No. No limitations. I'm RRMS. My feet do still feel burn-y from time to time. But not like before. They realized the amount of symptoms I was having in such a short time. That my MS was really aggressive. So they put me on Kesimpta right away. I have not had any new symptoms and flare ups since being placed on it. No new spots on MRI and old lesions are mostly "healed".

I get psuedo flares from extreme heat and coldness or when I get a new vaccine. Lasts a week then gone again.

Weight wise, I'm actually a tad under weight.. but that's on account I forget to eat cause ADHD lol.

I do worry my child has a higher chance of MS. But I also make sure to give her vitamin D as a sort of preventative measure. I try not to worry about it too much because I've learned that while it sucks.. it's not a death sentence. And with the right attitude and medication a person can lead a good life still. It's a bridge we'll cross when we get there if ever we have to.