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Hi all, my name is Bill and I’m a 58 year old male from MA. Thank you for adding me here. I was diagnosed with MS in April 2019. I am now on my fourth DMT (previously on Tecfidera, Vumerity and Copaxone). I’m currently on Briumvi infusions. I had my first infusion this May, and had my second infusio...

Hello, I'm just wondering if anyone else has had trouble with medication. When I was pregnant I was on copaxone which my skin had a bad reaction too and then on avonex but had bad flu symptoms when I took them for 3 hours. Then I change to tecfidera when I was no longer pregnant and took for 3 mon...

Hello 🫶🏻 I’ve recently stopped Copaxone after starting to react to it and have just been approved for Kesimpta and Ocrevus-I can choose which I’d prefer to go with. As someone who has quite a lot of anxiety around taking medication the controlled hospital environment and longer periods between the...

Hi, after 3 years of Brabio/Copaxone (glatiramer acetate) injections I have to switch to Mavenclad as my neurologist found 2 new lesions on my brain. I’m very nervous to make this switch, it’s hard to hear that the medication you’re taking is not working. Does anyone have any advice or want to share...

So I recently had my annual appointment and MRI. Luckily nothing new picked up on the spine but unfortunately the same can't be said for my brain, as the scan showed a huge new lesion was found. Therefore, my doctor decided its time to switch from Copaxone to Myelenea (Mayzent). Can anyone share th...

Hi 👋 everyone, I have been on Tysabri for 2 years now and just been told I am JCV positive.It's a high measure so my health team have advised me to come off it. I would like to have another child in the next year or so but worried that this might not be an option now if I switch drugs. U was on Cop...

I had my son in February and I was told during my pregnancy that I was high risk of relapsing in the first 3 months Post partum. Ofcourse my body decided to have that relapse in the April. I was on steroids and finished the, then had to have an MRI. Unfortunately my MS was still active after the ste...

My ms nurse just phoned me- I’m having my infusion next month then I’m having my injection next year. It will be in the tummy before take antihistamines, Paracetamol and a steroid tablet. It will take 10 minutes probably have to wait view minutes to see how you are. Never had a infection in my tumm...

i take my own injection myself its so easy taken its i feel better its good for me im looking forward taken its again on wednesday

Hello again everyone. I’m still bloomin ill. Had a test and I’ve had/got campylobacter. My injection was due last Sunday. My nurse advised to delay it and said to get back to them if it’s delayed by over a week. I’m still not 100%. Much better than I was but still nauseous and my stomach is defini...