Affordable Care for the CIRS Biotoxin and Mold Illness Epidemic - Chronic Inflammation Support

[@NutritionwithJudy]

You can learn more about CIRS here: www.nutritionwithjudy.com/cirs

[@jasongendron8309]

Is mycobind as affective as Welchol or cholysteriamne ?

[@msbolt99]

I appreciate the point you made about taking a break from obsessing over wellness content. That can really start to drive me crazy sometimes when I feel like I need to keep researching constantly to try to get better

[@NutritionwithJudy]

The wellness space has a lot of good and bad. It can be overwhelming for anyone and why we recommend our clients and patients to get off the internet often. Fear tactics can sell well- not that everyone does it, but it happens more often than we’d like ❤️‍🩹

[@camreymosimann7126]

My heart goes out to people who don’t have the resources to get proper treatment or to make their environment safe. 🙏🏻 This is a disease that requires SO much. Great advice Judy! I’ll be sharing this with some friends who have failed the VCS but feel stuck due to finances.

[@olgasantiago-agirlfriendsguide]

❤I appreciate your concern because I’m trying to navigate through CIRS and Long Covid at the same time. I’m not well enough to work and savings is gone. It’s disheartening that the law is written in a way that landlords CAN get away with not remediating the home and I can’t afford to move yet I can’t afford to stay. It’s hard.❤. Thanks to Judy Cho, Lord-willing, I can find some healing.😊❤

[@BubbleBuster]

I fixed my CIRS without the toxic pharmaceuticals. It can be done. Spent thousands on CIRS and shoemaker protocols and didn't get any better. Almost ended up homeless cause of the thousands those crooks took me for. Took food from my family to try to save me. It took a long time and a lot of suffering to learn that we are our own healers. The body makes NO mistakes. God bless anyone watching this. Just know your family doesn't have to go hungry to heal. I healed through limbic work, moved from the moldy building, healing and sealing the gut, natural binders, and mega dosing thiamine. I can now go into moldy buildings and my symptoms don't return. The healing began when my relationship with God began. When they diagnose you it's casting a spell. Don't listen. I had the dreaded mold gene HLADR (that cost thousands to find out) and was told I'd always have to be scared and avoid. Nope. Don't fall for the spell. A diagnosis is just a spell casted to keep us sick. You are your own healer. Judy is a wealth of information.

[@annebeck2208]

I think the right food is a key factor!!!

[@katstaff317]

Thank you for posting this! That is absolutely absurd and unacceptable you almost went homeless to get better. That is why I'm not a huge fan of anyone who follows a protocol or tells me what to consume, especially pharmaceuticals. Who did you go to for limbic work? I am interested in exploring this further.

[@BubbleBuster]

@@katstaff317 I went with the Dynamic Neural Retraining System. Thank you for your kind words

[@BubbleBuster]

@@annebeck2208 honestly carnivore didn’t work for me till I implemented the fat soluble thiamine and brain retraining

[@sannamuh985]

@@BubbleBusterwhich brand and type of thiamine did you dose with? What amount worked for you, out of curiosity (of course the amount is individual for each person)? Which source did you use to learn and follow brain limbic training? Thank you for sharing your story, God Bless you.

[@annebeck2208]

I am so blessed that I got God led me to Carnivore and you Judy! It started 20 years ago with crazy bleeding. I went from clotting to not. Hemotologists diagnosed Von Willebrands, but not the cause. I managed it with pressure bandaids and tampons and it got better slowly. Then we were in Hurricane Katrina and there was mold everywhere! I thought the stress was making me bleed more. Our house was mostly fine and we had a whole house dehumidifier, we fixed it up and I got better. 10 years ago we moved into Military housing in North Dakota and thru a crazy comedy of errors (my husband's fault, not the military's), we lived in a house that had no air exchanged for 6 months. Add to that a high water table and Round-up ready crops, we had high mold and Glyphosate in the water. I was physically a mess. I gained 40 pounds in 6 months, no mater what I ate. My children developed a severe peanut allergy as did several other children on base. I went home to stay with my parents and lost 40 pounds in 6 months, eating more than normal. Back to my sweet husband and I gain that 40 pounds right back in the next 6 months and get all the health problems.back. I looked and looked for what could cause this. GAPS seemed like it might help, but the restricted amounts and lack of any organic anything in ND I decided not to try it. I did find several great books and articles on Mold, one very well written and free on Kindle. The author reminded me that mold needs humidity to grow, that a good dehumidifier would at least keep that amount of mold down. An Air purifier would help kill mold spores and help me feel better. Both did, the bleeding had returned, but we took all of that with us to the next house. I did read the Shoemaker Protocol but wasn't Carnivore and only partially healed. We did Oral Immuno Therapy for peanuts for my children and theri immune system calmed down and they eat peanuts everyday. But it has only been since trying Carnivore that I am truly healing. It is slow and we just had another mold exposure in this house, because the roofers dislodged the bathroom fan vent and hot damp air was venting into the attic. We had the house fogged, with a hydrogen peroxide product that gets into every crack and crevis, and within a week everyone felt 100% better. I do love the fogger system, with someone super reputable, if the house is actually water tight and any wet drywall has been removed and after leak swere fixed. We still use the dehumidifiers to keep mold down and dust mites down, but Carnivore has been the biggest game changer! In fact, we started it about the same time as we had the mold fogged and so it is actually hard to tell which made us feel better. I still need some healing as I still have some mold symptoms. Bless you Judy.

[@msbolt99]

I have von willebrands as well but I never thought to associate it with mold stuff and my other health issues related to digestion. I’ve never met someone else with that condition before.

[@NutritionwithJudy]

@@msbolt99we test for von W when someone is suffering from CIRS.

[@NutritionwithJudy]

Yes!!! Carnivore + mold protocol is so powerful together. We see improved benefits with the combination as well. So glad you have the answer and your family can heal ❤️‍🩹. Everyone that suffers from chronic illness should be on a meat-based diet. 🥩

[@annebeck2208]

@@msbolt99 The last step on the Shoemaker talks about Von Willebrands factor. I make it and make good, but CIRS messes with it. I have 2 other redheaded female friends that had hysterectomies because of Von Willebrand bleeding, when I think it was severe mold exposure. I just would not have the surgery. Now I know it was because every severe mold exposure...I started bleeding and stopped clotting, it always slowly got better as i moved or got a dehumidifier and remediation.

[@ciao2315]

Thank you for making this video. I understand Drs time is worth money for sure but also it becomes unattainable if you’re unable to work because you’re so sick. Thanks for giving advice that can help

[@happyone444able]

Thank you so much Judy! Very helpful content ESPECIALLY since I am dealing with this again most likely due to a move to SC. I was getting very overwhelmed and feeling extremely defeated, as the cost of getting well can be very difficult. Also, your reminder about limiting or ceasing the researching for the “next best thing” was very important for me. I have tried so many things and spent so much time, effort and $$ trying to help myself. I just need to strengthen my faith, take a break from all the”research” and do what I can. So thankful that I found your channel. God Bless!

[@brandonjackson1434]

Good deal, I am happy to have found this channel, just getting started with testing,the first time 6 years ago I got started in treatment things went bad ,i found breath work,ice water exposure,grounding,diet and as many other practices I could fit in helped with symptoms,but the last few years things have progressively caught up with me,so know a little more informed i move forward,Thank you Judy

[@gailivey2015]

This is a great video to share. The most expensive part of CIRS is just living in a clean, non-toxic environment. I'm still dealing with remediation, since there is only 1 company in my town that does it, and they don't value my time or my state of illness very much. After getting remediation done on the biggest problem areas, it still tested positive for active mold spores. Now, I'm waiting for them to come back and get it completely done. If they don't, I'll be forced to do it myself.

[@kvje3456]

Thank you Judy, I absolutely loved this video. If possible I would love to see a slower breakdown of the products and systems you use to to make your room ultra safe. It was a little fast for me to keep up and understand fully. I'm from the UK, so it might be that we use different terms.😊

[@brandonjackson1434]

That would be a great video,the cleaning products ,and the types of filters for air quality,and water quality,maybe add in emf correcting devices

[@heyjace7213]

If you don’t have a gallbladder you can ask your PCP for cholestyromine to soak up the bile. I told my doctor I wanted to start intermittent fasting but the bile build up in my stomach was making me nauseous and I had to run to the restroom the minute I ate lunch. I asked for it and he was like sure! No problem! I’ve been taking it for about a week and today I notice a huge difference in my concentration. And for the past few nights I haven’t had to get up in the middle of the night to go to the restroom and leg cramps have been minimal as well! Big changes.

[@insertmyidentityhere]

Most people can't tolerate that.

[@robertmarking817]

Great overview! Thanks!

[@vitalijussivakovas334]

Thank you 🙏

[@mandy-rf9gu]

Thanks!

[@candacekerr4139]

I so appreciate that you say, don’t listen to a lot of content! My daughter tells me that a lot. But I will always listen to you😊 I do have one question, if you have histamine issues, should you eat red meats?

[@huna1950]

Most people I know with CIRS that binder didn’t work but VIP peptide is really good

[@iAlwaysSpeakTheTruth]

VIP is imperative to restore MSH & VIP restoration to turn off inflammation. The chronic inflammation of CIRS is due to damaged MSH & VIP production.

[@franciscafazzo3460]

Nothing I do works.I got hyperbaric therapy.I'm living in a hotel NE veteran who's broke from the a*******Did charge me tens of thousands of dollars?I wake up with headaches , distorientation and depression

[@micaineseeley5339]

Unfortunately the only thing that works is environment. Plasmalogens maybe but it hasn't been shown scientifically yet. Once you get out of the environment you'll notice improvement.

[@insertmyidentityhere]

It's evil that most normal people can't afford to treat this.....

[@micaineseeley5339]

​@@insertmyidentityhere government involvement has increased the cost of health care multiple times that of CPI and is evil. Agreed

[@heatherrhodge2588]

As stated in previous comment, I've been unable to find a Dr willing to acknowledge my EXTREMELY SEVERE symptoms. No one I've seen has heard of or will bother learning what CIRS is. When i started elementary school, I stayed sick with strep throat regularly for at least a couple yrs & ended up getting scarlet fever despite being given penicillin. My Dr @ the time decided i was "allergic" to penicillin & I'm told I was given something to counteract it? Whatever it was, it finally cleared my throat up, my rash went away & I didn't have strep again for many yrs. Since learning about CIRS, I've wondered if its possible for pennicillin not to work in people with the defective HLA genes? I did some research & learned that scarlet fever comes from not treating strep throat in time. I recall taking pennicillin for awhile b4 developing scarlet fever, so it makes me wonder if I was really was allergic to it or if it coulda actually been due to my immune system not recognizing pennicillin? I realize pennicillin isn't the same as the mold, but still can't help but wonder, since it's made from it if that could be the case? If so, that'd be a good indicator that I carry a defective gene variant, ya know?

[@heatherrhodge2588]

I'm grasping at straws here. I've been too sick 2 even work since I was 26. I'm 40 now & consider it a good day if I manage to eat once. It takes every bit of energy I can gather just to feed myself. I spent so many yrs holding onto hope of finding a Dr who'd help me & trying to get help but eventually became too worn down to even try anymore. I haven't watched the entire video yet cuz I came to read comments, but I saw a lot of ppl commenting about how you said to take a break from researching. Well it's normally not even possible for me to research, bc most of the time I'm so mentally exhausted that I can't think straight enough or find it in myself to pick up my phone and type anything. I'm just so beyond my breaking point & I worry how I'm gonna make it. I'm totally stuck & need a breakthrough at this point. This illness is the definition of evil & anyone who hasn't experienced it could never begin to understand the agony & emotional turmoil that comes along with being totally crippled by it. I'M ALWAYS PUSHING MYSELF AS HARD AS I POSSIBLY CAN. Everyone around me is always telling me I just need to push myself more, blah blah. I wish they cld see that sadly it does take ever fiber of my being just to do the simplest things, like walk to the bathroom, or continue to stand in the kitchen& cook when my body is screaming at me that I need to lay down.

[@b.mary94]

Sounds like what my brother has... very difficult situation... know that you are not alone... just figuring out about all of this stuff too... and in my family... I pray you are holding on 🩵🙏 did you look at the video is there something you can do or get?

[@heatherrhodge2588]

@b.mary94 you're an amazing sis to research this illness in attempt to understand and help your bro!! Nobody in my family has even bothered to listen when I've tried reading stuff about it to em. They all think I'm just exaggerating my symptoms & choosing to be lazy or something! (As if anyone would choose to stay stuck in their bed for YEARS, never leaving the house for anything, let their child's entire childhood go by without taking them to do fun activities, etc)! I cant recall if I finished watching this or not, but it matters little, since I don't even have a budget. I get NO INCOME or financial support whatsoever. My mom lets me live with her & that's the extent of help I can hope to get. She's elderly w fixed income & can't afford rent anywhere else. Rent here is 4x cheaper than even 1 BR apts, but the house is so moldy & dilapidated, it should be condemned!! My 58yr old brother decided to move in here about 4yrs ago. He's the biggest POS I've ever met. He's a narcissist & my mom's his enabler. She's afraid of him & never learned how to set boundaries. He holds onto all of her cards, debit & credit & uses them as he pleases. She actually gave him all her cards b4 he even moved in here. She became too ashamed and lost all confidence in herself 2 use them after she accidentally slid a card thru backwards at walmart & my bro made a big deal about it, saying cruel, hateful remarks to her right then& there, embarrassing her in public. She's a very timid, self-conscious person. He knows that, & it was likely his intent to make her stop using her debit card. He already had all her credit cards at the time, just not her debit. He'd maxed them all out tho. I had the bright idea to get her a balance transfer card over a decade ago. I explained how she'd save money on interest that way, if she transferred her balances from her Belk and Sears cards & stopped using them. She was too afraid to ask him for the card info on those cards tho & ended up just giving him the balance transfer card to use as he pleased. I tried another time after that, getting her another balance transfer card (after asking her if she wanted me to) & yet again, she never bothered transferring any balance & just gave it to him!! I was adopted. He was 18 when I was born. When I turned 18, I planned on buying myself a car. I had saved up a little over 13k from working since I was 14. When my dad took me to look at a car I was interested in buying, (an older Accord at the Honda dealership), he ended up buying me a brand new Accord (bc he'd just gotten $ from his dad passing away). She was with us & witnessed me pleading with him not to waste his money getting me a car. My parents have always been poor & he spent nearly all his inheritance on that car. She even caught me sitting outside in the car a day or 2 later, bawling my eyes out. She got in the car and asked me what was wrong. I told her how awful I felt that daddy had blown his money getting me the car, bc I knew they rly needed that money. I also explained how I'd saved my money all those yrs so I could pay for my own car & that I'd been prepared to spend it all. I just felt SO bad about it. She told me that my dad really wanted to do that for me & made me swear not to tell a soul that he had bought that car, instead to act like I was making payments. I asked her why I needed to lie about it n she said bc it'd hurt my brother's feelings if he found out. So, I lied to everyone, pretending like I was paying4 the car for 9yrs. The car got totalled in an accident after 7yrs. At that time, I'd been considering filing bankruptcy bc I'd racked up medical bill debt from not having insurance. (Not due to that wreck). My bro convinced me that the court could force me to sell whatever car I ended up getting & offered to let me put whatever car I was gonna buy in his name, to prevent them from doing that. At the time I had no idea he was a narcissist & would screw me over, so when I got a car to replace the Honda, I put it in his name the day I paid cash for it. Not even 3 mts later, he stole my car & there was nothing I could do about it. I was in debt, had no transportation & had recently quit my job (doing hair, bc my medical issue made it too difficult). I ended up having to move in with my parents, which is when my CIRS symptoms started getting more and more extreme. He finally told me one day that my mom had told him since day 1 that my dad bought me that car! I explained to him how she'd been the one who insisted that I lie about it. There's so much more I wanna get out about the whole situation, but I'm exhausted just from typing all this. Thx, if you've bothered reading all this. I just needed to vent a Lil.

[@b.mary94]

@@heatherrhodge2588 hi there Heather it's okay you can vent. Sounds like a rough live. If you have a discord or telegram you may add me there to talk if you ever feel like it. Wish I could help you in any other way but at least (or most) I'll keep you and your family in prayer... we are not promised an easy life sadly...

[@heatherrhodge2588]

@b.mary94 I know that's the truth!! I honestly wish I wasn't such an empathic person. I'd be so much better off if I had no conscience and cld take advantage of ppl, like my brother (& half sister). I was adopted within my family, by my biological moms aunt. My mom had just turned 17 when I was born & my great aunt acted like she was just trying to help my mom out by helping care for me. After a few mts, she told her she needed some type of authority over me, in case of emergency(like I had to go to the ER & she had to make decisions) & offered to adopt me. She promised she'd tell me about my biological family situation when I got old enough to understand. Well, once the paperwork was done, she stopped letting my mom & gma (my aunts sister) have anything 2 do with me. She even refused gifts they tried to give me. I found out I was adopted at 15 by my dad, during an argument. My half sister is 4yrs younger than me & lives with my gma. She's never wrkd & has been spoiled all her life. She basically calls all the shots as far as our gma is concerned. Like, my gma just gives her her cards to go buy anything she wants etc. I'm sure they ended up doting on my sis bc of the way I was practically stolen from them. They made up for what they weren't able to do for me with her (& likely guilt from giving me up). If my sister was in my position, sick needing help paying to see a functional medicine Dr, I'm sure my gma (& likely biological mom as well) would do anything they could to make sure she got the help she needed. But I'm stuck here, ganged up on by my mom n bro, going without even essential everyday items. I can't even get tampons, papertowels, razors, ANYTHING AT ALL bc my brother controls every dime of my moms money. My biological family, while still in my family, never was able to bond with me, so they don't really care & are too worried about giving Tiffany anything she wants to consider my needs. (Not that I think they shld do anything 4 me. In fact, it really really bothers me to have anyone do anything 4 me. Even as a teen, when my mom and I went to eat or something, I paid, bc I just don't like taking from people. It makes me happy to do things for others, not the other way around.) I've been unable to do anything 4 even myself for so many yrs now & I have no happiness in my life except4 my daughter, which really, I always feel terrible cuz she's depressed by the fact that we have no transportation & she never gets to go anywhere, like even to a store. I can't buy her anything & she goes without just as much as I do. We watch tv together & when I feel well enuf, I cook with her and do crafts. She's 9. She sleeps in the bed with me cuz since my bro moved in, she can't have her own room. Our bed is so old and gross. I can't even get help cleaning around here bc my moms too busy washing all my bros dishes and she's just old n not doing very well to be honest. I've seen a big decline in her health, esp mentally since my bro moved in, but she won't let me take up for her to him. She lies 4 him all the time & it's just psycho!! My dad passed away in 2016. I actually believe he was suffering from CIRS as well for many yrs b4 he passed. I remember lots of times when my mom would get bk from going somewhere with my bro & tell my dad that he bought her this and that etc. My dad wld get mad at her and say stuff like "ur really gonna keep trying to convince me that he'd do anything 4 you like that?! Come on woman, I'm not stupid. I know he's a piece of shit." I didn't even really understand why he acted like that at the time but it makes total sense now. I know my mom is intimidated and afraid of my bro, but I still don't understand why she worships him the way she does & lets him get away with all he does. I honestly believe my dad prob decided to get me that car bc he knew I was a giving person (nothing like his biological son) & that's why he wanted to help me. I know if he was still around, my bro wldnt be living here.

[@sophie.v.]

Hi Judy 💕 can you make a video on decontaminating a car when there’s no active mold. I just bought a 3 year old used car and I need to buy a Hepa Vacuum (I have no idea which is best for cleaning in the car and in a home) and figure out which cleaner is best to use on the whole inside of the car. I can’t find any videos on KZbin of people recommending a specific vacuum for cirs and suggestions/step by step for decontaminating cleaning for Homes/Trailers/Cars.

[@judyactonayala3074]

Thanks, Judy! Do you know about the HiTech machines that decontaminate homes and buildings and disappear the mold?

[@heavychevy4616]

thanx & god bless

[@EthanJonas-uk9mh]

do you suggest fermented and probiotic foods with the carnivore diet

[@felixaudet5860]

What can be done to counter the homocysteine buildup caused by a high protein diet/carnivore diet? What B vitamin works the best to convert that homocysteine into cysteine?

[@douggrant3431]

What if someone doesn’t get better on the shoemaker protocol after three attempts what would be your opinion and suggestion?

[@marybraud8718]

So helpful

[@iAlwaysSpeakTheTruth]

Marcons is TOUGH to clear!

[@jerryiwanski256]

I tried the CVS version of cholestyramine and it just about wrecked me. I seem to be handling the compounded version ok.

[@tealpatt]

Hi, Judy .. I love your work! Where is the interview you did with doctor Alan Gruning? I can't find it...any more

[@rorehmani]

HERTSMI-2 is the test recommended on a tight budget. What would be the most ideal test if cost for home testing isn't an obstacle? I want to see if i can gift that to my parents. Thanks!

[@JamieR]

Fantastic video, Judy. What do you recommend if carnivore makes one sweat like crazy? I just can't eat carnivore 😅 and what if we have MCAS and other things on top? And do you take on international clients?

[@jasongendron8309]

My practitioner only uses mycobind as a binder. Is it as effective?

[@iAlwaysSpeakTheTruth]

Yes. About 25% of CSM.

[@annebeck2208]

Urgent Question: Can you do MOLD allergy shots or mold Sublingual drops (SLIT) if you have CIRS? Both use mold, one is injected and one is swallowed. I would hate to be cleaning out the mold with expensive Rx, while I am putting more mold in my body with SLIT. I get a stuffy nose from mold outside, when the counts are high, SILT calms that and helps me breath, but I don't want it to cause other problems. I have no idea how or who I would ask, current Dr. does not know. (The SLIT one popular for Texas is usually CedarX, but there are others for other zones and allergens on Amazon. )

[@LessJunkMoreHealth]

Do you ever recommend "true" commercial ozone treatments for the living space? Even for temporary relief?

[@user-xo9vd7qm6p]

@judy How can someone with GERD and gastritis eat a high fat diet?

[@chasethehorizonx]

Betaine HCL and oxbile

[@agreeablegraylife]

I cleaned out my gallbladder with the amazing gallbladder liver flush. Did it 3 times so far. Feeling better each time and fat is getting easier to digest.

[@agreeablegraylife]

But first, I used healing herbs to get the inflamation down, and that took about 9 months.

[@Bhatmann]

Can ringworm on my skin be the cause of or contribute to CIRS?

[@user-mw2sm6sm5u]

If you think others in family have CIRS.... Does everybody have same Halo types? Since it comes from Original gene? I can't find any info on this. Thank you so much for everything you do.❤❤❤❤❤

[@at0miclaughter]

I have the mold susceptibility and chronic lyme susceptibility and my mom has the Multi-susceptibility and chronic fatigue gene

[@user-mw2sm6sm5u]

Thank you. Did any brothers or sisters get Cirs? Or even your cousins?

[@at0miclaughter]

@user-mw2sm6sm5u I believe all my family members have it but only my mom (the most sick) was open to getting herself tested

[@LessJunkMoreHealth]

Do you recommend an ozone treatment in the space?

[@lindyb4509]

@nutritionwithjudy if you pass the vision test is it more likely that you don't have cirs?

[@jerryiwanski256]

I passed it and still have severe CIRS.

[@drgeraldrapp]

Can CIRS be cured?

[@jelenanuhanovic2855]

What does CIRS abbreviation stand for? Thank you

[@Bhatmann]

Chronic inflammatory response syndrome (CIRS)

[@sonicaudio777]

OKRA PEPSIN BINDS