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Ok this is probably a bad idea to post as people will judge but it is called fun drugs so it must be on others people's minds too so here it goes anyway. I used to be the biggest party animal ever from my teens trough my twenties. I'm Dutch and all thing that are party feeling enhancing are readily ...

So since I had COVID almost a year to the day and had the fun delta variant I've noticed my legs retaining water. I tried more potassium, lower my salt intake, drink more water, water pills both over the counter and prescribed, compression socks but all to no avail. So my neurologist after trying al...

I have traced my first symptoms back 1989. I was officially diagnosed this past January. I went to different doctors and E.Rs over the years, but I was always told they had no idea what was wrong with me and that the issues will probably just go away.... UGH!! I now know that the different issues ...

I was diagnosed RRMS in Dec 2020, the neurologist believes I've had it for 11 years. I've had 2 relapses in 2 years and currently have 1 active lesion (great way to end the year!) I have narrowed my choice of DMT down to Brabio 3xweek or Tecfidera, I like that Tecfidera is more effective and a pill ...

Hi all Is there anybody who has tried both of these drugs to help with spasms (I dont mean at the same time!) I have been on Baclofen for months, my balance is all over the show and very sleepy, dont know if thats worsening of symptoms or the Baclofen? Am trying Tyzanidine, will let you know ...

Hey peeps 👋 Billy from Shift.ms here. I wanted to get your thoughts and opinions as we've had lots of new members join us recently. I feel like I got quite lucky with picking my MS treatment. My neurologist in London recommended three DMTs to me (Ocrevus, Tysabri, Tecfidera) and patiently explaine...

Hi just been diagnosed and not sure what to think/do. Neurologist has recommended three different drug therapies. Tecfidera Plegridy Copaxone. His preference is for Tecfidera, but as you know nothing comes for free and the side effects with that seem worse than the other two, and neither of them ...

Hello, I am new and joined this group. I have been diagnosed with RRMS September 2016, it have been hard but with time and support, things will be good. & I have decided today which treatment to go for and I have decided with Avonex (Interferon Beta 1a) as it is safe for me. I could not go for...

I didn’t think MS could still humiliate me. I feel bad about how I’m effecting those around me and how I am going to be a greater burden on my family. I lost it and tore into my wife. I was in such a haze that I can’t remember what I said. I acutely remember the feeling of being mortified. Of c...

Does anyone smoke cannabis or use cannabis to relieve their symptoms