About Us
Fight Like Skye is an organization created to help bring awareness to the Sickle Cell Disease.
We are honoring Autumn Skye, a 14-year-old girl who is fighting the disease every day. Our mission is to educate people about Sickle Cell Disease and to provide support to those affected by it. We believe that with awareness and support, we can make a difference in the lives of those living with Sickle Cell Disease.
​
Our organization is committed to providing reliable information and resources to help individuals and their families manage the physical, emotional, and social challenges that come with Sickle Cell Disease.
We offer educational materials, support groups, advocacy efforts, and community events to bring people together, share experiences, and create a sense of belonging.
​
We recognize that raising awareness is only part of the solution. Fight Like Skye also actively supports scientific research and medical advancements to improve the lives of those with Sickle Cell Disease.
We collaborate with medical professionals, researchers, and other organizations to promote funding and further research towards finding a cure.
​
Join us in our fight against Sickle Cell Disease.
Together, we can provide hope, increase awareness, and ultimately make a positive impact on the lives of individuals and families affected by this condition.
​
Fight Like Skye is here to fight alongside you, raising our voices, and advancing our cause until Sickle Cell Disease is conquered.
About Autumn Skye
Autumn Skye Collins is a 14 year-old native of Nashville, Tennessee.
Autumn was born on December 3, 2010 to parents Briana Cooper and Alonzo Collins.
Autumn enjoys singing, dancing, creating YouTube videos and playing with her dogs, "Little T" and "Lola" (Rest In Peace).
​
On the day Autumn was born, the doctors brought news that no one could’ve ever have imagined. Her parents were told that their then, only child has a blood disease. Autumn Skye was diagnosed with Sickle Cell Anemia SS.
Neither parent knew much about the disease but both parents were carrying a Sickle Cell trait with no complications their entire lives.
​
Her mother took immediate action.Researching. Asking Questions. Trying to find a way to cure her daughter, Autumn Skye.
​
In March of 2016, Autumn Skye’s mother decided to start a foundation honoring not only her daughter but in an effort to honor everyone affected by this blood disease and to bring awareness to people all over the world!
Autumn Skye knows she is a “Special” child.
​
Her doctor’s visits are 3 times more frequent than a healthy 14 year-old and over night stays are quite the norm.
As of the Summer of 2025, Autumn Skye has received 4 blood transfusions to help her live and play with little to no restrictions!
Click Below To Hear Autumn's Story
