I just got the diagnosis in June of last year and started Tecfidera in August. My latest MRI showed quite a few new lesions in my brain (I only had one visible lesion when I was diagnosed). My neuro is going to get another MRI in 4 months then make a decision about possibly switching to Tysabri. I will go in sometime soon to get the JC virus test.
I am wondering about what the infusions are like and how long it lasts and can you go back to work right away? I don't like the idea of missing work once a month - would it be feasible to get the infusions in the morning and be back after lunch, for example? No one at work knows about my MS, so getting this time off will be awkward. And it would be harder to explain monthly absences.
I am wondering about what the infusions are like and how long it lasts and can you go back to work right away? I don't like the idea of missing work once a month - would it be feasible to get the infusions in the morning and be back after lunch, for example? No one at work knows about my MS, so getting this time off will be awkward. And it would be harder to explain monthly absences.
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