Cancelled Podcast
Region: US
Tuesday 29 April 2025 05:17:02 GMT
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stella hahn :
i have elhers danlos it’s so common and it’s so exhausting
2025-04-29 19:11:01
249
meadow🪼 :
i have hyper mobile ehlers danlos syndrome. it’s actually way more common than you would think, the worst kind you can have is the cardiac version but that is extremely rare.-
2025-04-29 19:15:06
8986
Chandler 🤍 looratak 🤍 :
Wait the sitting on the floor thing??? someone explain that one to me. I think I might relate pretty please
2025-07-15 20:33:06
0
arealpaigeturner25 :
how do people not know what ehlers danlos is,??
2025-04-30 05:10:10
19
Charlotte Rose :
Can someone tag me In the compilation video I can’t find it I’ve seen it before
2025-04-29 23:47:22
0
Cass :
i have it too lmao and i’ve never heard of that life expectancy
2025-04-29 23:20:03
9
That one lesbian :
It’s very common in women, a lot of people who have this or POTS saw it appear after Covid
2025-04-29 18:01:01
1140
★ jenna aimee :
It is SO harmful when a public figure is uneducated on rare diseases and decides to use their platform to call one of the most life altering syndromes “mild” when it is in fact debilitating.
2025-04-30 04:17:33
510
Cacia Gooden :
just got diagnosed last year! it's classified as rare only bc its hard to get diagnosed
2025-04-30 06:14:45
3
motherhen_chloe :
I have POTS and apparently it's common to have ehlos dahlos too
2025-04-30 23:51:07
0
Addy 🏳️⚧️ :
Finding out I have this thing from Tana is wild….
2025-04-30 00:45:58
0
Brinlee22 :
I have it 90 percent of people have the hypermobile one life expectancy is very normal
2025-04-29 20:58:31
0
𝔅𝔲𝔯𝔫𝔢𝔯𝔟𝔯𝔦𝔱𝔱 🕷️ :
Please don’t say that the hyper mobile version of EDS is the mild version. I have it and it is not mild at all. I suffer so much and you saying that just diminishes what me and others like me have to
2025-04-29 23:44:38
70
kayla carnelli :
my best friend has it, she’s 19 and has been diagnosed with it for many years now
2025-04-30 03:58:18
0
mariah carey💅🏽😘😤 :
It’s genetic so you have to be diagnosed by a geneticist it’s not actually that common because of it being genetic but
2025-04-30 17:28:15
2
mari :
my sister has vascular ehlers-danlos which is a fatal type. it’s nice to have awareness made of the illness as a whole, and i appreciate brooke for doing research but making it a bit is uncomfortable-
2025-04-30 22:35:27
1
cece 🦢 :
lowkey this is similar to how emma chamberlain got diagnosed with pcos in the middle of a hair salon
2025-04-29 17:02:30
17678
SabOlive :
i have hEDS, you’re chilling girl
2025-04-30 04:28:45
9
mark.questionn :
I saw a video of a girl saying she thought Tana had this! Years ago
2025-04-29 18:30:30
2
Meags :
The amount of people not understanding that something can be debilitating but still be medically “mild”. That does not take away from your struggles. It’s just a medical definition of a scale on how
2025-05-01 20:37:26
1
Brittany Rose :
I have it. Don’t go get diagnosed. Doctors don’t do anything about it anyways. Nothing makes you feel better. Docs still gaslight you. And it just makes it more difficult to get life insurance.
2025-04-30 11:08:01
1
Karson :
Hi Tana! I have Hyper mobile Ehler Danlos! You can go get tested for it, it’s a physical test! Everyone has different issues. I literally dislocated randomly (once in my sleep, worst one yet)..
2025-04-30 01:29:15
0
Alyson Lowman :
I have this! It’s genetic!
2025-04-30 02:36:24
6
Jaclyn Paige :
Eds has different subtypes, but not all of them can be found w genetic tests. My drs have pretty much told me that it’s not worth going for a diagnosis because there really isn’t treatment besides PT
2025-04-29 20:43:02
0
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