Questions for the lovely and supporting people here:
- Has anybody tried the herb maca? It’s quite expensive here in Australia, but if people with fibromyalgia and CFS (or one or the other) have had good experiences with it, I’m willing to shell out.
- Also, I’d love to read some opinions on A Hummingbird’s Guide-merely the ramblings of conspiracy
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The article is here, there are 300 comments. Hopefully they will print some letters in reply this week.
http://www.newscientist.com/article/mg20126997.000-when-illness-is-mostly-in-the-mind.html
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2. I don't gel well with the Hummingbird's guide website and it's view of CFS always being a misdiagnosis (even if I believe ME is a more appropriate name). But I don't doubt that there is a lot of other useful information presented.
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