Let's be brave though, with loving respect.....this is happening from the cvd shots, too. Not just the infection, but the injection as well. People have to know.
That's why when Covid started and Doctor wanted me to take the shot I, refused because i had been diagnosed with Mcas in 2019 and was afraid of my body reacting to this shot and who knows what would happen? Even though my Dr tried to shame me, I wouldn't have it.
Anything the natural infection causes. The vaccine infection can cause too. The vaccine tells your body to make the exact same Spike proteins that the virus damages your body with. Evidence is coming out that the vaccine might lead to higher spike protein loads in the body because there's no off signal to tell your body to stop making the spike protein from the shot. I just want to know how come the WHO, and people who created this bioweapon haven't even seen a jail cell or end of a pitchfork.
My methods for my body include low histamine foods, antioxidants, vitamin C, fasting, binders clay and charcoal higherdose minerals and vitamins, and adaptogenic herbs. Be aware of the implications of latent dental infections, gut disbiosis, parasites, mold exposures and heavymetals.
Started working at an office building with a moldy basement. For 9 months, I suddenly gained 16 lbs , stopped sleeping, cortisol crashed, testosterone crashed, ferritin plummeted to single digits. My body has gone haywire. The only visible symptoms are lethargy, constant rhinosinusitis. I quit this week. Let’s pray for me to get better.
I had to diagnose myself & thankfully I did. They gave me antibiotics so the first thing I tackled was my immune system which they destroyed. I also started taking Quercetin & NAC & went back to fasting. I knew that what I had was related to Covid but my doctor & emergency doctors diagnosed me with dermatitis. They were clueless. I'm so much better now but I will keep working at it. And after little sleep for a month, I'm now getting a lot of healing deep sleep, which helps a ton.
Wow! What a great informative talk. My journey started in April 2016. Broke out in hives, which was all over my face, trunk, arms and even a spot on my butt. Went to a dermatologist. Took oral steroids for a month. Connoted having rashes, and finally got a referral in November. By January I saw a rheumatologist. He wanted my top 10 concerns. There were so many more than that. He did a boat load of tests, sent me for some x-rays, then called me a week later and told me I had primary Sjogren's. I thought I had lupus. The problem with the medical system is that they no longer have critical thinking skills. The medical industrial complex has made rules that diagnosis comes from test results. I was put on hydroxychloroquine. Over the years, I continued to have various symptoms. Symptoms that were outside the realm of Sjogren's. I did lots of research into the symptoms. I highly suspected MCAS. One year, I would see the MD. The next year the PA. When I tell the PA about my symptoms, I am gaslighted. I finally asked my internist if he would partner with me to follow my Sjogren's. He said yes, so I cancelled my appointment with the rheumatologist. Several days later, my internist had a medical emergency and retired. Got a new internist, but I decided I did not want to be sent to another rheumatologist to treat me. It has been a year and a half since I stopped the hydroxchloroquine. The MCAS symptoms continue, but gaslighting rules the medical field. I decided I will suffer in silence. Too little knowledge and too little concern.
Take breaks and keep trying to find a real human Dr. I’ve been in this circle and been injured In surgery and a procedure and I will not give up until I see a major reduction in my inflammatory symptoms.
I have severe dry eyes. This started after menopause (complete at age 45, after a couple years of high stress) and after living in a moldy house. I've been working on healing for over 5 years. I think I'm on the right track, and then I seem to go backwards. Thank you for your information...on many videos. 🙏
Boy oh boy, do I ever wish I'd seen this at the beginning of my histamine intolerance journey! At 50 I "suddenly" had a severe asthmatic response to any and all histamine even to the point of not being able to eat ANYTHING because of the involvement of histamine in stomach acid production. Of course, I quickly learned how to fast after I put that together. And, I learned about the toxin portion of the problem and started eating nearly 100% organic, whole/minimally processed (as in cooked), low histamine food. After about 5 months of fasting (intermittent and prolonged 3- to 5-day) and eating super clean my asthma abated. I stayed on a low histamine diet and continued IF for about a year, and I guess that reduced my bucket load to the point where I can eat high histamine food, again, and not have any trouble. I never had covid or took the v-shot (seems everyone I know who took it is "sick all the time" now), so I guess it had to have been a slow filling up of my bucket over my lifetime, and that does make sense - I always had seasonal and a few food sensitivities that I thought were "normal" and I recently learned that my propensity to motion sickness and migraines were also histamine related, most likely. Oh, and I took two Thorne gut tests along the way, one 3 months into my recovery experience and one a year later. My disbiosis is WORSE now?! BUT, the good news is I guess I reduced my bucket load to the point where my disbiosis isn't causing it to overflow anymore. I probably wrecked my gut forever with antibiotics I took every year for 20 years for chronic bronchitis. Thank you very much for putting this information together, Dr. A. It explains the extreme difficulty I had navigating this and that's extremely comforting.
Dr. Anderson Makes 100% sense. I wish there was more docs like this on TH-cam, many wannabes just spread pseudo. I would be most interested in the role of gut microbiota and the foods that could modulate it towards the most eubiotic conditions - this is a vast and complex topic though but probably the primary way we could affect the cells participating in the disorder. So, please focus more on the flora and gut and the food. As it is closely related to immune system anyways. Thanks!
Don’t know if this will be seen: Doc mentioned “Lutein” as a flavonoid to treat MCAS. Did he misspeak; Did he possibly mean Luteolin… which is used to treat MCAS (and, I take). I have never heard about the use of “Lutein” for MCAS. Thank you.
Thank you Dr. Anderson! I was just diagnosed with MCAS and this is so incredibly helpful and informative. Thank you for making this easier to understand. I look forward to watching more videos and sharing this information with my patients. I’m in healthcare and, like you said, I think this is more common than originally thought. I have been telling my PCP for 10 years that I think something is wrong with my gut. I’ve seen every specialist. My food allergies and enhances were just getting worse over the years. This year, my PCP ran blood tests, showed I have an MTHFR gene mutation, and she put me on methyl folate without any other supplements to facilitate the methylation process. One month later, I couldn’t eat 90% of foods due to strong histamine reaction, and unable to sleep due to heart palpitations, and very low blood pressure. I spent dozens of hours researching…I’m working with a functional medicine doctor now and it is changing my life! 🎉 I’m also wondering about the relationship between gut health, candida, overgrowth, and MCAS. I will comb through your other videos.
excellent video for trying to explain this to someone who all of a sudden in the past 7 weeks has developed chronic insomnia after some periods of stress. we are seeing a functional psychiatrist and a naturopathic doctor and they are looking at everything from toxins to gut healing to mast Cell activation. we're hoping that following these anti-inflammatory protocols and the fact that he has removed sensitive foods from the diet will help get his body back in check the insomnia is extremely debilitating. I wonder if the doctor could do a video on insomnia and mast cell activation
Brillant breakdown. Sincerely appreciated. Here in Australia there doesnt seem to be any doctors with this level of understanding. My 64yr old sister is suicidal. She has severe symptoms that scream MCAS or severe histamine intolerance. Doctors have had her on high levels of cortisones and other pharmaceuticals for decades and she now has a range of symptoms from those drugs on top of it. On top of that she is an ideological vegetarian - she is absolutely resistant to the idea that vegetables, fish, chocolate etc may be the cause of a lot of her symptoms. She has literally said she'd rather die than eat meat so she has no where to turn. It is so depressing. My last hope is to find someone that can try her on the type 1 and 2 anti-histamines I have been hearing about but there is no one in AUstralia.
I'm glad you're finding the videos helpful. That sounds like a very tough situation. You might try the links in video description to find an integrative doctor for help. Best of luck - Team Dr. A
"a billion other 'straws' " ??? That's overwhelming. Excellent talk/explanation. Helped me a lot. Did you do another VIdeo talking about how/where to get help? My bucket is overflowing at a flood rate. I have a medical background... but am in a town that is so deficient of any kind of cognizance or willingness to actually "go the distance" to fully help. (Their after the bucks). Thanks again.
Recently found your channel. I don't have all the words to express how much I am enjoying your videos. I have been on a long health journey that is too complex to express in a couple of sentences, but needless to say that everything got a whole lot worse after C. I am still dealing with Long-C and do multiple things to help with all my symptoms. I am also a zebra (EDS). That I am sure you know comes with that. Anyhow...I just wanted to say thank you. I am at that part of my journey where most of the things I read about and watch videos of are not informative for me anymore. Your videos that I have watched so far have provided some new information for me. :)
I watched your videos and other, read articles...but I haven t found information about real and sustainable heal of this disease. Is it possible or I have to tell me I have to live now with all these symptoms all my life. Thanks
Thank you Dr.Anderson. Does the burning sensation from being allergic to an environmental allergen fall under this bucket? I feel like I’m running away from my self and don’t know if the histamine blockers will help as it feels like a third degree burn on my skin. Ty again
Thanks for the info dr. I wonder if you would know why the histamine symptoms get worse during a woman’s period and how to help my body feel better. Thanks
Thank you for the simple and brilliant explanation. A lot of blood pressure medication increase histamine. If you take antihistamines, your blood pressure goes up. It is a viscous circle. Some times you have to take pain killer or antibiotics. Those increase histamin too. How do you manage these medications?
I started having eczema and urticaria symptoms when I got Covid. They got worse about 6 months ago, with palpitations when I ate. Went on antihistamines for 5 months or so then stopped them because I started feeling hungry non-stop. I believe it is a side effect of the fexofenadine. I am hungry since the end of May and stopped them at the end of June. The hunger did not go away even two months after I stopped them and I am getting desperate. My urticaria is worse than when I started them as well.
Why does MCAS cause constipation? I'm just getting diagnosed with MCAS (& POTS, EDS, ADHD, Autism..). Ive had severe constipation for 40 yrs (I'm 51), & it's so bad now I have no choice but to use exlax daily. Ive been thru 30+ yrs of doctoring, specialists, medication, supplements, massage, energy healing, castor oil packs, dietary changes (or not eating at all cause I feel WAY better if I dont), etc.. and WHAT to do for the constipation so I can poop like a normal person?
Hi Dr. Anderson, thank you for your videos. I am being seen by allergy/ immunology now. Confusing as I tested in the normal range for Tryptase but elevated Leukotriene E4, U, I am also being considered as having POTS (after a tilt table test) , I don't have a formal diagnosis for MCAS yet, but all signs are pointing to POTS and MCAS, I have tachycardia and I am in a holter monitor cascade for 30 days. I am trying to go out on my own and learn about histamine foods and correlation, so I can have some relief, I faint after LARGE meals, not all the time but sometimes, I was diagnosed with rapid gastric emptying after an all day study, I went 36 years before I was diagnosed , I have been discarded multiple times. Its been a wild ride for me, sorry to overshare on the feed here but any insight would be valued. So do you see any correlation with these three things I mentioned above? Thank you! Oh and I have AMAG with high gastrin levels and metaplasia in my stomach and small intestine. And last but not least, Hashimotos Disease.
POTS and MCAS can certainly be related. Best of luck with your journey and recovery. It would be best to get an integrative doctor on your team to help give you specific advice - Team Dr. A
3 years ago i have a dengue infection (a virus transmitted by mosquito) the evolution of clinical state was bad, the immune system destroyed all blood platelets
Make sure to check the links in video description to find an integrative doctor. She should work closely with a doctor she trusts to get the most help. Best - Team Dr. A
Firstly, thank you, they started testing for cancers and are now removing a nodule from my thyroid...TOMORROW, RFA so that is good, because it's over my trachea not in my Thyroid lobe, so I am lucky but EVERY symptom that I came in with a couple yrs ago and then acutely last year, still exists...SKIN breakouts, eczema, bone pain, extreme limb fatigue, brain fog, bad gut, colon, the bucket theory and keep that low, is what I've been watching and it helps, Histamine Intolerance. I also have insomina, so I take antihistamines every night, as my Pharmacist is the one who told me...maybe that. It helps or have a strict anti-histamine foods...I am better. I need to say, yes, I had OG Covid and long-covid for sure...but I got myself well after about a year and JUST said to myself, whoa, feeling like ME AGAIN and then this all started after the vaccine...I am not that person, but it is just seems to be true, after the 2nd it ramped-up, for me. I am unrecognizable. Anyway, 2 colonoscopies, endos, because IBS, bad gut, but they say I don't have it, YET I have it. Heart palps from just ANYTHING. I feel best when I am home, no smells, no people, don't touch anything and do not eat. It's nuts...like I'm allergic to everything. Pun intended. I have given up on my GP as they told me they cannot test for allergies if they do not know what they are testing for. A Direct quote. I was stunned, because it was the dumbest thing I've ever heard. So, antihistamines and prayers, and I'm agnostic so...
Dr Paul, is quite possible to have MCAS without cutaneous manifestations, right? I have been diagnosed with eEDS, ADHD and there is a huge suspicion of MCAS. Good guess? My symptoms get out of control every damn time I eat something, usually within 15-30 minutes. By the way, amazing content, very much appreciated. Thank you!
about bucket oveerflowing and Covid: I thought for about a year Covid caused MCAS. Then I realized I had histamine problems long before, and Covid worsened it. THEN I realized over a span of several months I had MCAS all along for about at least 12 years, as far as I can remember. probably longer. and it probably triggered my Ankylosing Spondylitis that I have since ~2007, I suspect. Or the other way around. What do you think is more likely?
I have a really weird TNFRSF13B (TACI/BAFF) Deficiency (Homozygous) that likely led to MCAS/MCAD and SFN and Fibromyalgia and Grave's Disease and Sjogren's etc...I want my immune balance back...I presently have hypogammaglobulinemia....low in Ferritin....No measurable Molybdenum....little guidance...I know you cannot comment on my case specifically but generally what would you recommend for someone like me? I am taking Cromolyn Sodium and using Red Light Therapy and Hyperbaric O2 and Compression and trying to get in nature occassionally for Green Light Therapy etc..... Generally speaking....anything you can suggest? Oh I am taking Methylene Blue too...and a number of other medications....
You're not alone. MCS too. After about 5 years of use and was told it was mast cell attacks when I was in severe tolerance, or withdrawal. Caused MCS too. I'm tapering and my MCS is going away.
2008 was when benzoes were listed as a front line mast cell med. Makes sense with all the Dysautonomia, neuropathy, tinnitus and wd suffering people are developing.
Thank you for your validation. I'm so frustrated. I have all of them, and it's maddening. Im hopefull I can get more open and educated doctors on my team so far I have 1, my dermatologist. I see new allergist this week and work with a natural pathetic on line. The food change has been a game changer. Absolutely mentally and emotionally taxing!! Grateful I have my background and knowledge in holistic mentally practices. Doing what I'm calling a system reset right now and it's beyond difficult going it alone.
Is there a doctor in the St. Louis area that works with Mast Cell? I have been eating three foods for 3 years, can't tolerate anything without symptoms.
I haven't been able to get anybody to take a serious look in the StL area. They all immediately jump to substance abuse as the cause and antipsychotics as the solution.
@bjornolson21 6 minutes ago So, how can all this immune deregulation and mast cell release not show up on a blood test. Hscrp, Ig levels, histamine levels, other mast cell levels?
"Extremely rare" turns out to be maybe almost 5% of the population. General practicionere should not be in charge of epidemiology based on their erroneous assumptions.
Do u have thugs in your family, it's possible that we have to help them make it, it would explain the iffyness in our lives that we can't wrap our heads around, better we don't know them & what they did, it makes it harder , but who r we to say , they can't make it, & their goes your heart, 💝 little kids not safe with them , the problem, we were little kids too , & gosh baby the struggles He must have dealing with us ! 💝👣👑💒
We're skinny for a reason but it sure helps in avoiding all these iffy things u get from diluting your inner parts, were not sapossed to push that hard our tummys & they be happy & give us heads up when they full , it's a beautiful relationship & comforting to not be in thst heavy wt fight ! 💝🚴♀️🥑🥭🥦🍅🍉
Let's be brave though, with loving respect.....this is happening from the cvd shots, too. Not just the infection, but the injection as well. People have to know.
That's why when Covid started and Doctor wanted me to take the shot I, refused because i had been diagnosed with Mcas in 2019 and was afraid of my body reacting to this shot and who knows what would happen? Even though my Dr tried to shame me, I wouldn't have it.
Totally ❤
Anything the natural infection causes. The vaccine infection can cause too.
The vaccine tells your body to make the exact same Spike proteins that the virus damages your body with.
Evidence is coming out that the vaccine might lead to higher spike protein loads in the body because there's no off signal to tell your body to stop making the spike protein from the shot.
I just want to know how come the WHO, and people who created this bioweapon haven't even seen a jail cell or end of a pitchfork.
Absolutely 💯
😉👍🏻
My methods for my body include low histamine foods, antioxidants, vitamin C, fasting, binders clay and charcoal higherdose minerals and vitamins, and adaptogenic herbs. Be aware of the implications of latent dental infections, gut disbiosis, parasites, mold exposures and heavymetals.
Can you share with me the resource you used for low histamine foods? I am finding mixed things online.
@@mrs.g4997check out Leanne Hopkinson ( Australia)
@@mrs.g4997 Dental infections can cause MCAS ?
He failed to mention mold. That is what triggered mine
That's a good point, definitely a common trigger - Team Dr. A
Started working at an office building with a moldy basement. For 9 months, I suddenly gained 16 lbs , stopped sleeping, cortisol crashed, testosterone crashed, ferritin plummeted to single digits. My body has gone haywire. The only visible symptoms are lethargy, constant rhinosinusitis.
I quit this week. Let’s pray for me to get better.
He has in other videos
I had to diagnose myself & thankfully I did. They gave me antibiotics so the first thing I tackled was my immune system which they destroyed. I also started taking Quercetin & NAC & went back to fasting. I knew that what I had was related to Covid but my doctor & emergency doctors diagnosed me with dermatitis. They were clueless. I'm so much better now but I will keep working at it. And after little sleep for a month, I'm now getting a lot of healing deep sleep, which helps a ton.
Thank you for this information and god bless your recovery
From now on, I will refer to you as Professor. You have an incredible ability to explain complex issues so effortlessly!
This is the best explanation of MCAS. Thank You.
Wow! What a great informative talk. My journey started in April 2016. Broke out in hives, which was all over my face, trunk, arms and even a spot on my butt. Went to a dermatologist. Took oral steroids for a month. Connoted having rashes, and finally got a referral in November. By January I saw a rheumatologist. He wanted my top 10 concerns. There were so many more than that. He did a boat load of tests, sent me for some x-rays, then called me a week later and told me I had primary Sjogren's. I thought I had lupus. The problem with the medical system is that they no longer have critical thinking skills. The medical industrial complex has made rules that diagnosis comes from test results. I was put on hydroxychloroquine. Over the years, I continued to have various symptoms. Symptoms that were outside the realm of Sjogren's. I did lots of research into the symptoms. I highly suspected MCAS. One year, I would see the MD. The next year the PA. When I tell the PA about my symptoms, I am gaslighted. I finally asked my internist if he would partner with me to follow my Sjogren's. He said yes, so I cancelled my appointment with the rheumatologist. Several days later, my internist had a medical emergency and retired. Got a new internist, but I decided I did not want to be sent to another rheumatologist to treat me. It has been a year and a half since I stopped the hydroxchloroquine. The MCAS symptoms continue, but gaslighting rules the medical field. I decided I will suffer in silence. Too little knowledge and too little concern.
Are you also hyper mobile ?
Take breaks and keep trying to find a real human Dr. I’ve been in this circle and been injured In surgery and a procedure and I will not give up until I see a major reduction in my inflammatory symptoms.
I have severe dry eyes. This started after menopause (complete at age 45, after a couple years of high stress) and after living in a moldy house. I've been working on healing for over 5 years. I think I'm on the right track, and then I seem to go backwards. Thank you for your information...on many videos. 🙏
Best of luck to you on your journey, and thank you for the support! - Team Dr. A
How did you solve
Boy oh boy, do I ever wish I'd seen this at the beginning of my histamine intolerance journey! At 50 I "suddenly" had a severe asthmatic response to any and all histamine even to the point of not being able to eat ANYTHING because of the involvement of histamine in stomach acid production.
Of course, I quickly learned how to fast after I put that together. And, I learned about the toxin portion of the problem and started eating nearly 100% organic, whole/minimally processed (as in cooked), low histamine food. After about 5 months of fasting (intermittent and prolonged 3- to 5-day) and eating super clean my asthma abated. I stayed on a low histamine diet and continued IF for about a year, and I guess that reduced my bucket load to the point where I can eat high histamine food, again, and not have any trouble.
I never had covid or took the v-shot (seems everyone I know who took it is "sick all the time" now), so I guess it had to have been a slow filling up of my bucket over my lifetime, and that does make sense - I always had seasonal and a few food sensitivities that I thought were "normal" and I recently learned that my propensity to motion sickness and migraines were also histamine related, most likely.
Oh, and I took two Thorne gut tests along the way, one 3 months into my recovery experience and one a year later. My disbiosis is WORSE now?! BUT, the good news is I guess I reduced my bucket load to the point where my disbiosis isn't causing it to overflow anymore. I probably wrecked my gut forever with antibiotics I took every year for 20 years for chronic bronchitis.
Thank you very much for putting this information together, Dr. A. It explains the extreme difficulty I had navigating this and that's extremely comforting.
Thank you for sharing ❤
I really appreciate hearing hormones can have a huge impact
Really struggling five months post partum 😢
Dr. Anderson
Makes 100% sense. I wish there was more docs like this on TH-cam, many wannabes just spread pseudo.
I would be most interested in the role of gut microbiota and the foods that could modulate it towards the most eubiotic conditions - this is a vast and complex topic though but probably the primary way we could affect the cells participating in the disorder.
So, please focus more on the flora and gut and the food. As it is closely related to immune system anyways. Thanks!
That's a great idea, thank you - will pass it along! - Team Dr. A
Can we talk about ME/CFS please?
Don’t know if this will be seen: Doc mentioned “Lutein” as a flavonoid to treat MCAS. Did he misspeak; Did he possibly mean Luteolin… which is used to treat MCAS (and, I take). I have never heard about the use of “Lutein” for MCAS. Thank you.
Yes, it's luteolin for mast cells. Lutein is for your eyes.
The most brilliant mind on the matter! Thanks Dr. A! You've gotten me through the last 6 months since my MCAS started up for the first time. 🙏
Glad you're benefitting from the videos! Thank you for the support. - Team Dr. A
Thank you Dr. Anderson! I was just diagnosed with MCAS and this is so incredibly helpful and informative. Thank you for making this easier to understand. I look forward to watching more videos and sharing this information with my patients. I’m in healthcare and, like you said, I think this is more common than originally thought. I have been telling my PCP for 10 years that I think something is wrong with my gut. I’ve seen every specialist. My food allergies and enhances were just getting worse over the years. This year, my PCP ran blood tests, showed I have an MTHFR gene mutation, and she put me on methyl folate without any other supplements to facilitate the methylation process. One month later, I couldn’t eat 90% of foods due to strong histamine reaction, and unable to sleep due to heart palpitations, and very low blood pressure. I spent dozens of hours researching…I’m working with a functional medicine doctor now and it is changing my life! 🎉 I’m also wondering about the relationship between gut health, candida, overgrowth, and MCAS. I will comb through your other videos.
excellent video for trying to explain this to someone who all of a sudden in the past 7 weeks has developed chronic insomnia after some periods of stress. we are seeing a functional psychiatrist and a naturopathic doctor and they are looking at everything from toxins to gut healing to mast Cell activation. we're hoping that following these anti-inflammatory protocols and the fact that he has removed sensitive foods from the diet will help get his body back in check the insomnia is extremely debilitating. I wonder if the doctor could do a video on insomnia and mast cell activation
Oh wow, this is 100 percent my situation. I'm so happy to find this video!!
Thank you again for another calm & coherent review
of the many facets of this condition.
Thank you for the kind words, glad you are enjoying the videos! - Team Dr. A
Thank you Dr. Anderson. I recently watched many of your videos on histamine intolerance and MCAS.
That's great to hear, glad you're enjoying the content! - Team Dr. A
Brillant breakdown. Sincerely appreciated. Here in Australia there doesnt seem to be any doctors with this level of understanding. My 64yr old sister is suicidal. She has severe symptoms that scream MCAS or severe histamine intolerance. Doctors have had her on high levels of cortisones and other pharmaceuticals for decades and she now has a range of symptoms from those drugs on top of it. On top of that she is an ideological vegetarian - she is absolutely resistant to the idea that vegetables, fish, chocolate etc may be the cause of a lot of her symptoms. She has literally said she'd rather die than eat meat so she has no where to turn. It is so depressing. My last hope is to find someone that can try her on the type 1 and 2 anti-histamines I have been hearing about but there is no one in AUstralia.
I'm glad you're finding the videos helpful. That sounds like a very tough situation. You might try the links in video description to find an integrative doctor for help. Best of luck - Team Dr. A
😮
"a billion other 'straws' " ??? That's overwhelming. Excellent talk/explanation. Helped me a lot. Did you do another VIdeo talking about how/where to get help? My bucket is overflowing at a flood rate. I have a medical background... but am in a town that is so deficient of any kind of cognizance or willingness to actually "go the distance" to fully help. (Their after the bucks). Thanks again.
Anaphylactic reactions to almost everything. Nice to see more information on this :)
Recently found your channel. I don't have all the words to express how much I am enjoying your videos. I have been on a long health journey that is too complex to express in a couple of sentences, but needless to say that everything got a whole lot worse after C. I am still dealing with Long-C and do multiple things to help with all my symptoms. I am also a zebra (EDS). That I am sure you know comes with that. Anyhow...I just wanted to say thank you. I am at that part of my journey where most of the things I read about and watch videos of are not informative for me anymore. Your videos that I have watched so far have provided some new information for me. :)
That's really good to hear. Glad you're benefitting from the videos -Team Dr. A
100% me. Thank you I'm not crazy
I watched your videos and other, read articles...but I haven t found information about real and sustainable heal of this disease. Is it possible or I have to tell me I have to live now with all these symptoms all my life. Thanks
Next level on this content. Refreshing to hear the depth of understanding.
Really glad you're enjoying it, thank you for the support - Team Dr. A
Thank you Dr.Anderson. Does the burning sensation from being allergic to an environmental allergen fall under this bucket? I feel like I’m running away from my self and don’t know if the histamine blockers will help as it feels like a third degree burn on my skin. Ty again
Thanks for the info dr. I wonder if you would know why the histamine symptoms get worse during a woman’s period and how to help my body feel better. Thanks
Thank you for the simple and brilliant explanation.
A lot of blood pressure medication increase histamine.
If you take antihistamines, your blood pressure goes up.
It is a viscous circle. Some times you have to take pain killer or antibiotics. Those increase histamin too. How do you manage these medications?
I started having eczema and urticaria symptoms when I got Covid. They got worse about 6 months ago, with palpitations when I ate. Went on antihistamines for 5 months or so then stopped them because I started feeling hungry non-stop. I believe it is a side effect of the fexofenadine. I am hungry since the end of May and stopped them at the end of June. The hunger did not go away even two months after I stopped them and I am getting desperate. My urticaria is worse than when I started them as well.
Great video! I learned a lot! Thanks Dr Paul 😊
Glad you liked it! - Team Dr. A
What about the spike protein and lipid nano particles?
Why does MCAS cause constipation? I'm just getting diagnosed with MCAS (& POTS, EDS, ADHD, Autism..). Ive had severe constipation for 40 yrs (I'm 51), & it's so bad now I have no choice but to use exlax daily. Ive been thru 30+ yrs of doctoring, specialists, medication, supplements, massage, energy healing, castor oil packs, dietary changes (or not eating at all cause I feel WAY better if I dont), etc.. and WHAT to do for the constipation so I can poop like a normal person?
Thank you very much, ould you pese let us know if you have a book or going to have one soon. ❤
Eat Right 4 Your Type for foods that may be taxing. Diet can look genetic when it’s cultural, But the two do go together.
Hi Dr. Anderson, thank you for your videos. I am being seen by allergy/ immunology now. Confusing as I tested in the normal range for Tryptase but elevated Leukotriene E4, U, I am also being considered as having POTS (after a tilt table test) , I don't have a formal diagnosis for MCAS yet, but all signs are pointing to POTS and MCAS, I have tachycardia and I am in a holter monitor cascade for 30 days. I am trying to go out on my own and learn about histamine foods and correlation, so I can have some relief, I faint after LARGE meals, not all the time but sometimes, I was diagnosed with rapid gastric emptying after an all day study, I went 36 years before I was diagnosed , I have been discarded multiple times. Its been a wild ride for me, sorry to overshare on the feed here but any insight would be valued. So do you see any correlation with these three things I mentioned above? Thank you! Oh and I have AMAG with high gastrin levels and metaplasia in my stomach and small intestine. And last but not least, Hashimotos Disease.
POTS and MCAS can certainly be related. Best of luck with your journey and recovery. It would be best to get an integrative doctor on your team to help give you specific advice - Team Dr. A
I have MCAS and Mastocytic Enterocolitis
3 years ago i have a dengue infection (a virus transmitted by mosquito) the evolution of clinical state was bad, the immune system destroyed all blood platelets
My daughter is 33, has had chronic lyme or maybe still does, has MCAS, and has dying ovaries. What can she do?
Make sure to check the links in video description to find an integrative doctor. She should work closely with a doctor she trusts to get the most help. Best - Team Dr. A
Firstly, thank you, they started testing for cancers and are now removing a nodule from my thyroid...TOMORROW, RFA so that is good, because it's over my trachea not in my Thyroid lobe, so I am lucky but EVERY symptom that I came in with a couple yrs ago and then acutely last year, still exists...SKIN breakouts, eczema, bone pain, extreme limb fatigue, brain fog, bad gut, colon, the bucket theory and keep that low, is what I've been watching and it helps, Histamine Intolerance. I also have insomina, so I take antihistamines every night, as my Pharmacist is the one who told me...maybe that. It helps or have a strict anti-histamine foods...I am better. I need to say, yes, I had OG Covid and long-covid for sure...but I got myself well after about a year and JUST said to myself, whoa, feeling like ME AGAIN and then this all started after the vaccine...I am not that person, but it is just seems to be true, after the 2nd it ramped-up, for me. I am unrecognizable. Anyway, 2 colonoscopies, endos, because IBS, bad gut, but they say I don't have it, YET I have it. Heart palps from just ANYTHING. I feel best when I am home, no smells, no people, don't touch anything and do not eat. It's nuts...like I'm allergic to everything. Pun intended. I have given up on my GP as they told me they cannot test for allergies if they do not know what they are testing for. A Direct quote. I was stunned, because it was the dumbest thing I've ever heard. So, antihistamines and prayers, and I'm agnostic so...
Mine began with a traumatic tooth removal???
You didnt mention the people who have hEDS ! MCAS often goes with hEDS. And some have 2 copies of the tryptase gene.
He did mention genetics
Dr Paul, is quite possible to have MCAS without cutaneous manifestations, right? I have been diagnosed with eEDS, ADHD and there is a huge suspicion of MCAS. Good guess? My symptoms get out of control every damn time I eat something, usually within 15-30 minutes.
By the way, amazing content, very much appreciated. Thank you!
Glad you're liking it! Yes MCAS can present with many different symptoms that aren't just cutaneous - Team Dr. A
about bucket oveerflowing and Covid: I thought for about a year Covid caused MCAS. Then I realized I had histamine problems long before, and Covid worsened it. THEN I realized over a span of several months I had MCAS all along for about at least 12 years, as far as I can remember. probably longer. and it probably triggered my Ankylosing Spondylitis that I have since ~2007, I suspect. Or the other way around. What do you think is more likely?
How do peptides work for mca? cjc 1295 ipamorelin
Is it the same as CIRS? Pple that claims to have long Covid, could it be MCAS, CIRS or both?
I was first diagnosed with cirs, from mold.
I have a really weird TNFRSF13B (TACI/BAFF) Deficiency (Homozygous) that likely led to MCAS/MCAD and SFN and Fibromyalgia and Grave's Disease and Sjogren's etc...I want my immune balance back...I presently have hypogammaglobulinemia....low in Ferritin....No measurable Molybdenum....little guidance...I know you cannot comment on my case specifically but generally what would you recommend for someone like me? I am taking Cromolyn Sodium and using Red Light Therapy and Hyperbaric O2 and Compression and trying to get in nature occassionally for Green Light Therapy etc..... Generally speaking....anything you can suggest? Oh I am taking Methylene Blue too...and a number of other medications....
I developed MCAS after being poisoned by a benzo drug for 4 years.
You're not alone. MCS too. After about 5 years of use and was told it was mast cell attacks when I was in severe tolerance, or withdrawal.
Caused MCS too.
I'm tapering and my MCS is going away.
2008 was when benzoes were listed as a front line mast cell med. Makes sense with all the Dysautonomia, neuropathy, tinnitus and wd suffering people are developing.
Oh
And those coming off of benzoes develop histame intolerance and mcas.
I just was thinking if that could have been my case too! 😢
Omg the worst of my symptoms started towards the end of my taper
Lol thought this was another Boeing 737 MAX discussion!
Does LDN have a positive impact on MCAS????
Yes many find it helpful with inflammatory conditions like MCAS - Team Dr. A
Thank you for your validation. I'm so frustrated. I have all of them, and it's maddening. Im hopefull I can get more open and educated doctors on my team so far I have 1, my dermatologist. I see new allergist this week and work with a natural pathetic on line. The food change has been a game changer. Absolutely mentally and emotionally taxing!! Grateful I have my background and knowledge in holistic mentally practices.
Doing what I'm calling a system reset right now and it's beyond difficult going it alone.
What to do when a gene was turned on? Are we just f*cked? Happened to me after being moxed/floxed.. :( and its pretty bad.
Is there a doctor in the St. Louis area that works with Mast Cell? I have been eating three foods for 3 years, can't tolerate anything without symptoms.
I haven't been able to get anybody to take a serious look in the StL area. They all immediately jump to substance abuse as the cause and antipsychotics as the solution.
@bjornolson21
6 minutes ago
So, how can all this immune deregulation and mast cell release not show up on a blood test. Hscrp, Ig levels, histamine levels, other mast cell levels?
Ace 2 re recpters were targeted
why did my mcas make me lose my periods?
The vax probably did that if you got it
Can the autoimmune disorders be caused by covid shots not just getting covid?
"Extremely rare" turns out to be maybe almost 5% of the population. General practicionere should not be in charge of epidemiology based on their erroneous assumptions.
🙏🦋🙏💖🙏
Do u have thugs in your family, it's possible that we have to help them make it, it would explain the iffyness in our lives that we can't wrap our heads around, better we don't know them & what they did, it makes it harder , but who r we to say , they can't make it, & their goes your heart, 💝 little kids not safe with them , the problem, we were little kids too , & gosh baby the struggles He must have dealing with us ! 💝👣👑💒
We're skinny for a reason but it sure helps in avoiding all these iffy things u get from diluting your inner parts, were not sapossed to push that hard our tummys & they be happy & give us heads up when they full , it's a beautiful relationship & comforting to not be in thst heavy wt fight ! 💝🚴♀️🥑🥭🥦🍅🍉
He didn't give a brief of what MCAS is. Watching any further is pointless for me, js. Bye
You can see his other videos where he goes into great detail.