Thanks for watching everyone! Please post your questions and comments below⬇, I look forward to hearing from you! To shop for any of the Supplements described in the video: 🧡dr-rajsrees-public-supplement-store.myshopify.com
Can vitamin B9(folate/L-5-MTHF), B3, B12, ZINC, vit A, vit C, vit D, Quercetin Which of these supplements be taken in conditions like too much urination and UTI?
amazing ,I've had urticaria for 35 years I've been to more doctors hospitals and specialists than a sickly gazelle. I've learned more from your videos than what any of them know. I have been only using antihistamines( chlorphenamine) as it's the only thing that kinda works for flare ups. But over time I was finding I was having to take 18+ tablets a day to ease symptoms. I diagnosed myself with histamine intolerance through your videos and tried diamine oxidase supplement. Now I only take one antihistamine when I get a bad flare up. I'm currently working on detox and gut rebalance and I gotta admit I feel like I've found the elixir of youth as I feel 10 years younger. All thanks to you. Thankyou so much for your effort and time masking these videos.
This is the best video I have seen so far on these frustrating issues. Thank you for taking the time doc. Your depth of care in responding to comments is so appreciated too. Wish you were in my neighbourhood in Australia. We need more of you
@@drrajsree Can vitamin B9(folate/L-5-MTHF), B3, B12, ZINC, vit A, vit C, vit D, Quercetin Which of these supplements be taken in conditions like too much urination and UTI?
Thank you so much this video, this is the best ever informative video I've ever seen about MCAS. This is exactly explaining all of my symptoms and I'd experienced most of these symptoms without any diagnosis. I've visited Gastroenterologist, endocrinologist, PCP, cardiologis, pulmonologist etc. Lately I am getting allergy shots, lactose free , gluten free histamine free diet, H1 and H2 blockers. I am not suffering GIsymptoms like before. My unexplained diarrhea, colic pain , vomiting suddenly stopped after the second allergy shut. I still suffer deep muscle and joint pain after every allergy shot along with nausea, several times vomiting. I am more energetic than ever before. My allergy dr told me my allergies might be through mast cells.
Thank you for calling out EMF’s. That’s a very real trigger for me and it gets pretty exhausting hearing people and Dr’s not believe it’s real. They cause inflammation and trigger flares, it’s black and white for me and would be for others that experience it too.
@@kimberlynormandy2690 Thanks, sadly there's a growing number of us. I did discover if you google mast cell degranulation and EMF's there's a few limited studies showing EMF's do cause degranulation! As well as studies linking microglia activation in the brain. So at least some researchers agree there's a connection there. Hope more research can help better understand why some of us are affected more than others and what we can do about it. For now I just plug everything in and distance myself from strong signals (which is sometimes hard to do).
Amazingly helpful video! I was just diagnosed with Classical EDS today (which I was expecting). What I didn't expect was that my practitioner said in all likelihood I also have MCAS! So I've been prescribed H1 and H2 inhibitors plus Prevacid for a month and we'll go from there. This video explained things so that the average person can have a better understanding of what we've been experiencing so thank you so much for that. I'll also be sharing this video with my family members who I now believe are dealing with this as well!
This should be mandatory for every Dr to watch and get educated on MCAS and histamine intolerance.. Thank you for a great video easily explained,I wish you lived in the San Francisco Bay Area.😊
I developed this as an allergic reaction to the covid vaccine... I have been suffering with this for 2 y and a half. I am taking antihistamine to help and I am on low histamine diet, gluten and lacto free and no processed food but I still get symptoms from any physical effort or stress etc... my symptoms: brain Inflammation, dizziness, nausea, brain fog, confusion, disorientation, shaking, twitching, neck problems, gluten intolernace, lacto allergy intolerance and histamine intolerance. if I eat something high in histamine I get bad brain fog, panic attacks, feels like my blood pressure is going crazy.. the reactions are different depends on what I do and what I eat. mainly the brain fog is the issue that gets worse when I walk or eat more food and it gives me confusion and disorientation... I really hope that there is a fix for this.
I also got my first flare up after te covid vaccine! for two years i did not feel that much untill I got another trigger from another injection. It's so tiring to try so hard to eat clean and doing everything you can and still react to almost everything :(
@maartjek9691 , I understand you. I'm in the same situation for 3 years. I have flares every time my body gets in contact with different triggers (meds, insect bite, viruses...).
Just...wow! Informative, concise, easy to understand, thorough. You deserve an award!! Thank you for all of your research, time and editing. You've created an extremely helpful video.
I got MCAS post covid, my throat and mouth were ´burning´ for 8 months until I got on Cromolyn, its life saver. Also, Ketotifen helps me a lot and Quercetin. I wish it could just go away though. I had inflamed thyroid and still have pain in bones and joints, the only thing ever helped was Prednisone 40 mg. Still on my way to proper treatment, its been 4 yrs
OMG, I’ve been having burning mouth symptoms for over a year now and never tied it post Covid problems. I’m hoping I can find that supplement online, here in the US
Thank you Dr. Rajsree. This is the best information on MCAS i have found. Having MCAS i do find this video incredibly helpful. Thanks a lot for your hard work and information you shared. ❤🎉🎉🎉
Hi Dr, this was a very great and complete video ( exposé). I just recognised myself and all the membres of my family. Unfortunately many doctors dont know thé mcas ans they must of thé Time get anoyed during thé consultation and just dismiss us. It is really difficult to find one that is knowledgeable in this area. Anyway i will keep surching until i find the help i need. Thank you very much for this Great video that i Hope will help Many of us suffering from MCAS . God bless you and your family
Thank you for sharing this once in a lifetime information; which is extremely rare to find and can help thousands of people who are often misunderstood. 🙏🏻💐
Wow. You just painted the exact story I’ve been desperately trying to solve for years. I pray every day that I will get better. I feel no one understands, both medically and personally. It’s so difficult to voice my symptoms efficiently. I truly believe this will help me get help I desperately need. Thank you for your dedication and passion! Any recommendations on doctors on the east coast?
A doctor I saw recently suspects MCAS and hEDS at the root of POTS for me. So until I’m able to work again and afford specialists and treatment, at least now I can attempt to avoid mentioned triggers and try supportive supplements to hopefully see some relief finally thanks to your comprehensive video. Thank you so very much!
Great presentation and eye opener! Thank you very much. Since 2 years I am suffering from several stomach and small intestine issues (Helicobacter, SIBO), which possibly caused histamine intolerance and probably MCAS. 10 months on diet, but my symptoms are progressing lately and I am still looking for triggers. I am very grateful for all your work and helping us all over the world. Greetings from Poland 🙏
Dear Dr.Rajsree , Black tea ,prickles inhibit DAO and thus triggers the MCAS.so tea and MCAS are mutually exclusive. Please discuss the role of DAO supplements ,dietary intake of organ meat like kidney which contain DAO. Vitamin B6 in form pyridoxal 5 phosphate 100mg really helps in mitigating symptoms since it involve in metabolism of histamine.benfotamine also has role in gut adhesion of cellular lining .thanks for making awesome video on this topic .regards,farhan
Thanks so much for watching! 😊 Yes DAO supplements can help some people with histamine intolerance to better tolerate high histamine foods. I didn't mention it in the video because they are from porcine kidneys and are expensive and have limited efficacy. Often taking Digestive Enzymes can offer a more significant benefit. By healing the gut, a person is able to restore their own DAO production most times. Yes B6 is part of the methyl B complex that I recommended and is a co-factor for DAO and therefore can be helpful.
@@drrajsreeI can’t seem to tolerate b vitamins (including methyl forms). I’m wondering if this means I should stay away from them or if it’s paradoxical.
I've always had allergies here and there. A few years ago I started getting hatd with Anaphylaxis and that is brutal!! Swollen etc. but no one says how dang sick a person gets......loss of sight, total body weakness, throwing up, diarrhea, losd of voice, loss of consciousness. Im seeing an Allergist Immunologist the first of June. I have no idea what I'm so allergic too. I have Epi, Prednisone and liquid Benadryl with me all the time. I get so angry because no one seems to understand how sick. The ER and paramedics have been great though. When I learned the anaphylactic symptoms like sweating, tingling, overwhelming body heat and lip sweating.....I thought on crap, I've been doing this thinking it was related to my IBS! Now I know the "IBS" was a start of a reaction.........thanks for posting info.
Hi Judy, Same here, and still figuring it all out, I think I got MCAS and histamine intolerance just realising a few days ago and this video again seems to back it up. Just seen a doctor (specialising in allergies..) and just got told i just have uticaria and edema. which only means swelling and are basically only symptoms.. that's all she gave me and wanting to prescribe anti-histamines. I read somewhere that anti-histamines is onlyl for short term and not good in the long-term. Also I just read from your comment that you use steroids. Please become aware of TSW. I've been through hell getting that from prednisone, only just after a few rounds. Best thing is to avoid steroids. It's not even worth the risk of getting TSW as it's extremely bad and will disrupt your life majorly. just wanted to let you know. All the best
@@irisvandijk570 not doing Prednisone very often at all. This is a good Immunologist and Im impressed with her. She is looking at the Mast Cells and Thyroid. She doesnt believe its food related. Also, antihistamines will not stop Anaphylaxis at all. Two of my worst attacks I had Claritin in my system daily. Benadryl will not stop Anaphylaxis, only an Epi will stop the progression until medical care is given. It is given after the Epi. Its going to be a lot of testing and in the end there may be no answer, its the Idiopathic Anaphylaxis . Just keep the Epi or two by you at all times!!
I apologize I can't advise you personally on what to take. You're welcome to learn more about the supplements on my store and decide: dr-rajsrees-public-supplement-store.myshopify.com/
Amazing video. Best one I've seen on the subject. Thank you for producing this. I wish I could get my doctor to watch it. I've seen nearly a dozen providers, including four immunologists, and none of them know any of this. I will definitely check out your store. I need to heal my gut. I react to almost everything. By the way, what are your thoughts on Black Seed Oil (Nigela Sativa)? Helpful for MCAS or no?
Thank you Dr Rajsree l am lerning so match frome your video and l am very greatful that your sharing so much knowledge GOD bless you and your family 🙏🏾
Yes tennitus can be seen in both! I did come across in my research that sometime anti-histamine ear drops can help. Please check with your doctor. Thanks so much for watching! 😊
Could you please tell me what might be happening to me? For the past 5-6 years, I've been experiencing an allergy whenever I do something that causes my body temperature to rise, such as working out, walking fast, eating (I assume digestion increases body temperature), or going out in the sun. A sudden, agonizing itch starts from head to toe, and it only happens during the winter months. In the summer, I'm as healthy as a normal person. Country: india Age: 19 Gender: male
Thank you for the Video! I think it's so helpful how you make your Videos and how you always have a step-by-step plan, cause you can feel really lost with all the information out there and I often get confused and that therefore really helps! I also love how you breakdown those diseases and how you complain them so easily that even a child could understand them! Thank you so much for your work!!! I also have MCAS and I really hope this can help me next to my other things I get from my doctor! :) Also I am from Europe and wanted to ask, if there's a way to ship your supplements to my country too? :) I also wanted to ask for maybe other topics for other videos: xsyndrom of loss of bile acids and xType A Gastritis (also if you have an ulcer cause of that and how to treat that. Normal medications can't really help there, cause theres already too little stomach acid, but because of the ulcer I also cant take betain, although I would need it, cause Im having really bad problems with digesting my food. Do you have there also some alternative recommendations and what someone can do than?) I have another doctors appointment this week again, but maybe you have some tips there too! Thank you again for your videos and I wish I could become one of your patient too! ;)
Thanks so much for watching! 😊 We ship our supplements throughout the United States. Unfortunately, we do not ship to other countries yet due to challenges with shipping abroad. Hopefully someday! Thanks for watching! Best wishes, RN
Hello Dr ,I just discovered your channel,so interesting! Just a gentle note,if I may:(again,thanks for the great infos) for me,struggling with mcas,me cfs,brain fog and dysautonomia,the little hand writing on the video is quite a strong signal and makes it a bit difficult to continue watching ,as I am sensitive to these quick stimuli,along with the music,as it is quite dense information requiring concentration.So maybe considering a gentler,quieter visual would be great! Just a thought.kind regards from the South of France
Wonderful to hear from you in France! My videos can also be listened to (like a podcast) if that would be better tolerated. But thank you for watching and for your feedback.
MCAS has made me allergic to corn. Corn is in every vitamin supplement - either as magnesium stearate or cellulose capsules. Is the answer to get everything compounded??
Hi- thank you. I have Sjogrens disease. I know there is a connection with EDS but have you seen a connection with Sjogren’s? Also, I see in the comments that you said G.I. map has false positives with H pylori . I had the gut zoomer and SIBO and candida came up however my breath test for SIBO is negative. Is it your experience that vibrant wellness also gets false positive with SIBO and candida? I was listening to the expert on MCAS., Dr Theoharides and he said he doesn’t put much stock in those gut tests. Do you? Thanks so much lots of questions I know.
Hello Dr. My brother was diagnosed with MCAS recently. I have symptoms of itchy skin but no rash, insomnia, anxiety, depression and have a runny nose most of the time. I don't feel I am sensitive to food, medication or products. Is it possible I have it as well?
Thank your for this amazing video! If a person had SIBO / Dysbiosis / Leaky Gut prior to Long Covid, is it possible that these conditions lead to the development of long covid, because the immune system and mast cells where already triggered and weakened? Thank you!
Very possibly yes! 70% of our immune system is in our gut, so if there is gut microbiome dysfunction, this could weaken our ability to fight and overcome common viruses. Thanks so much for watching! 😊
With MCAS there is a rise in the tryptase level during a flare and reactions are to many things other than foods (as seen in Histamine Intolerance). MCAS involves gene changes in Mast Cell Genes that are acquired by a trigger (stressor). Histamine Intolerance is often acquired due to gut microbiome issues that reduce production of the DAO enzyme.
The #1 most informative and thorough video on RUclips! 🫶🏾I hope the universe gifts you your hearts desires. Instead of baiting me into a pricy protocol with a practitioner, you share real life options for wellness. I am grateful for every second of this video, and the other videos referenced.
We check nearly every box in the video and are doing most of the “treatments” with not much success. How do we find someone great to work with around us?
Dr. Laurence Afrin is the doctor who wrote the book on MCAS and has a lot of experience. I don't know him personally but I did see he offers consultations: aimcenterpm.com/dr-lawrence-afrin/
Is it possible to be diagnosed based on symptoms and reaction to antihistamines and medications? I have EDS/POTS and I get the severe flushing and POTS symptoms along with stomach issues and skin allergies to chemicals, and migraines from fragrances. But my Tryptase and urine test came back normal. Thank you so much for this informative video.
Oh my God I think I might have MCAS. For about a year I noticed white stars in my POV appearing, especially when going to sleep. Then I started to get big infected pimples which just never went away and were constantly bleeding. After that I noticed that the lymph nodes in my neck and under my jaw ballooned and my throat became inflamed. Shortly after all those things the sleeping problems and heart palpitations 24/7 came, which worsened when trying to sleep. I later found out I had massive mold infestation INSIDE the wall, which was also the reason for the dampness and odd smell in my room. I could not sleep for days and was about to kill myself unironically. I literally had to book hotels just to be able to catch some sleep. Fast forward a year to today and I still struggle with heart palpitations and insomnia when having contact with even trace amounts of mold. This disease is one of the worst there is and I don't think that I'd wish it on my worst enemy. Also take mold seriously! This shit could fuck you up just like it did for me!
Thank you for this video Dr. Rajsree! I have A LOT of the symptoms of MCAS but I can tolerate Spinach and Tomatoes just fine. How can that be explained that these two high histamine foods do not trigger a reaction?
This is interesting. I first had dermatographism when I was 14. I’m 51 now and noticed it went away like 3-4 years ago. Around the same timeframe, I started getting itchiness all over my body like every 3-4 months. Do you know if dermatographism can go away and change into itchiness? It’s like I’m being bitten by lots of tiny bugs or being gently poked by needles that cause extreme itchiness. With that said, would you be able to tell me which of your products I can try? Thanks in advance!
Sorry to hear this. If I had to pick one product it would be Histamine Support. We get great feedback on this one for histamine symptoms like itchy skin. It's best taken at a dose of 2 capsules twice a day. Thanks for watching! You can shop for any of our supplements here: dr-rajsrees-public-supplement-store.myshopify.com/
Interesting. I have hEDS. I had an inset with a severe vaccine reaction which led to Lyme disease diagnosis. I’ve had POTs, vagus nerve syncope, simple partial seizures often triggered by showers. But I have cold intolerance so I have to make them hot. I would add I think severe nausea in pregnancy- which I had in all of mine. I also had obstetric cholestasis- itching like no other. Leaky gut, estrogen dominance- endometriosis, ovarian cysts, liver issues…. Luckily I found a good doc that has been understanding. My family thinks this is all in my head.
Wonderful to hear from you! Unfortunately, we currently only ship within US and Canada due to challenges shipping supplements abroad. If you have any relatives visiting here we can ship to any US address and they can bring it to you.
Hi I have reflux, hiatus hernia, astmasymtoms, dry caugh. My face and chest turn red(flushing) several times every day. And inside my mouth my chin swells. My brother died from cancer last year and since then I've been so afraid to get sick by my self. I went to the doctor to get some bloodtest done. Cromogranin A and 5-HIIA and they came back normal. I also did an CT of my neck, thorax, and abdomenal. No cancer was found. I wonder now if I can trust the tests and the CT ? My doctor doesn't think my symtoms has nohing to do with Histamin when I asked her about it. The only answear I get is it's becaus of trauma and stress. What do you think?
I just discovered I'm afflicted. I have all of the symptoms noted all the time I've had this problem all of my life. I used to get hives and difficulty breathing when I was a kid. I remember the first time it happened I was exposed to poison ivy the real one not poison oak. I was a kid and a poison ivy had caterpillars all over it and I played with them for a few minutes and had a very serious mast cell activation event. Ever since that day my immune system was altered. All related to my allergies that presented when I was about 6 and I'm now 59. It's destroyed my vision by about 45. I've always had perfect vision and for no known reason I need a 2.25 prescription now. My main symptom is swollen watery eyes and brain fog. Varying degrees of inflammation all over my body. Constant stomach upset. Basically the most severe symptoms because I'm so sick and I've never treated the disease. One medication that helped me was Doxycycline. I've been diagnosed with somatoform disorder. I started taking Cetirizine, Vitamin C and Bromelain.
I have IBS, GERD, chrinic gastritis, SIBO and anemia. My dr saud to start 63mg of iron from ferritin daily. I knew I couldnt take the regular iron supplements so I researched it and found 65mg carbonyl iron w vit C. Been on it couple weeks with no additional abdominal/GI symptoms. Iron ferritin can cause nausea and constipation which is what my Dr told me to try. Not a very good idea if you already have a lot of GI issues.
It comes in a capsule you swallow with water. You can learn more about it in this video covering my Herbal Protocol for SIBO, which you can find here: ruclips.net/video/zHATkKdznIA/видео.html&t=3s
Can mold be the cause of my very low levels of DAO? My symptoms are reflux, dermatitis and lungs\chest pain. Do they look more like MCAS or histamine intolerance? Thanks 😊
Have you had any patients (or heard of cases) of myoclonus, chorea, dystonia or any other movement disorder caused by either POTS, MCAS, mastocytosis, SIBO, GERD, candida, EDS or any diseases/syndromes you mention in this video?
Doctor, i m a woman, a few thick hair grow on upperlip and jaw. What is the cause and how to get rid of them permanently through diet and lifestyle only.
I have MCAS, I have a problem with Hashimoto's disease and hypothyroidism. I should take Levothyroxine but I have very strong histamine reactions to it. What am I supposed to do?
I've had issues since birth. Severe anaphylaxis multiple times, joint and muscle pain, fatigue. Hypermobile joints made me conclude that I've had hEDS since birth. That then developed into MCAS somewhere down the line and that led to my M.E. diagnosis. I'm still trying to get both hEDS and MCAS confirmed but keep getting dismissed. Funnily enough, one of my more severe allergies that showed up from nowhere disappeared after the Covid vaccines. I just got GERD diagnosed (after 5 years of suffering), but I'm allergic to all antacids.
I can take all these at the same time or should it be different times of the day? I have a reaction to literally every food even if it’s just burning at the lips. Idk what to eat anymore.
Thoughts on using low dose doxycycline as a mast cell mediator and calm over active microglia? Ie 20mg EOD for MCAS that seems specific to gut pain and neuro inflammation, very little histamine specific events, like rashes or allergies. But neuro inflammation after certain foods and activities.
I was diagnosed with Urticarial Vasculitus years ago and doctors just keep putting me on Immunosuppressant drugs, and i still suffer with alot of these symptoms MCAS causes
We carry essential magnesium that is really popular. Thanks for watching! You can shop for any of our supplements here: dr-rajsrees-public-supplement-store.myshopify.com/
EoE is generally true IgE allergy mediated so you definitely want to have and IgE food panel done. Some patients with MCAS also have true IgE allergies as well so it's possible.
@@drrajsree Strange thing Autism. I saw a review of a real good study connecting poor nutrition and the severity of autism. Poor nutrition = low vit D3, low magnesium, low..... The study even showed amazing improvements from getting essential vitamins up to good levels on the marginal autistic participants.
Hello Dr. I have 13month old baby boy. He suffering from this infection from his 4 month old age. Now i stopped medicine. Can i start cetirizine drops ?
Great question. I talk about Histamine Intolerance vs. MCAS in the video. No, generally Histamine Intolerance does not turn into MCAS. MCAS is different in etiology (genetic predisposition + trigger that causes mutations in mast cell regulatory genes).
Quick question Doc! If I have MCAS due to SIBO, will curing the SIDO in turn cure the MCAS? Or will I have to do two different protocols? Any guidance or help would be greatly appreciated. My symptoms just started about a year ago but they are progressing pretty fast. Please and thank you 🙏🏼
I would address the SIBO first since gut healing is key in MCAS. Thanks so much for watching! 😊 You might also like my video on my Herbal Protocol for SIBO, which you can find here: ruclips.net/video/zHATkKdznIA/видео.html&t=3s
@@drrajsree thanks Doc! And I actually watched your sibo protocol video right before this one. Thanks for the reply and clarification. Keep pumping out these informative videos!
I got cholinergic urticaria after either a polio vaccine, food poisoning in Thailand, chronic PPI use, or severe stress from my education, or due to any combination of these. Having a dual Campylobacter jejuni and Toxoplasma gondii infection from food poisoning triggered an extreme amount of additional strange symptoms on top of this. I’m quite sure SIBO, which I tested positive for, plays a role in this, either causal, or a result. Do you think it’s possible to calm the mast cells down in this case of a trigger which can’t be reversed. I mean, I can’t go back in time to avoid the triggers… and treating SIBO with rifaximin and prokinetics didn’t work. It came right back. what are your thoughts? Any input from anyone reading this would be appreciated!
Every individual is different. I believe there is always hope to heal the body. Finding and working with a knowledgable provider to guide you step by step would be very helpful. I do have a video on my herbal protocol for SIBO if you are interested: ruclips.net/video/zHATkKdznIA/видео.html&t=3s
Hi Dr I live in the OC. How could I see you for a consultation? I have been dealing with what I believe to me MCAS and also digestive problems for the past 6 years. I was hoping you could work with me to find a solution.
I apologize I'm not taking new patients at this time. I hope some of the tips in this video can help you. To search for a functional medicine provider, please go to IFM.org Best wishes in your health, RN
I feel as if I’m allergic to everything. Well a lot of things. I began to react to the sensitive skin arm and hammer detergent etc. I have always had sensitivity and allergies etc but after Covid it got rediculous . After I had that insane cytokine storm so many more things flare me up. I took an Uber and just stepping into the vehicle I got a severe allergic reaction to the “little trees “ air freshener. Unscented stuff is used in my house. I can’t even clean with most cleaners anymore and I used to be able to. One thing though is it’s not the hot as you were mentioning about hot showers. It’s the cold. The heat is almost like a soothing feeling. It helps with pain, allergies you name it. Along with the tree (only prarie naturals) shampoos etc. but the cold causes a release of histamines etc. In fact the cold causes physical pain if my skin comes in contact with it. Ugh I live in Canada too which is not ideal. I’ve never heard of mast cell syndrome till recently.
Can anything help with a prickly itching, stinging pins and needles sensation my daughter is having in the body which comes and goes. It is making her depressed
Thanks for watching everyone! Please post your questions and comments below⬇, I look forward to hearing from you! To shop for any of the Supplements described in the video:
🧡dr-rajsrees-public-supplement-store.myshopify.com
😅P😮⁰
Can vitamin B9(folate/L-5-MTHF), B3, B12, ZINC, vit A, vit C, vit D, Quercetin Which of these supplements be taken in conditions like too much urination and UTI?
❤😊😊
amazing ,I've had urticaria for 35 years I've been to more doctors hospitals and specialists than a sickly gazelle. I've learned more from your videos than what any of them know. I have been only using antihistamines( chlorphenamine) as it's the only thing that kinda works for flare ups. But over time I was finding I was having to take 18+ tablets a day to ease symptoms. I diagnosed myself with histamine intolerance through your videos and tried diamine oxidase supplement. Now I only take one antihistamine when I get a bad flare up. I'm currently working on detox and gut rebalance and I gotta admit I feel like I've found the elixir of youth as I feel 10 years younger.
All thanks to you. Thankyou so much for your effort and time masking these videos.
Ghaxxuloo9
Dr d1 o🎉@@neerajsainidob26
This is the best video I have seen so far on these frustrating issues. Thank you for taking the time doc. Your depth of care in responding to comments is so appreciated too. Wish you were in my neighbourhood in Australia. We need more of you
Thanks so much for watching! 😊 I'm so glad it was helpful.
This video describes me to a "T" and have been suffering from symptoms for decades 😢 Thank you for explaining it so easily and completely ❤
I'm sorry to hear this, but hopefully this video can help bring some explanation to your symptoms! Thanks so much for watching! 😊
@@drrajsree Can vitamin B9(folate/L-5-MTHF), B3, B12, ZINC, vit A, vit C, vit D, Quercetin Which of these supplements be taken in conditions like too much urination and UTI?
Thank you so much this video, this is the best ever informative video I've ever seen about MCAS. This is exactly explaining all of my symptoms and I'd experienced most of these symptoms without any diagnosis. I've visited Gastroenterologist, endocrinologist, PCP, cardiologis, pulmonologist etc. Lately I am getting allergy shots, lactose free , gluten free histamine free diet, H1 and H2 blockers. I am not suffering GIsymptoms like before. My unexplained diarrhea, colic pain , vomiting suddenly stopped after the second allergy shut. I still suffer deep muscle and joint pain after every allergy shot along with nausea, several times vomiting. I am more energetic than ever before. My allergy dr told me my allergies might be through mast cells.
Thanks so much for watching and best wishes in your health! 😊
Thank you for calling out EMF’s. That’s a very real trigger for me and it gets pretty exhausting hearing people and Dr’s not believe it’s real. They cause inflammation and trigger flares, it’s black and white for me and would be for others that experience it too.
Yes indeed! Thanks for watching.
Also a trigger for me too. It is real thing for sure and you are not alone!
@@kimberlynormandy2690 Thanks, sadly there's a growing number of us. I did discover if you google mast cell degranulation and EMF's there's a few limited studies showing EMF's do cause degranulation! As well as studies linking microglia activation in the brain. So at least some researchers agree there's a connection there. Hope more research can help better understand why some of us are affected more than others and what we can do about it. For now I just plug everything in and distance myself from strong signals (which is sometimes hard to do).
No, not alone
Amazingly helpful video! I was just diagnosed with Classical EDS today (which I was expecting). What I didn't expect was that my practitioner said in all likelihood I also have MCAS! So I've been prescribed H1 and H2 inhibitors plus Prevacid for a month and we'll go from there. This video explained things so that the average person can have a better understanding of what we've been experiencing so thank you so much for that. I'll also be sharing this video with my family members who I now believe are dealing with this as well!
Thanks so much for watching! 😊 Best wishes in your health, RN
This should be mandatory for every Dr to watch and get educated on MCAS and histamine intolerance.. Thank you for a great video easily explained,I wish you lived in the San Francisco Bay Area.😊
I have hEDS and have essentially put my mcas into remission. Don't settle.
I developed this as an allergic reaction to the covid vaccine... I have been suffering with this for 2 y and a half. I am taking antihistamine to help and I am on low histamine diet, gluten and lacto free and no processed food but I still get symptoms from any physical effort or stress etc... my symptoms: brain Inflammation, dizziness, nausea, brain fog, confusion, disorientation, shaking, twitching, neck problems, gluten intolernace, lacto allergy intolerance and histamine intolerance. if I eat something high in histamine I get bad brain fog, panic attacks, feels like my blood pressure is going crazy.. the reactions are different depends on what I do and what I eat. mainly the brain fog is the issue that gets worse when I walk or eat more food and it gives me confusion and disorientation... I really hope that there is a fix for this.
I'm so sorry to hear this. I hope your health improves! Best wishes, RN
I also got my first flare up after te covid vaccine! for two years i did not feel that much untill I got another trigger from another injection. It's so tiring to try so hard to eat clean and doing everything you can and still react to almost everything :(
@maartjek9691 , I understand you. I'm in the same situation for 3 years. I have flares every time my body gets in contact with different triggers (meds, insect bite, viruses...).
@@maartjek9691look at Tina Peers MCAS videos
@@maartjek9691look at Tina Peers MCAS videos and f l c c c
Just...wow! Informative, concise, easy to understand, thorough. You deserve an award!! Thank you for all of your research, time and editing. You've created an extremely helpful video.
Thanks so much for your kind support! 🙏 I really appreciate hearing from you! Best wishes, RN
I got MCAS post covid, my throat and mouth were ´burning´ for 8 months until I got on Cromolyn, its life saver. Also, Ketotifen helps me a lot and Quercetin. I wish it could just go away though. I had inflamed thyroid and still have pain in bones and joints, the only thing ever helped was Prednisone 40 mg. Still on my way to proper treatment, its been 4 yrs
I'm so sorry to hear this. I hope your health improves! Thanks for watching. Best wishes, RN
Where to buy cromolyn?! It's not available in the US 😢
@@virginiastephenson3086 Im sorry, Im in middle Europe and have to buy in Austria or Czech republic. Maybe online?
@@drrajsree Thank you dear
OMG, I’ve been having burning mouth symptoms for over a year now and never tied it post Covid problems. I’m hoping I can find that supplement online, here in the US
Thank you Dr. Rajsree. This is the best information on MCAS i have found. Having MCAS i do find this video incredibly helpful. Thanks a lot for your hard work and information you shared. ❤🎉🎉🎉
Thanks so much for watching! 😊 Great to hear this video was helpful!
Hi Dr, this was a very great and complete video ( exposé). I just recognised myself and all the membres of my family. Unfortunately many doctors dont know thé mcas ans they must of thé Time get anoyed during thé consultation and just dismiss us. It is really difficult to find one that is knowledgeable in this area. Anyway i will keep surching until i find the help i need.
Thank you very much for this Great video that i Hope will help Many of us suffering from MCAS . God bless you and your family
Thanks so much for watching! 😊 I really appreciate your kind words and blessings.
Awesome video!! I've shared it with a few of my family members that just dont understand what I"m going through. Thank Yo so much!!
Thanks so much for watching! 😊 Glad it was helpful.
Thank you for sharing this once in a lifetime information; which is extremely rare to find and can help thousands of people who are often misunderstood. 🙏🏻💐
Thanks so much for watching! 😊
Wow. You just painted the exact story I’ve been desperately trying to solve for years. I pray every day that I will get better. I feel no one understands, both medically and personally. It’s so difficult to voice my symptoms efficiently. I truly believe this will help me get help I desperately need. Thank you for your dedication and passion!
Any recommendations on doctors on the east coast?
drtaniadempsey.com/lawrence-afrin/
Dr. Lawrence Afrin is the expert on MCAS and is in NY.
A doctor I saw recently suspects MCAS and hEDS at the root of POTS for me. So until I’m able to work again and afford specialists and treatment, at least now I can attempt to avoid mentioned triggers and try supportive supplements to hopefully see some relief finally thanks to your comprehensive video. Thank you so very much!
Thanks so much for watching! 😊
You could try ginger. It helps me stopping the heart palpitations and insomnia
@ Thank you! I’ll have to give it a shot 🙏🏼
Best video! You know how to explain it well and the pictures work well with it.
Thank you very much!
Absolutely the best explanation in one video.
Thanks so much for watching! 😊
Brilliant, logical explanations. I've heard many vids on MCAS, methylation et al. This is the best. Thank you for doing your videos.
Thanks so much for your kind support! 🙏 I really appreciate hearing from you! Best wishes, RN
Great presentation and eye opener! Thank you very much. Since 2 years I am suffering from several stomach and small intestine issues (Helicobacter, SIBO), which possibly caused histamine intolerance and probably MCAS. 10 months on diet, but my symptoms are progressing lately and I am still looking for triggers. I am very grateful for all your work and helping us all over the world. Greetings from Poland 🙏
Great to hear from you in Poland! Thanks for watching.
I have mcas but now I have a fear of eating incase I am ill again 😔 sweet potato is the only food i will willingly eat now
I'm so sorry to hear this. I hope your health improves! Best wishes, RN
I'm searching for MCAS for awhile now. This is perfect.... thank you 😊
Thanks so much for watching! 😊
I've done alot of research on MCAS, this was a beautifully made video.
Thanks so much for your kind support! 🙏 I really appreciate hearing from you! Best wishes, RN
This video is a miracle for me! Thank you so much.
Thanks so much for watching! 😊 I'm so happy to hear my MCAS video was helpful to you!
This is a very well prepared video of what my daughter suffer.
What do you charge for a consultation for. 40 year old that is very very sick.
Dear Dr.Rajsree , Black tea ,prickles inhibit DAO and thus triggers the MCAS.so tea and MCAS are mutually exclusive. Please discuss the role of DAO supplements ,dietary intake of organ meat like kidney which contain DAO. Vitamin B6 in form pyridoxal 5 phosphate 100mg really helps in mitigating symptoms since it involve in metabolism of histamine.benfotamine also has role in gut adhesion of cellular lining .thanks for making awesome video on this topic .regards,farhan
Thanks so much for watching! 😊 Yes DAO supplements can help some people with histamine intolerance to better tolerate high histamine foods. I didn't mention it in the video because they are from porcine kidneys and are expensive and have limited efficacy. Often taking Digestive Enzymes can offer a more significant benefit. By healing the gut, a person is able to restore their own DAO production most times. Yes B6 is part of the methyl B complex that I recommended and is a co-factor for DAO and therefore can be helpful.
@@drrajsreeI can’t seem to tolerate b vitamins (including methyl forms). I’m wondering if this means I should stay away from them or if it’s paradoxical.
Thankyou so much! Your videos are so thorough and easy to understand ❤
Thanks so much for watching! 😊
Great video, thorough, informative and positive. Thank you 🙏🏻
Thanks so much for watching! 😊
I've always had allergies here and there. A few years ago I started getting hatd with Anaphylaxis and that is brutal!! Swollen etc. but no one says how dang sick a person gets......loss of sight, total body weakness, throwing up, diarrhea, losd of voice, loss of consciousness. Im seeing an Allergist Immunologist the first of June. I have no idea what I'm so allergic too. I have Epi, Prednisone and liquid Benadryl with me all the time. I get so angry because no one seems to understand how sick. The ER and paramedics have been great though. When I learned the anaphylactic symptoms like sweating, tingling, overwhelming body heat and lip sweating.....I thought on crap, I've been doing this thinking it was related to my IBS! Now I know the "IBS" was a start of a reaction.........thanks for posting info.
Thanks so much for watching! 😊 I hope your health improves!
Hi Judy, Same here, and still figuring it all out, I think I got MCAS and histamine intolerance just realising a few days ago and this video again seems to back it up. Just seen a doctor (specialising in allergies..) and just got told i just have uticaria and edema. which only means swelling and are basically only symptoms.. that's all she gave me and wanting to prescribe anti-histamines.
I read somewhere that anti-histamines is onlyl for short term and not good in the long-term.
Also I just read from your comment that you use steroids. Please become aware of TSW. I've been through hell getting that from prednisone, only just after a few rounds. Best thing is to avoid steroids. It's not even worth the risk of getting TSW as it's extremely bad and will disrupt your life majorly. just wanted to let you know. All the best
@@irisvandijk570 not doing Prednisone very often at all. This is a good Immunologist and Im impressed with her. She is looking at the Mast Cells and Thyroid. She doesnt believe its food related. Also, antihistamines will not stop Anaphylaxis at all. Two of my worst attacks I had Claritin in my system daily. Benadryl will not stop Anaphylaxis, only an Epi will stop the progression until medical care is given. It is given after the Epi. Its going to be a lot of testing and in the end there may be no answer, its the Idiopathic Anaphylaxis . Just keep the Epi or two by you at all times!!
I definitely have mcas, histamine intolerance, leaky gut, sibo, Mthfr. Should I just take all of the supplements you mentioned in the video?
I apologize I can't advise you personally on what to take. You're welcome to learn more about the supplements on my store and decide:
dr-rajsrees-public-supplement-store.myshopify.com/
Amazing video. Best one I've seen on the subject. Thank you for producing this. I wish I could get my doctor to watch it. I've seen nearly a dozen providers, including four immunologists, and none of them know any of this. I will definitely check out your store. I need to heal my gut. I react to almost everything. By the way, what are your thoughts on Black Seed Oil (Nigela Sativa)? Helpful for MCAS or no?
Thanks so much for watching! 😊 I haven't read much about Black seed being beneficial in MCAS.
I have done all the lab test and was negative but I responded to cromolyn very well
Thank you Dr Rajsree l am lerning so match frome your video and l am very greatful that your sharing so much knowledge GOD bless you and your family 🙏🏾
Thanks for watching my new video Tess! Your kind words are always so uplifting! Appreciate your blessings and support always!
Awesome video ! Do you find tinnitus to be a common or possible symptom of HI or MCAS?
Yes tennitus can be seen in both! I did come across in my research that sometime anti-histamine ear drops can help. Please check with your doctor. Thanks so much for watching! 😊
C'est très bien expliqué, merci, en France, les médecins sont ignorants... Je souffre d'un MCAS depuis 40 ans
Thanks so much for watching! 😊
Could you please tell me what might be happening to me? For the past 5-6 years, I've been experiencing an allergy whenever I do something that causes my body temperature to rise, such as working out, walking fast, eating (I assume digestion increases body temperature), or going out in the sun. A sudden, agonizing itch starts from head to toe, and it only happens during the winter months. In the summer, I'm as healthy as a normal person.
Country: india
Age: 19
Gender: male
Very informative and thoughtful presentation.
Thanks so much for watching! 😊
Thank you for the Video! I think it's so helpful how you make your Videos and how you always have a step-by-step plan, cause you can feel really lost with all the information out there and I often get confused and that therefore really helps! I also love how you breakdown those diseases and how you complain them so easily that even a child could understand them! Thank you so much for your work!!! I also have MCAS and I really hope this can help me next to my other things I get from my doctor! :)
Also I am from Europe and wanted to ask, if there's a way to ship your supplements to my country too? :)
I also wanted to ask for maybe other topics for other videos:
xsyndrom of loss of bile acids
and
xType A Gastritis (also if you have an ulcer cause of that and how to treat that. Normal medications can't really help there, cause theres already too little stomach acid, but because of the ulcer I also cant take betain, although I would need it, cause Im having really bad problems with digesting my food.
Do you have there also some alternative recommendations and what someone can do than?)
I have another doctors appointment this week again, but maybe you have some tips there too!
Thank you again for your videos and I wish I could become one of your patient too! ;)
Thanks so much for watching! 😊 We ship our supplements throughout the United States. Unfortunately, we do not ship to other countries yet due to challenges with shipping abroad. Hopefully someday!
Thanks for watching!
Best wishes,
RN
Hello Dr ,I just discovered your channel,so interesting! Just a gentle note,if I may:(again,thanks for the great infos) for me,struggling with mcas,me cfs,brain fog and dysautonomia,the little hand writing on the video is quite a strong signal and makes it a bit difficult to continue watching ,as I am sensitive to these quick stimuli,along with the music,as it is quite dense information requiring concentration.So maybe considering a gentler,quieter visual would be great! Just a thought.kind regards from the South of France
Wonderful to hear from you in France! My videos can also be listened to (like a podcast) if that would be better tolerated. But thank you for watching and for your feedback.
MCAS has made me allergic to corn. Corn is in every vitamin supplement - either as magnesium stearate or cellulose capsules. Is the answer to get everything compounded??
So sorry to hear this. Yes unfortunately compounding is often a helpful option for MCAS patients.
Hi- thank you. I have Sjogrens disease. I know there is a connection with EDS but have you seen a connection with Sjogren’s? Also, I see in the comments that you said G.I. map has false positives with H pylori . I had the gut zoomer and SIBO and candida came up however my breath test for SIBO is negative. Is it your experience that vibrant wellness also gets false positive with SIBO and candida? I was listening to the expert on MCAS., Dr Theoharides and he said he doesn’t put much stock in those gut tests. Do you? Thanks so much lots of questions I know.
I find the GI Effects stool profile to be most accurate (by Genova diagnostic).
Such an eye opener hat's off to you
Thanks so much for watching! 😊
Hello Dr. My brother was diagnosed with MCAS recently. I have symptoms of itchy skin but no rash, insomnia, anxiety, depression and have a runny nose most of the time. I don't feel I am sensitive to food, medication or products. Is it possible I have it as well?
You and I have very similar symptoms. I’ve been diagnosed with fibromyalgia but I’m starting to wonder…
Thank your for this amazing video! If a person had SIBO / Dysbiosis / Leaky Gut prior to Long Covid, is it possible that these conditions lead to the development of long covid, because the immune system and mast cells where already triggered and weakened? Thank you!
Very possibly yes! 70% of our immune system is in our gut, so if there is gut microbiome dysfunction, this could weaken our ability to fight and overcome common viruses. Thanks so much for watching! 😊
What does an acquired disorder mean for MCAS and how is it determined to acquire MCAS opposed to acquire histamine intolerance? Thank you.
With MCAS there is a rise in the tryptase level during a flare and reactions are to many things other than foods (as seen in Histamine Intolerance). MCAS involves gene changes in Mast Cell Genes that are acquired by a trigger (stressor). Histamine Intolerance is often acquired due to gut microbiome issues that reduce production of the DAO enzyme.
@@drrajsree thank you.
@@drrajsree Dr. If the trigger or stressor is identified and removed than can you recover from MCAS ?
This was exceptionally helpful. Thank you for sharing your knowledge!
Thanks so much for watching! 😊
This was such an informative video. Thank you so much for your efforts. 🙏🏼
Thanks so much for watching! 😊
The #1 most informative and thorough video on RUclips! 🫶🏾I hope the universe gifts you your hearts desires. Instead of baiting me into a pricy protocol with a practitioner, you share real life options for wellness. I am grateful for every second of this video, and the other videos referenced.
Thanks so much for your kind support! 🙏 I really appreciate hearing from you! Best wishes, RN
Very well explained and detailed.
Thanks so much for watching! 😊
We check nearly every box in the video and are doing most of the “treatments” with not much success. How do we find someone great to work with around us?
Dr. Laurence Afrin is the doctor who wrote the book on MCAS and has a lot of experience. I don't know him personally but I did see he offers consultations:
aimcenterpm.com/dr-lawrence-afrin/
Try cutting out high oxalate foods. It made a huge difference for me with my MCAS.
thank you very very much . great video
Thanks so much for watching! 😊
Is it possible to be diagnosed based on symptoms and reaction to antihistamines and medications? I have EDS/POTS and I get the severe flushing and POTS symptoms along with stomach issues and skin allergies to chemicals, and migraines from fragrances. But my Tryptase and urine test came back normal. Thank you so much for this informative video.
Oh my God I think I might have MCAS.
For about a year I noticed white stars in my POV appearing, especially when going to sleep. Then I started to get big infected pimples which just never went away and were constantly bleeding.
After that I noticed that the lymph nodes in my neck and under my jaw ballooned and my throat became inflamed.
Shortly after all those things the sleeping problems and heart palpitations 24/7 came, which worsened when trying to sleep.
I later found out I had massive mold infestation INSIDE the wall, which was also the reason for the dampness and odd smell in my room.
I could not sleep for days and was about to kill myself unironically. I literally had to book hotels just to be able to catch some sleep.
Fast forward a year to today and I still struggle with heart palpitations and insomnia when having contact with even trace amounts of mold.
This disease is one of the worst there is and I don't think that I'd wish it on my worst enemy.
Also take mold seriously! This shit could fuck you up just like it did for me!
Thank you for this video Dr. Rajsree! I have A LOT of the symptoms of MCAS but I can tolerate Spinach and Tomatoes just fine. How can that be explained that these two high histamine foods do not trigger a reaction?
Great question! Every individual with MCAS is different, so it's good to listen to your body. I'm glad you tolerate those foods!
I ❤ your videos! Thanks to you & your team for making this content.
Thanks so much for your support!
This is interesting. I first had dermatographism when I was 14. I’m 51 now and noticed it went away like 3-4 years ago. Around the same timeframe, I started getting itchiness all over my body like every 3-4 months. Do you know if dermatographism can go away and change into itchiness? It’s like I’m being bitten by lots of tiny bugs or being gently poked by needles that cause extreme itchiness. With that said, would you be able to tell me which of your products I can try? Thanks in advance!
Sorry to hear this. If I had to pick one product it would be Histamine Support. We get great feedback on this one for histamine symptoms like itchy skin. It's best taken at a dose of 2 capsules twice a day. Thanks for watching! You can shop for any of our supplements here:
dr-rajsrees-public-supplement-store.myshopify.com/
@@drrajsree thank you! I just ordered Histamine Support!
If someone takes betaine hcl/pepsin along with digestive enzymes, can they take histamine h2 blockers?
Yes! Thanks for watching.
Hyy dr pls post a vedio on vitiligo with type1 diabetic pls its gives a hope on so many life's
You might like my video on Autoimmune Disease:
ruclips.net/video/loIbxqmNOwc/видео.html
Thank u. So informative.
How long can you take the Natural Antihistamine Doc?
A lot of my patients take it for months with no problems.
Interesting. I have hEDS. I had an inset with a severe vaccine reaction which led to Lyme disease diagnosis.
I’ve had POTs, vagus nerve syncope, simple partial seizures often triggered by showers. But I have cold intolerance so I have to make them hot.
I would add I think severe nausea in pregnancy- which I had in all of mine. I also had obstetric cholestasis- itching like no other.
Leaky gut, estrogen dominance- endometriosis, ovarian cysts, liver issues….
Luckily I found a good doc that has been understanding.
My family thinks this is all in my head.
I'm glad this was helpful. Best wishes in your health, RN
Those who got it from the vax, have you detox the spike protein?
Wow thank you for these video. Very complete
Thanks so much for watching! 😊
Hyy dr rajsree, i am from india u r the best doctor i have seen so far ,i need to purchase u r supplements so pls guide how to purchase thanks a lot
Wonderful to hear from you! Unfortunately, we currently only ship within US and Canada due to challenges shipping supplements abroad. If you have any relatives visiting here we can ship to any US address and they can bring it to you.
Hi
I have reflux, hiatus hernia, astmasymtoms, dry caugh. My face and chest turn red(flushing) several times every day. And inside my mouth my chin swells. My brother died from cancer last year and since then I've been so afraid to get sick by my self.
I went to the doctor to get some bloodtest done. Cromogranin A and 5-HIIA and they came back normal. I also did an CT of my neck, thorax, and abdomenal. No cancer was found.
I wonder now if I can trust the tests and the CT ? My doctor doesn't think my symtoms has nohing to do with Histamin when I asked her about it. The only answear I get is it's becaus of trauma and stress. What do you think?
You might want to get a second opinion from another doctor.
I just discovered I'm afflicted. I have all of the symptoms noted all the time I've had this problem all of my life. I used to get hives and difficulty breathing when I was a kid. I remember the first time it happened I was exposed to poison ivy the real one not poison oak. I was a kid and a poison ivy had caterpillars all over it and I played with them for a few minutes and had a very serious mast cell activation event. Ever since that day my immune system was altered. All related to my allergies that presented when I was about 6 and I'm now 59. It's destroyed my vision by about 45. I've always had perfect vision and for no known reason I need a 2.25 prescription now. My main symptom is swollen watery eyes and brain fog. Varying degrees of inflammation all over my body. Constant stomach upset. Basically the most severe symptoms because I'm so sick and I've never treated the disease. One medication that helped me was Doxycycline. I've been diagnosed with somatoform disorder. I started taking Cetirizine, Vitamin C and Bromelain.
I'm so sorry to hear this. I hope your health improves! Best wishes, RN
Wow it seems like me. I always have pain. Chronic migraines divorce IBS I always have issues.
Thanks so much for watching! 😊 Hope this video helps bring some insight.
I have MCAS. Is there an association between MCAS and sarcoidosis which I was diagnosed with 20yrs ago. I also have hypothyroidism.
I have not heard of an association between MCAS and sarcoidosis in my research. Hope your health improves! RN
Excellent video and info thanks!
Thanks so much for watching! 😊
Every time i go to the doctor they thinks im crazy
I'm so sorry to hear this. I hope your health improves! Best wishes, RN
Hi , doctor
Can I take iron supplements with ibs and sibo pain, will it make it worst?
Iron is often hard on the gut. You can try a low dose one to see how it affects you.
I have IBS, GERD, chrinic gastritis, SIBO and anemia. My dr saud to start 63mg of iron from ferritin daily. I knew I couldnt take the regular iron supplements so I researched it and found 65mg carbonyl iron w vit C. Been on it couple weeks with no additional abdominal/GI symptoms. Iron ferritin can cause nausea and constipation which is what my Dr told me to try. Not a very good idea if you already have a lot of GI issues.
Great video!
This was helpful, thank you!
Thanks so much for watching! 😊
Dr madam oregeno oil how to drink sibo patient... Water mix or
It comes in a capsule you swallow with water. You can learn more about it in this video covering my Herbal Protocol for SIBO, which you can find here:
ruclips.net/video/zHATkKdznIA/видео.html&t=3s
Dr thanks for letting everyone know you have just nailed it from Johannesburg South Africa 🇿🇦
Thanks so much for watching! 😊
Can mold be the cause of my very low levels of DAO? My symptoms are reflux, dermatitis and lungs\chest pain. Do they look more like MCAS or histamine intolerance? Thanks 😊
Have you had any patients (or heard of cases) of myoclonus, chorea, dystonia or any other movement disorder caused by either POTS, MCAS, mastocytosis, SIBO, GERD, candida, EDS or any diseases/syndromes you mention in this video?
No I have not. Thanks so much for watching! 😊
Doctor, i m a woman, a few thick hair grow on upperlip and jaw. What is the cause and how to get rid of them permanently through diet and lifestyle only.
Sometimes this is from high testosterone. You might like my video on PCOS:
ruclips.net/video/ouAOGSC0GVk/видео.html
@@drrajsree Thanks doctor.
is mcas the same as cirs?
It's different. Thanks for watching.
I have MCAS, I have a problem with Hashimoto's disease and hypothyroidism. I should take Levothyroxine but I have very strong histamine reactions to it. What am I supposed to do?
Please watch my video on Hypothyroidism where I talk about Tirosint, a hypoallergenic version of T4.
Im also suffering from mast cell activation syndrome please suggest medicine madam im from india .
She described me perfectly
Thanks for watching. Sorry to hear this; hope your health improves!
@@drrajsree I am following the protocol and I believe it is working. Thank you for the work you do. Blessings.
I've had issues since birth. Severe anaphylaxis multiple times, joint and muscle pain, fatigue. Hypermobile joints made me conclude that I've had hEDS since birth. That then developed into MCAS somewhere down the line and that led to my M.E. diagnosis.
I'm still trying to get both hEDS and MCAS confirmed but keep getting dismissed.
Funnily enough, one of my more severe allergies that showed up from nowhere disappeared after the Covid vaccines. I just got GERD diagnosed (after 5 years of suffering), but I'm allergic to all antacids.
I'm so sorry to hear this. I hope your health improves! Best wishes, RN
I can take all these at the same time or should it be different times of the day? I have a reaction to literally every food even if it’s just burning at the lips. Idk what to eat anymore.
I love your videos , you are the best ❤
Thanks so much for your kind support! 🙏 I really appreciate hearing from you! Best wishes, RN
Thoughts on using low dose doxycycline as a mast cell mediator and calm over active microglia? Ie 20mg EOD for MCAS that seems specific to gut pain and neuro inflammation, very little histamine specific events, like rashes or allergies. But neuro inflammation after certain foods and activities.
I have not come across low dose doxycycline in my research on MCAS. Thanks for watching.
When my son was younger he was allergic to his own hair once cut....big welts ..we're looking into mcas now
Thanks so much for watching! 😊
I was diagnosed with Urticarial Vasculitus years ago and doctors just keep putting me on Immunosuppressant drugs, and i still suffer with alot of these symptoms MCAS causes
I'm so sorry to hear this. I hope your health improves! Best wishes, RN
what magnesium do you suggest to take at night?
We carry essential magnesium that is really popular. Thanks for watching! You can shop for any of our supplements here:
dr-rajsrees-public-supplement-store.myshopify.com/
I am sure I have this. I was just diagnosed with EOE which I feel is tied to this? Do you think that’s possible?
EoE is generally true IgE allergy mediated so you definitely want to have and IgE food panel done. Some patients with MCAS also have true IgE allergies as well so it's possible.
MCAS fits my symptoms well … so during an episode I had tested my tryptase but the result was only 4. Is this a definitive test?
Tryptase can miss MCAS sometimes. Some MCAS specialists can run more extensive tests from the urine.
Hello Dr. Is there a connection with Autism and Mast Cell disfunction?
Great question! I didn't come across that in my research, but I wouldn't be surprised if there was a connection.
@@drrajsree Strange thing Autism. I saw a review of a real good study connecting poor nutrition and the severity of autism.
Poor nutrition = low vit D3, low magnesium, low.....
The study even showed amazing improvements from getting essential vitamins up to good levels on the marginal autistic participants.
Hello Dr. I have 13month old baby boy. He suffering from this infection from his 4 month old age. Now i stopped medicine. Can i start cetirizine drops ?
Please discuss with his doctor. I apologize I can't advise on his health.
Can histamine intolerance turn into MCAS?
Great question. I talk about Histamine Intolerance vs. MCAS in the video. No, generally Histamine Intolerance does not turn into MCAS. MCAS is different in etiology (genetic predisposition + trigger that causes mutations in mast cell regulatory genes).
Quick question Doc! If I have MCAS due to SIBO, will curing the SIDO in turn cure the MCAS? Or will I have to do two different protocols? Any guidance or help would be greatly appreciated. My symptoms just started about a year ago but they are progressing pretty fast. Please and thank you 🙏🏼
I would address the SIBO first since gut healing is key in MCAS. Thanks so much for watching! 😊 You might also like my video on my Herbal Protocol for SIBO, which you can find here:
ruclips.net/video/zHATkKdznIA/видео.html&t=3s
@@drrajsree thanks Doc! And I actually watched your sibo protocol video right before this one. Thanks for the reply and clarification. Keep pumping out these informative videos!
I got cholinergic urticaria after either a polio vaccine, food poisoning in Thailand, chronic PPI use, or severe stress from my education, or due to any combination of these. Having a dual Campylobacter jejuni and Toxoplasma gondii infection from food poisoning triggered an extreme amount of additional strange symptoms on top of this. I’m quite sure SIBO, which I tested positive for, plays a role in this, either causal, or a result.
Do you think it’s possible to calm the mast cells down in this case of a trigger which can’t be reversed. I mean, I can’t go back in time to avoid the triggers… and treating SIBO with rifaximin and prokinetics didn’t work. It came right back. what are your thoughts? Any input from anyone reading this would be appreciated!
Every individual is different. I believe there is always hope to heal the body. Finding and working with a knowledgable provider to guide you step by step would be very helpful. I do have a video on my herbal protocol for SIBO if you are interested:
ruclips.net/video/zHATkKdznIA/видео.html&t=3s
Hi Dr I live in the OC. How could I see you for a consultation? I have been dealing with what I believe to me MCAS and also digestive problems for the past 6 years. I was hoping you could work with me to find a solution.
I apologize I'm not taking new patients at this time. I hope some of the tips in this video can help you. To search for a functional medicine provider, please go to IFM.org
Best wishes in your health,
RN
Have you noticed a relation to Mcas and endometriosis?
There is a correlation between endometriosis and SIBO, but I haven't heard of a correlation of MCAS with endometriosis.
I feel as if I’m allergic to everything. Well a lot of things. I began to react to the sensitive skin arm and hammer detergent etc. I have always had sensitivity and allergies etc but after Covid it got rediculous . After I had that insane cytokine storm so many more things flare me up. I took an Uber and just stepping into the vehicle I got a severe allergic reaction to the “little trees “ air freshener. Unscented stuff is used in my house. I can’t even clean with most cleaners anymore and I used to be able to. One thing though is it’s not the hot as you were mentioning about hot showers. It’s the cold. The heat is almost like a soothing feeling. It helps with pain, allergies you name it. Along with the tree (only prarie naturals) shampoos etc. but the cold causes a release of histamines etc. In fact the cold causes physical pain if my skin comes in contact with it. Ugh I live in Canada too which is not ideal. I’ve never heard of mast cell syndrome till recently.
I'm so sorry to hear this. I hope your health improves! Best wishes, RN
Can anything help with a prickly itching, stinging pins and needles sensation my daughter is having in the body which comes and goes. It is making her depressed
I have heard this can be related to histamines; but please also discuss with her doctor.
@ thank you 🙏🏾 do you send any of you products to UK?
I need so much help, but don't have stable housing yet or money