there are a lot of moldies here:
/www.mypatientmatch.com/posts/mold-testing-apartment-for-dummies-39169I just grabbed the first thread in a search, but there might be better threads. Lots of mast cell, CFS,fibro, and lyme patients there are affected by mold. A lot of us there have Mast Cell Activation Syndrome/MCAS or Mastocytosis, and that is probably why mold is such a challenge for us.
I select "community", then "global" to look at the forum. Its better for me to see all groups cuz mast cells and mold are important to me. Not as busy as your lyme board here.
I remember one friend there posting an interview about
mold in the home that Chris Kresser did...maybe a youtube podcast, but his site likely links to it. It was an interesting interview with the guy who inspected his home.
(if anyone wants mast cell info, do a search for "reference" at mypatientmatch (up above). My thread will come up. Titled: Reference thread for sharing mast cell info. My posts are
open to the public. The site is private in some respects. You have to join to see some other peoples posts/threads if they set their's up as private from the general public.