We now have nearly 700 people who subscribe to the MS forums but most of you don’t say very much. I’m curious about who’s here. Why did you join us? What information are you looking for? Are there things we should be doing that we aren’t? Don’t be shy – John and I, and I’ll bet a bunch of your fellow MSers, want to hear from you.
I joined because I was looking for others with MS and their experience with CBD, though I’m sure there are other topics that will interest me. There might be some topics that I can contribute useful experience, suggestions and/or advice for 🤗
I use CBD when I haven’t got the real thing! Think it has an effect but this could be just placebo. As for the real stuff drink it at night with cocoa [now always get marijuana oil] as it helps me sleep and reduces the muscle pain I often get in my right arm. Was part of the post-sixties generation that took drugs recreationaly. Its strange that MS has meant that its no longer for fun but survival!
Multiple Sclerosis News Today is strictly a news and information website about the disease. It does not provide medical advice, diagnosis or treatment. This content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this website.