@trifecta_collective: Mast cell issues, including mast cell activation syndrome, are a symptom. They are NOT a root cause. We are seeing a lot of practitioners only focus on the mast cell side of things vs understanding and looking at the bigger picture of what is triggering the mast cell themselves. Often, this is a complex answer. Toxin overload issues, dysregulated nervous system, gut overgrowths, drainage pathway dysfunction, etc are often heavy hitters contributing to mast cell issues. You’ll also hear a lot of people talking about DAO, quercetin and vitamin c supplementation. All of these may feel supportive to help with mast cell stabilization BUT these can also flare up more sensitive individuals. Note that there are over 20 different mast cell stabilizers that we know about and each person may respond to them differently. Different ones can also feel supportive in different ways depending on symptoms. Some of the ones we commonly use are fisetin, perilla, luteolin, PEA and pycnogenol. If you suspect you are dealing with mast cell issues (or you already know you are) and want to dive deeper into WHY you are having these issues so you can understand where to start in supporting your body appropriately so you no longer have to deal with these, let’s chat. We offer free consultations. Use the link in our bio to book yours. #mastcell #mastcellactivationsyndrome #moldtoxicity #chronicstress #histamineissues

Megan l Root Cause Healing
Megan l Root Cause Healing
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Thursday 27 August 2026 13:19:30 GMT
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mandalubu
MandaLuLu :
I’ve suffered from 12-37 before we finally tried a MCAS med as a trial and the same day I started feeling normal. I’m incredibly happy to figure it out but I’m so sad at times that I was gaslit so long and made to believe I was just crazy with anxiety I couldn’t control.
2026-08-27 21:26:37
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paperandfireworks
Julia :
What are your thoughts on this situation: Itching and flushing improved with Zyrtec. Tryptase not elevated. 24 hr urine test didn't show anything, but no flare during it. Diagnosed hEDS, chronic migraines (can't find a med that helps much; strangely, Sudafed helps a little), chronic nerve and muscle pain, FND, Orthostatic Hypotension. Syncope. Lots of abdominal pain, diarrhea, constipation. 2 concussions with post-concussion syndrome. The question is: should we pursue additional MCAS diagnosis and treatment, and might it help with some of the symptoms? Her allergist has acknowledged that it's hard to diagnose. I'm not sure if cromolyn sodium or ketotifen is something we should ask about.
2026-08-27 19:15:13
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