I’m on tec & have been for the last 2yrs. The flushing never went away. My biggest prob is I’m prone to infections, I’ve never had as many since being on tec. Now, my neurologist has advised me everytime I hav an infection to stop takin tec so my point to her was I’m off it more than on it. They seem to be reluctant to change my treatment as any new lesions on my brain & spine hav been insignificant. I’m awaiting another appt for brain & spine MRI I see my neurologist on 24th & would like to speak to her about dif options bcos before I just let everyone else decide wat they think I should do. Would like to have tried cannabis to help wiv pain & spasms in my arms legs & hands but I hav young children & live alone with them, social workers are involved & explained its illegal & I cud actually lose my children if I do use it. I’ve tried dif types of cbd oil which haven’t helped either. My hair has definitely thinned also. I’m exhausted both physically & mentally & don’t know what else I can do to help myself. I think this is the most I hav spoken about my RRMS since my diagnosis in 2014