How To Treat MCAS Naturally | Healing Mast Cell Activation Syndrome 

Here’s a video about the MCAS medication which really helps me! 😊 ru-vid.com/video/%D0%B2%D0%B8%D0%B4%D0%B5%D0%BE-SB1b2KJzWmw.html

Hello, just want to pass along, as a fellow MCAS sufferer, with me, vitamins and supplements, the excipients, dyes and fillers are often the problem and *not* the active ingredient. Even things like microcrystalline cellulose can trigger problems with a lot of people that have MCAS. Obviously, we are all totally unique so what triggers issues with me does *not* mean it will with you or anyone else, but it's just something to consider and look into. Anyway, great channel, it's no doubt helpful for many people and I hope you can improve. :)

Thank you for this Georgina! The warmths and hope that you present in your videos continues to inspire me! Curious to know, where did you get your glasses from? They are sooo cute!

it sounds like we're going through similar things: so many systemic illnesses (i have hEDS and POTS and very probably MCAS) have lots of overlapping conditions and what might help one condition might adverse, completely infuriatingly affect another... also completly impossible to do scientific studies on what helps and what doesn't as there are just too many parameters... I find it hard to know what makes me sick as pain, heat and even low level stress will set it off, if i do a test to see if a supplement or eliminating something from my diet works it's impossible to know if it was this change that made a difference or something else non-related! it's all such a pain in the ***, completely infuriating!

another video of yours that feels tailor-made for me :') love you, georgina !

Was diagnosed with MCAS quite a few years ago. Went thru many many many tess and was finally able to narrow it down and get put on medication. I see folks commenting that they take Quercetin. Little side note: quercetin is found in onions.

Just started mestinon for pots and it has done wonders for my gastroparesis. Definitely something to think about. Has HEALED my nausea and vomiting.

I don't know if it'd still help, but I've used something called Ester-C here in Canada, and it's vitamin C buffered with calcium, which is supposed to be easier on the GI tract than ascorbic acid.

Did you do any other videos on mcas? You are incredible and beautiful ❤❤❤❤

Congratulations on the diagnosis! I hope it ends up being a quality of life improvement! Do you know why they took you off the fish oil? If it helps, I have a certificate in plant based nutrition and some vegetarian sources of omega-3s are: chia seeds, hemp seeds, walnuts, and flaxseeds. With the flaxseeds, they need to be ground in a coffee grinder to make the omega-3s bioavailable, but they're definitely the cheapest option. Canola oil also has a somewhat decent omega-3 content so using that for your cooking oil could be helpful too. Personally, I just take an algae oil supplement, which is the same form of omega-3s as in fish oil. The other supplements I take for my MCAS are an olive leaf extract supplement (a natural H1 blocker) and a mangosteen pericarp supplement (a natural mast cell stabilizer). If I'm getting digestive symptoms, which are rare for me, I'll take a peppermint leaf supplement (a natural H2 blocker). My doctor okayed these because I was getting side effects from the antihistamines I was on before. I hope you're doing well and that your symptoms are better controlled now. :)

I don’t have MCAS diagnosed but I take 1000mg Vitamin C and 2,200mg fish oil daily for my fibromyalgia that is caused by hypermobility (doctor recommended dosage for me). I am now sorta looking at my past and wondering if I had mild MCAS. (Being sick daily or near daily, lots of rashes, etc.) I really appreciate your videos. I hope you find something that is able to help you. I always take my vitamin D and vitamin C after eating. If I take them without eating right before I throw up.

Thanks for this! I'm having some weird stress symptoms at the moment and I'm more convinced than ever that I have a MCAD. Like you, I thought you had to have severe respiratory issues and need to carry an epipen etc. I have an HSD diagnosis. I have chronic allergic rhinitis and have used a nasal spray for over 20 years. I can't sleep without it. The stress symptoms I have are a dermatitis flare/sore itchy rashes on my hands, under my arms, my earlobes and now my eyes which are swollen, itchy, prickly and sore. I've noticed this with my eyes when I've been stressed before. I take vitamins C and D3 daily but I may try increasing the d3 as it is a relatively low dose. I'm also bruising even more easily than usual. I have some mild GI issues too which I've always had. I have no idea how to broach the subject with my GP though without sounding like a hyperchondriac! 😂

My geneticist prescribed high dose vitamin C for me but I’ve been lazy and haven’t taken it. My GP prescribes high dose vitamin D because I’m deficient. I haven’t tried the fish oil. I have suspected MCAS but not confirmed but I would love any improvement in the sick department. I’m done to barely being able to eat anything and I’m so over feeling sick and having to not eat another thing I enjoy. Hoping to start fish oil and see an improvement!! I don’t even know if I flush like I used to. I never knew when it was happening until people asked me if I was okay because I was all blotchy red. I notice the ones on my stomach that come and go and usually correlate with eating something that my body rejects. Also, you look so gorgeous (more than you always do) in the pst clip. Your skin is super glowy. But, of course, you’re always gorgeous :) Thanks for this video!!

What kind of vitamin c is it? I could only do calcium acsorbate myself Omega 3 is the best.. I do hemp seeds on my meals, chia and hemp powder in smoothies definitely notice a difference 💚🌱

sometimes high dose vitamin C can cause promblems in ME patients because it activates the immune system and ME has an autoimmune component, so basically it just gives the body ammunition to attack itself. I have severe ME and also got very unwell after trying high dose vitamin C, I wasn't sure if it was related or not but now I'm starting to think it might be (I'm also hypermobile, have POTS and suspect I have mast cell problems)

I was vegan, had a deviated septum which caused sinus disease from untreated sinus, which is what I think has caused mass cell activation syndrome, along with nutrient deficient

Vitamin C and D have no miraculous effect on me either, and I use the bio-available vitamin C (Ester-C). Oddly, exercise helps.

Also vit c with ascorbic acid is a no go for mcas . Camu camu is best source of vit c for mast cellS

I'd love to know how you are going now! The supplement I love the most is quercetin (I make sure mine has no bromelain because personally I react to that.)

I’m going to try vegan omega 3 and see if I notice any improvements with that. Thank you for sharing! It’s so hard to get appointments with specialists 💚

I am very allergic to fish and seafood so I can not take the fish oil supplements. Wondering if there is a substitute?

These are all natural MCAS treatments, the first two are recommended by professor Aziz & have successfully treated lots of people. This video is about my experiences, ofc everyone reacts to things differently, so it’s up to you whether you’d like to watch this or not 😊

Hey Georgie! Omega-3 is fat-soluble, if you have any problems with it, maybe you have EPI. I haven't done a test for EPI myself yet, but enzymes like Creon are definitely a plus for me. BTW vitamin D is fat-soluble too.

I take vitamin C and another called Quercetin which I recommend looking into. I'm not super sure of their efficacy yet as I had another medication change ontop of adding these recently. Also MCAS Diagnosed

Check if there is sulfites or preservatives in your supplements. Those trigger MCAD and are in sooooooooooo many products we ingest.

RDA or recommended daily allowances are only enough to keep you from getting scurvy. I take about a 1000 mg to 2 g of fish oil, primrose oil, and borage oil day and you can take 2 or 3000 mg of Vit C a day easily and when you're sick your body needs more.

Vitamin C causes me to have horrible abdominal pain and explosive diarrhea.

Hi, I am putting in here that vitamin D is super important to take for your general health regardless if it does anything to your MCAS. So I recommend that you try it in spray form. The brand name is BetterYou. And I am buying it from a local supermarket in Ireland. Pretty sure that you will find it in any health food shop in UK. Choose the spray with D+K2. The vitamin K2 helps with absorbition and that the D-vitamin work better in your body. You spray it to your mouth, under your thong and it tastes peppermint and is very sweet. Also check other vitamins which can be sprayed to your mouth. Helps so much with everything!

YOu need to be careful taking Fish oil with MCAS as one of the symptoms with MCAS is Bleeding and Clotting problems. Have you tried B-6?

Worry, anxiety, obessive thoughts, obsessive veganism or vegetarianism can cause stomach upset and digestion problems.

I have to be so careful with vitamin and supplements, I have had some that caused me so much GI pain. I recently started on oral cromolyn sodium and that of all the things has made the biggest difference for me, my abdomen had been SO swollen, i looked 8 months pregnant all the time and over the first 2 weeks of treatment it just kind of melted away. Eating one of my trigger foods will cause it to puff right back up though. Quercetin helps me a lot, and liposomal vit C.

I think you need to read about the leaky gut bc it the cuse for histamine problem

Umm this is a misleading title!! You don’t have a treatment for MCAS please don’t clic bait 😑

I was in course for antibiotics few weeks ago and Mast cell has come back anymore tips

Also, I take quercetin, Vitamin D, and Vitamin C and don't see any improvement at all, really. Also, may I ask how you were diagnosed? Which kind of doctor? My general practitioner said he does not test for that.

My biggest mast cell symptoms among other things is severe abdominal pain and swelling and I can’t seem to find any relief .

Vitamins are not medications for mcas.

Takes a while for stomach to get used to it I take 4000 mg now but it took few weeks

Vegetarian healing from mcas bonne chance

When you have mold toxicity and Lyme that triggered it. Its not so simple