@drdavidmorris: Why do POTS, MCAS, and EDS often appear together? POTS, Mast Cell Activation Syndrome (MCAS), and Hypermobile Ehlers-Danlos Syndrome (hEDS) are frequently discussed together because they may affect multiple body systems, including the autonomic nervous system, connective tissue, immune function, circulation, and joint stability. Learn why recognizing symptom patterns across different systems may be an important part of understanding complex chronic conditions. 👇 Would you want a healthcare provider to look at the whole picture instead of just one symptom? 💬 How many specialists did you see before someone connected your symptoms? #POTS #MCAS #EDS #EhlersDanlos #dysautonomia #mastcellactivation #hypermobility #functionalmedicine #murfreesboro #magnoliamedicalcenter #rootcause #fyp #viral

Dr David Morris
Dr David Morris
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Region: PH
Wednesday 29 July 2026 12:00:00 GMT
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jillerrs
jillerrs :
Respectfully, put this on my doctors’ fyp instead of mine?
2026-07-30 16:04:29
4416
se.khara
Mariah🌵 :
Autism + MCAS + EDS + Endometriosis
2026-07-29 15:29:41
1317
kmarlo777
KMArlo777 :
Sounds like there’s no cure.
2026-08-18 01:59:24
1
echoofdissent
echoofdissent :
Question, is it common for it to be painful with IVs if someone has all three? My daughter says it burns and is incredibly painful.
2026-08-18 01:24:44
0
unkabell
Unkabell :
the women have figured it out. unfortunately we need ✨️referrals✨️
2026-07-30 22:50:07
1041
tiffanylbell1
Tiffany Bell :
I have all of the above and it’s so annoying
2026-08-17 17:40:01
1
armstrong.jess
Jess :
But why does it suddenly become a problem? I went from 20 years of running and 10 in CrossFit to struggling to go for a walk..
2026-07-30 11:56:26
1321
tater_snackz
tater_snackz :
“Find someone who really listens” sir that is the problem
2026-07-31 18:10:21
359
darling_dahlia
darling dahlia :
we're also seeing women with these 3 are more likely to have endometriosis
2026-08-17 19:37:06
1
lucia_vh
Lucia :
NEVER GO TO A CHIRO AS AN EDS
2026-08-10 18:03:51
14
poshnpolished
Emma 💅 :
The nurses and the PTs are seeing it but the Drs refuse to consider!
2026-07-30 12:07:40
1522
sharono227
Sharon Andrea :
You know what would be helpful? If someone would put together a nationwide list of doctors who understand and are willing to work with us AND take insurance.
2026-08-11 15:35:48
55
nomadic_wolf
Leah :
“Find someone who’s willing to listen” and that’s where we already lost
2026-08-17 23:49:53
10
trudyjo64
Trudy💕 :
And add autism, adhd, pcos, endo. I'm tired of my alphabet soup
2026-07-30 19:03:46
145
sailor_snowwy
🌸♐❄️Snowwy Girl❄️♐🌸 :
Neuro Behcets here. I have fibromyalgia. Everyone states that I'm quite hypermobile except my PCP. My face gets bright red when I'm stressed, overheated, or eat certain foods. I also have POTS and ADHD. 😭😂
2026-08-17 01:42:27
1
jessibender
HorsesJesusFamily😇 :
ha we had doctors looking up how to put my jaw back in the right way on Google! and still messed up when they put it back in
2026-08-17 04:41:53
1
magic_knitter
Magic_Knitter :
I’ve given up on the EDS dx. Can’t get anyone to take me seriously cause I don’t “look” like what they expect. I’m trying the allergist next, see if I can get the MCAS and then try to corner the cardiologist. I swear they just won’t listen and if I get told “loose some weight and it’ll all get better” one more time….
2026-08-03 23:15:34
28
pips.books00
Pip’s.Books✨ :
Collectively we need him
2026-08-10 10:04:18
58
kathryn2121
Kathryn :
I have all 3 diagnosed, and I have specialists for all 3, but unfortunately it's never made the slightest difference in terms of treatment or symptom improvement.
2026-08-11 10:25:00
8
social_justice_now
JenJen :
TikTok is my doctor at this point.
2026-07-30 04:37:11
632
mollyjanehitstheroad
Molly Jane :
Getting an IV in my hyper mobile veins can make the most confident, best nurse, EMT, Paramedic cry and question their skill.
2026-07-30 19:41:12
226
thepurplemama
vics✿ :
sprinkle Dysautonomia into the mix and we have a winner ✨️
2026-08-13 00:02:36
34
littlechelise
Chelise :
Might as well throw CPTSD and Long Covid.
2026-08-01 01:13:24
26
alexpaxon
AlexPaxon :
I have the.. not as unique addition of (likely) ME/CFS which is regularly written off as “just fatigue” but it is literally a mitochondrial issue. I have yet to find anyone that actually knows that yet and it would make a huge amount of sense if that ALSO tied into everything else.
2026-08-03 19:41:09
7
lilithai
Lilithai 爱 :
why dont they teach doctors this???
2026-08-10 18:11:13
11
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