treatment after VCS?
Is the VCS test enough to start self-treatment?
Unfortunately, I’m unable to afford further testing as I’m only 16, and my parents don’t believe in mold exposure causing this much symptoms. They believe that because my ordinary blood tests at the doctors have come back normal, I should be fine. However, I’ve been dealing with debilitating symptoms for over a year, many of which I believe correlate with mold exposure and CIRS.
I initially used the free VCS test from vcstest.com, which came back positive with a biotoxin score of 62/90. Just to be sure, I also purchased the $15 test from SurvivingMold.com, which came back as “failed” in both eyes and also indicated positive symptoms.
I was told that if the VCS test comes back positive, there is reportedly a very high likelihood of having CIRS. I’m now getting to the point where these symptoms are significantly affecting my everyday life, and I’m struggling to cope with how long this has been going on.
Has anyone here gone mainly based on the VCS test alone and then self-treated with binders such as CSM (cholestyramine), or other treatments? I’m not sure what would be the safest or most appropriate approach, especially when I can’t afford further testing.
If anyone has been in a similar situation or has any advice, I’d really appreciate hearing about your experience.
Thanks!