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Please help,

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Hi LDN family, I have followed this group for the last 4 months learning and reading all the juicey advice and details daily.

Hope you can help me, I'm 34 with FM & have been on LDN for 4 months and feeling better. I have 90% of the symptoms of Canadida and did the spit test which if is accurate I do have it! I have researched so much about it but confused not sure what to do from here, what to take or who to see? I dont have insurance and understand most docs are not even familiar with Canadida.

Any advice I would appreciate,

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