Hey all, had my post relapse appointment yesterday and have agreed to start on oral Tecfidera starting in the coming weeks. Feeling positive about this but maybe not the first few weeks, I'll try keep a diary. Anyone used anything to tackle any side affects (stomach or flushes), just in case it'd be good to know.
Make sure you eat properly. That is all I can think of. My flushes were minimal and only lasted minutes. My ms side effects are worse than the meds ?
Thanks Naomih, eating has never been a problem!!! When do you take them? Morning and tea time or later? Sure the box will tell me when they arrive!!!