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Myasthenia Gravis For support and discussions on Myasthenia Gravis, Congenital Myasthenic Syndromes and LEMS. |
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05-01-2023, 08:43 PM | #1 | ||
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Hello! It's been a while since I've been on here, I hope everyone is doing decently well!
I was curious if anyone has experience with MG and using CBD products, and how it affects your MG? |
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05-07-2023, 04:28 PM | #2 | ||
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Hi. Out of desperation for help with nerve pain in my left face I tried lowest strength CBD oil as one tool to help. I was getting increased pressure to use less Hydrocodone I had to look for options. I can’t use a strength more than 17 mg and it works so well I can use a little on my fingers on left face and Occipital Nerve spots like above my ear. I do not use it for tight even spasmed muscles especially Chest. In a push for relief I have on a couple Occasions depressed my breathing by over applying. Daughter bought me stronger Oil by mistake and wow that made me weaker all over. I am careful to use a high quality product that is also used for Seizures by children. Sculptor 44
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05-08-2023, 06:59 PM | #3 | ||
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On last message from me I wanted to mention my very complicated vision and Brain and it’s affects on my writing. So when I went into uses I put the word NOT in before talking about Spasms. Opps. My Eyes are a lot worse. On Spasms which I get severe it is Excellent. And it is Fast!! Again some on my fingers and apply on skin at spasm and it starts to relax. This CBD is the one Dr Sanjay Gupta documented so Well on his CNN series. Be well. Sculptor 44
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05-18-2023, 05:21 PM | #4 | ||
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Oh good to know! I know CBD has been associated with anti-inflammatory effects and can help with some autoimmune dz's like RA, but I sure don't want to make my muscles weaker! Thank you!
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