When do you feel your dmt has worn out, My next round of Ocrevus is August, when do you start feeling like it running out? I'm not getting wobbly yet that usually the first sign that it wearing out.
I recently had my MRI results and (as I kinda suspected after a rough few months) had new lesions.
I'm currently on Plegridy (moved from Tecfidera as I'm JCV positive and my lymphocytes lowered a lot). Tecfidera worked ok for me, but Plegridy obviously hasn't been as effective.
Due to the hard fe...
Hi all.. do's anyone else feel let down by their doctors..
My consultant is more bothered about how far I can walk than anything else, I have vision problems but to them it's not a problem to me it's a nightmare and all they keep throwing at me is physio to help my walking... I'm not on DMT as my bo...
Hi all, in a few weeks I’m going to go on holiday for the first time after diagnosis and recovering from a relapse. I’d like to ask what are the things to consider or that might be useful to bring ? I have done a travel insurance but I’m thinking if should ask the ms team for a certificate of the di...
So I went to the doctor my lession on my brain hasn't progressed so that's good but, I was concerned because I asked my doctor why haven't I been sick yet, my main worry was how often I would get sick due to it supposedly suppressing my immune system but, I have not maybe due to my other autoimmune ...
Hey has anyone else had problems with friends and family understanding the treatment. I’ve spent time with my friends and family explaining the treatment and truly thought they understood. I had my first full treatment of Ocrevus yesterday and a friend has texted asking when will the treatment start...