← Return to Doe anyone with Myelofibrosis suffer musscle spasm?

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I have CMT, which is a rare neuropathy and affects my entire body, that was diagnosed in 2022. The muscle spasms have been so severe that I can't move or walk and sore for several days. I am on magnesium and muscle relaxers. Staying hydrated is supposed to also help. Doctor suggested drinking a bottle of Pedialite every day. I use a powder form of electrolytes in water that helps. These spasms come on so suddenly, day and night, that I knew I needed something that would help immediately. What has been working for me when I feel one coming on is pickle juice. I carry it with me everywhere and have by my bed It truly has been a blessing. It doesn't interfere with the meds and stops the spasms before it goes to the "I can't take it anymore stage." I hope this helps you as it has me. Prayers for you all.

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Replies to "I have CMT, which is a rare neuropathy and affects my entire body, that was diagnosed..."

Thank you for info re muscle spasms, you do get to stage where Can't take it anymore. have not found secret to stop it yet - but very debilitating