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Turns out I had non-specific lesions on my brain. I was having neuro symptoms when they found them, but they found them to be so “unimportant”…they LEFT IT OUT OF MY FINAL MED REPORT…..then slapped me with a psych diagnosis….now 2.5 years later my symptoms are worse and I’m disabled….im pissed. I’ve...

Could anyone recommend an insurance provider who is reasonable? I am having difficulty finding a provider who won't gouge me because of my diagnosis.

Hi everyone, I'm new here, got diagnosed about 2 months ago after optic neuritis and 4 months of waiting for the results. I feel relieved to have the diagnosis but also feel like I'm "fake" and "guilty" seeing as my only symptom is my eye problem. Has anyone had similar experiences/feelings after th...

1. Vitamin B12 Deficiency Symptoms Numbness, weakness, balance problems, brain fog, very similar to MS. Diagnosis Blood tests measuring B12 and methylmalonic acid levels. Why it is different Caused by a vitamin shortage rather than immune attack. Symptoms improve with supplements instead of immun...

My first post, so let me introduce myself, in case it helps someone who’s closer to the beginning of this difficult journey. I’ve had RRMS for over 20 years and been on DMTs for around 15. I’m still walking and working, but get tired easily, and I still drive, just with a blue badge in the car. So,...

Hi everyone! Today was another big day in my new MS journey since my diagnosis in February 2025. It has been confirmed I have relapsing remitting MS and I will begin my medication in approx 6 weeks - short wait whilst the NHS sort this out. How did anyone find the medication I'm being moved on ...

it’s been rough since the diagnosis. My relationship ended because of it, even if it wasn’t the only reason. A lot of little things stacked up, but when things got tough, she left. Just moved out over the weekend let her keep the apartment. I’ve been trying to reach out to the MS community, see if I...

I’ve got my first appt tomorrow with the MS nurse, I’ve read up on DMTs and pretty much made my decision. I’m happy to hear what my neurologist recommends based on his meeting with the MS MDT I’ve got a list of questions and a list of symptoms but my main question is - when can I start treatment! ...

I was diagnosed March 31st, 2025, And I don't know how to get my family to realize I might never be better... I understand that it's only been a few months, the first year of diagnosis is the first, and this is hard on them too. I am blessed to have a family who can assist me and help provide for ...