Google
Trusted Resources: News & Events
Latest announcements and gatherings
Dr. Doris Wethers, 91, on Front Lines against Sickle Cell, Dies
Dr. Doris L. Wethers, who broke racial barriers in the medical world before gaining renown for research and advocacy that helped lead to mandatory testing of all newborns for sickle cell anemia, died on Jan. 28 in Yonkers. She was 91.
The cause was complications of a stroke, her daughter-in-law Lisa Booker said.
In 1965, Dr. Wethers became the first black chief of a medical department at a New York City voluntary, or private nonprofit, hospital when she was named director of pediatrics at Knickerbocker Hospital in West Harlem.
Knickerbocker, which had a history of refusing to admit black patients, was renamed Arthur C. Logan Memorial Hospital before it closed in 1979.
+myBinderRelated Content
-
Thalassaemia and Sickle Cell Society of AustraliaThalassaemia and Sickle Cell Australia (...
-
Contrary to expectations: seasonal variation in sickle cell crisis – a nation wide data analysisBackground: Sickle cell crisis is a pain...
-
Altered Functional Connectivity in Sickle Cell Disease Exists at Rest and During Acute Pain ChallengeOBJECTIVES: Sickle cell disease (SCD) is...
-
Sickle Cell Disease Association of America Michigan Chapter, Inc.The vision of Sickle Cell Disease Associ...
-
Today’s Faces of Sickle Cell Disease: Linda Thomas WadeLinda Thomas is a health care educator, ...
-
Velvet Brown-WattsVelvet L. Brown-Watts, is the Founder-...
-
New Hope for Our Youth: 2021 Indiana Sickle Cell Conference – Virtual EditionFriday, April 23, 2021 8:30am – 12:30...
To improve your experience on this site, we use cookies. This includes cookies essential for the basic functioning of our website, cookies for analytics purposes, and cookies enabling us to personalize site content. By clicking on 'Accept' or any content on this site, you agree that cookies can be placed. You may adjust your browser's cookie settings to suit your preferences. More Information
The cookie settings on this website are set to "allow cookies" to give you the best browsing experience possible. If you continue to use this website without changing your cookie settings or you click "Accept" below then you are consenting to this.
Powered by
Support for this site is provided by
This platform is made possible through a partnership with the Sickle Cell Disease Association of America, Inc. (SCDAA) and its member organizations. SCDAA's mission is to advocate for people affected by sickle cell conditions and empower community-based organizations to maximize quality of life and raise public consciousness while advancing the search for a universal cure.