Ehlers-Danlos Syndrome: Young Kiwi teen's fight to be believed | RNZ
Ehlers-Danlos Syndrome: Young Kiwi teen's fight to be believed | RNZ
RNZ ·
Ehlers-Danlos Syndrome: Young Kiwi teen's fight to be believed | RNZ
RNZ ·
finally some coverage for EDS. my cousin went years without a diagnosis, told she was just dramatic. system's broken for rare conditions.
facts, took my sister 8 years. 8 bloody years of being told she was depressed.
absolute nightmare trying to get doctors to listen when you're young and look fine on the outside. this kid is brave for speaking up.
my mate has this and he dislocates his shoulder putting a t-shirt on. it's wild ppl think it's fake just cos it's rare.
lol cope, some people do fake it for attention. but yeah not everyone obviously
yeah nah get stuffed with the 'it's just anxiety' diagnosis. happens way too often to women and young people.
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get stuffed with that attitude. why would anyone fake this hell.
can't believe it takes a media story for doctors to start taking patients seriously. what a joke of a system.
exactly. when you've seen a kid cry from a simple touch you know it's real. heartbreaking.
had to fight for 6 years to get my daughter diagnosed with something similar. the gaslighting from specialists is real. sending love to this whānau 🤍
reading these comments as a med student and honestly we need way more training on rare diseases. this shouldn't be this hard for patients.
good on you for wanting to do better. that's the kind of doctor we need.
bendy joints and chronic pain is not a personality flaw Janice. maybe listen to patients instead of your ego.