, patching the hole would make all my problems go away.
I do have a cough but its not dry and I do smoke a lot. 3. I do have psoriasis, psoriatic arthritis and gout. 4. Negative antibody test at week 4. Negative Rna Pcr quantative test at week 5. negative antibody at week 5. Negative AG/AB 4th generation at week 7. Negative rapid POC antibody at week 9. I don't know what to do. With all the symptoms ive been having wouldn't I have tested positive by know if I was infected? My body temps have been all over the place.
I have arthritis in both knees and hands. The doctors say it is not RA , they think maybe psoriatic arthritis since I now have psoriasis of the scalp that was brought on during treatment for hep c (clear) My question is that I have heard of another arthritis associated with autoimmune disorders but they didn't have a name for it. Does anyone else here have psoriatic arthritis and what are your symptoms the doctor told me that it resembles RA and is crippling.
granular tissue consistent with Psoriatic Arthritis. (I was diagnosed with psoriasis at age 14).
He referred me to a rheumatologist who started me on Humira.
I then moved from CO to SD.
The rheumatologist in SD simply tried adding Methotrexate and an NSAID to the Humira, which was not doing anything for my pain.
After a few months of worsening pain, the SD doc replaced Humira with Enbrel in addition to the Methotrexate and Mobic.
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