@livchronically: If you have POTS and hEDS and haven’t been able to get to the root cause of it and nothing seems to be working, you might want to get your atlas checked! #potssyndrome #potsawareness #chronicillness #atlas #uppercervical #uppercervicalcare

livchronically
livchronically
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Region: US
Tuesday 20 May 2025 17:38:52 GMT
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fransprat
Frances Spratley :
It’s funny you said this because I get pain at the base of my skull and have mentioned it several times. MRI showed nothing. I have pots
2025-05-20 19:40:19
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christinaiscrafty
Christina is Crafty🆘🇺🇸 :
I had an atlas adjustment once because I kept getting ear pain without infections. It was the loudest adjustment I’ve ever had. My brain echoed. Zero ear issues since.
2025-05-21 06:12:07
232
timeisindifferent
timeisindifferent :
Omg I am able to crack the right side of it does that mean anything
2025-07-31 12:28:28
0
yahushaloveskourtney
Kourtney :
Not me diagnosed with POTS just a few months ago but MANY years ago having a chiropractor telling me that my head literally isn't on straight
2025-05-20 23:53:47
800
youbetchabottomdollar
youbetchabottomdollar :
Is this why I get that strange crinkly sound from the back of my neck? Like someone crinkles up paper right before the sound of something flowing.
2025-05-22 03:14:14
134
realblairhuddy
realblairhuddy :
I just discovered my atlas is off by 5 degrees and my nervous system is SHOT and having dysautonomia symptoms. Just started with a Blair technician yesterday.
2025-05-21 00:23:58
717
pinkbbunnies
e :
Every day I talk about how I can FEEL the weight of my head
2025-06-16 18:36:05
658
beadliciousjewelry
Keychain Bling Bar LA :
And what kind doctor would you see to ask about this ?
2025-05-21 01:05:51
38
nishabhandaru
dr. nish :
This is what I’ve been telling my patients! A lot of them said their other doctors have always looked at them crazy when they said they felt nauseous or dizzy with head movements but no pain.
2025-07-31 02:28:55
0
ciaraheden47
ciarah :
My physical therapist kept telling me I had so so many deep knots in that area too. I've had pots for 10+ years, and have constant pain where my skull connects to my neck. I just say my head is too fat for my body.
2025-05-21 17:42:05
93
lisasandoli
lisasandoli :
Would this show up on a MRI for CCI? Getting an mri because I also have hEDS w pots and mcas
2025-05-20 19:06:24
89
ashbljs
Ash :
Getting my atlas adjusted has helped! But I also encourage people to research stallate ganglion and/or vagus nerve blocks if the adjustments alone don’t work!
2025-05-20 18:46:14
833
minicaseyaussie
Casey-Zoey :
Everyone: stop looking down at your phones so much, purposely look at the sky to stretch your neck, do chin tucks, use something like a neck pillow to relax the muscles and decompress at least 5-10 minutes a day
2025-05-21 18:31:21
543
aubricado
Aubs :
ur telling me that the giant knot that hasnt gone down in a decade is not just a silly little thing I have? the continous popping of my neck???? its at this part of my neck 😭
2025-05-21 19:42:44
820
brand.new.sky
Suki :
THIS likely explains why I began having POTS - violent symptoms- after a car accident. They only improved with time and years of meds. My neck(when misaligned-often in sleep) gives me issues. I also have hEDS
2025-05-21 04:06:46
170
_urdead2me
Lana⛓️🖤 cosmic crybaby :
Would you have pain here? Cause that’s exactly where I have pain and like a knot, hard bump that never goes away
2025-05-21 03:09:14
297
sidequestswpheez
SIDEQUESTSWPHEEZ :
Why is living so hard
2025-06-16 09:52:47
148
brittnderson157
Brittany Anderson :
how can this be effected/ changed by chiari malformation? I have pots and heds and currently waiting to be check for chiari malformation bc my son just got diagnosed with CM
2025-05-22 02:23:49
9
laurelleaflane
LaurelLeafLane :
So my Atlas is split in half. so fun. I've had it carefully adjusted & many of my allergies went away.
2025-05-20 20:58:45
127
bballmom32
Bballmom3 :
I agree!! Been doing NUCCA for 3 years. Be sure to also check for Eagle’s Syndrome that can also block blood flow to jugulars and cause POTS and Dysautonomia. My atlas adjustments were helping drain venous congestion at the base of my skull and also helped with intracranial pressure. Just had right Styloid removed and haven’t needed NUCCA since and Dysautonomia is gone
2025-06-06 21:38:56
1
stef_on_ya
Stef :
How do you find out if it’s the atlas causing everything? A iPad.
2025-07-16 01:05:31
0
mjasfaith
MJa :
I’m being treated by a ln upper cervical chiro yet my immense pain continues in the c1,2,5,6… and trigeminal region. I’m
2025-07-24 04:54:25
0
elladir
Elladir :
pretty sure my Chiro keeps trying to adjust it, but every time I walk out of there 5minutes later it's stuck edgeway again...I was given exercises
2025-07-12 22:15:34
1
ballisticbrunette
𝑫𝒐𝒎𝒊𝒏𝒊𝒒𝒖𝒆✨ :
I think I messed mine up after a serious concussion. Shorty after I developed dysautonomia.
2025-05-20 22:17:58
32
allisonlee.dng
Allison Lee :
Absolutely insane…. 2 years ago i got a concussion accompanied by a telescoping neck injury. I developed pots symptoms once i tried to go back to work and had been SUFFERING since. Like i could not drive in the car for more than 5 minutes without an ice pack tucked in my headband. I got nerve blockers, injectable migraine meds, muscle relaxers, beta blockers, and whatever else you can think of to try and remedy it with no luck. One day I accidentally “clicked” my neck back into place and 99% of EVERYTHING I’ve struggled w vanished. I’m wondering if this is a key to the puzzle 😭
2025-05-21 03:57:58
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