Hi - just wondering if people on tec have urine tests done every 3/6 months along with their blood tests? So far I’ve only had blood tests.
Thanks 
Nope, just bloods in the 2 years plus I’ve been on it.
never heard of urine tests for tecfidera.
Thank you all. Good to know others are just having bloods too. I hadn’t realised some places do both until I read it somewhere the other day.
Your hospital sounds fab Val!
I didn’t know that so many people had both done.
Good idea because as we all know UTIs lead to relapses.
I used to have urine tests, but since covid just bloods. I’m impressed you get your results online. I phone up the next day to get mine. If I didn’t phone up I would have no idea as not automatically told here.
I have bloods (and the last couple of times urine) taken at GPs. If the nurse ticks a box the results are available through GPS patient access. Otherwise letter sent to me and GP. I assume if there is anything dramatic my MS Nurse will contact me.