dry
@drytski • 25,796 subscribers
streamer, artista e não sou grossa (não tenho intestino grosso)
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9:08
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YODA REAÇOESKKKKKKKKKKKKKKKKKKKKKKKKKKKKKKKKKKKKKKKKKKKKKKKKKKKKKKKKKKKKKKKK lindo isso galera
dry141,923 views • 1 month ago
0:40
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1:56
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MINHA MAE ACHOU A ENTREVISTA Q A GENTE FEZ NA TELEVISAO. isso foi 2 anos atrás, qnd tinhamos recém tido o diagnóstico e eu tinha aberto uma vaquinha (foi essa a minha 1 vaquinha q a gnt acabou nao conseguindo nem 20% da meta, e eu encerrei e consegui ser transferida pro HA)
dry616,401 views • 8 months ago
1:00
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só queria expor isso aq pq já deu né, tava quieta até agr pq pensei que iam parar alguma hr mas não param de encher meu saco. então eu vou contar oq vem acontecendo, e com isso so quero q denunciem em massa pra conta dessa galera cair ( até pq a twitch deles caiu mas voltou)
dry443,792 views • 8 months ago
O MINERVA STALKEANDO MEU TWITTER EM LIVE NUNCA FIQUEI COM TANTA VERGONHA NA VIDA
dry36,848 views • 1 month ago
48:09
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1:36
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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
dry74,307 views • 9 months ago