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
2022 Annual Advocacy Day Event – SCDAA
Sickle Cell Disease Association of America, Inc. will host its 2022 Annual Advocacy Day event virtually on April 5, 2022. Join us and learn how to #BeASickleCellAdvocate!
Advocacy Day is an opportunity for patients and caregivers affected by sickle cell disease to learn how to advocate for issues that are important to them. Participants will learn about the key legislative issues that are important to individuals living with SCD and their families, including promoting stable funding for research, better healthcare access and increased education and awareness for the sickle cell community throughout the country.
We invite individuals representing our 53 member organizations and affiliates from 29 states to participate in this virtual advocacy training and raise awareness of sickle cell disease.
This event has ended.
Related Content
-
people & placesBrenda Martin, CPNP-PCBrenda Martin is a pediatric nurse pract...
-
people & placesLeroy Hughes, JrLeroy Hughes, Jr. joined Public Justice ...
-
videos & visualsSickle Cell – Wanda Whitten Shurneyhttps://www.youtube.com/watch?v=vgZ6QmA4...
-
people & placesSickle Cell Association of Hillsborough CountyThe Sickle Cell Association of Hillsboro...
-
people & placesBridges Pointe Sickle Cell FoundationThe Bridges Pointe Sickle Cell Foundatio...
-
news & eventsKNOWvember Webinar: A grandparent’s voice – Advocacy and support for chronic pain familiesWhile parents are often the prim...
-
education & researchAddressing Sickle Cell Disease: A Strategic Plan and Blueprint for ActionThis consensus study report was commissi...
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.