OK guys so I am basically guinea piging Myself with magic mushrooms. I’ve heard a lot about people micro dosing to help them with all kinds of stuff, but I do have a high Tolerance so I will not be micro dosing. This is my first time and it’s all in hopes that it helps with neuroplasty. Has anyone ...

Hi all! After 6 years, I’ve finally found a consultant who will prescribe Fampridine for me! I live Liverpool, UK where it is not available on the nhs so I’m paying privately! Don’t get me started on the postcode lottery of this!!!! Anyway, thankfully, other than the initial consultation fee I am ge...

Just a question that's been on my mind 🤔 How do those of you with MS who live in hot countries manage your day to day life? Does the heat make your symptoms worse or have you found ways to adapt? Love to hear your experiences, routines and any tips that help you cope.

Does anyone take choline supplements and does it help with your MS

First post here. I've been going through a flare up for over a month now but been told I can't be given steroids as I'm waiting to start treatment, waiting being the key word here since no one seems to know what's going on it feels like. I've been dealing with hand numbness and spasticity and other ...

My days have been quite painful since summer’s start. As a result I’m asleep soon after and the days now become nights 😅 the fun find is that I’m darn near pain free all night until the sun comes up. So freaking weird! I can tell the sun has come up by the tightening of my leg muscles as well as ...

Hey peeps, I've noticed that my symptoms increase/worsen when there are rapid or drastic changes in the atmospheric pressure. When the pressure starts rising rapidly or gets above 1025mb I feel awful. Start experiencing worse vertigo and headache. Does anyone else check the pressure and notices ...

I feel like every since my diagnosis I've been limiting myself mentally with what I can do. Prior to being diagnosed I knew something was wrong and I just kinda pushed through everything and dealt with it. Now im quicker to relax and not push myself which is good, but my problem is I've lost most of...

I’m not sure if uncaring is the title I really want for this rant/observation but I started thinking of the years since my diagnosis (2002) my family members even my grown children I don’t think any one of them has really been curious enough to read about my symptoms the things I deal with daily and...