How did CSM work out for you? Did you notice a difference quickly? I fail the vision test and REALLY suffer cognitively since getting sick, hoping to find a CIRS doctor soon.
@@michaelthelen1 it was heavy on my stomach.. I felt muscle relief the first 2 nights, it was wonderful, but I couldn't take it anymore, it's harsh chemicals.. get a clean CSM from a compound pharmacy or get Welchol
Hypermobile, mitral valve prolapse, dysautonomia, inflammation, GERD, bile reflux, gastroparesis, IBS, joint pain, FATIIIIIIIIIGUE, horrible head/neck pain, undifferentiated connective tissue disease, lots of CIRS and MCAS symptoms (also possibly Bartonella from cat bite at age 2) ... at 16 years old. She is almost healed. Grain/dairy-free. LOTS of magnesium, Vitamin D, multi, Biocidin, digestive enzymes, natural dessicated thyroid, LDN, and finally...NeuroProtek (NP). NP has made a HUGE difference for headaches and fatigue. Don't give up and keep on learning.
@@leestevenson2873 Possibly! She has a history of UTI's from age 3-7. I need to get medical records from another state. However, her brother has several symptoms as well.
Yes I was and it was the final straw. It took me years to start healing because the information in this video was not out there. A lot of this information is on my blog but I and many others had to work together on Facebook figuring out how to heal. I am glad to see they are figuring it out now. I got ill even though I lived in a moldy environment. Then I had to get a Dtap shot for my job. I got very ill then next day and I just kept getting sicker and sicker. I ended up getting diagnosed with Lyme which did makes sense because most of my life I would experience boughts of mental confusion for no reason. They gave me antibiotics and I started feeling better. But after a while they would quit working and they would have to change them. Will all antibiotics quit working after a while and the Lyme made me so ill that they had to rush me in an ambulance. They gave me an IV of cipro. I felt better after a few hours. I thought finally I am rid of this Lyme. Then after a couple days all heck broke lose. My health started to dramatically declined and if I wouldn't have posted my symptoms on Facebook and someone had recognized them I most likely would still be bedridden. I was bedridden for months while I an many others worked together figuring out how to heal from it. I still have symptoms come up once in a while but I am almost healed from them. I still live in a moldy environment and it doesn't effect me. I am very careful about getting bit with ticks now though. What I believe set all this off is I ran a coal fired furnace. They refused to supply us with respirators so their was not way to avoid breathing in the smoke and dust from it. Most others who ran it died from strokes or heart attacks. I seen what was happening to them so I quit and found another job but things never seemed quit right. I believe the coal fired boiler was the trigger to set things in motion.
Evie, I'm in a real bad way...mold exposure via my CPAP machine and now extreme, full body eczema ...beyond brutal. Naturopath has me on detox drops, 400mg of mg, 3000 mg vit D, 2000 vit C, and a very restricted diet of just root veggies and fish/chicken...but nothing is working. What FB group is it that you're speaking of...I'd like to join? Tyvm!
I had SIRS that turned to MODS...in 2014/2015. Listening to you, I believe I now know I'm stuck in CIRS. With this knowledge, health is achievable. Thank you.
I pray healing (complete healing) all throughout your mind & body in Jesus name. May a supernatural peace come over you & you be filled with hope knowing a full restoration is near & this affliction will not last. May the answers & resources your seeking be given to you quickly & with clarity.
Start an elimination diet. Carnivore (maybe even doing OMAD) for 90 days strict, then start to expand to see if certain foods cause a negative effect from there. I am not a doctor but this has worked for many many people including Mikhaila Peterson and family.
I had mold, Lyme, and related infections. My life went through a meat grinder., along with my family. Know it’s not just 1 thing. I’m the most difficult group you speak of 😞
I am also in this difficult group. In the process of healing still, but set back by repeated re-exposure to mold. Hoping to conquer that once and for all soon. But I see light at the end of the very dark, very difficult and lonely tunnel.
A LOT of information and amazing to have a doctor have a ever-expanding mind to go above and beyond helping their patient. It's too bad there aren't more doctors like this.
What about supplementing Glycine to raise VIP? In the study, The Effects of Glycine on Subjective Daytime Performance in Partially Sleep-Restricted Healthy Volunteers, "Glycine increased AVP and VIP expression 4.2- and 3.2-fold, respectively, during the light period".
BiotoxinJourney Great article, and to me it's worth trying. I have 'immeasurable antidiuretic hormone' and very low VIP. No practitioner has mentioned trying glycine. Thanks for this tip. I'll mention, too, that I've visited your site many times and found lots of helpful info! (You probably won't see this...)
I couldn't finish the treatment video because 1. I cannot convert the precursors in things like flax seed oil to actual omega 3 and 2...wheat germ oil...talk about inflammatory response!
I live in Chicago and have been treated by multiple functional medical doctors and I continue to decline. Does anyone know an actual doctor that treats this?
Hello one of the videos talks briefly about CIRS could be from a dental issue where can I find more info on that my mom has CIRS and is from mold but she also have Trigeminal neuralgia but some neurologists says its not confirmed TN she had a bad dental issue and her illness started after that dental issue.
My doctor recently informed me that the FDA will no longer allow the sale of VIP. Is this the case? Are there alternatives to VIP? Any info would be greatly appreciated.
If you don't already have a CIRS-literate doc near you, then make one. Find a good Functional Medicine doc who's willing to learn. Tell them about CIRS. Provide links to this lecture series. Start with some of the basic tests. There are also health consultants online who may be able to help. In the US, you can order many labs these days without a doctor.
Great information but in your Sx Cluster Analysis I have seen people who had high glyphosate levels or who were vaccine injured display most of those symptoms. How do you factor those variables into your analysis? I have also seen these symptoms in those who have been injured by fluorquinlones.
I got the H1N1 flu vaccine and I went downhill! I’m wondering now if this is what’s wrong with me. Maybe I don’t have Fibromyalgia???? Need to watch all 3 videos.
@@stephaniekeller4449 I posted on my blog about vaccine injury and correcting it. The flu vaccine has caused this to occur in many but the Dtap is much much worse. The Dtap vaccine is what almost killed me.
Not a single doc could figure out why I have biliary dyskinesia. Did a year of searching and medical tests to find mold toxicity. I get RUQ pain and burning legs/arms.
I have CIRS due to black mould and the worst part is that due to such a long period of exposure I now am allergic to VOC so shopping is a painful experience. So over it all.
Both are relatively new. Think of MCAS as downstream of CIRS (worry about repairing CIRS first). My opinion of course. Judy Cho has a podcast or two on it that are pretty good
So if I have this and go through treatment and heal …..I still have the genetic weakness meaning I can get sick again right? Am I supposed to live in a bubble now? Or does he go over preventative/supportive measures one can do to strengthen the body?
What you want me for is an electronic document and the name and the code you want it is required from your email signature or email signature or or not by the way you do the job to get the documents to the email that will will help me with my employment in a timely way that will be sent by my client as they are required for my application and the contract will not complete and they may be sent directly from legal legal authority on my legal application and legal action for legal purposes as I have not yet been made to be granted an appeal letter of authority in accordance to their policy in respect to their employment and the name and number they have given in my employment letter and letter dated 6th July as proof for your consideration for for further proceedings as I have to be grateful grateful if they will help with this matter or the relevant documentation as they are are required for me and the council will also not charge the deposit until after payment made by me as they were not issued to you as the tenant was sent out of court order from a colleague
I know many people who live in severe mold and they are perfectly healthy, and they have the genes that are supposed to make them more susceptible. Why are they not effected by the mold?
They mention that sometimes a trigger is required-like an illness or injury that stresses the body and suppresses the immune response. It’s kind of like walking a tightrope-someday you fall but until then you’re fine.
@@leestevenson2873 I got food poisoning, then that developed into chronic nausea, and then that developed into anxiety, depression, migraines, fatigue, and then memory issues. I think without the initial food poisoning it never would have caused that snowball effect. Just my POV
@@HurtsSoGood347 Yep something similar happened to me and that was when the mold really started to effect me. I got Lyme disease. Once I got my viral load down I could start handling the mold again. I do take supplements to prevent the mold from making me ill but once something happens to weaken the body the mold will really nail you.
@@mohammedabdulkadir2004 Carnivore alone reverses lots of things. Adding in intermittent fasting or OMAD can turbocharge it sometimes. Lots of info on carnivore finally being allowed to escape the Food/Pharma giants info trap.
Dr Heyman was at the 2019 Fort Lauderdale Mold Congress where the offer was made for these "Shoemaker doctors" to proceed in connecting CIRS with the Holmes 1988 "Chronic Fatigue Syndrome". Which is an official CDC created syndrome so they obviously recognize their own creation as medically valid. As opposed to CIRS that is nothing more than a name invented by Dr Shoemaker. Dr Heyman and the group declined to act on the offer. Perhaps they fail to understand that "Mold at Ground Zero for CFS" means that toxic mold is part of the CFS syndrome. Or maybe they think that they are such Mighty Gods of Medicine that they can get the CDC to accept CIRS and throw out CFS. For whatever reason, their lack of response indicates low comprehension that a doctors duty is to "respond to evidence" and "connect the dots" My confidence in the Shoemaker group was misplaced. They don't deserve to be trusted.
@@at0miclaughter I gave these researchers the opportunity to receive information vital to solving the mystery of a famous syndrome. They threw that opportunity away.
Maybe they didn't see the benefit of spending their time and resources on proving something they already know to be true. Maybe they thought it would be better spent furthering the research. Clearly the protocol works, so...
![Blox Fruits Dragon Rework Update [Full Stream]](http://i.ytimg.com/vi/EqDAp8udhm0/mqdefault.jpg)
What a lecture 👏🏻 started CSM 2 days ago, let's hope this is my closure from this illness.
How did CSM work out for you? Did you notice a difference quickly? I fail the vision test and REALLY suffer cognitively since getting sick, hoping to find a CIRS doctor soon.
@@michaelthelen1 it was heavy on my stomach.. I felt muscle relief the first 2 nights, it was wonderful, but I couldn't take it anymore, it's harsh chemicals.. get a clean CSM from a compound pharmacy or get Welchol
Who did you see, needing help..
@@opedromagicodid you end up trying welchol or did you end up continuing on with the CSM
@@opedromagicohow are you doing now?
Brilliant talk. The guys on the ball!
Hypermobile, mitral valve prolapse, dysautonomia, inflammation, GERD, bile reflux, gastroparesis, IBS, joint pain, FATIIIIIIIIIGUE, horrible head/neck pain, undifferentiated connective tissue disease, lots of CIRS and MCAS symptoms (also possibly Bartonella from cat bite at age 2) ... at 16 years old. She is almost healed. Grain/dairy-free. LOTS of magnesium, Vitamin D, multi, Biocidin, digestive enzymes, natural dessicated thyroid, LDN, and finally...NeuroProtek (NP). NP has made a HUGE difference for headaches and fatigue. Don't give up and keep on learning.
Sounds like you were injured by fluoroquinolones or choroquine.
@@leestevenson2873 Possibly! She has a history of UTI's from age 3-7. I need to get medical records from another state. However, her brother has several symptoms as well.
Yes I was and it was the final straw. It took me years to start healing because the information in this video was not out there. A lot of this information is on my blog but I and many others had to work together on Facebook figuring out how to heal. I am glad to see they are figuring it out now. I got ill even though I lived in a moldy environment. Then I had to get a Dtap shot for my job. I got very ill then next day and I just kept getting sicker and sicker. I ended up getting diagnosed with Lyme which did makes sense because most of my life I would experience boughts of mental confusion for no reason. They gave me antibiotics and I started feeling better. But after a while they would quit working and they would have to change them. Will all antibiotics quit working after a while and the Lyme made me so ill that they had to rush me in an ambulance. They gave me an IV of cipro. I felt better after a few hours. I thought finally I am rid of this Lyme. Then after a couple days all heck broke lose. My health started to dramatically declined and if I wouldn't have posted my symptoms on Facebook and someone had recognized them I most likely would still be bedridden. I was bedridden for months while I an many others worked together figuring out how to heal from it. I still have symptoms come up once in a while but I am almost healed from them. I still live in a moldy environment and it doesn't effect me. I am very careful about getting bit with ticks now though. What I believe set all this off is I ran a coal fired furnace. They refused to supply us with respirators so their was not way to avoid breathing in the smoke and dust from it. Most others who ran it died from strokes or heart attacks. I seen what was happening to them so I quit and found another job but things never seemed quit right. I believe the coal fired boiler was the trigger to set things in motion.
Evie, I'm in a real bad way...mold exposure via my CPAP machine and now extreme, full body eczema ...beyond brutal. Naturopath has me on detox drops, 400mg of mg, 3000 mg vit D, 2000 vit C, and a very restricted diet of just root veggies and fish/chicken...but nothing is working. What FB group is it that you're speaking of...I'd like to join? Tyvm!
@@PfizerIsKillngMe if you listen to all of his series you will understand, watch them 10 times like me to understand.
I had SIRS that turned to MODS...in 2014/2015. Listening to you, I believe I now know I'm stuck in CIRS. With this knowledge, health is achievable. Thank you.
This is motivating I’m ordering my treatments today, have you began this protocol yet ?
Keep us updated
What is mods
Just tested positive for lyme, CIRS, and Marcons. My head and neck hurts so bad. Its all awful. I pray we all heal and find peace
I pray healing (complete healing) all throughout your mind & body in Jesus name. May a supernatural peace come over you & you be filled with hope knowing a full restoration is near & this affliction will not last. May the answers & resources your seeking be given to you quickly & with clarity.
Add heavy metal toxicity and you have my story and I healed. It might not feel that way now but it will happen…
How are you doing now? Did you start the shoemaker protocol?
Start an elimination diet. Carnivore (maybe even doing OMAD) for 90 days strict, then start to expand to see if certain foods cause a negative effect from there.
I am not a doctor but this has worked for many many people including Mikhaila Peterson and family.
Ordered my tests because of the pain like yours. People just don’t get it and dismiss our complaints too casually. It’s real. Hope your doing well
I'm so glad I found this! So many things finally make sense about my own struggle.
I wish I learned about CIRS years ago… I hope that more patient suffering from Lyme disease find out about CIRS 😢
Is there a way to get access to the presentation download? So much great information!
I had mold, Lyme, and related infections. My life went through a meat grinder., along with my family. Know it’s not just 1 thing. I’m the most difficult group you speak of 😞
Have you tried this protocol ?
How are you now
I'm with your girl. Hang in there.
did you heal?
I am also in this difficult group. In the process of healing still, but set back by repeated re-exposure to mold. Hoping to conquer that once and for all soon. But I see light at the end of the very dark, very difficult and lonely tunnel.
I have mold, lyme. MCAS, EBS, CMV, etc. I totally get it.
A LOT of information and amazing to have a doctor have a ever-expanding mind to go above and beyond helping their patient. It's too bad there aren't more doctors like this.
Thank you for what you do.
Our pleasure!
What about supplementing Glycine to raise VIP? In the study, The Effects of Glycine on Subjective Daytime Performance in Partially Sleep-Restricted Healthy Volunteers, "Glycine increased AVP and VIP expression 4.2- and 3.2-fold, respectively, during the light period".
BiotoxinJourney have you found any answers to this ?
VIP is only used at the very end of treatment
@@spectator59 Yes, but it's the most critical part of the treatment. I'm very interested in this possibility
BiotoxinJourney Great article, and to me it's worth trying. I have 'immeasurable antidiuretic hormone' and very low VIP. No practitioner has mentioned trying glycine. Thanks for this tip. I'll mention, too, that I've visited your site many times and found lots of helpful info! (You probably won't see this...)
This is a GREAT observation! I could really use a consultant to get started with CIRS stuff, wish you were available for a chat.
I couldn't finish the treatment video because 1. I cannot convert the precursors in things like flax seed oil to actual omega 3 and 2...wheat germ oil...talk about inflammatory response!
Great presentation! Are the dietary recommendations forever or just until symptoms improve?
keto carnivore alleviated a lot of my symptoms! got me back to exercising, taking care of my appearance, lost 26kg too.. fatigue got a lot better too
I live in Chicago and have been treated by multiple functional medical doctors and I continue to decline. Does anyone know an actual doctor that treats this?
Hey i live in Chicago as well! Did you end up finding a good doctor?
Same 😢
Great lecture.
We're glad you enjoyed it!
Hello one of the videos talks briefly about CIRS could be from a dental issue where can I find more info on that my mom has CIRS and is from mold but she also have Trigeminal neuralgia but some neurologists says its not confirmed TN she had a bad dental issue and her illness started after that dental issue.
I had/have all of these same things. I pray she heals!
I'm from brazil, how can i have this kind of treatment here?
Why is the Nanotrap test no longer available?
Someone can help me?
My doctor recently informed me that the FDA will no longer allow the sale of VIP. Is this the case? Are there alternatives to VIP? Any info would be greatly appreciated.
what is VIP?
Susan Horton, if you listen to all videos, VIP is explained. Think it is a nasal spray.
Anyone from india got the cirs panel done?
Where can we get treatment?
If you don't already have a CIRS-literate doc near you, then make one. Find a good Functional Medicine doc who's willing to learn. Tell them about CIRS. Provide links to this lecture series. Start with some of the basic tests. There are also health consultants online who may be able to help. In the US, you can order many labs these days without a doctor.
@@spectator59 they dont know this he says.....they give supplements they dont correct the iisues.
Great information but in your Sx Cluster Analysis I have seen people who had high glyphosate levels or who were vaccine injured display most of those symptoms. How do you factor those variables into your analysis? I have also seen these symptoms in those who have been injured by fluorquinlones.
I got the H1N1 flu vaccine and I went downhill! I’m wondering now if this is what’s wrong with me. Maybe I don’t have Fibromyalgia???? Need to watch all 3 videos.
@@stephaniekeller4449 I posted on my blog about vaccine injury and correcting it. The flu vaccine has caused this to occur in many but the Dtap is much much worse. The Dtap vaccine is what almost killed me.
Yes...Mold in cars is an issue.
LabCorps range for alpha MSH is still 0-40 pg/mL
How can we make an appointment with this doctor? My daughter has mold she is 19 and is very sick.
Where are you? How to contact?
Not a single doc could figure out why I have biliary dyskinesia. Did a year of searching and medical tests to find mold toxicity. I get RUQ pain and burning legs/arms.
Is it possible to access the presentation slides anywhere?
Just get out of mold ??? What if you can afford to move ????
Where are helps
do you have links to this powerpoint deck?
Who is this n how do i see them
I have CIRS due to black mould and the worst part is that due to such a long period of exposure I now am allergic to VOC so shopping is a painful experience. So over it all.
What’s VOC?
@@alexcasey351volatile organic compounds - gases that become airborne
What about lyme co-infections why ignore that or root canal infections
What is difference btw CIRS and mast cell activation syndrome? (besides mcas is only recently recognized?)
Both are relatively new. Think of MCAS as downstream of CIRS (worry about repairing CIRS first). My opinion of course. Judy Cho has a podcast or two on it that are pretty good
So if I have this and go through treatment and heal …..I still have the genetic weakness meaning I can get sick again right? Am I supposed to live in a bubble now? Or does he go over preventative/supportive measures one can do to strengthen the body?
Where are the doctors who will listen to this as a possibility to our " mysterious " situatuons
You can try functional medicine doctors or practioners.
What you have been meaning on to make me laugh out what is happening on my way in to be
What you want me for is an electronic document and the name and the code you want it is required from your email signature or email signature or or not by the way you do the job to get the documents to the email that will will help me with my employment in a timely way that will be sent by my client as they are required for my application and the contract will not complete and they may be sent directly from legal legal authority on my legal application and legal action for legal purposes as I have not yet been made to be granted an appeal letter of authority in accordance to their policy in respect to their employment and the name and number they have given in my employment letter and letter dated 6th July as proof for your consideration for for further proceedings as I have to be grateful grateful if they will help with this matter or the relevant documentation as they are are required for me and the council will also not charge the deposit until after payment made by me as they were not issued to you as the tenant was sent out of court order from a colleague
one good thing about having a broken blood brain barrier is that GABA supplement enters and people with anxiety don't need to take benzodiazepines.
I suffer from severe anxiety I have tried almost everything is this a problem within the gut itself
@@nylakhan5658wondering the same thing bc I have horrible anxiety and my medication does hardly anything for me. Feels like my gut is messed up!
EBV igg over 600 and range is 0-17.9
I know many people who live in severe mold and they are perfectly healthy, and they have the genes that are supposed to make them more susceptible. Why are they not effected by the mold?
Maybe they don’t have the genes, could be same family but who knows,
They mention that sometimes a trigger is required-like an illness or injury that stresses the body and suppresses the immune response. It’s kind of like walking a tightrope-someday you fall but until then you’re fine.
@@t1mpani yep exactly, they need to identify the triggers that brought them to that point.
@@leestevenson2873 I got food poisoning, then that developed into chronic nausea, and then that developed into anxiety, depression, migraines, fatigue, and then memory issues. I think without the initial food poisoning it never would have caused that snowball effect. Just my POV
@@HurtsSoGood347 Yep something similar happened to me and that was when the mold really started to effect me. I got Lyme disease. Once I got my viral load down I could start handling the mold again. I do take supplements to prevent the mold from making me ill but once something happens to weaken the body the mold will really nail you.
I'm gonna give my neurologist a call I think.
Can fasting cure this ?
Fasting can reduce inflammation, but it won't reverse CIRS.
Prolonged peridic fasting, carnivore and hot climate reverse it for sure
@@mohammedabdulkadir2004 Carnivore alone reverses lots of things. Adding in intermittent fasting or OMAD can turbocharge it sometimes.
Lots of info on carnivore finally being allowed to escape the Food/Pharma giants info trap.
LOOK INTO Anakinra (Kineret)
I couldnt even see the lines on many...😑
what is the link to the visual acuity test?
what is MHS?
Mental Health system
It’s a hormone he describes at 33:31
If you don’t money you no what to do
Breast implants also cause all of this.
Yeah but there's no clinical practitioner that's this available this guy's not a connection where the f*** do you go to get help
I’m sure I have drain bamage.
Thanks, let’s get successful
Just get out of mold??? What if yo
Dr Heyman was at the 2019 Fort Lauderdale Mold Congress where the offer was made for these "Shoemaker doctors" to proceed in connecting CIRS with the Holmes 1988 "Chronic Fatigue Syndrome". Which is an official CDC created syndrome so they obviously recognize their own creation as medically valid.
As opposed to CIRS that is nothing more than a name invented by Dr Shoemaker.
Dr Heyman and the group declined to act on the offer. Perhaps they fail to understand that "Mold at Ground Zero for CFS" means that toxic mold is part of the CFS syndrome.
Or maybe they think that they are such Mighty Gods of Medicine that they can get the CDC to accept CIRS and throw out CFS.
For whatever reason, their lack of response indicates low comprehension that a doctors duty is to "respond to evidence" and "connect the dots"
My confidence in the Shoemaker group was misplaced. They don't deserve to be trusted.
Elaborate
@@at0miclaughter I gave these researchers the opportunity to receive information vital to solving the mystery of a famous syndrome.
They threw that opportunity away.
Wow? And I am trying to get help 🆘 somewhere, I am in mst. Anyone out there can respond?
Maybe they didn't see the benefit of spending their time and resources on proving something they already know to be true. Maybe they thought it would be better spent furthering the research.
Clearly the protocol works, so...
He may have good information but try to get help like this somewhere right you get sick you're f*****
No one helps
His a rude man. had to threaten legal action to get my money back. he was a prick to me.
You where treated by him ? Why did you want your money back
@@donaldpasserelli3529 read what i wrote