@kimberlyrhoades112: ✨POTS TALK✨ #chronicillness #potssyndrome #pots #awareness

Kimberly Rhoades
Kimberly Rhoades
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Region: US
Tuesday 13 August 2024 16:07:41 GMT
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fishboyjustin
fishboyjustin :
question can you take a circulation supplement for the pooling?
2024-08-13 19:18:43
5
snburkholder
Shelby Burkholder :
Everyone always said I was faking my leg pain 😭 when I got diagnosed my mom felt sick bad.
2024-08-13 21:35:35
3
mountain_mama_710
Mountain Mama🐔🍃💨 :
thank u for bringing light to all this! people are too quick to judge rather than inquire or educate themselves. ur a peach! much love ❤️
2024-08-13 16:17:18
3
shut_ur_damn_mouth08
shut_ur_damn_mouth08 :
i got diagnosed with POTS just recently and before i got diagnosed i had to go on the Manitou Incline, it took me so long to get to the top and it was horrible 😀
2024-08-13 21:49:24
3
_aphr0dite
Aphrodite (OGCC) :
Thank you for following me you actually made my month Kim. My legs always feel weak and ache
2024-08-13 21:05:36
3
holley483
Memphis Michael :
Chronic Venous Insufficiency (CVI)
2024-08-14 03:14:51
1
mrsstamper071220
Serena Stamper :
I never knew about POTS until til I seen your videos. It’s really important to learn about other people’s disabilities and understanding conditions in life. 🥰
2024-11-03 08:32:49
0
alycemarie677
alycemarie677 :
How did you get diagnosed?
2024-08-23 18:31:14
0
ruby._201
Ruby :
I don’t have POTS, but I enjoy seeing people who do have POTS telling everyone how it feels and what all comes with it! Thank you for sharing your experience!!
2024-08-13 16:15:41
17
ur.hoez.luv.bryce
ur.hoez.luv.bryce :
I love how you openly relate
2024-08-13 16:13:58
12
chrissynicolebooks
Chrissy Nicole 🍉🏳️‍🌈 :
It’s like have heavy weights wrapped around my legs mixed with the feeling of bruises constantly mixed together
2024-08-13 16:26:05
8
helenblaineduhon
Helen Blaine Duhon :
I have Guillain Barre Syndrome & I walk funny due to pain and/or neuropathy (I was paralyzed for a year)sometimes I have to use a walker at 34 & I hate the way ppl stare at me so I feel your pain🫶🏻
2024-08-13 23:03:04
4
amyviece
axcivite :
is it varicose veins?
2024-08-13 19:40:21
2
ladycr0w123
CrowBoutique :
I have EDS and POTS and honestly POTS is probably the most debilitating part of this. I use a wheelchair so I don’t pass out and hit the floor. Get yourself some nice compression socks babe❤️
2024-08-14 17:43:47
1
willywonkasleftpinkytoe
◌ :
i have been diagnosed with POTS for a couple years now (and i have had it for a few years), but i only recently stumbled onto the POTS side of tiktok and i am learning so many things i have experienced that i didnt know were my POTS (ig i was still grieving and hoping itd have gone away after a year, so i never did my own research) i usually just try to power through and take the mind over matter approach, but it always ends up making it feel worse and last longer
2024-08-14 08:08:18
1
savy_scarlet
Savy :
I don't have pots but I have several autoimmune disorders that cause pain and other symptoms and seeing other, especially younger and look "normal", really help me feel less alone
2024-08-14 03:23:30
1
maxsavage666
Max Savage :
why did I show this to my partner and her respond with "you sure that's not your legs?" 🙃 I feel your pain/struggles. I've been using a cane since April and contemplating a walker
2024-08-13 20:35:24
1
jacedakotah
Jacedakotah :
Thank you for spreading awareness ❤️
2024-08-13 20:16:26
1
medicallymadison
Madison Shreve, LCMHCA :
GET IT OFF UR CHEST BABE
2024-08-17 04:19:03
0
jadiewadie98
JadePerks98 :
❤️❤️❤️❤️❤️❤️
2024-08-22 13:53:10
0
alliecatlives
Lexifer :
@That's-So-Raven
2024-08-22 10:13:11
0
hernandez_house
K- Hernandez :
I have been watching you all night on fb. 🤣 but now I’m convinced I have POTS. I’m curious how the pain feels in the legs? And also does it feel like you can’t breathe when you stand?
2024-08-20 09:59:57
0
p0hl1n
T1LY4 :
Help i thik i have pots i have 23 signs
2024-08-18 10:40:56
0
supermonkeyballer
supermonkeyballer :
Ken Carson
2024-08-17 22:30:19
0
raven_and_munson
Tess & Munson 🐶 :
I have these veins too and sometimes my legs hurt as well. Thanks for letting me know I’m not alone! I haven’t been diagnosed with POTS though…🤔
2024-08-23 00:39:49
0
system.of.chaos.and.hope
🌎✨The Collective Kingdom✨🌎 :
No I felt this so hard 😭
2024-08-15 15:19:10
0
fashnme
Cristal Rodriguez :
Thank you for speaking up on Potsies 😭🌷♥️
2024-08-14 12:39:02
0
kangarose8
Mama rose 🌹🇺🇸 :
🥰🥰🥰
2024-08-14 04:05:49
0
emmyemc
🦋 🦋 Emily 🦋 🦋 :
I don’t have pots but I have liver issues. I deal with red spots on my legs when my platelets are low. Lately my legs have HURT really bad. Like the muscles are bruised up and my RLS has been spicy.
2024-08-14 03:39:42
0
holley483
Memphis Michael :
Wear compression socks
2024-08-14 03:15:15
0
natalieann625
Natalie :
I was in the vyvgart trial and when I was getting the infusions my leg pain and blood pooling was 100% gone. I’m so bummed the trial got terminated.
2024-08-14 02:27:51
0
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