Sickle Cell Disease
Co-Pay Relief Program Fund Notices
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Approved and Donation Ready
This fund has been developed in response to patients who have contacted PAF for help with their medication expenses and could not find help. While this fund has been fully designed and we are ready to provide needed support to these patient communities, this fund is not yet able to accept applications for assistance as we are still working to secure charitable donations that will allow us to open it.
If you, or someone you know, would like to contribute to this fund, please visit our Donors page for more information on how to provide critical support for patients in need.Fund Type
Co-Pay, Co-insurance & Deductible (medications and office visits), Medical Insurance PremiumsMaximum Award Level
$10,000 Per Year
- Household Income Requirements 400% or less of Federal Poverty Guideline (FPG) (adjusted for Cost of Living Index (COLI) and number in household)
- Insurance Requirements All Insurance Types
- Must reside and receive treatment in the United States.
About Sickle Cell Disease
Sickle cell disease is a group of inherited disorders that affect red blood cells. People with sickle cell disease have red blood cells that contain mostly hemoglobin*S, an abnormal type of hemoglobin. These atypical red blood cells become rigid and sticky and are shaped like sickles or crescent moons. Early cell death causes a shortage of healthy red blood cells impairing the body’s ability to deliver oxygen to the tissues. Periodic episodes called crises, are caused by the blockage of blood flow, resulting in pain. There are five types of sickle cell disease – In HbSS, the patient inherits two sickle cell genes (“S”), one from each parent, is commonly referred to as sickle cell anemia, this is the most severe form of the disease. Other types include Hemoglobin SC disease, Hemoglobin SB+ thalassemia, Hemoglobin SB-zero thalassemia, Hemoglobin SD, hemoglobin SE and Hemoglobin SO. Symptoms usually begin in early childhood, and people with sickle cell disease have ancestors that came from sub-Saharan Africa, Mediterranean countries, Saudi Arabia, India or from Spanish-speaking regions in the Western Hemisphere. Sickle Cell Disease is also called HbS disease, Hemoglobin S Disease, SCD, Sickle cell disorders, Sickle cell anemia, SS disease and Sickling disorder due to hemoglobin S.