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 ...

Does anyone suffer from a high heart rate while in enclosed areas with heat and no ventilation? My heart rate usually goes up could reach up to 130/140 on my watch I feel nauseous and as if I will faint Is that only me or a common MS thing?

That’s partly what gaming is for me. I can jump online, play a few games, talk absolute rubbish with people and switch my brain away from MS for a while. It’s basically my pub, except the beer is cheaper and occasionally a 12-year-old calls me shit at Fortnite. There’s even research suggesting surge...

I have just increased my dulloxetine to assist with fatigue and ever morning I take it, I seem to get very itchy hands. Not sure if they are connected neither are the nurses/pharmacist. Anyone else had this?

I've just informed the DVLA about my RRMS diagnosis. I have no symptoms that affect my ability to drive, and my consultant said I was fine to continue doing so. I'm still scared they will revoke my licence 🙈 I have 3 children who I have to drive to and from school as we don't live near it so this w...

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 ...