The @MartinCenter CEO says #sicklecelldisease advocacy is a social justice and a clinical fight. “We found that this disease was killing people ... But society said, ‘Who cares? They're Black people, we don't care.’" https://t.co/kS2izAcwQM via @Farah_Yousrym
It’s official: SCDAA’s 2022 Advocacy Day will be held virtually on April 5! Join us to learn how you can stand up for sickle cell and make a difference: https://t.co/5txxi9Iacl #BeASickleCellAdvocate
Love your dedication to our young warriors and your concern for all SCD warriors throughout their lifespans. We are so happy to have you on our side, Dr. Jacob!
“I want my patients to be able to live their best lives. Because diseases like sickle cell disease should not define or limit our children. They deserve better, and I know my mission is to help make that happen.” – Dr. Seethal Jacob #IWD2022#WomenInMedicine
Kids ages 7-16 with #sicklecell disease - and their siblings - can climb to new heights this summer at @indiana_htc's Camp Silver Moon! We're now accepting registrations at https://t.co/1X5CWm0YWu for campers to join us June 19-24.
We are expanding our #sicklecell team @RileyChildrens!
If you are an RN, who wants to work with a passionate, collaborative, and fun team while caring for an amazing population of kids, please check out the link below!
#NurseTwitter#Pediatrics#PHODocs
https://t.co/gVRZWoSeAJ
Kids across Indiana are looking forward to summer camp at Camp Silver Moon! Register your child for an unforgettable week at IHTC's outdoor adventure camp, June 19-24! Kids ages 7-16 with sickle cell disease and their siblings are invited. Register at https://t.co/1X5CWm0YWu
Dr. Charles F. Whitten is Black History. Founder and President Emeritus of the @SCDAAorg. Today on his posthumous 100th birthday, we remember and cherish his legacy, dedication, commitment to SCDAA and to those living with Sickle Cell disease. Dr. Whitten is Black Excellence.
The @RedCross is experiencing a drastic blood donation shortage. Blood donors who are Black play a critical role in helping people with sickle cell disease. It is essential that the blood they receive be the most compatible match possible.
Donate today, https://t.co/GzbT2PEOHk
Amazing to see so many #sicklecell centers/providers coming together to improve #access and quality of care for patients with SCD across the lifespan!
Excited to be a part of this alliance and looking forward to what may come.