Tips on Tecfidera?
So I was diagnosed with RRMS in November of last year (2021) and the treatment recommended to me was Tecfidera. I have not taken any yet even though I was prescribed it a few months ago as I have been trying to finish my last year at university.
I have never been good at taking any medication because I am scared of side effects, especially feeling or being sick as I have a phobia.
Just looking for some advice or words of encouragement as I will be starting treatment in the next few weeks. I am constantly asking my nurses the same questions over and over but it would be good to hear from people who have experince with it.
Thanks x