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Old 02-18-2008, 05:42 AM
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Question M.E/C.F.S

Hi Everyone, this is my first post. Ive had severe M.E for 6 years, 3 of them bedbound, now I manage to get out the house now and again but am still really ill. Ive been reading about MMS the last week and am really excited about trying it. Im waiting for it to arrive. I was just wondering if anyone had had any success with using MMS for M.E/C.F.S? Thanks, Leis.
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Old 02-18-2008, 06:17 AM
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Welcome Leis. It's good to have you here. Have you been to the blog https://www.healthsalon.org/

On the left column, click on MMS testimomials, then scroll down till you come to Testimonial number one. - that includes information about ME - CFS. There are some cautionary tales too - worth reading those! Good luck
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Old 02-18-2008, 06:35 AM
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And be sure to read the Klinghardt protocol found on this forum in the MMS thread.
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Old 02-20-2008, 03:23 AM
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Thanks for the replies Xania and Arrowwind
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Old 02-20-2008, 05:17 AM
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Welcome Sproket. 21 years ago, I developed CFS from too much exercise while on a severely restricted diet. I was able to recover with good nutrition and a more reasonable exercise regimen. I do occasionally have a relapse if it over extend myself. When this happens, I take a stiff dose of Beta 1,3/1,6-D-Glucans at bedtime, and I usually am fully recovered in the morning.
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Old 03-06-2009, 07:14 AM
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Quote:
Originally Posted by sproket View Post
Hi Everyone, this is my first post. Ive had severe M.E for 6 years, 3 of them bedbound, now I manage to get out the house now and again but am still really ill. Ive been reading about MMS the last week and am really excited about trying it. Im waiting for it to arrive. I was just wondering if anyone had had any success with using MMS for M.E/C.F.S? Thanks, Leis.

Hi Leis,

I too was diagnosed with ME/CFS and have been ill for over twenty years now. However two years ago I found that all my symptoms are due to lyme disease and I have recently started MMS to help with my symptoms.
It would be worth you getting a blood test for lyme and I think many ME sufferers have been misdiagnosed and mistreated for year!
If you want to email me privately on [email protected] I can advise you further.
best wishes,
Shelley
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