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Hey! I was diagnosed with RRMS in sept 25, following main symptoms of right sides leg numbness and weakness, with sporadic arm numbness. I also had some foot numbness and other symptoms before and after the leg symptoms. Since June ive been mostly symptom free. I started octrevus at the end of octo...

I’m new here. I was just diagnosed with rrms with chronic seizures on my birthday 10/16 after having it for 17yrs I had my first steroid infusion treatment today day 1 of 5 I would love any advice any one would like to give. I just turned 38. I’m a mom of 3.

Hello, I was diagnosed in 2024 after 9 years (apparently an earlier MRI taken then could have meant an earlier diagnosis but I had a less competent neurologist then). Anyhow, I have been on Kesimpta since last summer and didn't have any notable side effects.I also take high doses of vitamin D and om...

Hi everyone, i’m newly diagnosed. I have yet to even see neurology outpatient. I went into the ER thinking I was having a stroke and my MRI results showed a different story. They did a spinal tap so I’m waiting for those results to come back. I’m here because I’m not really Sure what to expect with...

I got diagnosed with RRMS in the month of June. I didn't had a clue about this disease or the symptoms. I'm still figuring out the symptoms that I'm experiencing by searching on the internet. All new terms and symptoms to understand. Recently I've been facing a lot of Cognitive issues, feels terribl...

Officially was diagnosed Friday with MS. I did three sounds of 3 days of IV steroids, which did havoc on my body. They are starting me on infusions , just waiting on the insurance. My questions are ... Help me prepare for my infusion... What to wear/ bring ? What snacks to bring ? Your experience wi...

Im newly diagnosed and I feel so emotionally all over the place. I feel like a prisoner in my own body because of my symptoms. I didnt have early signs... or I missed them so I went from being fine one day to literally broken the next. My emotions are all over the place! Im so mad and depressed...

My doctor is starting me on samples of Ocrevus next week and I'm scared after hearing the horror stories related to it he told me I've got an aggressive primary progressive ms which you never want to hear from your doctor aggressive 😭 but now I'm accepting everything it's horrible and my poor mothe...