Sudden Multiple Schlerosis in 2021? I wonder why 💉
(media.greatawakening.win)
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I've had MS since 2000. I went through the double vision, facial paralysis, walking with a cane and eventually a wheel chair. Now, if you saw me, you'd never guess I have MS. I give credit to meds I now take. My neurologist tried to get me to take the jab and I refused. Now they think I made the right choice.
So, what meds are you taking?
I've been on Avonex, Beta-Seron, Tecfedera, Tysabri and now Ocrevus. Ocrevus is a bi-annual infusion. I have an MRI scheduled in two weeks to see if Ocrevus is still doing its job.
I'm glad to hear your symptoms are mostly in remission and that the drugs are helping. There may be supplements that help also and/or that reduce the chance of side effects from the drugs; you've probably already researched that topic but here's a resource worth knowing about:
https://www.lifeextension.com/protocols/neurological/multiple-sclerosis
Another thing that comes to mind for me is that the contrast agent injected into patients before an MRI can cause serious side effects; someone I know had an MRI last year and until then I'd never heard of that. As with other procedures and drugs being prescribed, the side effects are often downplayed or simply not mentioned. Some contrast agents are more likely to cause problems than others; it may be worth your time to look into the topic.
https://www.qwant.com/?q=MRI+contrast+agent+side+effects&client=brz-brave&t=web
Best wishes for your health.
Thank You