Cooley's Anemia Foundation, Inc.

/ New York /

Cooley’s Anemia Foundation

Cooley's Anemia Foundation is a US nonprofit dedicated to serving people with all forms of the genetic blood disorder #thalassemia. Cooley’s Anemia Foundation is a U.S. non-profit serving people with various forms of thalassemia. The mission of Cooley’s Anemia Foundation is to increase life expectancy and enhance the quality of life for those impacted by thalassemia, a class of genetic blood disorders, most of which require regular blood transfusions and aggressive management of chronic iron overload, the predominant cause of early death. We do so by funding medical research to advance treatment and curative approaches, by supporting and advising patients and their families and advocating on their behalf, and by educating medical professionals and the general public. Every day, we strive for longer and healthier lives for all patients with thalassemia until a universal cure is found.
111971539
IČO
1954
Založeno
New York, NY 10001 USA
Adresa
thalassemia.org
Web
cooleysanemia
Twitter (1622)
CooleysAnemiaFoundation
Facebook (6100)
2205264
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Poslední komentáře

❤️ Proud to support the Cooley's Anemia Foundation! Their commitment to enhancing the lives of those affected by thalassemia is truly inspiring. Let's work together for a cure! #ThalassemiaAwareness
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Just signed up for the 14th Annual Care Walk! Excited to contribute to a cause that really makes a difference in the lives of patients and their families. 🥳🌟 #WalkForACure #CooleysAnemiaFoundation
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Poslední diskuze

- How can we further raise awareness about thalassemia and its impact on patients' lives within local communities?
Odpovědí: 3, Naposledy před 1 den detail
- What innovative funding strategies could the Cooley's Anemia Foundation implement to enhance its support programs for patients and their families?
Odpovědí: 3, Naposledy před 1 den detail

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- 212, G80, E61, H01 -

Milestones Miracles Medical Grants Fellowships What is Thalassemia. Downloadable Brochures on Thalassemia How Can I Support CAF. Event Registration CAFs 14th Annual Care Walk FDA Approves Gene Therapy for Beta Thalassemia CAFs Social Media Patient Registration 70 Years of Leading the Fight Against Thalassemia Donate NowPatient Registration Advancing Care Inspiring Hope Empowering Patients CAFs Story We Are All Connected by Blood Newsletter Signup Popup Configuration Delay Timer The popup is set to appear 5 seconds after this page has loaded. Cookie Expiration The popups cookie is set to expire after 5 days.

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