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Off Topic Fibromialga

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I know this is off topic, but has anyone here had any experience with SCD

helping Fibromialga? My mom has it and it's been really painful for her

lately. I told her it could be yeast and to try the diet, but her Doctor

told her that was a bunch of bologna. Doctors can be so stupid sometimes.

I thought if I could show her that it has helped others with Fibromialga

that she may be more likely to try the diet. I would appreciate any of your

thoughts or experiences.

Thanks,

Kim-Mom to Noah 2yrs old SCD 1yr ASD

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