I’m 31, was diagnosed with MS 4 years ago, but I’ve learned to basically live with it with no medications. Now as of last week I’m experiencing just awful symptoms. I’m so dizzy i can hardly stand. Has anyone had success with diet changes? I’m reading two books right now (well, my husband is for me I’m too dizzy) and they talk about MS being absolutely healed due to killing all the yeast in their bodies. Any thoughts??? Has anyone had good experiences with this???
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Members responded to a question about diet changes for MS by sharing personal experiences and practical insights, with several pointing to Dr.... Read more
Stem cell is a process but I believe it would benefit a lot of people dealing with autoimmune disease. I'm no scientist but if you look into it , it sounds very promising. We would all just have to keep hoping for a miracle. 🙏
I read others comments on stem cells and from what I have read and from one person I know that has had it, There is strong reports of a definite improvement after treatment but it fades with any or all improvements gone after 3 years or so.
I would know that ! Before getting diagnosed I had multiple flare up's and since I was only 15 years old my mom had to take me into the hospital. She got tired of taking me and saying I was lying because the doctors kept telling her I was fat or on drugs. So I had to learn how to know my body and when to let it rest or what no to feed it. I know medicine is a must with MS to slow it down, but Medicine is also the cause of many other illnesses.
Happy to hear your MS is leaving you mostly alone,I tried the theory of diets and life style changes . I fully recommend medication , remember it is about limiting damage ,what ever happens is there for ever so try and minimize it while you can . Living with it and ignoring it hoping it goes away isn't the best idea , I tried it for a few years after I was diagnosed and thought it was a better option ... till it wasn't.
Yeah that is very ture. But when I asked my doctor about it she said that they are only testing it at the moment. Also, that they would only do it to people who are already at their worst. My father lives in Spain and they are more advanced with MS over there.