DISCLAIMER
The information and materials accessed through or made available for use on any of our Sites, including, any information about diseases, conditions, treatments, or medicines, are for informational purposes only. The Content is not intended to be and is not a substitute for professional medical advice, diagnosis, or treatment, and your participation on our Sites does not create a healthcare professional-patient relationship. You should consult a doctor or other qualified health care professional regarding any questions you have about your health or before making any decisions related to your health or wellness. Call your doctor or 911 immediately if you think you may have a medical emergency.compose your message
message sent
email sent successfully
Trusted Resources: News & Events
Latest announcements and gatherings
Readout From the First Lady’s Roundtable on Improving the Lives of Americans Living With Sickle Cell Disease
First Lady Melania Trump and the Health and Human Services Department (HHS) hosted a roundtable on “Improving the Lives of Americans Living With Sickle Cell Disease” in recognition of National Sickle Cell Disease (SCD) Awareness Month. For the first time since 1983, the White House has elevated this important issue with a Presidential Proclamation issued by President Trump on August 31, 2020.
The First Lady opened the roundtable by reaffirming the goal of finding a cure and highlighted the children’s well-being pillar of her Be Best initiative, noting that the effects of SCD often begin in early childhood. Mrs. Trump also pointed out that progress has been made through early identification and new life-saving therapies, but noted that there is still much more to do.
Related Content
-
Community CenterFoundation For Sickle Cell Disease ResearchThe Foundation for Sickle Cell Disease R...
-
videos & visualsMiai & Ama Talk About Sickle Cell Diseasehttps://www.youtube.com/watch?v=7bUFGux-...
-
Community Center@sicklecelldocTwinmom, wife, and pediatric hematologis...
-
people & placesSickle LifeSickle Life is a sickle cell disease adv...
-
news & eventsRare Disease Day Symposium at the Quinnipiac Frank H. Netter MD School of MedicineSince 2015, the Frank H. Netter MD Schoo...
-
people & placesSickle Cell Disease Association of Florida, Inc (SCDAF)The Sickle Cell Disease Association of F...
-
education & researchA Guide to Living With Sickle Cell Disease: Define Yourself, Define Your LifeDefine yourself, define your life. No ma...
send a message
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.
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.