The Know Your Type Program.
The HEAL Program by Raremark Foundation is a health systems initiative focused on improving…
Sickle Cell isn’t a curse. It’s a chronic disease that isn’t getting the coverage it needs. At Raremark Foundation, we get that, and we’re here with one goal: to help you discover more about Sickle Cell disease and build a community of advocates.
We sift through the noise, delivering expert-vetted sickle cell info through a real-life lens. We’re here to support and inspire, so you can take action every day to live your best life. Whether we’re talking pain episodes, breakfast, breathing, or mental health, you can trust that all Raremark Foundation (CHF) content is evidence-based, science-backed, and crafted from real life experiences.
You can also trust us to talk honestly about mental health, sickle cell health, relationships, race, and gender, with empathy and inclusivity at the forefront of everything we do.
The HEAL Program by Raremark Foundation is a health systems initiative focused on improving…
An initiative by Raremark Foundation, this program exists for one reason: to give Warriors living…
The HEAL Program by Raremark Foundation is a health systems initiative focused on improving…
Warriors
received life-changing hip replacement surgeries through the Hope for Warriors Fund.
people
screened for their genotype.
Carriers
identified and counseled.
people
empowered to make informed health & family planning decisions.
112 members
47 members
40 members
Not every day does the SCD community witness a moment like this! Uganda officially commissioned the country’s first Hydroxyurea manufacturing plant at Quality Chemical Industries
The launch of the Africa CDC Continental Plan for Sickle Cell Disease (SCD) and other inherited blood disorders is a historic turning point in the
Join us as we explore the journeys of those living with rare diseases, the challenges they face, and the breakthroughs that bring hope.
Because every story matters. 💙 #SickConversations #RaremarkFoundation
