SCDAA Nevada Chapter
HeLp Us Support Our Rare Disease Community During COVID-19
The SCD and Rare Disease Communities are some of our most vulnerable to COVID19, your generous support will help us provide the essentials that these patients and families may not be able to get out to retrieve due to the increased risk this virus poses to their already compromised health. Thank You for your Support!
COVID19 Relief for Rare Families
#MakeSickleCellPopular
Sickle Cell Awareness Month
This month, find a Sickle Cell Organization like Dreamsickle Kids and donate, volunteer, wear burgundy or register to donate bone marrow via Be The Match or blood via Red Cross. These actions help children and adults affected by SCD throughout the US.
.jpg/:/rs=h:650,cg:true,m)
COVID-19 Focus Group
COVID-19 Focus Group
Virtual COVID19 Focus Group
A virtual talk to discuss COVID19 and the affects and understanding of this pandemic on the African-American community of Las Vegas
About DreamsiCkle Kids Foundation
Misson
What is Sickle Cell?
Misson
Our mission is to #MakeSickleCellPopular by increasing awareness, educating ,and advocating for long term changes for the SCD population of Nevada to improve Equity and access to care for those affected by SCD and other Rare Diseases while also addressing health disparities.
Vision
What is Sickle Cell?
Misson
To be a community leader in advocating for those affected by Sickle Cell. Our vision will be achieved by bringing communities together through social events that provide support, education, resources and awareness for Sickle Cell Disease.
What is Sickle Cell?
What is Sickle Cell?
What is Sickle Cell?
SCD is a group of inherited red blood cell disorders. Healthy red blood cells are round, and they move through small blood vessels to carry oxygen to all parts of the body. In someone who has SCD, the red blood cells become hard and sticky and look like a C-shaped farm tool called a “sickle”. The sickle cells die early, which causes a con
SCD is a group of inherited red blood cell disorders. Healthy red blood cells are round, and they move through small blood vessels to carry oxygen to all parts of the body. In someone who has SCD, the red blood cells become hard and sticky and look like a C-shaped farm tool called a “sickle”. The sickle cells die early, which causes a constant shortage of red blood cells. Also, when they travel through small blood vessels, they get stuck and clog the blood flow. This can cause pain and other serious problems such infection, acute chest syndrome and stroke.
It is estimated that:
- SCD affects approximately 100,000 Americans.
- SCD occurs among about 1 out of every 365 Black or African-American births.
- SCD occurs among about 1 out of every 16,300 Hispanic-American births.
- About 1 in 13 Black or African-American babies is born with sickle cell trait (SCT).
Dreamsickle Kids Foundation, Inc. Board Members
Executive Director
Executive Director
Executive Director
Georgene' " Gina" Glass
(Las Vegas, Nevada)
Sickle Cell Advocate & Aspiring Author
Mother to child with Sickle Cell. Georgene' founded Dreamsickle in 2018 to support children and families with Sickle Cell Disease in Nevada.
Originator of the #MakeSickleCellPopular movement.
President
Executive Director
Executive Director
Jennifer Riddle
(Las Vegas, Nevada)
Owner, NV'D Beauty
Account Manager, Barclaycard
Secretary
Executive Director
Secretary
Destiny Morris, Michigan City, In
Director
Director of Public Relations
Director of Public Relations
Jasmine Grafton
(Illinois)
Treetop Products, Inc.,
Certified Holistic Nutritionist
Cosmetologist
Director of Public Relations
Director of Public Relations
Director of Public Relations
Nykolette Boyd
(Los Angeles, California)
Transaction & Marketing Coordinator, Grand B Realty
Owner/Operator, Donnisha FX
Donate Now
Your generous donation will help Dreamsickle Kids Foundation continue to #MAKESICKLECELLPOPULAR and help provide access to resources for children and families affected by Sickle Cell Diseas and all Rare Diseses in Nevada.