I take Black Seed Oil, Seamoss, Paleo diet.

MS gym with Trevor Wiken, MS moves with Mandy. Both available on YouTube and they have excellent platforms for all things MS related. Movement is medicine. 🌻🧡

Yes but until you know what you're dealing with, everything is going to be a guess. It's a process. It stinks. But to treat it and get some help you have to know what the problem is. Leave "DR. INTERNET " alone for the moment. Get a firm diagnosis and go forward with that in mind. Internet medical information is not a good thing. If I'd believed Dr. Internet I'd have been probably trying to howl at the moon or bathing in sheep poop to treat my leprosy! My point is until you know your status and get a firm diagnosis, you just won't know. You'll drive yourself crazy because Dr Internet says you probably have to. Go easy on yourself now. There's going to be time to work on the solution once you know what the problem is.

If it wasn't for the internet I wouldn't know about a study done that I shared with my neuro. I'm now getting botox for my extreme spasticity. Everything isn't for everyone. Being your own best advocate means educating yourself so you don't leave feeling your concerns are not being heard. Use your discernment and good old fashioned common sense. Fight on warrior, in whatever way honors your life. We all have MS. But we are so very different. Our lifestyles, demographics, etc, etc. I'm sending you positive vibes and good energy 🌻 🧡

I have felt I was losing my mind or imagining symthoms reading these post have given me strength and a voice. I really thank everyone and hope you continue to share.

I'm having problems remembering words Since covid in January I have been in a horrible MS flar getting more tests than tomorrow