Humira and neuropathy

@seniormed, Sorry to hear about the adverse neuropathy side effects from taking Humira. Hoping members with some experience can offer what worked for them. I did see a Mayo article on the topic but not sure if it will help.
-- Adjusting psoriatic arthritis medications: Advice from a Mayo Clinic expert
https://mcpress.mayoclinic.org/psoriatic-arthritis/adjusting-psoriatic-arthritis-medications-advice-from-a-mayo-clinic-expert/
@dadcue posted an article on alternatives for psoriatic arthritis in another discussion here - https://connect.mayoclinic.org/comment/1010415/ that might be helpful. Are you able to discuss possible alternatives with your rheumatologist?

@johnbishop

I don't remember posting this but the links are both the same. I was on Humira for about 3 months for a condition similar to psoriatic arthritis. I have reactive arthritis with uveitis which are in the same family of disorders with psoriatic arthritis.
https://www.medicalnewstoday.com/articles/psoriatic-arthritis-vs-reactive-arthritis-comparison
My only problem with Humira was that it didn't work well for PMR. Had I not had PMR, Humira might have worked for me.
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I don't know the connection that neuropathy has with autoimmune disorders. I definitely have neuropathy but mine is called idiopathic. For all I know, my neuropathy could be autoimmune too.
https://autoimmune.org/disease-information/peripheral-neuropathy/

Sorry Mike @dadcue and @seniormed, I messed up the link to your post in another discussion and just now fixed it. This was the post that I should have linked - https://connect.mayoclinic.org/comment/1010415/.