Google
Trusted Resources: News & Events
Latest announcements and gatherings
WNY Girl Gets First Pediatric Bone Marrow Transplant for Sickle Cell in Buffalo
Kayla Rushing is the first pediatric patient to receive a bone marrow transplant for Sickle Cell Disease in the City of Buffalo.
The procedure took place through a partnership with Roswell Park and Oishei Children’s Hospital.
Dr. Steven Ambrusko is the Director of Sickle Cell and Hemoglobinopathy services program. He says this procedure is the first step toward a larger initiative to ensure children with Sickle Cell Disease in Buffalo get the care they need.
+myBinderRelated Content
-
Gene Therapy: What You Need to Know (Warrior FAQs)Two gene therapies were recently approve...
-
5th Annual World Sickle Cell Day 24-Hour Sickle Cell-a-ThonCayenne Wellness Center and Children's F...
-
Cure Sickle Cell FoundationCure Sickle Cell Foundation, Inc. is a 5...
-
Blood Transfusions: What You Need to Know and Do (Part 2: Blood Matching)https://www.youtube.com/watch?v=bs4bRApy...
-
Sickle Cell Disease: Why Is It Hard to Talk About Our Pain?https://www.youtube.com/watch?v=63pgiclv...
-
Rae BlaylarkRae Blaylark is a passionate and genuine...
-
Hemoglobinopathy Counselor Training Course – VIRTUALUPDATE! 2020 Hemoglobinopathy Counselor ...
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.