Cancelled Podcast
Region: US
Tuesday 29 April 2025 05:17:02 GMT
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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
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Brinlee22 :
I have it 90 percent of people have the hypermobile one life expectancy is very normal
2025-04-29 20:58:31
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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
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Frankie :
EDS is more common in women because testosterone helps the development of cartalidge and other connective tissues so symptoms aren’t as notable.
2025-04-29 17:43:29
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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
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des :
the reason why they don't diagnosis it as much as they should is because everyone has some of the symptoms but the difference is that people with eds is we have multiple symptoms but more people have+
2025-04-29 20:20:15
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Kaytlynn Briann :
I think I have it but I don’t know what to do to find out
2025-04-30 14:49:18
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★ 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
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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
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maggie :
girl go see a rheumatologist 😭 it’s not scary you’ll probably just get a prescription for physical therapy
2025-04-29 18:04:48
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Emily Foxx :
my sister was CONVINCED I had marfan syndrome i have like almost all the symptoms
2025-06-12 09:02:51
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Kadee Kopinski :
I feel like drs just give eds diagnosis when they don’t want to figure out what’s actually wrong cuz how do like 40% of women have it then?
2025-04-30 03:37:35
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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
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Alyssa :
Brooke trying real hard being careful to not get cancelled is killing me 🤣🤣
2025-04-29 22:26:07
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Kekeponyo :
I have Ehlers Danlos Syndrome. Everything is a mindset and you just have to keep pushing and be strong. It’s an autoimmune disease so that means it’s incurable and just gets worse w age. I hope u can
2025-04-30 22:16:19
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Bees :
I’m so glad that Tana is looking into this.🖤
2025-06-16 15:53:17
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highimkimberr :
They absolutely diagnose it but most doctors don’t believe you and it has to do with faulty collagen. Also, Tana, you would have very stretchy joints that are easily dislocated. I don’t think you have the vascular form of it, which is very dangerous.
2025-04-30 04:29:02
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Ashlynn :
Omg i have that toooo it sucks i can’t work fast at all and there is no real disability support system
2025-06-22 00:17:02
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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
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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
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catahfqko2m :
Her experience sounds like POTS for sure. However, there are many causes for pain (& secondary POTS) that should be ruled out long before EDS. Even hEDS can be severe and require life altering changes
2025-04-30 15:31:31
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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
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natalia :
i wish tana would’ve googled it before talking abt it again 💀
2025-04-29 23:15:41
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Alyson Lowman :
I have this! It’s genetic!
2025-04-30 02:36:24
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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
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