slayadragon
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I have heard an increasing amount about the idea of the issue of mast cells problems being related to ME/CFS over the past few years, but am not sure if this so far is a hypothesis or if people are actually succeeding with treating this with drugs or in other ways. And I don't have time to read through all the threads on this forum.
So I'm wondering if someone would be willing to summarize what experiences people with ME/CFS have had using this approach. (Other than, of course, avoiding problem substances, which obviously can be helpful to people with this disease.)
Thanks much for your help!
Best, Lisa
So I'm wondering if someone would be willing to summarize what experiences people with ME/CFS have had using this approach. (Other than, of course, avoiding problem substances, which obviously can be helpful to people with this disease.)
Thanks much for your help!
Best, Lisa
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