Our Mission
The Ree Wynn Foundation provides education and promotes awareness of the rare blood disorder TTP to reduce the mortality rate and enhance the quality of life of those living with the disorder.
Upcoming Events
A TTP diagnosis often surprises and confuses those who are diagnosed. Because the disorder is so rare, patients and their families often feel isolated. The TTP support group brings patients and their families together to share their experiences and provide support to one another to reduce feelings of hopelessness and isolation.
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