Intro to CIRS: ruclips.net/video/aU_krpHnWA8/видео.html. Learn more about Chronic Inflammatory Response Syndrome (CIRS): www.nutritionwithjudy.com/cirs
I am 67 and have Primary Progressive Multiple Sclerosis, I’ve been bedridden for near 10 years; diagnosed almost 20 years ago, PPMS just kept getting worse until 2021 when I started eating carnivore. I had never heard of the carnivore diet but I knew what I wanted to eat; nothing but meat. I’ve been full carnivore for over one year. I eat almost exclusively beef and eggs. I use a lot of ghee and sea salt, and that’s about it. I try to maintain a ketosis level of 6.5; I keep that high for healing. The benefits have been great; I was unable to take care of myself at all. A few months back I started to shave myself, dress myself, and cut my own nails. Further, I was able to shower myself and I can now whistle again; my lungs have been too weak to provide forceful air for whistling. Other benefits over the past year plus, I have noticed cognitive decline for years; with carnivore I truly believe I am beating it. I had years of nasty indigestion, constipation and high B/P, that is all fixed, down at least 70 lbs, hand tremor gone, age spots gone. I just started being able to get up on my feet without assistance.
You might benefit from a GAPS Version of the same carnivore diet. Ie. Adding bone broth or tiny bits of live sauerkraut juice might be huge for you. Look up natasha Campbell mcbride. So happy for your improvement!!
Fabulous! My father died of complications of MS (most likely med side effects and concurrent Candida). I would also recommend IgG food sensitivity testing. I did it and found #1 allergens: EGGS AND BACON! Could help further boost your recovery, and I applaud the strides you have made, they are phenomenal!
I too, am very grateful to Judy because Kelly is my daughter-in-law, and I know how very difficult her journey has been and how much better she is feeling now. I am very impressed with Judy's extensive knowledge and her open mind and heart. Her expertise in the CIRS disease allows her to zero in and listen to her clients. I know Kelly's struggle are real. I had no idea what a challenge these issues could be, but I am very thankful that Judy has been able to recognize them. . It's amazing to me how common this is. Thank you Judy! Congratulations Kelly!!
Thank you, Sharon! I haven't met you yet but I looking forward to the day I do. Kelly is an amazing human being and I know her significant other is too!. ❤
My doctor is having my tested tomorrow for mold, metal toxicity and hormone balance. I’ve been keto and carnivore and my thyroid is still way off and I have high inflammatory markers on my lab results. There are some things that just aren’t getting fixed. That’s hard for something by people on the carnivore community to accept - they don’t want to believe you can still have issues after being a carnivore. This interview was helpful because I’ve tried everything too and I’m still all messed up!
We owe you so much gratitude, Judy You have helped so many of us who were suffering with CIRS and had no idea I'm glad I was already a part of the Carnivore Community so I could hear about this and seek help with healing I'm personally very thankful I am on my way to root cause healing!!
I think this was honestly the best interview i've ever seen during these 5 years and thats a big big thing. These positive vibes and no promoting. Thank you so much, both of you!
Awww such a great interview by Judy featuring my CIRS sister Kelly! You both are the best and I’m so happy to be going through this with you both ❤️🩹 your story will help so many 🤗
I'm in the CIRS Group with you both and judy helped me get there I am so thankful for all of you in this space I have asked a million questions and, at times, have doubted this entire protocol but I know I'm on the right track I finally passed my VCS test after 2 months on Protocol now if I can just get my blood pressure to go down!!! It will come, just got to have faith and continue on the journey
Hi Judy. I’m grateful I found this video! Kelly Ann is literally telling my story. This is me!! I am traveling that road now. I haven’t tried carnivore because it sounds so bizarre but after hearing her story and how much it is like my condition and what I am dealing with currently. I was just wondering if Kelly Ann has a public website or a blog where I can follow her. I know she said she is extremely private but agreed to come on this show with you, but I just feel such a connection with her because what she dealt with is so specific with what I am going through. Thanks Judy
I am so glad you mentioned the Cellcore products. I spent thousands and used all of them and did not get better. I’m so thankful I’m finally on the Shoemaker Protocol and on the road to healing. Looking forward to a story just like Kelly’s!
Hey Judy, 29 year old pilot in the army here. Been strict Carnivore for 3 months due to recent abrupt health issues. Military medical system has been little help. This video hit home for me and I believe this might be my issue. I took the eye test online and failed, it told me I likely have CIRS. Went to your website to get a consultation but it honestly confused me. Would love to reach out to you and work on my issues as I want to be healthy again.
I can relate to so much of this! 😥I was so wishing that carnivore would be a cure-all. Especially when you've tried so many different things.When you've had chronic issues for years just eating meat sounded and felt really simple. Carnivore has helped my gut but lately I'm going downhill again. I took the eye test in 2019 and didn't pass. Going to look into this again but to be honest it looks so complicated when you're laying in bed with terrible fatigue and tears. Thank you for doing this podcast. God bless.
You can email us. We try to make it as simple as possible so that you don't have to struggle. My only requirement is to really believe you can heal (and follow the protocol). The heavy lifting of learning the illness and what to do next is on the NwJ team.
Your not alone. I have followed Judy for couple years now and have tried every video. I'm still not healed. I have taken so many tests but never herd of this. Thus lady's story is just like mine less the MS. IM ACTUALLY excited. Never give up. I just completed my EMT school and start fireman training next month. I have many hard days just to keep going. This knowledge is amazing thank you. But where to start wow.
Be sure to avoid gluten with autoimmune. My theory is that the gut gets destroyed with antibiotics (I used to use them constantly) and then leaky gut causes confusion in the immune system. Prayer is powerful too!!!
I love these When Carnivore alone isn’t enough series. So true.. diet is impactful but there are times when my body just needs many angles of support beyond diet.
Great - where are people getting all this money to buy grass fed beef and pay for expensive doctors and treatments? Cuz being sick and not working makes all this impossible.
Thank you for sharing your story and Judy thank you for all the work you do on behalf of the CIRS community to educate and help people!! So encouraged by this interview as I’m just beginning my CIRS treatment.
It's standard when writing that the writer should define a term such as CIRS or AIP the first time they use it. This should be the practice in this format as well. When you use a term repeatedly without defining it, you're not helping those who don't know the terminology.
Thank you for the letters CIRS. I will be able to speak with my new Internist next month. I hadn’t read the whole title of the video, just the words carnivore and MS.
I’ve known about my CIRIS since 2016. If someone knows they have mold in their home and they are sick no matter what they need to tell the person that’s trying to help them heal because they will never heal while living in mold. A Lot of mold is hidden and you don’t always know, but if you do! For people that can’t afford the test I don’t see why you couldn’t start them on the protocol and if 3-4months later they are starting to heal then that’s good right. If they are not healing I don’t see how the protocol could hurt them. When someone might have CIRIS that’s basically rock bottom health so I don’t see what they have to loose by trying. The medication CIRIS protocol was not a magic potion for me but getting out of the mold was. I still struggle and I think I always will carnivore and all.
Bless you Judy!!! Healing is so important and I really appreciate this!!! The biggest problem with buildings and mold is that a building must balance air flow with energy efficency. It costs a lot more to have air flow in and out and around a building, dehumidify while not drying out the building....with the energy efficency laws we have to build buildings tight, tight, tight. I don't see a way out of this with building codes. Dehumidify may be the thing people have to do, since mold needs humidity to grow., reduce the humidity = reduce mold. But healing still needs to happen!
Judy & Kelly thank you both for this video. I was diagnosed 7 years ago with CIRS. I did the Shoemaker protocol & started keto / carnivore then. 6 months ago I gained weight overnight & slowly but surely my symptoms began to return. But because they weren’t as severe as they were originally I didn’t put 2&2 together. Until I heard this interview! Kelly’s story was my story & my name is also Kellie! I have tried every bio hack carnivore, fasting, saunas, red light therapy, sunrise, sunset, grounding, blue light blockers. You name it I’ve done it. It just occurred to me after hearing this I need to go back to my Dr. I made an appointment today. Thank you for all you do Judy. You’re marvellous!!❤
Hi! I never been diagnosed, even I had done brain scans and so on.. years ago. The pain I have, there are no words. The muscle rigidity and bone cracking and pain , mostly in my low back spine, sacro.. it goes down to my legs.. I have this pains since childhood… I’m always exhausted and I’m 32… I’m so tired of it. Been 1 year and a half in this diet and it’s going slow.. but I’ve seen changes in my mood, and gut. The biggest change is in my gut, feeling more present in my body as before the gut was not in a good state. Now it’s staring to improve and in feel more peaceful and present in my body but I still feel my body is so rigid, tired, in pain… sometimes I’m sitting and suddenly my leg is completely asleep, like I don’t feel any leg… and It takes some 30 seconds for it to come back to life… I have si much pain in my hips and sacro and legs.. pelvis … I hope this gets better! It heals!! I feel I’m waisting my life!
I recently listened to a book called "Could It Be B-12", which said some 60% of people diagnosed with MS, actually are just B-12 deficient. The longer one goes without a proper diagnosis, the more damage is done, that may not be reversible. I highly recommend the book to anyone diagnosed with MS.
She ate meat for years, which is high in B12, and also did the gut supports to ensure she was breaking down and absorbing the B12. It wasn't the solution for Kelly.
@@NutritionwithJudy I assumed you had checked this, but there were people commenting about being diagnosed with MS and I was thinking more about them, when i commented. It is apparently a scarily common misdiagnosis that leads to unnecessary debilitation and early death, when it could be easily treated.
I’m so happy to have watched this. I have chronic Lyme and have been eating carnivore for 6 months. I think I have CIRS after listening to this interview. Now I need to find out how to be tested- thank you!
I watched a video about a woman who had to move into her car to get away from her toxic home because she didn't have the money to remove the problem. Sad but she is cheerful because she feels better.
A friend of mine who works in a large grocery store described what she saw when her store was being remodeled… MOLD! Lots and lots of black mold, especially in the freezer/frig areas. When she told me that they left the mold there and just put in new refrigerators, etc, I told her that she should think about getting a new job… in some other sector. Also, I had a whole house dehumidifier installed about two years ago that helps keep my house very comfortable during hot, humid summer months, but also keeps the circulating air mold-free. The system is tied into the reservoir/pump on the main heating system and is emptied automatically via hosing into my garden.😊 If I recall correctly, the project cost was in the $1,000 range. Btw, I almost never need to run the air conditioner, (another mold potential), so imo, it’s worth the money. Last, ditch as many chemicals (environmental insults) as you can. When conditions permit, I hang my laundry outside in the sunshine and fresh air. The sun is a natural sanitizer, and who doesn’t love that wonderful smell that you have on your bed the first night after a line dry!?!?!!! It fixes everything.☀️
Great info ! Had no idea acs were mold potential * e two grocery stores I frequent (I’m on an island options are limited) have OBVIOUS green and black mold on the ceilings above the freezer areas. I can’t believe they just leave that there. Guess few people look up lol...not funny I know.
@@foxyauragems6146 An air con system was the reason for Legionnaires’ Disease that killed people several years ago in Philadelphia, PA. Though technically it was not mold, it was bacteria which has similar origins to mold.
God bless you and THANK YOU Judy, for highlighting a little-known and often devastating condition that can remain hidden for years. I have CIRS from mold, and carnivore has been a God-send. Most of my pain, brain fog, numbness, anxiety and irritability are just gone after only 5 wks of eating carnivore. I'm just so much happier and calmer, and I've even lost 19# (after mold gave me a 43# weight gain on top of being overweight to begin with). My hormones have even started to normalize on their own. I'm well familiar with the Shoemaker protocol, and I was using that as well but I had plateaued on that after a slow year of improvement until I found carnivore. Anyhow I believe the body is so brilliantly designed we can heal from so many things that mainstream medicine has told us are mystery diseases or deemed "incurable". Thanks again!
I really hope both Judy and Kelly Anne get this message. First of all thanks for sharing this, it is what a lot of carnivores need to hear! Carnivore can’t fix everything but it sure as hell helps a lot of things! Re the MS has Kelly ever been tested for heavy metals like a Hair Tissue Mineral Analysis? I have a mother who has MS and we are pretty sure it is from Mercury poisoning. Not long after I was born she was diagnosed. I found Mercury and Arsenic in my hair after trying to find what was causing my Hashimotos. Mold plus heavy metals is a force multiplier. It is ridiculous how much it can impact your health, and yet it is crazy how little it is tested for. If you have any dental work with metals in it e.g. amalgam fillings, then you likely have Mercury, and any vaccinations unless you specifically asked for no mercury, will probably have mercury in it as it is used as a preservative. I hope you get better soon Kelly! You’re in good hands with Judy, I can imagine her losing sleep over trying to work things out because that is how I am too 😂
Was she on a Benzodiazepine? Does anyone know? Because the symptoms she was describing and the "My body not acting like everyone else's" screams Benzo induced Neurological Dysfunction which I recovered from. People have no idea how bad Benzodiazepines are taken longer then 2-4 weeks they change your body in the worst way possible. I personally had hundreds of symptoms which doctors couldn't figure out. Everything she mentioned sounds word for word like my experience give or take hundreds of other symptoms I had
This is the first I've heard of CIRS. I've been aware that mold is toxic, but not realised what symptoms can be indicative of it. Thank you for this info. It occurs to me that tobacco smoking could be a contributor? They do talk of the possibility of mold growing on tobacco, and since it needs a certain degree of moisture to be suitable for smoking it could be that all tobacco has a certain degree of mold? I notice that if I can tolerate a couple of puffs, but if I have three or more I usually get cold feet and hands, and it goes to my head and makes me a bit unstable on my feet. I am also wondering if mold can grow on house-dust?
The broken-down particles of mold spores (when they dry up and break down into fragments) hang out in the dust and in any porous material. That's most of what gets people sick. It's not just mycotoxins and not always the active mold that smells like mildew. So yes, it can be in the house dust. All environmental toxins can exacerbate a worsened-state immune system (including smoking, plant toxins, plastics, etc). Getting to root cause will help you become more resilient.
Thank you so much for this interview Judy. After 7 months of carnivore with symptoms coming back I knew there was something else. After 6 months testing yes I have CIRS. I'm pretty academic and wow did I struggle with the diagnosis. Slowly it's sinking in, I'm believing it and now I'm about to start the protocol. I related to everything said here. 5 stars to you, I've listened to ALL your work and devoured your book. Xx
I have all of those symptoms including mold sensitivity and I feel horrible. I cannot afford the test for the autoimmune disease. I feel like I’m dying at times.
I just read a list online of almost 40 CIRS symptoms and I thought I was reading my autobiography! Yikes! Starting carnivore March 1st, currently preparing such as gathering recipes, and we shall see if I improve any. I've been ill for 16 years so hopefully I will find some relief! (Not so) funny that she has MS and I had suspected I could have MS because of various symptoms I have. But I also have symptoms that look like POTS, lupus, CFS, Fibro, MCAS, EDS, and any other number of illnesses. Having such a huge symptom list has made it so providers do not want to deal with me, I've had multiple admit that I must have more than one condition given the symptoms but they are at a loss and I've even been told to find a new provider because they can not help. I have a 2nd appt with a new provider next month, I'll bring the list of CIRS symptoms with me and check off the ones I have (almost all) and see what her thoughts are.
Wow i had to find what this CIRS because am just having more and more issues even on carnivore. My lymp nodes are swollen and hurting and am always tired so i better get to a dr. Thankyou for such and awesome video because not everyone is the same.
Judy, I love all your episodes so thank you. I've started with keto like 3 years ago and eventually landed doing meat only for about a year. One major issue I'm having is histamine reaction. I had it so bad that I ended up at the ER and since then non stop itching everywhere. I feel like I'm extremely sensitive to even other meats and it's very annoying 😞
Is there a mold test for dwellings that's reliable? My daughter was diagnosed with Hashimoto with escalatibg symptoms and has lived in her apartment for 17 months. I'm suspicious anyway.
Been carnivore for 16 months but could stop the hot flashes. Saw a Steak &Butter Girl video about how she cut out salt and pepper. Did the trick for me!! I can’t believe that’s what was causing the problem!!
I've had RA for over 40 years, but after listening to this entire interview, I'm pretty sure it's really not ciRS. I did find this discussion very interesting, though. Thank-you!
ONE QUESTION - when you say "hormone health" are you referring to just estrogen and progesterone? Wikipedia says we have more than 50 hormones (!) so how do I know if my hormones are "balanced"? I'm 64. Thank you again for all your amazing content.
CIRS primarily affects androgen hormones, cortisol, and the thyroid from an autoimmune perspective. Androgen hormones are the DHEA, testosterone, FSH, LH and estradiol. All sex hormones work together so it will impact progesterone and estrogen.
Hey Judy, really nice video! I was wondering if I can help you to edit your videos and create some highly engaging shorts out of them. Looking forward to hear from you. Thanks
Judy, how long did Kelly have to take the cholestyromine binder before she saw progress in her ability to reintroduce plant foods? I don't think that was mentioned in the video. And THANK YOU so much for bringing this information to the public.
Just a guess, but, would a person with Ehlers Danlos Syndrome be one of those "more susceptible" people? I also have several autoimmune diagnoses. I've been a strict carnivore for about a year, but I just can't break through that healing ceiling. I am greatly better than I was a year ago. But, I hit a plateau in every category after about 5 months.
Thank you for this very informative episode. I have a feeling you're going to get a lot of traffic on the website, that's includes me! I'll be looking for the next s interview
So if a person suspects CIRS and has medical insurance, can we just go to a basic family doctor to get tested? Or if we go through you how does this work?
She's had Dr. Shoemaker on previously, he was the one that came up with the protocol. On surviving mold there is a list of providers that follow the correct protocol to heal. Others don't follow the correct steps. Judy does have CIRS testing etc. on her site and many recommend, but she does refer to a Shoemaker phys.
My C4a was high in January. I have CIRS and have been treated for it via binders and supplements. I mentioned my incessant allergies to my NP but she didnt mention MCAS and histamines at all. Ive slowly been learning about this. I suspect histamine intolerance with some foods. Im on day 2 of no coffee and I actually feel better which is insane because Ive been relying on coffee for so long. I didnt realize coffee tends to have mold mycotoxins in it.
Sorry I’m not trying to be annoying but we are super poor doing the best we can. We live in a mobile home and can’t afford to move and we can’t make modifications. Im feeling a little discouraged. If anyone has suggestions I’m open to hear it. Thank you.
What’s missing for me with CIRS protocol, and I’ve watched Dr. Shoemaker interviews, is nutritional supplements and eating cleanly, sans gluten no fried foods etc. See ‘osteoporosis of the skull’ per Dr. Joel Wallach. What about vegans?
What's happening with me is that I started keto dropped weight and then got stuck, always having some amount of digestive issues that progressively got worse until I finally went carnivore, then felt awful until I added more fat, but butter is now bothering me. I'm still going to bed with something off in my gut. I've had US done on my GB and pancreas and nothing is off. Now I need a gastroscopy and colonoscopy soon. I feel like her in that I keep eliminating food and feel better initially but then I feel symptoms coming back and still can't lose weight. I have had mold/water damage in my home. And had one winter where I thought I was dying I was sick so many times. I live in a dry climate where it only rains in the winter. But it was enough to cause problems. My issues are mainly digestive but I had a rare breast tumor that was cancerous that started as a cyst and developed very quickly into a huge lump. And this was on a no sugar, keto, and IF diet.
Why does optimal health cost so much? Doesn’t seem fair to those of us that can’t afford testing, home remediations, meds, so many providers with different opinions.
The only thing I feel is that just because a food isn't causing you to react doesn't mean it's ok or healthy. The goal for me would be a proper human diet protocol even if i could theoretically eat everything.
Man I so relate to this and hVe had criticism. "You cant just try for a week and expect it to work", or "you need to cut out X, Y, Z, or quit binging." Uuuugh. I tried Keto for a year and carnivore for 4 months and kept loosing more sleep. I was so wired and tired.
I’m still strict carnivore after 2+years, but like yourself, have been unable to reverse IBS symptoms. A good night of sleep happens once in a while but rarely. Frustrating.
Hi Judy. I have been CV for 1 year but now I have started to develop Xanthelasmata under my eyes. I have a family history of high Cholesterol and without having any tests I would imagine mine is now sky high. my body isn’t handling cholesterol and fats very well. This is evident as I also have a low tolerance for fat in my diet. When I try to go over 60-65% I get terrible digestive issues. I have tried Ox Bile which only makes it worse. So I am having to eat a higher protein version of CV. I am eating 10+ eggs a day. Any thoughts?
Neal try using beef suet or tallow for cooking. It has been clinically proven to not increase cholesterol. Could it be possible your bumps were misdiagnosed? You could be detoxing from OXALATES. These crystals can push out of the body when you’re no longer ingesting them. Check out Sally K Norton for more on that topic.
@@leannelollypop1869 beef tallow goes straight through me. I just can't handle and fats like I said. It's definitely Xanthelasmata too. Not everything can be blamed on oxilates lol.
I have Aspirin Exacerbated Respiratory Disease, Sjogrens, Hashimotos and I had Graves’ disease as a child. I’m 40 years old and on Dupixent a biologic. I’ve had 2 surgeries to remove nasal polyps. I’ve tried every diet and have now been on meat, fruit, and honey after doing AIP and carnivore. My joint symptoms are better but all my histamine issues like my sinuses, eyes and my cheeks turning red and hot are still going strong. I also have asthma. I’ve been tested for every allergy and the only thing that came up was Bermuda grass. I have insomnia so bad and I get less than 30 minutes of deep sleep a night. Im in bed for 10.5 hours and average 7-8 hours of sleep a night but still feel incredibly tired. Even my muscles feel weak. Im wondering if I have this CIRS.
Judy, is it possible to have the HLA-DR genes and HLA-B27? Or do we just have one type of hla? Also, I’m already getting CRP tested regularly. Is there a way to setup CIRS test that doesn’t duplicate that? How do I ask questions like this so I know which thing to buy?
Yes, our team is trained in DNRS and it's a part of our upcoming mind-body program that we believe all our CIRS community needs. (if they haven't done it already)
@@NutritionwithJudy Thank you for your response. I will keep an eye out for this program. I purchased DNRS in 2019 when I was diagnosed with CIRS, but never really got into it. Didn’t have any direction from the 2 practitioners I was working with at the time and my mind couldn’t focus enough to understand what I was supposed to do to get anything out of it. Have made good progress since then, but I feel I’m missing something and have been looking back into the neural component of healing.
Thank you Judy and your guest. Im gonna have to keep learning about CIRS as 2 year clean carni and still have hashimoto and weight creep. I cant even find a doc to do the tests for hashimoto so for the past 9 mos im just trying to eat meat that i can afford and settle for now
Is there any hope or help for people who can't afford any of this but are suffering for years? This all makes sense with my symptoms. I'm in the middle of screening for MS with MRI's. MS or not I am sure the shoemaker protocol would be so helpful. I know our past home was full of mold. No one in my family is sick like me. I can't afford these tests or care. My husband works so hard in ministry and I am too sick and fatigued to work any job. I feel hopeless sometimes as the mainstream Drs think I am crazy when I suggest this.
I was told that the carnivore diet is bad long term, and that I need all different plants for gut diversity??? Is this true?? I'm carnivore at the moment, but don't Wana stick with it if it's bad for my Gastritis/gut problems.. any info peps??
Wow. Pretty sure i have this considering my house has had water damage and I have all the symptoms this lady as mentioned (including 3 years on a carnivore diet). Just ordered a genie test….
Judy,I have been carnivore for almost 3 months. Doing it to handle a rash on my neck that Ive had for 4 months. It itches, burns, and pulls. Its really ruling my life. Could this be a symptom of CIRS? I have low energy too. But no other symptoms.
I always agree with Judy - and this time too. Most come to Carnivore have CIRS ... I have always been sensitive to medications, paint, cold hands, histamines and after I had Covid, I was more sensitive for a while. Getting back to normal. But it takes time ... meat heals but takes time.
Could there be any indication with regular hematology/chemistry/urinalysis tests that could tell you one could be a candidate for CIRS? I just had them all done, and waiting for the 4 point saliva cortisol results. Would my GP be able to give me the vision test? That's a lot of money for the CIRS test!
I’ve been diagnosed with PPMS 16 years ago and stopped progressing about 13 years ago when going on the paleo diet. I also have Hashimoto’s and am pre-diabetic. I decided to transition to carnivore 5 months ago but my body couldn’t handle ketosis. In spite of guzzling water and taking some electrolytes, I experienced extreme thirst and fatigue. I couldn’t function like that and gave up after about 10 days. I’d like to give it another try but need assistance/guidance in how to make the transition work. I’m also intrigued with the CIRS suggestion. Any suggestions on how to proceed? I live in Tampa.
I've been Carnivore for 2 months, been doing ruminants only for 3 weeks, just cut out ghee 3 days ago as I thought that was causing issues, and now I'm having palpitations while trying to sleep, what am I missing, I take magnesium and put redmonds salt on my ground beef.
@@connorjoe6700 yes, the common zero carbohydrate type thinking tends to lead to responses to your kind of query that initially follow the line of "are you getting electrolytes" / "you might need more fat" ...
I recommend you Google dr. Ken Berry and dr. Salvino discussing carnivore diet with fruit and honey. Doctor Salvino had palpitations and other things and had to increase the fat and add fruit and honey before he could tolerate carnivore.
Hi Kelly, throughout all of this, did you struggle with debilitating nausea, vomiting, diarrhea, and/or COMPLETE loss of appetite? If so, how did you overcome that? I'm in so much trouble. I can't keep the nutrients in to heal myself.
It seems like there is no Certified Shoemaker physicians in Denmark. Do I just die then? I have chronic back pains and inflammation. Im 4 years into carnivore. Eating only fresh grass fed/finished meat directly from the farmer. The back seems to worsen even though I eliminated histamines. I do have mold ind the appartment and waiting to get a new. But that dosnt help me right now. Today I had crazy reaction after scrubbing down the areas with mold in my bedroom, and painting it. 30 minutes after I was done I felt like i was gonne vomit for 2 hours, fell a sleep and got som joint pain afterwards as well. Now 3 hours later I feel much better. But im not sleeping in that room tonight! What can I do beside getting a new appartment? Air purifyer maby?
Judy, have you ever looked into helminthic therapy for autoimmune modulation? People with intense food sensitivities and other autoimmune symptoms that sound like cases of CIRS have had full remission with helminthic therapy, allowing them to eat more foods again. I have already inoculated myself, but it has not been long enough to theoretically experience any benefits yet. but I'm just learning about your channel now from the mikhaila peterson podcast. I can only eat meat. 6 months of carnivore has done nothing for me in regards to food sensitivities. Thank you for your work, I'm going to delve deep into your information and hopefully find a way out of this.
Ever since I became sick I have had chronically low testosterone. It started when I went vegan at 16, and I have literally tried everything under the sun to fix it. Name the most obscure method of raising testosterone that you can think of and I have very likely already tried it. Bull testicles, pine pollen, cold therapy, heavy weight training, DHEA, the whole 9 yards. Nothing works. Prior to seeing your content I have been considering TRT as I suspected that I have hypogonadism. But now im having second thoughts?
![Carnivore Diet Dangers? 2 Doctors Answer Questions [Dr Anthony Chaffee]](http://i.ytimg.com/vi/bVj_kYUM0Sk/mqdefault.jpg)
![Carnivore Diet Dangers? 2 Doctors Answer Questions [Dr Anthony Chaffee]](/img/tr.png)
Intro to CIRS: ruclips.net/video/aU_krpHnWA8/видео.html. Learn more about Chronic Inflammatory Response Syndrome (CIRS): www.nutritionwithjudy.com/cirs
Thank you for sharing this information. Bless you!
I'm falling into the category of carnivore isn't enough and have exhausted all avenues. Judy how do I start working with you? I think I may have CIRS.
@@mv8771 don't she's just a holistic doctor. That's like getting a degree from "definitely not a fake college"
@@chuckybang I'd trust Judy's care over any conventional doctor any day!
@@mv8771 It's your funeral
I am 67 and have Primary Progressive Multiple Sclerosis, I’ve been bedridden for near 10 years; diagnosed almost 20 years ago, PPMS just kept getting worse until 2021 when I started eating carnivore. I had never heard of the carnivore diet but I knew what I wanted to eat; nothing but meat. I’ve been full carnivore for over one year. I eat almost exclusively beef and eggs. I use a lot of ghee and sea salt, and that’s about it. I try to maintain a ketosis level of 6.5; I keep that high for healing. The benefits have been great; I was unable to take care of myself at all. A few months back I started to shave myself, dress myself, and cut my own nails. Further, I was able to shower myself and I can now whistle again; my lungs have been too weak to provide forceful air for whistling. Other benefits over the past year plus, I have noticed cognitive decline for years; with carnivore I truly believe I am beating it. I had years of nasty indigestion, constipation and high B/P, that is all fixed, down at least 70 lbs, hand tremor gone, age spots gone. I just started being able to get up on my feet without assistance.
That's remarkable. So happy you are seeing such progress.
Amazing story! Thank you for sharing- amazing after so many years bedridden.
You might benefit from a GAPS Version of the same carnivore diet. Ie. Adding bone broth or tiny bits of live sauerkraut juice might be huge for you. Look up natasha Campbell mcbride.
So happy for your improvement!!
Incredible story, Jim! I hope you continue to heal.
Fabulous! My father died of complications of MS (most likely med side effects and concurrent Candida). I would also recommend IgG food sensitivity testing. I did it and found #1 allergens: EGGS AND BACON! Could help further boost your recovery, and I applaud the strides you have made, they are phenomenal!
I too, am very grateful to Judy because Kelly is my daughter-in-law, and I know how very difficult her journey has been and how much better she is feeling now. I am very impressed with Judy's extensive knowledge and her open mind and heart. Her expertise in the CIRS disease allows her to zero in and listen to her clients. I know Kelly's struggle are real. I had no idea what a challenge these issues could be, but I am very thankful that Judy has been able to recognize them. . It's amazing to me how common this is. Thank you Judy! Congratulations Kelly!!
Thank you, Sharon! I haven't met you yet but I looking forward to the day I do. Kelly is an amazing human being and I know her significant other is too!. ❤
My doctor is having my tested tomorrow for mold, metal toxicity and hormone balance. I’ve been keto and carnivore and my thyroid is still way off and I have high inflammatory markers on my lab results. There are some things that just aren’t getting fixed. That’s hard for something by people on the carnivore community to accept - they don’t want to believe you can still have issues after being a carnivore. This interview was helpful because I’ve tried everything too and I’m still all messed up!
For those of us WITHOUT the financial resources for testing.......what are WE supposed to do ? I literally subsist on less than 1500.00 a month.
We owe you so much gratitude, Judy
You have helped so many of us who were suffering with CIRS and had no idea
I'm glad I was already a part of the Carnivore Community so I could hear about this and seek help with healing
I'm personally very thankful I am on my way to root cause healing!!
I think this was honestly the best interview i've ever seen during these 5 years and thats a big big thing. These positive vibes and no promoting. Thank you so much, both of you!
Awww such a great interview by Judy featuring my CIRS sister Kelly! You both are the best and I’m so happy to be going through this with you both ❤️🩹 your story will help so many 🤗
Corrie! I know both you and Kelly have healed so much with CIRS + Carnivore. I'm excited for others to heal as well. ❤
I'm in the CIRS Group with you both and judy helped me get there
I am so thankful for all of you in this space
I have asked a million questions and, at times, have doubted this entire protocol but I know I'm on the right track
I finally passed my VCS test after 2 months on Protocol
now if I can just get my blood pressure to go down!!!
It will come, just got to have faith and continue on the journey
Hi Judy. I’m grateful I found this video! Kelly Ann is literally telling my story. This is me!! I am traveling that road now. I haven’t tried carnivore because it sounds so bizarre but after hearing her story and how much it is like my condition and what I am dealing with currently. I was just wondering if Kelly Ann has a public website or a blog where I can follow her. I know she said she is extremely private but agreed to come on this show with you, but I just feel such a connection with her because what she dealt with is so specific with what I am going through. Thanks Judy
I am so glad you mentioned the Cellcore products. I spent thousands and used all of them and did not get better. I’m so thankful I’m finally on the Shoemaker Protocol and on the road to healing. Looking forward to a story just like Kelly’s!
Hey Judy, 29 year old pilot in the army here. Been strict Carnivore for 3 months due to recent abrupt health issues. Military medical system has been little help. This video hit home for me and I believe this might be my issue. I took the eye test online and failed, it told me I likely have CIRS. Went to your website to get a consultation but it honestly confused me. Would love to reach out to you and work on my issues as I want to be healthy again.
Hi Terry, reach out to us at Customersupport@nutritionwithjudy.com. We can help support you through this process. ❤
Thank you for your service! Best wishes to you on your healing journey
I'm only 13 minutes in and, so far, this is the most relatable interview I've ever seen.
Omg my heart is leaping thinking this may be it for me!! I’ve suffered for so long!!
That was so eye opening! I had a serious mold exposure in an apartment years ago. I don’t think I ever fully recovered. Thanks for the great info!!!
I can relate to so much of this! 😥I was so wishing that carnivore would be a cure-all. Especially when you've tried so many different things.When you've had chronic issues for years just eating meat sounded and felt really simple. Carnivore has helped my gut but lately I'm going downhill again. I took the eye test in 2019 and didn't pass. Going to look into this again but to be honest it looks so complicated when you're laying in bed with terrible fatigue and tears.
Thank you for doing this podcast. God bless.
You can email us. We try to make it as simple as possible so that you don't have to struggle. My only requirement is to really believe you can heal (and follow the protocol). The heavy lifting of learning the illness and what to do next is on the NwJ team.
Your not alone. I have followed Judy for couple years now and have tried every video. I'm still not healed. I have taken so many tests but never herd of this. Thus lady's story is just like mine less the MS. IM ACTUALLY excited. Never give up. I just completed my EMT school and start fireman training next month. I have many hard days just to keep going. This knowledge is amazing thank you. But where to start wow.
@@NutritionwithJudyI feel like I am dying Judy Please help if you think you can. I believe, but don’t know what to do. Thank you
Be sure to avoid gluten with autoimmune. My theory is that the gut gets destroyed with antibiotics (I used to use them constantly) and then leaky gut causes confusion in the immune system. Prayer is powerful too!!!
Command the body to stop attacking itself, too. And get rid of all fear.
look into oxalates for leaky gut
I love these When Carnivore alone isn’t enough series. So true.. diet is impactful but there are times when my body just needs many angles of support beyond diet.
Great - where are people getting all this money to buy grass fed beef and pay for expensive doctors and treatments? Cuz being sick and not working makes all this impossible.
Thank you so much for sharing a story that is so relatable and a such a difficult journey ❤
Thank you for sharing your story and Judy thank you for all the work you do on behalf of the CIRS community to educate and help people!! So encouraged by this interview as I’m just beginning my CIRS treatment.
Fascinating discussion, as usual! I always learn something new when you post... Great job, Judy!
Thank you! I hope it helps you or someone you love!
Oh my gosh, I’m having all these same issues, getting worse on carnivore, thought I was crazy? And so sad
It's standard when writing that the writer should define a term such as CIRS or AIP the first time they use it. This should be the practice in this format as well. When you use a term repeatedly without defining it, you're not helping those who don't know the terminology.
Thank you for the letters CIRS. I will be able to speak with my new Internist next month. I hadn’t read the whole title of the video, just the words carnivore and MS.
Judy, I love your channel! I have cirs lyme mcas etc etc and am finally getting better. After so many years! Thanks for the interesting interview!
So happy to hear! I hope you continue to heal!
What did you do to heal please
I’ve known about my CIRIS since 2016. If someone knows they have mold in their home and they are sick no matter what they need to tell the person that’s trying to help them heal because they will never heal while living in mold. A Lot of mold is hidden and you don’t always know, but if you do! For people that can’t afford the test I don’t see why you couldn’t start them on the protocol and if 3-4months later they are starting to heal then that’s good right. If they are not healing I don’t see how the protocol could hurt them. When someone might have CIRIS that’s basically rock bottom health so I don’t see what they have to loose by trying. The medication CIRIS protocol was not a magic potion for me but getting out of the mold was. I still struggle and I think I always will carnivore and all.
Bless you Judy!!! Healing is so important and I really appreciate this!!! The biggest problem with buildings and mold is that a building must balance air flow with energy efficency. It costs a lot more to have air flow in and out and around a building, dehumidify while not drying out the building....with the energy efficency laws we have to build buildings tight, tight, tight. I don't see a way out of this with building codes. Dehumidify may be the thing people have to do, since mold needs humidity to grow., reduce the humidity = reduce mold. But healing still needs to happen!
Judy & Kelly thank you both for this video. I was diagnosed 7 years ago with CIRS. I did the Shoemaker protocol & started keto / carnivore then.
6 months ago I gained weight overnight & slowly but surely my symptoms began to return. But because they weren’t as severe as they were originally I didn’t put 2&2 together. Until I heard this interview!
Kelly’s story was my story & my name is also Kellie! I have tried every bio hack carnivore, fasting, saunas, red light therapy, sunrise, sunset, grounding, blue light blockers. You name it I’ve done it.
It just occurred to me after hearing this I need to go back to my Dr. I made an appointment today. Thank you for all you do Judy. You’re marvellous!!❤
Wow, I bet this was almost unheard of 7 years ago! Was it difficult or a long process to finally be diagnosed?
Hi! I never been diagnosed, even I had done brain scans and so on.. years ago.
The pain I have, there are no words. The muscle rigidity and bone cracking and pain , mostly in my low back spine, sacro.. it goes down to my legs.. I have this pains since childhood…
I’m always exhausted and I’m 32… I’m so tired of it.
Been 1 year and a half in this diet and it’s going slow.. but I’ve seen changes in my mood, and gut. The biggest change is in my gut, feeling more present in my body as before the gut was not in a good state. Now it’s staring to improve and in feel more peaceful and present in my body but I still feel my body is so rigid, tired, in pain… sometimes I’m sitting and suddenly my leg is completely asleep, like I don’t feel any leg… and It takes some 30 seconds for it to come back to life…
I have si much pain in my hips and sacro and legs.. pelvis … I hope this gets better! It heals!! I feel I’m waisting my life!
I recently listened to a book called "Could It Be B-12", which said some 60% of people diagnosed with MS, actually are just B-12 deficient. The longer one goes without a proper diagnosis, the more damage is done, that may not be reversible. I highly recommend the book to anyone diagnosed with MS.
She ate meat for years, which is high in B12, and also did the gut supports to ensure she was breaking down and absorbing the B12. It wasn't the solution for Kelly.
@@NutritionwithJudy I assumed you had checked this, but there were people commenting about being diagnosed with MS and I was thinking more about them, when i commented. It is apparently a scarily common misdiagnosis that leads to unnecessary debilitation and early death, when it could be easily treated.
Actually vitamin D and a lack of sun exposure is the culprit...
If that was the case then everyone in Canada. Mn, Vermont etx would have MS
@@foxywhitetip7387 Not everybody, just a higher percentage of the population.
Can you do a healing process update interview with Kelly Ann? ♥️♥️♥️
I’m so happy to have watched this. I have chronic Lyme and have been eating carnivore for 6 months. I think I have CIRS after listening to this interview. Now I need to find out how to be tested- thank you!
I watched a video about a woman who had to move into her car to get away from her toxic home because she didn't have the money to remove the problem. Sad but she is cheerful because she feels better.
A friend of mine who works in a large grocery store described what she saw when her store was being remodeled… MOLD! Lots and lots of black mold, especially in the freezer/frig areas. When she told me that they left the mold there and just put in new refrigerators, etc, I told her that she should think about getting a new job… in some other sector.
Also, I had a whole house dehumidifier installed about two years ago that helps keep my house very comfortable during hot, humid summer months, but also keeps the circulating air mold-free. The system is tied into the reservoir/pump on the main heating system and is emptied automatically via hosing into my garden.😊 If I recall correctly, the project cost was in the $1,000 range. Btw, I almost never need to run the air conditioner, (another mold potential), so imo, it’s worth the money.
Last, ditch as many chemicals (environmental insults) as you can. When conditions permit, I hang my laundry outside in the sunshine and fresh air. The sun is a natural sanitizer, and who doesn’t love that wonderful smell that you have on your bed the first night after a line dry!?!?!!! It fixes everything.☀️
Great info ! Had no idea acs were mold potential * e two grocery stores I frequent (I’m on an island options are limited) have OBVIOUS green and black mold on the ceilings above the freezer areas. I can’t believe they just leave that there. Guess few people look up lol...not funny I know.
@@foxyauragems6146 An air con system was the reason for Legionnaires’ Disease that killed people several years ago in Philadelphia, PA. Though technically it was not mold, it was bacteria which has similar origins to mold.
That’s why they need Colloidal silver in them systems.
@@foxywhitetip7387 interesting. Ty.
God bless you and THANK YOU Judy, for highlighting a little-known and often devastating condition that can remain hidden for years. I have CIRS from mold, and carnivore has been a God-send. Most of my pain, brain fog, numbness, anxiety and irritability are just gone after only 5 wks of eating carnivore. I'm just so much happier and calmer, and I've even lost 19# (after mold gave me a 43# weight gain on top of being overweight to begin with). My hormones have even started to normalize on their own. I'm well familiar with the Shoemaker protocol, and I was using that as well but I had plateaued on that after a slow year of improvement until I found carnivore. Anyhow I believe the body is so brilliantly designed we can heal from so many things that mainstream medicine has told us are mystery diseases or deemed "incurable". Thanks again!
Thanks for sharing with us, may your healing continue!
I really hope both Judy and Kelly Anne get this message.
First of all thanks for sharing this, it is what a lot of carnivores need to hear! Carnivore can’t fix everything but it sure as hell helps a lot of things!
Re the MS has Kelly ever been tested for heavy metals like a Hair Tissue Mineral Analysis? I have a mother who has MS and we are pretty sure it is from Mercury poisoning. Not long after I was born she was diagnosed. I found Mercury and Arsenic in my hair after trying to find what was causing my Hashimotos.
Mold plus heavy metals is a force multiplier. It is ridiculous how much it can impact your health, and yet it is crazy how little it is tested for.
If you have any dental work with metals in it e.g. amalgam fillings, then you likely have Mercury, and any vaccinations unless you specifically asked for no mercury, will probably have mercury in it as it is used as a preservative.
I hope you get better soon Kelly! You’re in good hands with Judy, I can imagine her losing sleep over trying to work things out because that is how I am too 😂
Was she on a Benzodiazepine? Does anyone know? Because the symptoms she was describing and the "My body not acting like everyone else's" screams Benzo induced Neurological Dysfunction which I recovered from. People have no idea how bad Benzodiazepines are taken longer then 2-4 weeks they change your body in the worst way possible. I personally had hundreds of symptoms which doctors couldn't figure out. Everything she mentioned sounds word for word like my experience give or take hundreds of other symptoms I had
I've been on Xanax for years. How did you recover?
What an edifying discussion. Thank you.
Thank you. I hope it helps ❤
This is the first I've heard of CIRS. I've been aware that mold is toxic, but not realised what symptoms can be indicative of it. Thank you for this info.
It occurs to me that tobacco smoking could be a contributor? They do talk of the possibility of mold growing on tobacco, and since it needs a certain degree of moisture to be suitable for smoking it could be that all tobacco has a certain degree of mold? I notice that if I can tolerate a couple of puffs, but if I have three or more I usually get cold feet and hands, and it goes to my head and makes me a bit unstable on my feet.
I am also wondering if mold can grow on house-dust?
The broken-down particles of mold spores (when they dry up and break down into fragments) hang out in the dust and in any porous material. That's most of what gets people sick. It's not just mycotoxins and not always the active mold that smells like mildew. So yes, it can be in the house dust. All environmental toxins can exacerbate a worsened-state immune system (including smoking, plant toxins, plastics, etc). Getting to root cause will help you become more resilient.
Can’t mold grow in our coffee beans also?
Thank you so much for this interview Judy. After 7 months of carnivore with symptoms coming back I knew there was something else. After 6 months testing yes I have CIRS. I'm pretty academic and wow did I struggle with the diagnosis. Slowly it's sinking in, I'm believing it and now I'm about to start the protocol. I related to everything said here. 5 stars to you, I've listened to ALL your work and devoured your book. Xx
Wow I really enjoyed this interview, I’d love to take that test …sooner than later!
I have all of those symptoms including mold sensitivity and I feel horrible. I cannot afford the test for the autoimmune disease. I feel like I’m dying at times.
Great interview! Thank you both. 🙏🙏
I just read a list online of almost 40 CIRS symptoms and I thought I was reading my autobiography! Yikes! Starting carnivore March 1st, currently preparing such as gathering recipes, and we shall see if I improve any. I've been ill for 16 years so hopefully I will find some relief! (Not so) funny that she has MS and I had suspected I could have MS because of various symptoms I have. But I also have symptoms that look like POTS, lupus, CFS, Fibro, MCAS, EDS, and any other number of illnesses. Having such a huge symptom list has made it so providers do not want to deal with me, I've had multiple admit that I must have more than one condition given the symptoms but they are at a loss and I've even been told to find a new provider because they can not help. I have a 2nd appt with a new provider next month, I'll bring the list of CIRS symptoms with me and check off the ones I have (almost all) and see what her thoughts are.
Wow i had to find what this CIRS because am just having more and more issues even on carnivore. My lymp nodes are swollen and hurting and am always tired so i better get to a dr. Thankyou for such and awesome video because not everyone is the same.
Excellent interview! Thanks Judy.
Judy, I love all your episodes so thank you. I've started with keto like 3 years ago and eventually landed doing meat only for about a year. One major issue I'm having is histamine reaction. I had it so bad that I ended up at the ER and since then non stop itching everywhere. I feel like I'm extremely sensitive to even other meats and it's very annoying 😞
This sounds like me Judy. Exactly like me. Holy smokes. I’m going to try this!! Thank you so much Judy for this video!!
Is there a mold test for dwellings that's reliable? My daughter was diagnosed with Hashimoto with escalatibg symptoms and has lived in her apartment for 17 months. I'm suspicious anyway.
Been carnivore for 16 months but could stop the hot flashes. Saw a Steak &Butter Girl video about how she cut out salt and pepper. Did the trick for me!! I can’t believe that’s what was causing the problem!!
This sounds exactly like me!!! I’ve had MS for years. Abs all the symptoms she is describing is me to a Tee!!! I need this help!
I've had RA for over 40 years, but after listening to this entire interview, I'm pretty sure it's really not ciRS. I did find this discussion very interesting, though. Thank-you!
ONE QUESTION - when you say "hormone health" are you referring to just estrogen and progesterone? Wikipedia says we have more than 50 hormones (!) so how do I know if my hormones are "balanced"? I'm 64. Thank you again for all your amazing content.
CIRS primarily affects androgen hormones, cortisol, and the thyroid from an autoimmune perspective. Androgen hormones are the DHEA, testosterone, FSH, LH and estradiol. All sex hormones work together so it will impact progesterone and estrogen.
Love this thanks Judy
Hey Judy, really nice video! I was wondering if I can help you to edit
your videos and create some highly engaging shorts out of them. Looking
forward to hear from you. Thanks
Can you treat for CIRS without testing?
No, the whole process is pretty involved. They need to test you for Marcons as well. If you have that , it will need to be addressed first.
Well it looks like I have to look into Cirs!
We have lots of resources and handouts on our website.
Judy, how long did Kelly have to take the cholestyromine binder before she saw progress in her ability to reintroduce plant foods? I don't think that was mentioned in the video. And THANK YOU so much for bringing this information to the public.
Just a guess, but, would a person with Ehlers Danlos Syndrome be one of those "more susceptible" people? I also have several autoimmune diagnoses. I've been a strict carnivore for about a year, but I just can't break through that healing ceiling. I am greatly better than I was a year ago. But, I hit a plateau in every category after about 5 months.
The fact that she said she can’t sweat means that she had autonomic dysfunction. I have the same problem and hoping the CIRS treatment will help
I am relating to this, very much.
Very interesting! 🙏
Thank you for this very informative episode. I have a feeling you're going to get a lot of traffic on the website, that's includes me! I'll be looking for the next s interview
So if a person suspects CIRS and has medical insurance, can we just go to a basic family doctor to get tested? Or if we go through you how does this work?
She's had Dr. Shoemaker on previously, he was the one that came up with the protocol. On surviving mold there is a list of providers that follow the correct protocol to heal. Others don't follow the correct steps. Judy does have CIRS testing etc. on her site and many recommend, but she does refer to a Shoemaker phys.
In cases of mould in the house, is the solution to move out only or one could try remove mould ?
My C4a was high in January. I have CIRS and have been treated for it via binders and supplements. I mentioned my incessant allergies to my NP but she didnt mention MCAS and histamines at all.
Ive slowly been learning about this. I suspect histamine intolerance with some foods. Im on day 2 of no coffee and I actually feel better which is insane because Ive been relying on coffee for so long. I didnt realize coffee tends to have mold mycotoxins in it.
Sorry I’m not trying to be annoying but we are super poor doing the best we can. We live in a mobile home and can’t afford to move and we can’t make modifications. Im feeling a little discouraged. If anyone has suggestions I’m open to hear it. Thank you.
What’s missing for me with CIRS protocol, and I’ve watched Dr. Shoemaker interviews, is nutritional supplements and eating cleanly, sans gluten no fried foods etc. See ‘osteoporosis of the skull’ per Dr. Joel Wallach. What about vegans?
What's happening with me is that I started keto dropped weight and then got stuck, always having some amount of digestive issues that progressively got worse until I finally went carnivore, then felt awful until I added more fat, but butter is now bothering me. I'm still going to bed with something off in my gut. I've had US done on my GB and pancreas and nothing is off. Now I need a gastroscopy and colonoscopy soon. I feel like her in that I keep eliminating food and feel better initially but then I feel symptoms coming back and still can't lose weight. I have had mold/water damage in my home. And had one winter where I thought I was dying I was sick so many times. I live in a dry climate where it only rains in the winter. But it was enough to cause problems. My issues are mainly digestive but I had a rare breast tumor that was cancerous that started as a cyst and developed very quickly into a huge lump. And this was on a no sugar, keto, and IF diet.
I’m praying 4 u 💕
I also am the canary in the coal mine, my mother also, and I can see it in my daughters.
I just found you, I'm glad.
Oxalates can be easily observed under a microscope. Pretty easy to rule out. I'm still dumping through my forearms 2yrs later!
What exactly are you putting under a microscope to determine that? I want to learn more about this kind of testing
Through your arms?
@@flutingaround Just swabbed samples from the suspect area.
@@RepublicOfWesternCanadaNOW yes, through the skin. Appears as little bumps, sometimes itchy, sometimes not.
@@darkfieldcarnivore3928 wow that's crazy. I've been dealing with oxalates it's been awful.
I have no doubt I have cirs, but I can’t afford treatment 😢
Why does optimal health cost so much? Doesn’t seem fair to those of us that can’t afford testing, home remediations, meds, so many providers with different opinions.
This is the struggle of my life. The biggest expense is home remediation if it's required. (and some of the Rx meds)
Frustrating indeed
I don't understand... Did the grassfed/finished beef stop working?
I know MANY people who couldn't eat pork, chicken, eggs, etc, etc.
this literally sounds like me!!!!! i work sooo hard, for over a
decade!!
can someone contact me for testing and a session and review of my labs??
Judy is an angel 👼
The only thing I feel is that just because a food isn't causing you to react doesn't mean it's ok or healthy. The goal for me would be a proper human diet protocol even if i could theoretically eat everything.
Man I so relate to this and hVe had criticism. "You cant just try for a week and expect it to work", or "you need to cut out X, Y, Z, or quit binging."
Uuuugh. I tried Keto for a year and carnivore for 4 months and kept loosing more sleep. I was so wired and tired.
I’m still strict carnivore after 2+years, but like yourself, have been unable to reverse IBS symptoms. A good night of sleep happens once in a while but rarely. Frustrating.
Hi Judy. I have been CV for 1 year but now I have started to develop Xanthelasmata under my eyes. I have a family history of high Cholesterol and without having any tests I would imagine mine is now sky high. my body isn’t handling cholesterol and fats very well. This is evident as I also have a low tolerance for fat in my diet. When I try to go over 60-65% I get terrible digestive issues. I have tried Ox Bile which only makes it worse. So I am having to eat a higher protein version of CV. I am eating 10+ eggs a day. Any thoughts?
Neal try using beef suet or tallow for cooking. It has been clinically proven to not increase cholesterol.
Could it be possible your bumps were misdiagnosed? You could be detoxing from OXALATES. These crystals can push out of the body when you’re no longer ingesting them.
Check out Sally K Norton for more on that topic.
Carnivore is obviously not the right fit for you.
@@leannelollypop1869 beef tallow goes straight through me. I just can't handle and fats like I said. It's definitely Xanthelasmata too. Not everything can be blamed on oxilates lol.
Liver cholestasis sounds like
I have Aspirin Exacerbated Respiratory Disease, Sjogrens, Hashimotos and I had Graves’ disease as a child. I’m 40 years old and on Dupixent a biologic. I’ve had 2 surgeries to remove nasal polyps. I’ve tried every diet and have now been on meat, fruit, and honey after doing AIP and carnivore. My joint symptoms are better but all my histamine issues like my sinuses, eyes and my cheeks turning red and hot are still going strong. I also have asthma. I’ve been tested for every allergy and the only thing that came up was Bermuda grass. I have insomnia so bad and I get less than 30 minutes of deep sleep a night. Im in bed for 10.5 hours and average 7-8 hours of sleep a night but still feel incredibly tired. Even my muscles feel weak. Im wondering if I have this CIRS.
Judy to the rescue.
Judy, is it possible to have the HLA-DR genes and HLA-B27? Or do we just have one type of hla? Also, I’m already getting CRP tested regularly. Is there a way to setup CIRS test that doesn’t duplicate that? How do I ask questions like this so I know which thing to buy?
Judy, do you ever recommend any of your clients try neural retraining? Something like DNRS or The Gupta Program?
Yes, our team is trained in DNRS and it's a part of our upcoming mind-body program that we believe all our CIRS community needs. (if they haven't done it already)
@@NutritionwithJudy Thank you for your response. I will keep an eye out for this program. I purchased DNRS in 2019 when I was diagnosed with CIRS, but never really got into it. Didn’t have any direction from the 2 practitioners I was working with at the time and my mind couldn’t focus enough to understand what I was supposed to do to get anything out of it. Have made good progress since then, but I feel I’m missing something and have been looking back into the neural component of healing.
Thank you Judy and your guest. Im gonna have to keep learning about CIRS as 2 year clean carni and still have hashimoto and weight creep. I cant even find a doc to do the tests for hashimoto so for the past 9 mos im just trying to eat meat that i can afford and settle for now
Is there any hope or help for people who can't afford any of this but are suffering for years? This all makes sense with my symptoms. I'm in the middle of screening for MS with MRI's. MS or not I am sure the shoemaker protocol would be so helpful. I know our past home was full of mold. No one in my family is sick like me. I can't afford these tests or care. My husband works so hard in ministry and I am too sick and fatigued to work any job. I feel hopeless sometimes as the mainstream Drs think I am crazy when I suggest this.
I was told that the carnivore diet is bad long term, and that I need all different plants for gut diversity??? Is this true?? I'm carnivore at the moment, but don't Wana stick with it if it's bad for my Gastritis/gut problems.. any info peps??
Excellent interview..very insightful..your b9th amazing
Wow. Pretty sure i have this considering my house has had water damage and I have all the symptoms this lady as mentioned (including 3 years on a carnivore diet). Just ordered a genie test….
Judy,I have been carnivore for almost 3 months. Doing it to handle a rash on my neck that Ive had for 4 months. It itches, burns, and pulls. Its really ruling my life. Could this be a symptom of CIRS? I have low energy too. But no other symptoms.
Hmmm, sounds like she was listening to Stephanie Person for high fat low protein advice. Good you found Judy.
I always agree with Judy - and this time too. Most come to Carnivore have CIRS ... I have always been sensitive to medications, paint, cold hands, histamines and after I had Covid, I was more sensitive for a while. Getting back to normal. But it takes time ... meat heals but takes time.
Thanks, John❤
If most have CIRS, do you have CIRS as well? Can you get back to "normal" just being carnivore without doing Shoemaker protocol?
Could there be any indication with regular hematology/chemistry/urinalysis tests that could tell you one could be a candidate for CIRS? I just had them all done, and waiting for the 4 point saliva cortisol results. Would my GP be able to give me the vision test? That's a lot of money for the CIRS test!
I’ve been diagnosed with PPMS 16 years ago and stopped progressing about 13 years ago when going on the paleo diet. I also have Hashimoto’s and am pre-diabetic. I decided to transition to carnivore 5 months ago but my body couldn’t handle ketosis. In spite of guzzling water and taking some electrolytes, I experienced extreme thirst and fatigue. I couldn’t function like that and gave up after about 10 days. I’d like to give it another try but need assistance/guidance in how to make the transition work. I’m also intrigued with the CIRS suggestion. Any suggestions on how to proceed? I live in Tampa.
Hi supposedly bone broth would help with that. Sorry comment is late
I've been Carnivore for 2 months, been doing ruminants only for 3 weeks, just cut out ghee 3 days ago as I thought that was causing issues, and now I'm having palpitations while trying to sleep, what am I missing, I take magnesium and put redmonds salt on my ground beef.
Could be needing higher fat
@va8382 I'm having 200g of fat a day, can't imagine I would need more than that.
@@connorjoe6700 yes, the common zero carbohydrate type thinking tends to lead to responses to your kind of query that initially follow the line of "are you getting electrolytes" / "you might need more fat" ...
I recommend you Google dr. Ken Berry and dr. Salvino discussing carnivore diet with fruit and honey. Doctor Salvino had palpitations and other things and had to increase the fat and add fruit and honey before he could tolerate carnivore.
I think you’re referring to Paul Saladino MD. Not salvino
Hi Kelly, throughout all of this, did you struggle with debilitating nausea, vomiting, diarrhea, and/or COMPLETE loss of appetite? If so, how did you overcome that? I'm in so much trouble. I can't keep the nutrients in to heal myself.
It seems like there is no Certified Shoemaker physicians in Denmark. Do I just die then? I have chronic back pains and inflammation. Im 4 years into carnivore. Eating only fresh grass fed/finished meat directly from the farmer. The back seems to worsen even though I eliminated histamines. I do have mold ind the appartment and waiting to get a new. But that dosnt help me right now.
Today I had crazy reaction after scrubbing down the areas with mold in my bedroom, and painting it. 30 minutes after I was done I felt like i was gonne vomit for 2 hours, fell a sleep and got som joint pain afterwards as well. Now 3 hours later I feel much better. But im not sleeping in that room tonight!
What can I do beside getting a new appartment?
Air purifyer maby?
Get an ozone machine. Try adding fats fruit n honey to carnivore diet.
I cannot get on the links provided for CIRS. It’s telling me that it may be an unsafe location and it will not let me go forward.
Judy, have you ever looked into helminthic therapy for autoimmune modulation? People with intense food sensitivities and other autoimmune symptoms that sound like cases of CIRS have had full remission with helminthic therapy, allowing them to eat more foods again. I have already inoculated myself, but it has not been long enough to theoretically experience any benefits yet. but I'm just learning about your channel now from the mikhaila peterson podcast. I can only eat meat. 6 months of carnivore has done nothing for me in regards to food sensitivities. Thank you for your work, I'm going to delve deep into your information and hopefully find a way out of this.
Ever since I became sick I have had chronically low testosterone. It started when I went vegan at 16, and I have literally tried everything under the sun to fix it. Name the most obscure method of raising testosterone that you can think of and I have very likely already tried it. Bull testicles, pine pollen, cold therapy, heavy weight training, DHEA, the whole 9 yards. Nothing works. Prior to seeing your content I have been considering TRT as I suspected that I have hypogonadism. But now im having second thoughts?
Did Kelly Ann mention having to get rid of any belongings? Or could she still keep them but just remediate the house?