Hello
I’m Sally, I was diagnosed in April this year with rrms. I’m still coming to terms with this scary condition and trying not to over react to changes. This being balance, pins and needles, numbness, moments of feeling really weak and wobbly legged and various niggles. Which have all got worse since diagnosis- is this in my head (pardon the pun 🙂🙃) or is my ms getting worse?
Im on techfedera and got through the the stomach cramps and just have the burning hot flushes once or twice a day which is bearable.
Any advice about symptoms and what to do would be most welcome
I've been on tecfidera for 3 years now and my two mri's I've had have came back with no new lesions. I've been through similar experiences to yourself and it does take a bit of time to get used to but eventually I found myself in a better place through slight exercise and better diet. I think everyone had different experiences but please try and stick it out and hopefully.....and I know you will.....find yourself in a much better place. Thoughts are with you x
Thank you, it is getting easier to deal with. It’s mainly the balance gone wonky for the last week so I’m fearful that I’m having another relapse. I have two lesions in my brain stem so could it be they are flaring up?? In terms of excercise I don’t to bad in that I do running a lot and training for a 10k at the moment. I work full time, gardening, walk the dogs. I do get tired tho!! My diet isn’t perfect but I’m guessing it isn’t the worst xx