I am really interested in all the comments on Amantadine, mainly because I’ve got a box sitting in front of me but my GP prescribed it to be taken between 4-6pm and everything I’ve read says not after 2pm to prevent insomnia. My neurologist wrote to my GP to tell them to prescribe it, but I fee…

Good morning I’ve been having numbness in my right arm and hand tingling a couple of years ago never thought anything about it ,until April 2019 ,I started with the symptoms again . I can have several episodes a day they can come and go I get such a strange feeling then sometimes a rising feeling…

Hi everyone. Hope you’re all well. This is my first post and I hope it is shared in strict confidence. I am going to skip the details of diagnosis and move onto the biggest challenge I have faced since being diagnosed with MS. I would be so grateful of your opinions. I was diagnosed with M…

Hi all. Does anyone have any experiences of taking Amantadine for MS fatigue. I am currently taking modafinil x 2 100g first thing each day but still suffer from chronic fatigue in the afternoons. MS Nurse has recommended switching to Amantadine. I’m happy to switch but reluctant to give up mo…

Hi I AM 21 years old, I found out in March this year while 20 weeks pregnant I had MS. From 12weeks onwards Through pregnacy I got double vision I was bed bound I had no balance and alot more concerning problems. I have no MS in my family so was a shock! I had a CT scan that showed nothing, Lumber …

Has anyone out there given up eating nightshade plants. I just read a brief article that said nightshade plants are bad for some people with autoimmune diseases for even cause a auto immune disease. Some people are allergic to them, it said to quit eating them for two weeks and then introduce o…

Hi! I’ve been so miserable lately! 15 years since diagnosis & going down! Until now I was soo good! Can barley walk now… never been like that! Hate it! I’m tired of being tired! So scared to end up on a wheelchair 😢

Get excited when you’re about to start a new treatment, or is it just me? 😊 Maybe hopeful is more the word for it

Hi all this my first ever post on here im a single mum to my amazing daughter whos almost 13 from oswestry shropshire in the uk i. Not only have ms found out almost 3 years ago i have heart failure but as ive. Been. Such good girl and keep taking my meds my hearts improved so much i no longer need …

Hi All, hope you’re all well. Thought I’d join this site to share experiences re living with MS, potential treatments, life/work balances and relationships. My name is Vanessa, Scottish, diagnosed with RRMS 12 years ago. MS Didn’t give me any significant problems (recovered well after initi…