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
Sickle Cell Matters Virtual Walk 2021
The Sickle Cell Disease Matters Walk 2021 will engage the community and increase awareness about sickle cell disease, the need for better treatment throughout a patient’s lifetime and ultimately find a cure.
The Sickle Cell Disease Association of America Michigan Chapter is celebrating 50 years of service to individuals living with sickle cell disease and their families.
Unfortunately, due to the current COVID pandemic conditions we have made the difficult but necessary decision to make the walk completely virtual.
Date:
September 1, 2021 to September 30, 2021
Related Content
-
people & placesTonymay FoundationTonymay foundation is a non-profit organ...
-
people & placesSickle Cell Foundation of AlbertaThe Sickle Cell Foundation of Alberta (S...
-
Community CenterQ & A With Andre Marcel HarrisQ: When were you diagnosed with sickle c...
-
videos & visualsSickle Cell Disease: Taking Charge of Your Health Part 1 – Real-World Patient Perspectiveshttps://www.facebook.com/watch/?v=343267...
-
Community CenterSick CellsElevating the voices of the sickle cell ...
-
people & placesAndrea M. WilliamsAndrea Williams founded and leads the Ch...
-
videos & visualsOur Sickle Life Season 03 Episode 04 – Hear Our Storieshttps://www.youtube.com/watch?v=2uD-Y0t-...
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.