@dra_says: This is a relatively new condition that could explain alot of sympotms in patients that are not responding to treatment. Educational Purposes only #mcas #mastcellactivationsyndrome #mastcellactivationdisorder #mastcelldisease #fibromyalgia #pots #potssyndrome #palpitations #dizzy #dizziness #doxtor #doctor #privatedoctor #privategp #reflux #heartburn #antihistamines #histamine #allergy #allergycheck #ibs #irritableboweldisease #irritablebowelsyndrome #chronicfatigue #chronicfatiguesyndrome #tiredallthetime #tired #stress

Dr Ahmed
Dr Ahmed
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Region: GB
Monday 18 March 2024 14:28:02 GMT
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triceratops429
Laura 🦓♾️🐙🏳️‍🌈🍉 :
MCAS goes hand in hand with connective tissue disorders. Since the mast cells live in connective tissue. I have hEDS.
2024-03-18 19:35:42
1169
joshjhargreaves
Josh Hargreaves :
I’ve had mcas for 1.5 years now after Covid. Has to diagnose myself - was treated disgracefully by my GP. After working on healing my gut, microbiome etc, I’m mostly better.
2024-03-18 19:29:48
335
amyschapter
Amy :
I wish there was more GPs like you! Thank you for being so on the ball!
2024-03-18 22:12:03
479
prettiditzz
Tee :
yup, my Endo called it! I'm allergic to my menstrual hormonal fluctuations. I'm good for like a week out of the month. the rest I love on hydroxyzine around the clock...
2024-03-18 23:52:59
131
em_attempts
EmAttempts :
im 99% sure i have this. do people w mcas tend to get POTS? bc im 99% sure i have pots
2024-03-19 03:46:13
226
sophiemakesterrain
Sophie 🏳️‍🌈🇬🇧 :
I’m pretty sure I have MCAS after Covid. I’m doing a low histamine diet which is enormously helpful for the symptoms. But the diet itself is miserable.
2024-03-19 17:34:53
172
mummywhisperer
Mummy Whisperer 💖 :
Yes I have MCAS … nightmare as all ‘good stuff’ is bad for me … cold swimming, avocados, fish, exercise 🤦🏻‍♀️
2024-03-18 19:57:36
149
ilikepinemartens
3 pine martens in a trenchcoat :
If you have a connective tissue disorder like EDS there’s a big cross over with POTS/ dysautonomia and mcas which makes it even harder to get a diagnosis
2024-03-19 13:46:17
233
letamber31314
Lulu :
I wish I could get an appointment with you, my GP does not care at all. I’ve got so many issues and nothing being done
2024-03-25 01:21:42
18
scouthawkk
scouthawkk :
Yeah, doc told me MCAS isn’t evidentially supported yet; also wouldn’t consider eval for hEDS b/c “there’s no treatment”
2024-03-18 20:37:17
61
sophie.hassall0
Sophie Lou :
PLEASE STOP 😭 It's a running joke in my family that I'm just 'allergic to everything' - I constantly have a blocked nose, dry eyes, and suffer with dry, itchy skin all over that is triggered by EVERY
2024-10-11 21:28:53
26
samprettycore
Sam 🖤 :
I believe I've got MCAS. I get rashes for no reason, foods flare me up, heat triggers symptoms. I can skin write, it goes red. My GP won't do anything and blames it on fibro and M.E.
2024-05-28 12:15:02
33
chayden118
Chayden118 :
I mostly struggle with hives caused by stress and sudden temp changes, but the more obvious one is the swelling I get from minor scratches 😅 They itchy like crazy.
2024-03-18 20:12:18
30
justnic_73
Nickster :
I’m a fibromyalgia chronic pain sufferer with chronic migraines and b12 deficiency always hurting always tired
2024-03-18 15:48:14
33
donnalangdon
Donna :
I was diagnosed with fibro 10 years ago.had a 24 hour ecg for heart palpitations and dizziness whe I stand generally feel rubbish all the time. Still no answers
2024-03-21 19:39:46
9
gemgem5000
ChronicallyEmGem5000 :
YES ! I’M SOOOO HAPPY People in your position are finally recognising it!!!!
2024-03-18 21:20:50
16
chantelle_at
Chantelle :
A great gastroenterologist suggested I had this a few years ago. Such limited info and good dr’s to get help for it.
2024-03-25 13:55:44
7
naidsta
Naidsta :
So I hit diagnosed with fibromyalgia, which I was skeptical about, then endometriosis, I’m sure I have histamine intolerance, red face and hands after food !!! I get alllll these symptoms you said……
2024-03-18 18:35:45
49
bbopboojoo
bobbie jean :
I have MCAS. not new. having connective tissue disease, ehlers danlos is my cause I guess. but becoming more common. i think covid had a play in tbat. if u become allergic to random things u nvr were
2024-03-18 22:45:50
38
innovationcreators
INNOVATION CREATOR NETWORK :
Where are you based? How would I get an appointment with you?
2024-03-18 22:00:29
5
stanleychesterfield
stanleychesterfield :
I've had daily nausea, vomiting, lower middle abdominal pains, bloating, cramps, loss of appetite etc since October, cant eat, lost 65lbs (225>160)
2024-03-18 22:07:25
24
louiselayfieldclaire
Louise Layfield Clai :
You’ve just described me, for last 3 years. Been put on antihistamines
2024-06-15 21:15:26
5
stephiebee1986
Stephanie :
I’ve been having food sensitivities to most foods. Dizziness. Skin itching. Low blood pressure. Low heart rate.
2024-03-20 20:46:23
5
mand_again
Mand 🇬🇧 :
What do you do if your GP has you written off as a hypochondriac
2026-01-08 18:06:40
1
ophiotterkin
Skaləmən :
I can't convince doctors of my symptoms let alone possible diagnoses. My allergies keep increasing, so ya, MCAS on the radar.
2024-03-24 03:43:35
2
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