Dr Ahmed
Region: GB
Tuesday 31 March 2026 16:19:20 GMT
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ValleyGirl110 :
I was diagnosed with POTS and am under investigation for MCAS! 💙
2026-04-17 15:06:16
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cazzy4040 :
I’ve got it all going on 😂 And now I’ve found out I also have hashimotos 😳 All linked to immune system function maybe? Well apart from hEDS as it runs in my family.
2026-04-09 23:21:37
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Denise64leo :
Is there a treatment for MCAS? I thought there wasn’t. I have Long Covid but I also have all those symptoms you mentioned.
2026-03-31 16:38:17
1
sean Sean Turley :
ihave all those ,no long covid never got it ,had bad stress last year for 3 months ,its been driving me mad .im really fit eat healthy and this just started .how can i check please
2026-05-02 19:21:44
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Emma :
does mcas cause lichen planus and/or srojgrens?
2026-04-03 00:26:04
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Babaloo :
I have MCAS and APS
2026-04-10 12:16:10
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Eileen Thombs :
Could it help my gastroparesis? I have hEDS, gastroparesis, and STC. Not been diagnosed with MCAS, but wondering if I might.
2026-05-26 20:51:27
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Nathalie van Dijk :
but mcas is just a result, not the cause....
2026-05-09 18:40:27
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salkev22 :
They don’t see MCAS as anything in wales, my daughter has POTS and EDS xx
2026-04-10 16:05:23
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carolina_momma :
Lucky me! I have all four!!
2026-04-02 03:06:25
1
cathynicdhiarmada :
Have them all … but do i have mcas or a histamine intolerance…?
2026-06-20 23:01:23
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🖤💛Kerry💛🖤 :
when saying long covid, would that also include ME/CFS?
2026-05-05 20:46:25
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NikkiFit ~ The Wellness MisFit :
Can you do a video on Erythromelalgia it’s so hard to find good docs that know about it and hard to find info on it 🥺
2026-05-07 00:42:58
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Amanda Jukes :
Would this cause persistent raised neutrophils? With other symptoms ie post nasal drip, polymorphic light eruptions, chronic cough, hormone issues with hrt ie not tolerated very well after full hysterectomy, hypermobile, adhd, gastrointestinal issues, endometriosis, palpitations, etc
2026-03-31 16:30:40
1
Chuck :
But mcas is not in the nice guidelines?so NHS not wanting to know about it when you speak to doctors about it ?
2026-05-25 10:26:25
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𝔻an 𝔻an :
Hey Dr Ahmed, I’ve got all these symptoms but I have fibromyalgia and crohns 😐 Is it possible that I ca somehow have all of this going on along side my current conditions ?
2026-04-05 23:24:09
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michellemelton.gammyof9 :
How do you test for it?
2026-04-01 03:15:20
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okie512 :
That’s the same as fibromyalgia isn’t it
2026-04-04 12:58:07
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🔥 KJoy 🦋 :
Is there a specific lab test for MCAS?
2026-04-01 05:32:17
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Humanityfailed :
how do you get rid of this
2026-04-01 06:22:44
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Zoeee :
I think I have MCAS (I also have hEDS) but my GP keeps saying oh it's too rare and dismisses me straight away!!
2026-06-25 20:12:44
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MaryJane :
The gi symptoms are very debilitating. Thank you 💙 😊 💙 for your work! Grateful!🥰
2026-04-02 00:50:34
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eliiiiiiiiii :
Hubby has confirmed HEDS son has confirmed HEDS and multi system allergies not controlled by 120mg anti histamine but no mcas diagnosis despite lots of symptoms. Other son has symptoms of pits including racing heart, lightheaded and dark vision on standing but no diagnosis for HEDS or pots (not HEDS symptoms though Tbf
2026-04-01 18:08:53
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Jordan B 🧡 :
How can I get my doctors to listen I’ve got pots and heds and just had a call with doc and she told me mcas is fake and not to believe everything google tells me and if I was to lose weight and go swimming it would resolve all my symptoms 😫
2026-04-22 12:56:46
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Ozzie :
Is getting red faced when drinking alcohol associated with MCAS? I don’t have the Asian gene. If I also have sweat on my face sit too long my face will burn.
2026-04-06 18:43:35
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