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Hey, Previously on head mri results was some changes. Now I'm on hospital for the last 5 days. I have dizziness, lack of balance, fatigue and difficulty with balance and coordination. Doctor today said they still looking for results of lumbar puncture. The most I'm afraid of that if they will not fi...

If you've experienced retrobulbar neuritis before, can you share what symptoms you had and how it was diagnosed? I've visited the optician after having had pain in my left eye when moving my eye. No blurred vision or colour vision loss. The optician has suggested RN as a possibility and made an urge...

I have always thanked God that all my ms plaque is in my head so it doesn't bother my walking or my arms. We'll at my last neurologist appt. He showed my stepdaughter my mri an he told her I have a severely damaged brain like some one who has had multiple mini strokes. And that my brain is dying bec...

Hi everyone, I’ve been diagnosed with RRMS for four years now and have been on Tecfidera since the beginning. My latest MRI showed a bit of progression, and my neurologist has suggested switching to Siponimod. I was wondering if anyone here has any personal experience with this medication – how have...

I’m loosing hope I’m crying non stop everyday I can’t take it anymore. I can’t. I can’t. I can’t. I don’t have Ms because I can’t. My neurologist had to lying, I know he did when he said I have Ms. I want to be normal, I am normal I don’t have Ms.. I’m going on ocrevus soon but I genuinely can’t. Be...

To those that care about my health: I am stable. Still the same from 2021. My last MRI scan showing no progression of MS. God Is Good. Faith Works!

So I was originally diagnosed in 2022 however PCP never communicated with me, after much frustration I found a new PCP who suggested MRI in December 2024…. Came back MS. So he sent me to Neurologist who yesterday said not MS even after 3 MRIs with lesions, why because my oligocional bands are negati...

I have had MS like symptoms over the years. In March they really came back. I had an MRI with new lesions and they called it Dawsons fingers. Waiting on a neurology referral at this point. I’m just a little nervous because I’ve also heard it can be NMSOD. Very similar diseases. Has anyone else had ...

Think am have to go to the ER to get my MRI done . Am so scared to get back in there . The ER can give me something for my anxiety, and the fact that I’m claustrophobic..

I'm finally typing this out. I apologize for the length. I just signed up for this Ap, and want to vent about life a little bit. I got diagnosed with RRMS in 2022. Although like I'm sure most of you, I was struggling with mysterious symptoms for years leading up to it. My left hand went numb, li...