What are the symptoms of Mast Cell Activation Syndrome (MCAS) and how is it diagnosed?
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- Опубліковано 9 сер 2021
- Do you wonder if you have Mast Cell Activation Syndrome MCAS also called Mast Cell Activation Disorder (MCAD)?
Can you have MCAS and Histamine intolerance at the same time?
Would you like to know how it is diagnosed?
Check out this video where I explain all about MCAS.
Grab your free low histamine food guide: bit.ly/LowHistamineFoodGuide
Get the Happy Without Histamine Reboot, a 4-week meal plan with recipes, prep guides, and shopping lists. Get started on your low histamine diet the easy way. bit.ly/LowHistamineMeal
Watch my free Masterclass The 5-Steps to Healing From Histamine Intolerance hwh.luannehopkinson.net/5hist...
Find out more about histamine intolerance with free articles and recipes at www.happywithouthistamine.com
Join the Happy Without Histamine Facebook group for regular live videos like this one / histaminehappy
#Histamineintolerance #MCAS #MCAD #Mastcellactivation
Great overall assessment of general symptoms of MCAS. Thank you for doing the video. People that suffer from this, such as myself, *desperately* need others, mostly the medical establishment, to have some idea that this even exists, not to mention having an understanding of it.
You're welcome! As I have had this myself I am passionate about awareness and helping people with MCAS.
It is so true ❤
I fell into this after I have been researching for the last couple of days. My migraines are out of control and my sinuses are waking me up at 3:00 every morning. I itch continues all the time. Hives, temperature problems. And you just so happen to have the perfect name. I have only seen one other person who spelled Luanne like this. I am going to my Dr. Tomorrow I hope she will listen to me. Thank you so much.
Hi, Luanne you have the perfect name too!
I swear. I have this. I swear I do. I’ve been sick for the longest time. Sneezing 50-100 x a day. Constant runny nose with puffy blood vessels inside my nostrils, some food gives me a headache or migraine or makes me nauseous and instant diareah, runny poo 10-15 x a day some days, constipation, a rash that appears on my face and aches/burns and stings when I smell certain smells or eat certain foods, insomnia, brain fog, extreme fatigue, sleep apnea, dizziness, heart palpitations, mouth ulcers, fibromyalgia, MTHFR gene mutation, T cell imbalance, autoimmune conditions.. MCAS is what I have. I’m almost sure of it 😭
I've had all sinus issues 15 years but now main symptom is fybromyalgia symptoms I have hsd and Asperger's I've found late 43 since sins diagnosis is your fybro all over
I’ve recently diagnosed myself with MCAS after having problems for years. Today I went to see my GP expecting to have to talk her into accepting my diagnosis. Imagine my delight when she said “yes, you’re right, I have it too”.😊
@@annesimpson2146 your lucky there do you have pain or is it allergy sinus rash issues
FODMAP asap?
@@brakeme1 fodmap diet?
Thank you for this video. Very helpful!
Your welcome!
Summary:
Mast Cell Activation Syndrome (MCAS) is a condition characterized by a range of symptoms affecting various body systems, often overlapping with histamine intolerance and other disorders. Diagnosis is challenging due to the absence of a definitive test, with clinical history and exclusion of other conditions being key factors. Complementary medicine and holistic approaches can help alleviate MCAS-related symptoms.
Highlights:
- Mast Cell Activation Syndrome (MCAS) presents with diverse symptoms across multiple body systems.
- Common symptoms include headaches, anxiety, gut-related issues, skin problems, respiratory symptoms, and more.
- Diagnosis relies on clinical history, symptom patterns, and exclusion of other disorders.
- Serum tryptase levels can be an indicator, but not all MCAS patients show elevated levels.
- Complementary medicine, nutrition, and holistic approaches can help manage MCAS symptoms.
Thank you so much! Great work!
I have most of these symptoms but my dr is clueless .. I can’t take most medications as they give me severe reactions! I’m at my wits end 🤷🏻♀️
I was like this once too. Check out my brain food progam where I teach you the tools I used to to be able take medication and increase my foods! my.practicebetter.io/#/60e8fd2239803311b86622d3/bookings?r=6139b37c3980330a44025879&step=services
Check if you have hypomobility heds Asperger's add if so it's this causing it eds society lists things
I have this condition and I have to stop work cos of it. My major symptoms are the flashing and hives and also intolerance of heat. I can get a break from it for about 2 weeks and it hits me hard again. I did a lot of food test it came back as I was allergic to most food I eat. I stuck with eating just another nothing. I want to book a call with u . Thx
Hi, my 6-month program The Happy Without Histamine MEthod is full right now, but you can add your details to the waitlist, and I will let you know when it opens.p.bttr.to/3D9z8oc
Also If you would like to work with me on The nervous system my Nourish your Nervous system package is open for bookings. This was the secret sauces for me that helped me when I was at rock bottom. p.bttr.to/3iARLJR
@@luannehopkinson is this a Mindbody program
I'm afraid to eat anything. I lost so much weight since covid I have damm near everything you are talking about. What should I do? =[
Hi, I have been down to just a few foods and I found Brain retraining was the main thing that helped me slowly tolerate more foods and medication. You should still make sure you get Medical support, but this can help to change how our body functions. I teach this or you can use a program such as DNRS or Gupta programs:
DNRS
bit.ly/2Yepn9A
GUPTA
bit.ly/2lDEiGJ
My Neuroplasticity package p.bttr.to/3iARLJR
Have a look at those, It is all science-based and really worked for me and many others!
I would very much like to talk to you. I'm on the brink of death. I have cystic fibrosis and just beat covid and I think I had back in Dec 2019 cuz a lot of the symptoms I've had all along
Great information. I’m recovering from covid(day31), and I think I may have mast cell activation when I over exert myself now(exercise). I just started taking h1 and h2 antihistamines to see if it helps.
I am glad you find it useful, if you want more info I have a free low histamine food list and a Facebook group with more info. eepurl.com/dPeJAr
I would love to get in contact with you, I have one bed ridden that's been diagnosed with them Cass, and has fluid around her heart
Thank you for this video. I've been going through all of this for about 6 years now. I just found out I gave two MTHFR gene mutations and see that it can histamine issues. Do you have any information regarding this? ✌️
MTHFR can impact histamine breakdown however it is not the cause that the body has an excess of histamine. I find that the epigenetic expression of genes can be improved on as well.
Do you have fybromyalgia
I think I have mass cell activation disorder as well as histamine problems. How do I get in touch with you and how do I get a list of a list of the histamine diet
Hi you can find out more about me and get free recipes at happywithouthistamine.com Grab your free low histamine foods guide to easily start a low histamine diet at this link eepurl.com/dPeJAr I work with clients in my 6-month program The Happy Without Histamine Method, you can get on the waitlist here p.bttr.to/3Ma6bxS
I know for a fact I have this and the Histamine intolerance. Idk when I can get diagnosed but I seriously need your guidance desperately. Please give me a way to contact you. I belive I have the anaphylaxis stage also. Please respond
Hi Joshua, I am literally suffering with all of these horrible symptoms. My doctor says it's all driven by anxiety and all she has prescribed is antidepressants. If you don't mind me asking, how are you doing now? Can you please share with me if you have found a treatment that has helped you? I would really appreciate your response. Thank you.
What about strong body odor ?
I have post nasal drip, cough, mucus and throat clearing for almost 2 years after covid. Also Sleep disturbances, geographic tounge and very high IL 1B. Can it be MCAS?
It may be, there is also a strong connection with the nervous system and both MCAS and long covid or post viral issues.
We work on the underlying issues of the nervous system in BrainFood course which helps address the underlying root causes of the nervous system.
Check out https:happywithouthistamine.com
How do I get your low hystamine food list?
Grab your free low histamine foods guide to easily start a low histamine diet eepurl.com/dPeJAr
What can I do for now to survive until I am diagnosed by an allergist/immunologist?
Go on a low histamine diet you may only be able to eat a few foods to start out. You can try H1 and H2 antihistamines if you are having histamine symptoms.
I didn't go to doctor but when u see what trigger le inflammation, to me are grain and others but need to tested I'm ok with milk no grain no alcohol no beer, 😢, no yeast, just fruits veggy meat or fish and seeds try when u eat something in a hour my mouth get inflamed so u know what does wrong to u
Write everyday what u eat what u drink the time too
How may I work with you?
Hi Tim. I work with clients in the Happy Without Histamine Method program. It is currently closed. However you can join the waitlist for the next intake at the link for the free masterclass here hwh.luannehopkinson.net/5histamine-secrets/masterclass-on-demand
You can also join the BrainFood program which is currently open or grab the Kickstart course this options are here www.happywithouthistamine.com/
Thank you.