Kruzn for A Kure Foundation
Kruzn For A Kure Foundation | Funding SIOD Research
813843682
2016
MUSCLE SHOALS, AL 35662 USA
kruznforakurefoundation.com
Kruznforakure
KruznforaKure
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Novinky
Today is #NationalNonprofitDay! Celebrate #NationalNonprofitDay with us by helping to spread awareness about our mission! Today we challenge you to reach out to your friends and share your reasons for supporting KFK! ❤️ https://t.co/o2X1pzP4Mj (tw)
DID YOU SEE THIS?? 👀👀👀 ❕SEPT 6TH, LABOR DAY❕ Mark your calendar 📆 and FOLLOW Handy on the H20 on FB and Instagram!!! Details to come! BENEFITING KFK!!! 😍 https://t.co/NmUqknDqjK (tw)
Poslední komentáře
💙 Thank you, Kruzn for A Kure Foundation, for shining a light on SIOD and providing hope to families like the Davenports. Together, we can make a difference! #HopeForSIODdetail |
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🌟 It's inspiring to see such dedication to finding a cure for SIOD! Let's rally together and support this vital research. Kruz and Paizlee are true warriors! 💪 #KruznForACuredetail |
Poslední diskuze
1. What are some innovative fundraising strategies that NGOs like Kruzn for A Kure Foundation can adopt to raise awareness and support for rare diseases like SIOD?Odpovědí: 3, Naposledy před 1 den detail |
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2. How can partnerships with universities and research institutions enhance the effectiveness of organizations focused on funding research for rare genetic diseases such as Schimke Immuno Osseous Dysplasia?Odpovědí: 3, Naposledy před 1 den detail |
V okolí
2
4.5
MUSCLE SHOALS
O společnosti
- 256, E05 -
Finding a cure for Schimke Immuno Osseus Dysplasia SIOD Our Mission Our Purpose Providing a place of hope for SIOD families Meet Our Founders We are the Davenport family. As you can see we have the two of the cutest kids on the planet with the sweetest personalities. Kruz Paizlee rarely meet a stranger but their life is different from others. On June 30th 2016 our son was diagnosed with a rare genetic and incurable disease called Schimke Immuno Osseous Dysplasia SIOD.
Výzkumná ústavy a/nebo analýza veřejné politiky
