Google
Trusted Resources: News & Events
Latest announcements and gatherings
Artist Panteha Abareshi Opens Up About Sickle Cell Disease and Expressing Her Pain Through Art in “The Girl Who Loves Roses”
When you suffer from a chronic condition, whether it be mental or physical — every day can start to feel like a battle. The non-stop pain becomes a part of you, of the way you move through life and express yourself to the world and to others. And it can get exhausting — both physically and emotionally — to say the very least. No one understands this better than Panteha Abareshi, a 17-year-old artist from Arizona who was born with Sickle Cell Beta Zero Thalassemia, a genetic condition that causes her chronic pain and severely limits her physical activity. Imagine not being able to go on long walks on the beach, workout after a stressful day, or enter to run in a marathon. These are all things we often take for granted, but this is Panteha’s reality.
+myBinderRelated Content
-
Fighting Through Our Pain TV With Thomas J. Harrington MDhttps://www.youtube.com/watch?time_conti...
-
Social-Environmental Factors and Cognitive and Behavioral Functioning in Pediatric Sickle Cell DiseaseSickle cell disease (SCD), an inherited ...
-
Transition: Taking Charge of Your Health and Health CareTransition is the process of young peopl...
-
Sickle cell and pregnancy (what you should know)https://www.youtube.com/watch?v=Jyc90LgB...
-
Today’s Faces of Sickle Cell Disease: Deidra Flowers-WilliamsAt six months of age, Deidra Flowers-Wil...
-
Dora Clayton-Jones, RN, PhD, CPNP-PCDr. Dora Clayton-Jones is an Assistant P...
-
Magical Monday Motivation: Sickle Cell Warrior # 17Living with Sickle Cell disease requires...
To improve your experience on this site, we use cookies. This includes cookies essential for the basic functioning of our website, cookies for analytics purposes, and cookies enabling us to personalize site content. By clicking on 'Accept' or any content on this site, you agree that cookies can be placed. You may adjust your browser's cookie settings to suit your preferences. More Information
The cookie settings on this website are set to "allow cookies" to give you the best browsing experience possible. If you continue to use this website without changing your cookie settings or you click "Accept" below then you are consenting to this.
Powered by
Support for this site is provided by
This platform is made possible through a partnership with the Sickle Cell Disease Association of America, Inc. (SCDAA) and its member organizations. SCDAA's mission is to advocate for people affected by sickle cell conditions and empower community-based organizations to maximize quality of life and raise public consciousness while advancing the search for a universal cure.