Morning, I am new here and new to this cursed condition. Apologies for the long winded tale I'm about to go on! I was diagnosed with Psoriatic Arthritis in 2020 and was given a raft of poisons which didn't work until I was given the miracle drug Adalizumab. It was a revelation. All symptoms gone, all pain gone, even the quite atrocious nail psoriasis disappeared. Fast forward 3 years and I lose all feeling in my left hand side, like someone has deleted my nerves in a perfect line all the way down from my collar to my toes. Visit various NHS "professionals" only for a Chiropractor in Gateshead, formerly of the USA, (who refused to touch me and gave me my money back) to shout at my GP to arrange an MRI. Panicked messages from Rheumatology and my GP telling me to immediately stop the TN-f drug and wait for a Neurologist. Which brings me to now. Diagnosed at 38 with RR MS and once again suffering with arthritic flair ups with all the joys that come with this. Peripheral Neuropathy is listed as a side affect and there is loads of research articles basically saying that Rheumatological treatments are "causing" MS, yet the NHS will not confirm or deny this. Has anyone else experienced this?