Looking for
something specific?

So last week I started Kesimpta and i injected in my leg, the side effects were okay just flu like symptoms and my legs were dead weights, but this week I injected in the stomach in the evening before bed and suddenly my whole body heated up, my upper body had a rash and my arms had red patches. Luc...

I've got my yearly blood tests tomorrow what do they look for I use kesimpta just worried about what they are looking for anyone had there blood tests done

So I've been taking injections since 2021 first plegridy now Kesimpta No bleeding First blood today 😂 this time I've injected myself and drew blood 😅 I don't feel like I did anything different, top of the thigh. Though this is the first time I've been given the cotton swabs and wipes along wit...

Hi, new here. 👋🏻 Just looking to have conversations with others who understand what I’m going through on a daily basis. Anyway, I was dx in July 2018. By September 2018, I had started on Lemtrada. Only a few months after my 5 year DMT monitoring period concluded, my neurologist put me on Kesimpt...

It’s been a while that I haven’t posted hope your all feeling well. Quick update on myself during with my MS. I am doing ok thank god and also been told since starting the Kesimpta I am stable and which is good news to hear as I have been through a difficult situation lately as me and my partner hav...

I have had to delay my Injection by 8 days due to a chest infection and concern about it stopping working. My family keep saying its fine they factor in changes of dates and delays (they have no knowledge of MS) but I am not so sure. My parents said they probably only need you to do 10 Injections ra...

Hi all. I'm taking the kesimpta injection and it's going fine. Me and my partner are thinking about starting a family, me coming off birth control etc. This would also involve changing my medication. I'm just looking for some advice please?

So a few months ago I had Lymphipenia which means my lymphocytes were dangerously low. I was asked to stop and chose a new med, I have yet to start. Does anyone take it and what should I expect?

So just seen the neurologist and it’s confirmed as Tumification MS and rapid evolving MS (having had 3 episodes in 2 years). Reading everyone’s stories I think I’m lucky as it’s only been 7 weeks since my first scan and I have seen the neurologist and neurosurgeons. Now to look at DMD options, I’m l...