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dry

@drytski24,330 subscribers

não sou grossa (não tenho intestino grosso) e faço lives https://t.co/Ackssr53hd

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Oi gente eu sou a dry e em janeiro desse ano eu e meu pai fomos pros EUA buscar tratamento pra nossa condição rara e genética (PAF) a gnt foi sem bater a meta da vaquinha e ainda falta 67 mil pra pagar (pq sao 2 pacientes) e a mayo ta cobrando entao abri uma meta+

Oi gente eu sou a dry e em janeiro desse ano eu e meu pai fomos pros EUA buscar tratamento pra nossa condição rara e genética (PAF) a gnt foi sem bater a meta da vaquinha e ainda falta 67 mil pra pagar (pq sao 2 pacientes) e a mayo ta cobrando entao abri uma meta+

670,428 views

sinceramente, já desisti. Tenho 23 anos e NUNCA beijei. Assinei o Tinder Premium por 40 reais e não dei um match. Sinto que fracassei como mulher, os homens têm medo de mim. Minha família pergunta pq eu não namoro, e eu tenho que dar aquele sorriso dizer que é pq eu não quero

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sinceramente, já desisti. Tenho 23 anos e NUNCA beijei. Assinei o Tinder Premium por 40 reais e não dei um match. Sinto que fracassei como mulher, os homens têm medo de mim. Minha família pergunta pq eu não namoro, e eu tenho que dar aquele sorriso dizer que é pq eu não quero

37,011 views

Videos

PRECISO DA AJUDA DE VOCÊS PRA VIVER!
9:08

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PRECISO DA AJUDA DE VOCÊS PRA VIVER!

dry

4,793,723 views • 6 months ago

EU SÓ QUERO VIVER! me ajudem por favor
1:56

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EU SÓ QUERO VIVER! me ajudem por favor

dry

814,722 views • 4 months ago

minha última chance
48:09

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minha última chance

dry

182,751 views • 9 months ago

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Hey, I'm Dryka Brenda, and I'm facing a difficult battle against a rare genetic disease called Familial Adenomatous Polyposis (FAP). It's caused by a mutation in the APC gene, which my father and I both have, and it causes the growth of many polyps throughout the digestive system. FAP doesn't just affect the large intestine; it can also affect the stomach, duodenum, small intestine, and even other organs like the thyroid, liver, pancreas, adrenal glands, bones, and skin. It's a silent disease that spreads internally and, if left untreated, almost inevitably leads to cancer. We only discovered this mutation in 2023 when my father was diagnosed with two tumors in his intestine, one in the rectum and the other in the colon (synchronous tumors). After that, he and I underwent surgeries to remove our large intestines, but unfortunately, this disease is progressive and is now affecting our stomach and duodenum. This mutation has already caused a lot of pain in our family. My grandmother passed away from stomach cancer, my brother from leukemia, and now my father and I are in this fight. But there is hope: an experimental treatment and specialized follow-up at the Mayo Clinic in the United States (a world reference in rare and genetic diseases). Both my father and I will be treated there, and my mother will go along as our caregiver. We have already created a crowdfunding campaign to raise the necessary funds, but it is not enough, and we need to raise this amount by January 22nd, otherwise we will not be able to undergo the treatment. The Token fees will help me pay all the costs: passports, visas, tickets, food, accommodation, medical translations and unexpected costs that arise, and mainly, the treatment It's difficult to ask for help, but we are clinging to the chance to live with quality of life and the chance to control this disease. PAF requires continuous monitoring, and this could be a turning point in our treatment. Any amount is already a seed of hope. And if you can't donate or buy my token, sharing already helps a lot <3

dry

73,880 views • 5 months ago

A DOENÇA Q EU TENHO PRECISA DE VISIBILIDADE!!!
1:36

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e se fosse com vc?

dry

129,133 views • 1 year ago

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PRECISO DA AJUDA DE VCS!!!

dry

63,798 views • 1 year ago

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