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After the mess the last few weeks. No new lesions. No contrasting lesions on brain or spine. No active signs of disease.

I want to share my great news here, as I feel you all are the ones who will truly understand. I recently had my first post-DMT MRI and I have NO NEW LESIONS! 😁🙌

I received this letter.. I am pleased to report that your recent mri scan of the brain shows a significant impr5in the appearance in terms of the number of MS lesions seen. Small residual changes if MS are seen with most other lesions having almost totally resolved. No features of PML are evident....

R2WK41 - My MRI results are in and its GREAT NEWS www.tracyslemtradajourney.co.uk

I'm 5 weeks pregnant!! After being diagnosed almost a year ago interrupting any plans to start a family. I'm so excited to share this news and it is a reminder that MS doesn't have me and that my life can continue on a path that I choose. xx

Please my people listen to this conference when you have time Mercury: A Hidden Driver Of MS And Neuroimmune Issues by Mark Hyman, MD We have great news! The Multiple Sclerosis and Neuroimmune Summit starts tonight at 6:00 PM ET. >> When the Summit goes live, you can access it here. << https://sum...

Hi ☺️ currently I am on Tysabri, have been for 9 months since diagnosis with so far very positive results (no relapses, symptoms, JC negative, etc), however my biggest pain point is the monthly infusions. Having discussed this with my neurologist he has suggested that I could choose to switch to Ocr...

Hi all. I am so confused, in a good way I guess but still... I have been feeling absolutely awful all year. I ignored the signs for too long which resulted in me reaching breaking point in October and I had to stop work. I've been working really, really hard to get better and I am definitely miles ...

Interesting post from the MS Society today about the new antiviral/antibody treatment proposals for people in the UK with MS who contract COVID19. Apparently we'll get a PCR testing kit to keep at home and then be offered treatment if we're COVID positive. I had COVID in April 2020 and was lucky...

I was diagnosed with RRMS October 2020 after I had optic neuritis. It appears that my first realapse was 18 years prior to diagnosis where I lost use of my right side but nothing else until last year which then lead to diagnosis. When diagnosed my neurologist advised that I was in the mild scale and...