RISE To Defeat Sickle Cell Disease

Research, Intervention, Support, Education


Americans affected with SCD

1 in 13

African American babies born with SCT


Carry gene responsible for SCD worldwide

$1.1B +

Annual cost for medical care in US


Health care cost in US/ average patient with SCD reaching 45

about hina

Our family has experienced firsthand the difficulties and struggles that are associated by raising a child with Sickle Cell Anemia. Hina Patel Foundation is in memory of our courageous daughter who battled Sickle Cell Anemia for 17 years followed by the complications from a bone marrow transplant for two additional years. In spite of her struggles, her perseverance for an education, a positive attitude, and a jovial personality prevailed.


There are no upcoming events at this time.


Hina Patel Foundation
P.O. Box 21443
Bakersfield, CA 93390-1443

Non Profit 501(c)(3) Tax ID: 27-3672018

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Hina Patel Foundation for Sickle Cell Disease

Sickle Cell Trait Toolkit | NCBDDD | CDC

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