Hello all, I’m 45 and was diagnosed with MS in June following initially visiting the doctors in April due to experiencing electric shocks in my face and head when touching a trigger point on my face, usually when using an electric shaver, really horrible and incredibly scary. Thinking it was Trigeminal neuralgia initially but after all the tests it turned out to be a symptom of MS and I was given the diagnosis. So after discussion with the consultant and doing our own research, I’m due to start Kesimpta in March. Should I be concerned about possible side effects or anything bad?