So disappointing only 410 likes over two years later. EVERY doctor should see this. Having worked in the medical field over 20 years, and having had over 18 doctors attempt to figure out what's wrong with me, I've observed most doctors think they know everything when they're extremely ignorant and have done more harm than good. God bless Dr. Heyman.
I cant agree more! I feel like EVERY SINGLE DOCTOR should be forced to learn about this illness!! I've spent nearly half of my life bedridden, unable to leave my house, all the while begging Drs to help me figure out what's wrong. I had to finally find this info myself and I literally went to the the Dr today, pleading that he order appropriate tests. According to my current Dr (who's obv just as worthless as all the others I've seen) he's supposedly given me every test possible and ruled out any inflammatory causes for my symptoms . I started listing off the biomarker tests for CIRS & he acted like I was stupid, saying "those are just proteins, they can't tell you anything"! I'm pissed that my life has basically been lost all bc Drs won't take the time to learn about something they don't know about. They all seem to believe they know everything, take offense & insist the patient is crazy if they try explaining a concept they aren't familiar with! My life is over & its been over for >15yrs. It didn't have to be, if only Drs coulda been required to learn this illness is very real and seemingly more disabling than any other condition in the history of mankind!
@heatherrhodge2588 I totally agree and empathise. I'm 10 years into this life-destroying journey and I've lost so much. I'm unable to work, so I'm existing on UK welfare benefits - universal Credit and personal independence payment - which are not uprated with inflation. My income barely covers the most basic of basics, so I'm unable to eat a healthy diet, buy supplements, try some of the protocols I've heard that have good results. I'm stuck in a half life and I'm fed up!
I did too and that is common for most people with this and other related and complex health problems. You really have to become your own doctor nowadays, especially without a functional medicine practitioner. Unfortunately insurance does not pay for those, and our healthcare system is based on profit from disease instead of actually killing people. It is such a complicated health problems and hard to grasp your head around much less convincing friends and Family's you're not insane LOL. I hope you have found more answers or figured it out for sure! Best health and wishes to you and everyone with this and other health issues!
@@sbbailey10 do you have alot.of pain I've found alot out any hav had many symptoms over the decades pain now is worst problem ime hypomobile found out have Asperger's so ime susceptable to this
this was amazing, as I realized that my brain has been on fire for twenty years and to see the level of research that Dr. Heyman and his colleagues are doing will dramatically shift the entire field of chronic conditions
@@erinzellers5565 oh, they won't take the time to listen. I honestly believe that 100%. I've tried telling Drs about this illness, but not a single one has taken it seriously. My current Dr esp doesn't want 2 hear a word about it. Apparently, he thinks if it's not in his little device, it doesn't exist. What I don't understand is...Why hasn't this illness been added to the list of "known conditions" (whatever it's called). There seems to be much more proof it's a real illness than many that ARE listed. I mean, there are multiple biomarkers, proof that exposure causes symptoms (since it's been proven that after recovery, abnormal lab values & symptoms are triggered by reexposure). What else could the medical board need?! I'm beyond my wits end suffering from this crap! My life's been over for well over a decade, yet no hope in sight! I don't even have the energy or mental capability to advocate for myself at this point. Drs who know about this illness ought to advocate more for us, esp knowing what utter hell we endure. I honestly believe most of em, including Dr Heyman, are much more interested in keeping this info confined to those who'll pay 4 access. I mean, their sites are behind a pay wall, so what does that tell you?! If they truly cared about helping patients (more than lining their pockets), they'd allow access. They'd still make plenty from their seminars & patients paying out of pocket. They don't want knowledge going mainstream, cuz they're afraid it'd take $ outta their pocket! It's BS!
Have you tried the guy in this video? He learned at U of Mi and is practicing in VA. If you find one, let me know!!! They always present the problem, but no one actually gives you a solution! Look for mold certified doctors under in state. I found one if three right where I live. Granted, it’s cost me thousands of dollars. And I still don’t have a diagnosis for my son, but any functional medicine practitioner should have the labs that show what you have, or at least rule out parasites, etc. There are also thousands of types of ticks that if you’re bitten by them exacerbate any mold exposure to the maximum! Ask to me tested for tick borne or Babesia!!!
I took the cholestyramine for 3 months and it worked great. But I can't move from the moldy environment so the illness came back. It was so great to feel well for awhile.
I’m so sorry! Can you get more? You can also create a “safe zone” where you live, and stay there with an air purifier. I had to do that for a while. It’s horrible!
@@simonstones1918 I was recommended a Molecule, but I got a cheaper one. Make sure it pulls mold out if the air. I just found a Mooka on Amazon, and bought two.you can really see the stuff clinging to the filter!
It is to bad that if you go to the emergency room on a rainy day when it gets so bad, and tell them about this, they won't be able to help you and will tell you it is something else when you know that when you get away from the biotoxins things get so much better. Leaky ceilings are pretty deadly.
I went to the emergency room for two weeks straight and they actually told me to stop coming back.... it's sad. It's so hard living like this. God Bless you, and I hope you're feeling well.
In the UK, where I live, it took 7 years to find a GP who would officially diagnose CFS/ME, as it's still not taken seriously across the medical community. I have been researching CIRS, Mold Toxicity etc, as since moving into my current home in Oct 2018 I've been suffering from skin lesions and a worsening of my CFS/ME symptoms. When I mentioned mould to my GP, he looked at me as though I was speaking gibberish. He advised me not to believe everything I read on the internet, google is not medically trained. I explained I had been reading medical & scientific journals mainly published in the USA. He agreed to read a few, so I emailed him some of the peer-reviewed papers.......haven't heard back from him. I don't know what to do now, how do I get well when the NHS and UK medical community don't even know what I'm suffering from?
Oh I feel you. I'm about to go talk to my doctor about what I've discovered...been sick for 7 years. Wish me luck! How are you now? Did you find another doctor?
@@andreaokos5495 ime not in UK what community CFS 1997 fybromyalgia 6 pots years ago.truugred by a fall found out about have Asperger's hypomobility the gene for this or mcas pyroles
The show “ Monsters inside me “ has many episodes on various Aspergillus species ( season Five and Six have a few) They state that the CDC says Reported Cases are Rare!! Well of course they will be when Doctors are Not being taught more than Aspergillus can cause allergies or make you sick, proper testing is Not available in hospitals, and toxicology screenings are Not done on routine or teaching autopsies, which is the only way to distinguish between COPD and Asthma or Aspergillosis from Toxic Mold. 🤦♀️
Holy crap!! My house is covered in and filled with mold. I'm no expert but I've done more than my fair share of research, including microscopically examining spores and I can almost guarantee it's aspergillus. My dad supposedly died from COPD, but after seeing your comment, I'm wondering if he actually died from aspergilloma. It wldnt surprise me, that's for sure. I've been bedridden for 15yrs with what I'm sure has to be CIRS. no Dr will bother listening or agree to order appropriate lab tests, so I still can't say for certain, but everything else has been ruled out & I'm still so sick I can barely leave my bed; much less my house. It takes a week to recoup just going to a Dr appt.
@@heatherrhodge2588 sadly the proper tests aren’t available mainstream as I went toe and toe with labcorp/quest and I’m now banned from the patient portal only seeing tests they’ve done, but can no longer look up tests or codes. And Toxicology screenings necessary to determine fungi as the COD are not done, or RARELY done,on routine or teaching autopsies, even when requested as I did. I had to get a private autopsy or I would have never known, nor would I be here now. Get yourself a mycotoxin blood test. I used MyMycolabs you can order it yourself but you’ll need to hire a mobile lab for the draw. Please note NYS residents cannot have it sent to NY, drawn in NY, or sent back from NY. I did everything through another state.
As a low MSH and dreaded gene dual haplotype I went through hell for years. I became a nurse in my 30’s because of all I experienced and learned. I am figuring out what I am doing as a nurse, and I keep coming back to this information. I currently work in primary care at a community center and see so many patients I suspect with CIRS but the providers are simply not trained in this field. Any direction to help me open into the functional medicine field as either an RN or NP is appreciated.
@@monkeybearmax I was very sick. Fatigue, pain, neurological issues to put it plainly. I went to a naturopathic doctor for years and slowly recovered. Part of the recovery was dealing with the trauma I endured. I tried multiple holistic avenues and treatments and not one specific protocol. I am now in remission after three solid years of treatment, and I must remain vigilant to avoid mold and inflammation.
Great info. What does one do when they've been ill for 20+ years and can barely work, are functionally incapacitated and have no means to get money to pay for treatment? 😔
Johnny Power well, i cannot apply this right from the beginning to myself. He says ppl still miserable after being removed from moldy places and treated lyme.. once i moved out from moldy apartment, Right Away I felt soo much better
Hi! Congrats on feeling better. How long did it take to get better and what symptoms did you have before you got well. Have they all fully resolved? Last q: How long were you in the mold environment before you were able to move. Thank you for sharing!
@@theizzies1 ok so… my first moldy apartment was in 2017-18, 1,5 years. by the end of it i was bedridden literally. back then it took me 6 months to more or less recover. This time I was exposed 7 months and mold was much worse. i was out before i started to suspect it at all on vacation for 5 weeks total, on 4th week i start to feel slightly better. so i suspected something is wrong there. First thing i’ve done- urine great plain mycotoxins test, ermi, mold inspector.. it s all was like nightmare. I am still not sure if ever be able to fully recover mentally and emotionally
40:20 How do you pulse Myrrh? Thank you so much for this info!!!! My whole life, I was suffering from this-I realized from two days ago!! From childhood…now mid 40s! I’m so grateful to find out this info!!!!!! 🙏💜
Thankyou for posting these, I’m really having trouble organizing these videos to watch his talks in the proper order, can you please correct the titles on them so we know the correct order to watch and take notes
Hi there, thanks for your comment! We just finished retitling these videos to make the series more accessible. Here is how you might enjoy watching these videos in succession: ruclips.net/video/31Ftaa_PBRk/видео.html ruclips.net/video/Dl8lhfATgLg/видео.html ruclips.net/video/7dPNjLhe2OY/видео.html ruclips.net/video/5UQuYBr0Mqs/видео.html ruclips.net/video/uvNtf1lSp1k/видео.html ruclips.net/video/dsY123rGjz4/видео.html
Do not waste your time his office NEVER answer their phone. Also, he never there, there is a NP, and she NEVER answer the phone! His office is in Aldie, VA, but do not waste your time!
Standard process. .awesome sense $$$$ - Doc? What's the ICD for this? Any patien5s w/ trigeminal neuralgia? Facial? Dental pain? Tooth loss? ..... can u expand on your clinical experience on patients that present w/ these s/s. Curious.....
I have been taking Welcholl for 8 months. It made me very tired and eventually made my muscle start to break down. However I am feeling much better, than before I started, since using and stopping Welcholl. My home has been professionally remediated and I have replace all soft furnishings and thrown out all my books and washed linen and clothes with Borax. Has anyone started Phosphatidylcholine this late in the process has it helped? I have taken Nordic Naturals Omega 3 the whole 8 months.
Is there a Dr in Arizona that follows these protocols? I'm slowly degrading and possibly dying, I'm desperately in need of help, I've spent thousands in Drs, testing, medicine and supplements. I believe I'm on the right track, but need professional help
You need to move to a place where you can turn off the electric breaker box at night to stop the electromagnetic current that aggravates the condition. then you can heal. also, no wifi, or cell phones in the house. thanks so much for this lecture. God Bless you.
@@t5396 My doctor told me to flip off the breaker to the bedroom at night to reduce the additional problems EMFs cause to people with mold illness. She said to shut off the WiFi as well. There's lots of info online about this.
@@EMPalar-xf3ng You’re right. It does really aggravate the mold illness. I never heard of turning off the breaker box, though, I’ve just known about the phones, the headphones, turning off the WiFi at night, etc. You can put a timer on your WiFi. It really is all over the media. Everyone covers it up because you can’t see it. It scrambles people’s brains. It’s happening to my son right now.
I heard dr. Jill catnahan comment that all electromagnetics regardless of frequency increase groth rates of mold, but I'm sure certain frequencies are worse than others.
@@t5396 if you study TF and plants and animals you'll find that some frequencies kill and some heal them. DC seems to be the healthiest. The higher the frequency the more deadly. Water warms at 2Ghz that why they use it for microwave ovens, warm water breeds life ,like mold.
I sure af had heart failure but didn’t die. lol! The uncontrolled inflammation and pain caused too much stress on my heart leading to multiple heart attacks which damaged 1/3 of my heart with scarring and ischemia. Had the pain been treated I likely would have been okay though.
The guy who did the Mg deficiency said we need magnesium food, like bananas, you say dont take bananas.. I cant eat oxalates, so cant have magnesium rich foods... why no bananas?
@@autumngrace8541 I can't handle any fruit. I have molds and dcandida. If a fruit can naturally harbor mold, then it should be avoided. Something like cinnamon will not allow most molds to grow on it. It kills mold. That's a good agent for killing and suppressing mold. But fruits aren't like that. I can't think of any that have wide spread killing actions against broad types of mold.
No. CIRS is rarely active, systemic mold growth in the body. It is the accumulation of toxic end-products, cell/DNA/RNA fragments and other microbial toxins that are released when organisms within a water-damaged building are metabolically active or are actively dying. THESE ARE NOT living organisms. And even more frequently NOT even mold-related. Many people are affected by bacterial toxins more than mold within water-damaged buildings.
@@MSV667 LMFAO. But if people were actually healed from his protocol, I would hope that they would be able to give testimonials and balaxi provide evidence that they were actually sick and actually healed from following his protocol. That way people like me don't think that he is totally full of s***.
I am pretty sure this doctor is based in Virginia, but I could be wrong. Doctors may be willing to meet virtually. Check out Tressa Pinkleton in Seattle WA.
@@norainwanderlust Hi Nora. I'm in Seattle and looking for a doctor to work with. Does DR Pinkleton follow this protocol? Have you worked with her personally for CIRS?
@@christopherc2635 Hey there, yes I saw Dr. Pinkleton for some time. Although she is knowledgeable, I wouldn't recommend seeing her. She has so many clients, and our appointments felt very rushed, generalized, and really left me feeling like a number on her client list. And honestly, the treatment she provided didn't help. I went on to discover that Mast Cell Activation Syndrome was at the root of my problems. If you have CIRS, it is likely you do too. I am nearly healed. I highly recommend reading up on MCAS and the work of Dr Afrin in the field.
So disappointing only 410 likes over two years later. EVERY doctor should see this. Having worked in the medical field over 20 years, and having had over 18 doctors attempt to figure out what's wrong with me, I've observed most doctors think they know everything when they're extremely ignorant and have done more harm than good. God bless Dr. Heyman.
Yup arrogant ignoramuses and I’d like all my money back from them too
Sorry these idiots are godlike creatures in our society. Grow your own food and be all over magnesium L Threonate
I cant agree more! I feel like EVERY SINGLE DOCTOR should be forced to learn about this illness!!
I've spent nearly half of my life bedridden, unable to leave my house, all the while begging Drs to help me figure out what's wrong. I had to finally find this info myself and I literally went to the the Dr today, pleading that he order appropriate tests. According to my current Dr (who's obv just as worthless as all the others I've seen) he's supposedly given me every test possible and ruled out any inflammatory causes for my symptoms . I started listing off the biomarker tests for CIRS & he acted like I was stupid, saying "those are just proteins, they can't tell you anything"!
I'm pissed that my life has basically been lost all bc Drs won't take the time to learn about something they don't know about. They all seem to believe they know everything, take offense & insist the patient is crazy if they try explaining a concept they aren't familiar with!
My life is over & its been over for >15yrs. It didn't have to be, if only Drs coulda been required to learn this illness is very real and seemingly more disabling than any other condition in the history of mankind!
@heatherrhodge2588 I totally agree and empathise. I'm 10 years into this life-destroying journey and I've lost so much. I'm unable to work, so I'm existing on UK welfare benefits - universal Credit and personal independence payment - which are not uprated with inflation. My income barely covers the most basic of basics, so I'm unable to eat a healthy diet, buy supplements, try some of the protocols I've heard that have good results. I'm stuck in a half life and I'm fed up!
@@swoozle2378I am sorry to hear that. I totally feel you…😢
I hope you borrow money or something to get out of this situation…🙏
OH MY GOSH THIS IS ME!!!! I HAVE LIKE ALL OF THESE SYMPTOMS and never never knew why, been searching for 15 years
Me too! I'm just discovering. Just checking in to see if you've gotten better?!
I did too and that is common for most people with this and other related and complex health problems. You really have to become your own doctor nowadays, especially without a functional medicine practitioner. Unfortunately insurance does not pay for those, and our healthcare system is based on profit from disease instead of actually killing people. It is such a complicated health problems and hard to grasp your head around much less convincing friends and Family's you're not insane LOL. I hope you have found more answers or figured it out for sure! Best health and wishes to you and everyone with this and other health issues!
Me too. So happy to find this.
@@sbbailey10 do you have alot.of pain I've found alot out any hav had many symptoms over the decades pain now is worst problem ime hypomobile found out have Asperger's so ime susceptable to this
this was amazing, as I realized that my brain has been on fire for twenty years and to see the level of research that Dr. Heyman and his colleagues are doing will dramatically shift the entire field of chronic conditions
Have you found healing through any of the presented knowledge? Did you contact their office?
Thank you for making this information digestible and available to the public!!!
These videos are so important. LIFE SAVING.
We agree!
FANTASTIC! This completely mimics my experienced and healing journey with toxic mold. Tell ALL. THE MDs. Prayerfully, they take it to heart.
@@erinzellers5565 oh, they won't take the time to listen. I honestly believe that 100%.
I've tried telling Drs about this illness, but not a single one has taken it seriously. My current Dr esp doesn't want 2 hear a word about it. Apparently, he thinks if it's not in his little device, it doesn't exist.
What I don't understand is...Why hasn't this illness been added to the list of "known conditions" (whatever it's called). There seems to be much more proof it's a real illness than many that ARE listed. I mean, there are multiple biomarkers, proof that exposure causes symptoms (since it's been proven that after recovery, abnormal lab values & symptoms are triggered by reexposure). What else could the medical board need?!
I'm beyond my wits end suffering from this crap! My life's been over for well over a decade, yet no hope in sight! I don't even have the energy or mental capability to advocate for myself at this point.
Drs who know about this illness ought to advocate more for us, esp knowing what utter hell we endure. I honestly believe most of em, including Dr Heyman, are much more interested in keeping this info confined to those who'll pay 4 access. I mean, their sites are behind a pay wall, so what does that tell you?!
If they truly cared about helping patients (more than lining their pockets), they'd allow access. They'd still make plenty from their seminars & patients paying out of pocket. They don't want knowledge going mainstream, cuz they're afraid it'd take $ outta their pocket! It's BS!
I wish I could find a doctor who understood this disease at this level.
even current docs are graduating med school with zero knowledge of CIRS
Same
Have you tried the guy in this video? He learned at U of Mi and is practicing in VA. If you find one, let me know!!!
They always present the problem, but no one actually gives you a solution! Look for mold certified doctors under in state. I found one if three right where I live. Granted, it’s cost me thousands of dollars. And I still don’t have a diagnosis for my son, but any functional medicine practitioner should have the labs that show what you have, or at least rule out parasites, etc.
There are also thousands of types of ticks that if you’re bitten by them exacerbate any mold exposure to the maximum! Ask to me tested for tick borne or Babesia!!!
Wow, very informative and understandable for one going through it. Thank you!
Fyi, the Turmeric product he mentioned is Turmeric-Forte from Mediherb :)
I took the cholestyramine for 3 months and it worked great. But I can't move from the moldy environment so the illness came back. It was so great to feel well for awhile.
Did you slowly improve over those 3 months?
I’m so sorry! Can you get more? You can also create a “safe zone” where you live, and stay there with an air purifier. I had to do that for a while. It’s horrible!
@@Tinyteacher1111 what air purifier?
@@simonstones1918 I was recommended a Molecule, but I got a cheaper one. Make sure it pulls mold out if the air. I just found a Mooka on Amazon, and bought two.you can really see the stuff clinging to the filter!
@@Tinyteacher1111 thank you. I’ve never heard of those makes. I’m in the uk. Perhaps they don’t sell them here…
It is to bad that if you go to the emergency room on a rainy day when it gets so bad, and tell them about this, they won't be able to help you and will tell you it is something else when you know that when you get away from the biotoxins things get so much better. Leaky ceilings are pretty deadly.
I'm currently suffering. It's been a living hell.
I went to the emergency room for two weeks straight and they actually told me to stop coming back.... it's sad. It's so hard living like this. God Bless you, and I hope you're feeling well.
@@janedoe2596 me too. I've got bells palsy at the moment. I wish you all the best
yes and i have been working in a building with leaky ceilings for years. i just want my
health back😭
@@BridgetGuerrera what are your symptoms
In the UK, where I live, it took 7 years to find a GP who would officially diagnose CFS/ME, as it's still not taken seriously across the medical community. I have been researching CIRS, Mold Toxicity etc, as since moving into my current home in Oct 2018 I've been suffering from skin lesions and a worsening of my CFS/ME symptoms. When I mentioned mould to my GP, he looked at me as though I was speaking gibberish. He advised me not to believe everything I read on the internet, google is not medically trained. I explained I had been reading medical & scientific journals mainly published in the USA. He agreed to read a few, so I emailed him some of the peer-reviewed papers.......haven't heard back from him. I don't know what to do now, how do I get well when the NHS and UK medical community don't even know what I'm suffering from?
Oh I feel you. I'm about to go talk to my doctor about what I've discovered...been sick for 7 years. Wish me luck! How are you now? Did you find another doctor?
@@GrnEyedFirecrkr I have my son’s doctors letters and articles, and my son went crazy because I did. They probably never read them.
It took years for me as
Well (I am in US). Frustrating to say the least. I’ve learned more than I’d like to admit but here I am- getting well!!!!
How are you Susie? I hope you found by now the community who works with CIRS in the UK..
@@andreaokos5495 ime not in UK what community CFS 1997 fybromyalgia 6 pots years ago.truugred by a fall found out about have Asperger's hypomobility the gene for this or mcas pyroles
The show “ Monsters inside me “ has many episodes on various Aspergillus species ( season Five and Six have a few) They state that the CDC says Reported Cases are Rare!! Well of course they will be when Doctors are Not being taught more than Aspergillus can cause allergies or make you sick, proper testing is Not available in hospitals, and toxicology screenings are Not done on routine or teaching autopsies, which is the only way to distinguish between COPD and Asthma or Aspergillosis from Toxic Mold. 🤦♀️
Holy crap!! My house is covered in and filled with mold. I'm no expert but I've done more than my fair share of research, including microscopically examining spores and I can almost guarantee it's aspergillus.
My dad supposedly died from COPD, but after seeing your comment, I'm wondering if he actually died from aspergilloma. It wldnt surprise me, that's for sure. I've been bedridden for 15yrs with what I'm sure has to be CIRS. no Dr will bother listening or agree to order appropriate lab tests, so I still can't say for certain, but everything else has been ruled out & I'm still so sick I can barely leave my bed; much less my house. It takes a week to recoup just going to a Dr appt.
@@heatherrhodge2588 sadly the proper tests aren’t available mainstream as I went toe and toe with labcorp/quest and I’m now banned from the patient portal only seeing tests they’ve done, but can no longer look up tests or codes. And Toxicology screenings necessary to determine fungi as the COD are not done, or RARELY done,on routine or teaching autopsies, even when requested as I did. I had to get a private autopsy or I would have never known, nor would I be here now. Get yourself a mycotoxin blood test. I used MyMycolabs you can order it yourself but you’ll need to hire a mobile lab for the draw. Please note NYS residents cannot have it sent to NY, drawn in NY, or sent back from NY. I did everything through another state.
As a low MSH and dreaded gene dual haplotype I went through hell for years. I became a nurse in my 30’s because of all I experienced and learned. I am figuring out what I am doing as a nurse, and I keep coming back to this information. I currently work in primary care at a community center and see so many patients I suspect with CIRS but the providers are simply not trained in this field. Any direction to help me open into the functional medicine field as either an RN or NP is appreciated.
Were u very sick? Are you recovered? Did u follow this protocol?
@@monkeybearmax I was very sick. Fatigue, pain, neurological issues to put it plainly. I went to a naturopathic doctor for years and slowly recovered. Part of the recovery was dealing with the trauma I endured. I tried multiple holistic avenues and treatments and not one specific protocol. I am now in remission after three solid years of treatment, and I must remain vigilant to avoid mold and inflammation.
@@AAtkinson thanks for sharing. Glad u are well now.
@@AAtkinson Congratulations on the healing! I also have the low MSH and dreaded gene dual haplotype. It's a challenge dealing with this.
How does one know if mold ..if considered in all homes? And Inflammation how to keep down?
Great info. What does one do when they've been ill for 20+ years and can barely work, are functionally incapacitated and have no means to get money to pay for treatment? 😔
Johnny Power well, i cannot apply this right from the beginning to myself. He says ppl still miserable after being removed from moldy places and treated lyme.. once i moved out from moldy apartment, Right Away I felt soo much better
Hi! Congrats on feeling better. How long did it take to get better and what symptoms did you have before you got well. Have they all fully resolved? Last q: How long were you in the mold environment before you were able to move. Thank you for sharing!
@@theizzies1 ok so… my first moldy apartment was in 2017-18, 1,5 years. by the end of it i was bedridden literally. back then it took me 6 months to more or less recover. This time I was exposed 7 months and mold was much worse. i was out before i started to suspect it at all on vacation for 5 weeks total, on 4th week i start to feel slightly better. so i suspected something is wrong there. First thing i’ve done- urine great plain mycotoxins test, ermi, mold inspector.. it s all was like nightmare. I am still not sure if ever be able to fully recover mentally and emotionally
@@theizzies1 so yeah right away was a bit exaggeration, it took 4 weeks
@@instasupermamka what were your symptoms
40:20 How do you pulse Myrrh?
Thank you so much for this info!!!!
My whole life, I was suffering from this-I realized from two days ago!!
From childhood…now mid 40s!
I’m so grateful to find out this info!!!!!! 🙏💜
Thankyou for posting these, I’m really having trouble organizing these videos to watch his talks in the proper order, can you please correct the titles on them so we know the correct order to watch and take notes
Hi there, thanks for your comment! We just finished retitling these videos to make the series more accessible. Here is how you might enjoy watching these videos in succession:
ruclips.net/video/31Ftaa_PBRk/видео.html
ruclips.net/video/Dl8lhfATgLg/видео.html
ruclips.net/video/7dPNjLhe2OY/видео.html
ruclips.net/video/5UQuYBr0Mqs/видео.html
ruclips.net/video/uvNtf1lSp1k/видео.html
ruclips.net/video/dsY123rGjz4/видео.html
@@WholisticMatters Thankyou so much for all u do, wish I could give u a hug, love from boston
Where is this doctor practicing?! How can someone get in contact with him?!
Do not waste your time his office NEVER answer their phone. Also, he never there, there is a NP, and she NEVER answer the phone! His office is in Aldie, VA, but do not waste your time!
@@ashburnconnecttv7860 he has a new physician that practices with him. Maybe that will help.
I called yesterday and first try got a person named Heide that was super sweet and took my info for a consult call.
Standard process. .awesome sense $$$$ - Doc? What's the ICD for this? Any patien5s w/ trigeminal neuralgia? Facial? Dental pain? Tooth loss? ..... can u expand on your clinical experience on patients that present w/ these s/s. Curious.....
I have been taking Welcholl for 8 months. It made me very tired and eventually made my muscle start to break down. However I am feeling much better, than before I started, since using and stopping Welcholl. My home has been professionally remediated and I have replace all soft furnishings and thrown out all my books and washed linen and clothes with Borax. Has anyone started Phosphatidylcholine this late in the process has it helped? I have taken Nordic Naturals Omega 3 the whole 8 months.
Do you think this can be treated without the binder since it causes side effects ?
but folks stay tuned because towards the end he really does give you the cure. gotta love him 10000% x
Thanks so much ! Helpful!!!
Is there any harm in following the natural protocol for CIRs even if you may not actually have it?
Unbelievable. This is why my moldy house damn near killed me. I can’t believe my entire life’s suffering comes down to this condition. Unreal
Is there a Dr in Arizona that follows these protocols? I'm slowly degrading and possibly dying, I'm desperately in need of help, I've spent thousands in Drs, testing, medicine and supplements. I believe I'm on the right track, but need professional help
You need to move to a place where you can turn off the electric breaker box at night to stop the electromagnetic current that aggravates the condition. then you can heal. also, no wifi, or cell phones in the house. thanks so much for this lecture. God Bless you.
What evidence do you have to support this?
@@t5396 My doctor told me to flip off the breaker to the bedroom at night to reduce the additional problems EMFs cause to people with mold illness. She said to shut off the WiFi as well. There's lots of info online about this.
@@EMPalar-xf3ng You’re right. It does really aggravate the mold illness. I never heard of turning off the breaker box, though, I’ve just known about the phones, the headphones, turning off the WiFi at night, etc. You can put a timer on your WiFi. It really is all over the media. Everyone covers it up because you can’t see it. It scrambles people’s brains. It’s happening to my son right now.
I heard dr. Jill catnahan comment that all electromagnetics regardless of frequency increase groth rates of mold, but I'm sure certain frequencies are worse than others.
@@t5396 if you study TF and plants and animals you'll find that some frequencies kill and some heal them. DC seems to be the healthiest. The higher the frequency the more deadly. Water warms at 2Ghz that why they use it for microwave ovens, warm water breeds life ,like mold.
Does Dr. Haymen have an active practices? If so, where?
Yes! The Virginia Center for Health and Wellness in Aldie, VA
@@NickFoxer do you go there?
You might want to Google for reviews first! Huh!
What is the curcumin product that he recommends? That part confuses me. I’m not sure what product he’s talking about and at what dose...?
Any Turmeric product will work. Check the ingredients is 1000mg. Take twice daily
Its's a supplement
curcumin-galactomannoside complex
@@jeffm.8134who sells that? I can’t seem to find anything but curcumin phytosomes which looks different.
How much Okra and beets should you take daily?
Ok so what's the 1st step if I have this please
So.. does anyone die from heart failure/attack from CIRS?
I sure af had heart failure but didn’t die. lol! The uncontrolled inflammation and pain caused too much stress on my heart leading to multiple heart attacks which damaged 1/3 of my heart with scarring and ischemia. Had the pain been treated I likely would have been okay though.
The guy who did the Mg deficiency said we need magnesium food, like bananas, you say dont take bananas..
I cant eat oxalates, so cant have magnesium rich foods... why no bananas?
They want you low amalose, not sure I spelled that correctly, but potatoes and bananas have a lot of it.
No sugar. Mold feeds off of sugar, it's probably the worst thing to eat while trying to rid yourself from mold.
@@norainwanderlust fruit gets bad rap, not same sugar. All starches should not be eaten with any oils or fats.
@@autumngrace8541 I can't handle any fruit. I have molds and dcandida. If a fruit can naturally harbor mold, then it should be avoided. Something like cinnamon will not allow most molds to grow on it. It kills mold. That's a good agent for killing and suppressing mold. But fruits aren't like that. I can't think of any that have wide spread killing actions against broad types of mold.
What about starving out the mold of the body? Isn't the mold "alive" in the body?
Yes! Try Doug Kauffman’s antifungal diet. Mild can’t live without certain things.
No. CIRS is rarely active, systemic mold growth in the body. It is the accumulation of toxic end-products, cell/DNA/RNA fragments and other microbial toxins that are released when organisms within a water-damaged building are metabolically active or are actively dying. THESE ARE NOT living organisms. And even more frequently NOT even mold-related. Many people are affected by bacterial toxins more than mold within water-damaged buildings.
@@coreydeacon3131 yes a d we have to get passed the biofilms and fat protecting and storing these toxins. Our bodies are amazing.
Mycotoxins that the living mold produce are the problem. I dont think mycotoxins are alive.
@@coreydeacon3131 bingo
CIRS
Where are all these people who were allegedly cured by this protocol?
Hopefully out enjoying their lives. Its a dark history for those who make it out. Not something most would like to continue to engage in on any level.
@@MSV667 LMFAO. But if people were actually healed from his protocol, I would hope that they would be able to give testimonials and balaxi provide evidence that they were actually sick and actually healed from following his protocol. That way people like me don't think that he is totally full of s***.
@@t5396 Friend of mine reversed CIRS with Heyman. It’s real. I’m in the process of working on it. CIRS is a nightmare but I am improving.
@@iAlwaysSpeakTheTruth do we just relapse when we go out in the world and get exposed again?
@@monkeybearmax if you’re exposed king and bad enough yes but it takes a lot.
Me and my husband are dying from toxic mold and no doctor here in Virginia will help us they tell me I'm crazy. We're scared
I am pretty sure this doctor is based in Virginia, but I could be wrong. Doctors may be willing to meet virtually. Check out Tressa Pinkleton in Seattle WA.
The Morrison Center in NYC.
Get out of environment and change diet. Best thing you can do.
@@norainwanderlust Hi Nora. I'm in Seattle and looking for a doctor to work with. Does DR Pinkleton follow this protocol? Have you worked with her personally for CIRS?
@@christopherc2635 Hey there, yes I saw Dr. Pinkleton for some time. Although she is knowledgeable, I wouldn't recommend seeing her. She has so many clients, and our appointments felt very rushed, generalized, and really left me feeling like a number on her client list. And honestly, the treatment she provided didn't help. I went on to discover that Mast Cell Activation Syndrome was at the root of my problems. If you have CIRS, it is likely you do too. I am nearly healed. I highly recommend reading up on MCAS and the work of Dr Afrin in the field.
Huh!
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