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: Community Center
Online groups, photo galleries and blogs
Sickle Cell Community Health Network
Sickle Cell Community Health Network is a 501(c)3 non-profit corporation dedicated to serving people and families affected by Sickle Cell Disease. Sickle Cell Community Health Network (SCN) helps individuals and families become actively involved in the health and wellness of themselves and their loved ones who are affected by the disease through community outreach, education, youth and family-oriented programs. SCN is a primary resource for the Sickle Cell community for information and referral, support, and community building activities.
+myBinderRelated Content
-
news & eventsNational Sickle Cell Awareness MonthSeptember is National Sickle Cell Awaren...
-
people & placesSonja L. Banks, MPA, MBASonja L. Banks is the Chief Executive Of...
-
news & eventsRepresentative Johnson Files Four Sickle Cell Disease Related BillsState Representative Jarvis Johnson (HD ...
-
people & placesGreater Boston Sickle Cell Disease AssocationThe Greater Boston Sickle Cell Disease A...
-
news & eventsCayenne Wellness Center’s Support Group ProgramsWe organize programs through which clien...
-
news & eventsHealthcare advocates aim to better inform community on sickle cell realitiesOne in 2,400 are born with sickle cell d...
-
news & eventsQ&A With Regina Hartfield, New CEO of the SCDAARegina Hartfield is set to become the pr...
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.