Looking for
something specific?

I know its bad in the beginning but would like some more anecdotal experiences of colds and infections when on this long term - both good and bad experiences. Thanks

Hi everyone x How do you handle not feeling supported mentally, emotionally or physically? I live on the other side of the Atlantic from my family. They don’t visit. I’ve made peace with it. If they ever say it I’m like whatever. My mother never really took my MS stuff seriously. But she met a...

Hi all, hope somebody may have the answer and have some experience of this. Is it a simple case of just stopping the monthly injection or will I need to gradually wean off the medication. After 2 years of taking Kesimpta, the side effects (constant cold, runny nose and dry eyes) have taken its toll...

Took the first injection and I know some people get sidetracked effects and some that don't so let's hope I'm in the latter category 😂 I've got some paracetamol if needs be. Injection site a little achy but that's pretty normal

Hi Wondering if anyone has advice on taking vitamins with Kesimpta. I used to take the following but have since read some may be unsuitable. I stopped taking an immune supplement which contained C, D & Zinc. I got a cold for the first time in about 10 years. Taking D3, B12, Omega 369, D Mannose. Us...

Hi, I wasn't at home yesterday to sign for my Kesimpta package and just picked it up 10 minutes ago, the ice packs were melted and the prescription box that holds the injection wasn't very cold, is it still good to use on Nov. 8th, or should I call Kesimpta and let them know?

I’ve been taking kesimpta for over a year now and had no issues so far! But after my last injection 2 days ago, I’ve noticed some slight redness, swelling and itchyness around the injection site. Has anyone else experienced something like this?

Spoke to the MS nurse today about medications and I got a booklet describing all of the meds, I’m having a hard time choosing between these 2, kesimpta is 1 monthly injection but side effects look a bit rough and you aren’t monitored as much whereas Ocrevus is the 6monthly infusion still kind of rou...

Has anyone Had knee replacement after being diagnosed with MS