#mcas
Exit poll as MCAS reading comprehension for grownups
November 3, 2026 at 10:41 PM
[Medical BS]

I had another doctor who apparently treats a lot of folks with MCAS

Yet he was very Shocked Pikachu Face when I had an MCAS reaction to the medication he prescribed

Sir. Doctor. Sir. This is a classic MCAS problem.
October 30, 2026 at 3:33 PM
hEDS, MCAS, PoTS, ME/CFS und weitere Syndrome werden meist als Komorbiditäten bezeichnet. Diese treten aber in gewisser Hinsicht auf so unglaublich robuste Weise simultan auf, dass sich die Frage, wo genau die Fäden dieser Komorbidtäten zusammenlaufen,
link.springer.com/article/10.1...
The Relationship Between Hypermobile Ehlers-Danlos Syndrome (hEDS), Postural Orthostatic Tachycardia Syndrome (POTS), and Mast Cell Activation Syndrome (MCAS) - Clinical Reviews in Allergy & Immunolog...
In recent years, an association between hypermobile Ehlers-Danlos syndrome (hEDS), mast cell activation syndrome (MCAS), and postural orthostatic tachycardia syndrome (POTS) has garnered attention and...
link.springer.com
November 3, 2026 at 12:10 PM
[Medical BS]

I am glad don't have to explain chronic illnesses like POTS and MCAS to my doctors anymore

But also I'm...concerned about the number of doctors who have picked up frankly incorrect info about POTS and MCAS

(Not even just the "it's over diagnosed" bias)

#NEISvoid
October 30, 2026 at 3:27 PM
Can you request my MCAS be cured and also for Jack Campbell to be okay, thank you
November 3, 2026 at 1:31 AM
Gibt es hier noch jemensch, der/die ebenfalls Eingliederungshilfe von der Stadt oder dem Landkreis bekommt und an ME/CFS (und/oder MCAS, PoTS, kPTBS) erkrankt ist? Ich habe heute einen kleinen Leitfaden im Umgang mit mir und den Erkrankungen geschrieben. Würde den teilen, wenn das interessant ist.
November 2, 2026 at 4:10 PM
IBS can be MCAS! 😨
November 1, 2026 at 12:00 PM
är sååå tacksam att jag inte har mcas (vill absolut inte ha mcas så tänker utgå från att jag inte har det och inte kolla upp)
October 31, 2026 at 6:37 PM
[Medical BS]

I recognize there are more MCAS patients than there are MCAS specialists, and he was probably trying to help

But immunology is complicated!

And I kinda feel like if you don't even know the name of a common antihistamine then maybe you should let my immunologist handle it
October 30, 2026 at 3:38 PM
[Medical BS]

A doctor who sees a lot of MCAS patients was concerned my MCAS was affecting the thing he was treating me for

But then he was like, quizzing me on what meds I take?

He was trying to recommend cromolyn like I'd never heard of it, but did not recognize the name of my OTC antihistamine
October 30, 2026 at 3:36 PM
#Boeing #F/A-18 (all variants), #USA - Navy : Blue Angels (165780) by Andrzej Rejter (#Miramar MCAS / Mitscher Field) #Display Team #aviation #photography #avgeeks
USA - Navy : Blue Angels Boeing F/A-18 (all variants) 165780 at Miramar MCAS / Mitscher Field NKX / KNKX (Photo by Andrzej Rejter)
Photo of 165780 Boeing F/A-18 (all variants) of USA - Navy : Blue Angels at NKX / KNKX Miramar MCAS / Mitscher Field - USA - California © Andrzej Rejter Sep 25th 2026
airplane-pictures.net
October 30, 2026 at 6:47 PM
We could have had *decades* of research on cfs/me, pots, mcas, etc. if only doctors had LISTENED TO ALL THE SUFFERING OF WOMEN FOR FUCKING DECADES.
November 1, 2026 at 3:29 AM
ever been investigated for mcas?

sometimes it's not fixed IgE allergies but a more general… allergenicity, you might say. which can be treated more generally too
November 3, 2026 at 3:21 PM
That's incredible. Sounds like part of MCAS?
November 1, 2026 at 9:32 AM
TIL att extremt svullna ögon efter att man gråtit är en supervanlig EDS/MCAS grej och vill nu slå amerikanskan som klassificerade mig som ”not a pretty crier” 1994 i ansiktet. Med typ en stol. Som hon är allergisk mot
November 1, 2026 at 9:02 AM
I've seen a photo of someone with MCAS who went through the grid test and reacted to everything, including the control square.
November 3, 2026 at 3:37 PM
i forgot i have an extreme intolerance to alcohol due to eds/pots/mcas in this moment ok nevermind
November 1, 2026 at 1:30 AM
Common knowledge amongst the #MECFS and #LongCovid communities:

- with meds start low and go slow
- meds may trigger your MCAS anyway

Researchers on ME and LC:

- let’s start meds on a much higher dose and increase quickly
- don’t screen for MCAS
Nathan Fillion's Speechless 'Um No' Reaction
Alt: GIF apt Nathan Fillion's Speechless 'Um No' Reaction
static.klipy.com
October 29, 2026 at 4:15 PM
and POTS and MCAS and hEDS... not to mention having all those at once 😖
November 2, 2026 at 10:41 PM
Hey @jaimeharrison.bsky.social I hope you see what we are up against on social media everyday brother. These people are wild and we try. Respect you immensely and keep up the good work in South Carolina. Shout out to MCAS Beaufort! My first duty station
October 30, 2026 at 8:05 PM
När the shit hits the fan så kommer fan allt på en gång så nu tar vi en omgång MCAS-symptom också.
Hatar att få det på mina barnveckor eftersom jag vet hur rädd min dotter blir. 💔
November 3, 2026 at 5:52 PM
Okay so my comorbidities that are eds caused/connected:

Dysautonomia/pots, mcas, intracranial hypertension, cranial csf leaks, vascular stenosis, spondylolisthesis, gastroparesis, reoccurant sibo, ADHD, hernias, uterine prolapse, gerd, pcos
suspected: cci, hiatal hernia

I think that’s it lol
November 3, 2026 at 1:32 PM
It’s so common for pwME to have MCAS as well. I have 4 different antihistamines per day.
November 1, 2026 at 2:17 AM
If you are on FB, there are MCAS support groups, including an Aus one.
November 1, 2026 at 7:06 PM