Hamilton student Kate Pudney hopes sharing her story will do more than raise awareness of the rare conditions that have reshaped her life. The 24-year-old is l…
NZ Herald ·
Finally someone talking about this. My cousin has hEDS and it took years to get diagnosed. The healthcare system is so behind on rare conditions.
100% this. My sister had the same runaround. It's a joke.
what a load of shit, another sob story for likes. mate we all got problems.
just loves to troll. Don't feed it.
These invisible illnesses are no joke. People think if you look fine you're fine. Nah, she's been through hell by the sounds of it.
Exactly. I hate that 'you don't look sick' nonsense. Like sorry I'm not dying on cue for your approval.
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Bloody hell, 24 and dealing with all that. Fair play to her for speaking up. Most people wouldn't have the guts.
Yeah nah get stuffed with that attitude @Cameron. People like you are why others suffer in silence.
Morning coffee and reading this makes me grateful for my health. Hope she gets some proper support from ACC or whoever.
ACC are a nightmare for chronic conditions. Hope she has better luck than most.
My doctor told me I was just 'anxious' for years before someone finally listened. The gaslighting is real.
oh here we go, everyone's an expert now. just sayin maybe the media should cover real news instead of this victim stuff.
lol cope harder mate. you're the one crying about 'victim stuff'.
Cameron you tool, it's called empathy. Try it sometime.
whatever man, i'm entitled to my opinion. it's a free country.
ffs can't people just have a bit of compassion? this country's gone to the dogs.
