Sadly, great healers think this is really an issue due to limits in their fine training. After writing 3 mold books, working with a PHD in biochemistry and a master boulder, and am working on books 13 and 14 on tick and flea infections, I feel I might help in this issue.
1. Mold people talk about biotoxins from mold, bacteria like mold and others as if they are a long term issue.
Biotoxins are long term because the remediator is merely close, friendly, smart, excellent at marketing and DOES know some structure remediation skills. I have had people using the local “good expert” who then contaminate other locations like a new home, office, car, vacation place, etc. because the remediation was only “reasonable.” Who determined it was reasonable? They did a post test and told you? You felt better?
What is their training? I mean degrees, in biochemistry, toxicology, masters in biology. Where were they trained extensively in building, structure defect identification and repair? Where and when did they learn advanced AC systems?
Dr. Gary Rosen is a top Florida State trainer and knows all these areas profoundly. HE TRAVELS IN THE USA OR EUROPE AND ALL BIOTOXIN ISSUES ARE GONE. GONE! There is no eternal use of binders unless you are removing carcinogens, inflammatory chemicals or debris from dead bartonella or the “co-infections” Lyme bacteria and the single-cell parasite Babesia.
If you feel bad when you stop the fine binders in routine use in emerging medicine, it may be from a fair remediation, or these three sample other causes just mentioned.
In my mold section at personalconsult.com I mention scientists entering the Last Polish King’s burial tomb. All died quickly but one from these biological toxins.
WHY WAIT TO REMOVE POISONS FROM BACTERIA OR MOLD INFECTIONS?
2. This does not mean you sit and wait and ignore “Lyme.” Of course this titanically complex bacteria has a moving spiral active form, nut form, frozen perster and slime jello coated biofilm type. “Treating Lyme” means which form? My bias is not certain, but tends to stun, then lower the active form, and add low dose effective killers of the other three forms. They do not have identical treatments except in very rare innovation treatments few know.
3. You start at an invisible comfortable dose and never increase at a full tablet or capsule every 1-2 days. Never stop x as add y. That is LSD anti-science chaos. You will typically “feel” an unknown dose–it could be 1/5th the smallest capsule compounded or a dose so high the pharmacist needs to talk with the research clinician. Since Bartonella, Lyme and Babesia are everywhere, it is not helpful to “tell you what you will feel” when you are making dead infection particles and spiking inflammation chemicals.
I do not believe in the gold of the self, but if you feel a new discomfort, you are likely correct that it is infection debris or “gasoline” inflammation. Some tolerate effective doses but that has solutions too complex for this post. (Some are mentioned in my Destroy Depression book out January 30, 2026).
4. What is Lyme? Sure it is a bacteria in four forms, but it assumes ticks have sterile guts and saliva–except for Lyme. I have never seen anyone with merely Lyme bacteria. And I have no recollection of a patient with two infections. Though physicians smarter than me miss these often. Why? They do not PRE-KILL ALL POSSIBLE INFECTIONS TO MAKE MASSIVE PARTICLES and they use ONE LABORATORY. I love some select labs. But all miss things.
And when I find Bartonella (23 species 2025 Schaller) or Babesia, I treat each with one thing to kill only them. And increase the killing of Babesia, Bartonella and Lyme, alternating increases so none are ignored.
If you are the 1.4% dying of Babesia, we transfuse and move fast but that is not routine.
FYI if you wish to learn more, see my vast number of blog posts, books, facebook posts, videos and other social media.
Or far better, fill out the phone chat info at personalconsult.com.