@22:53-28::01  Once physical environment is clear, what to treat first?
-For Sensitive patients treat limbic system, vagal nerve system, and Mast Cell Activation Syndrone (MCAS) first!
 Then mold, then Lyme and co-infections if needed. (But listen to it for yourselves; this is a really important, informative discussion!!)
This is a critical understanding for those of us who have been struggling with chronic mold and Lyme.  Thank you!!

Since nothing is a quick fix, and leaving a moldy environment isn’t doable for many, what we need to know is what to expect for long term consequences for major organs or the brain, and how to best prevent those.  It seems a negative mindset, but who wouldn’t want to know whether they are in grave danger if they are truly trapped in their dangerous environment, particularly if money is an issue and things like applying for disability is a dead end.

Mold and lyme went misdiagnosed (by 11 doctors at a cost of several thousand dollars and down time)for several years. It was a EYEOLOGIST in Houston that hit the nail on the head. Look to an EYEOLOGIST for diagnostic accuracy.

So information! Thank you for hosting! ❤❤❤

Wifi makes my symptoms go thru the roof. This makes it difficult to find a wifi free work environment to make money to pay for treatment, so i can work.

This video is incredible! Thank you so much for doing this interview! This is exactly what I’m trying to figure out for myself is it mold, Lyme or Bartonella that’s causing my horrific burning (in brain, spine and hands) and joint symptoms. After 3.5 years of abx I’m still struggling. I need answers and this will definitely help me figure out what is the cause and how to reverse it. 🙏🏻

Incredibly in depth discussion, really appreciate it.  First time I have heard a discussion on all "mysterious" symptoms I have been dealing with. My original MD threw a lot of things at me from antidepressant to beta blocker to gabapentin of course nothing worked. Finally went to a naturopath doc and mold was his first thought. Low and behold my mold levels are very high. Now on binders for the past 4 months and symptoms have got so much better. What I find interesting is when I get sick those symptoms come flooding back. And my symptoms come back every now and then... I guess its going to be a long process to clear the mold out.
thank you for this discussion.

Thank you for your expertise. This will help me with my next visit.

Is there any literature on using TTFD as part of a chronic lyme protocol?

Almost always co- infections

Thank you
I am suffering major gut issues as I watch , black mould
The cramps , spasms are unbearable and I may have impaction
I have Mast cell activation / Ehlers Danlos / dysautonimia

The worst symptoms are the pain in gut but the overall inflammation in my already injured body
Cramps , spasms
Electric shock type pain in thumb joint

The hot flushing is horrid , but insomnia and outburst of rage
Do you think I screamed out for help ? Yes
Dod my doctors step up for me?
No
My sister owns this wet wet wet apartment ( she did ut know when she bought it ) should have had remediation. 18 mnths ago

Oh
I developed night time
BED WETTING

Volumes of urine but take me out of mould for a week and it does not happen

Did I miss where they mentioned the treatment?  Could someone timestamp me a link to where they talk about how to treat it?

How does one treat the limbic system and vagal

What kind of Doctors are  these please.

Tks a zillion! My son is one of the first declared case in Montreal, Quebec and we are really struggling to make him recover! Will dig into this new avenue. :thanksdoc:

I would like to know why they endorse the Hermie and the Hertz, because when the founder and maker of the Tess pacifically says do not use it in your home, was not it it’s not accurate for the home

It literally stachy mold. Nothing else needs attention.

Diagnosed with EBV and Borrelia burgdorfiri by Armin labs in Germany in March 2022. My GP and a cardiologist refuse to affirm my diagnosis, calling it fibromyalgia, NOT lyme!
Despite seeing a Lyme holistic doctor, my symptoms got worse. He ordered a hair analysis test which confirmed I had toxic levels of Barium in my body! Started a detox regimen, but just got worse because I couldn’t tolerate activated charcoal and herbals.😩 Wreaked havoc with my GERD and schotzches Ring/hurt all hernia. I then without knowing ingested a mold contaminated soy milk product, and I’ve been really struggling ever since. Digestion. Is terrible! Horrific pain in the solar plexus now and back/leg pain with weakness in my lower legs. Intermittent nausea, bloating /brain fog and random throbbing pain in the lymph glands from behind my ears, to my armpits/thighs and pelvis.
I can’t get anyone here in 🇨🇦 to acknowledge that ingesting mold from a contaminated beverage has any impact on my current health😢 Very frustrating 🤦‍♀️

Seems like most chronic diseaes are parisitic in nature/mold is in that category to.

I am a Lyme disease victim. 15 plus years and still counting. I'm from the suburbs of Chicago! I've been searching for a doctor to treat me properly and for all these aliments for years. I also started having seizures out of no where at the age of 35?! My doctor literally abandoned me after my first treatment. I've been ridiculed by every doctor I'd seen! Please if anyone knows a doctor or clinic near me to help with my Stage 3 Lyme disease and Mold toxins, I would greatly appreciate it.
Thank you Project Lyme!!! I think I can see a little light at the end of the tunnel again! :hands-yellow-heart-red::face-blue-wide-eyes: