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    360° SCD Hub
    360° SCD Hub
    • Home
      • Welcome & Overview
      • Top 10 Reasons to Sign Up for Free on the 360 SCD Hub App
    • Courses
      • Living with SCD
      • Medical Community
      • General Community
    • News
      • News
      • Calendar
      • 360° SCD Hub TV
      • Virtual Resource Library
    • KidZONE
      • Flashcards for Kids
      • 6 Point Body Map Challenge
      • How to Be an SCD Superhero for your Friends
      • Common Disorders with SCD Flashcards

    Category: Real Stories from the CDC

    Real Stories from People Living with Sickle Cell Disease: Tasha

    Tasha’s Story Tasha Hines is 39 years old, married, and a registered nurse at an internal medicine outpatient clinic. She also has sickle cell disease.…

    sickle-cell-foundation-of-arizona
    SCFA_Coach September 25, 2023
    0 Comments

    Real Stories from People Living with Sickle Cell Disease: Tristan

    Tristan’s Story I was diagnosed with sickle cell disease at 6 months of age in my hometown of Williamsport, Pennsylvania. At that time, I was…

    sickle-cell-foundation-of-arizona
    SCFA_Coach September 25, 2023
    0 Comments

    Real Stories from People Living with Sickle Cell Disease: Alissia Cofer

    Alissia Cofer’s Story Alissia Cofer is a former camp director at Camp Cell-A-Bration, a free, week-long camp in Burton, TX, for children aged 6–14 with sickle…

    sickle-cell-foundation-of-arizona
    SCFA_Coach September 25, 2023
    0 Comments

    Real Stories from People Living with Sickle Cell Disease: Blaze Eppinger

    Blaze Eppinger & Camp New Hope Each year, Blaze Eppinger, who works for the Sickle Cell Foundation of Georgia and is a strong supporter of those living…

    sickle-cell-foundation-of-arizona
    SCFA_Coach September 25, 2023
    0 Comments

    Real Stories from People Living with Sickle Cell Disease: Phillip Okwo

    Phillip Okwo’s Story Phillip Okwo is a former summer camp counselor at Camp Crescent Moon, a week-long sleep away camp for children with sickle cell disease…

    sickle-cell-foundation-of-arizona
    SCFA_Coach September 25, 2023
    0 Comments

    Real Stories from People Living with Sickle Cell Disease: Lametra Scott

    Lametra’s Story In September 2012, Lametra Scott gave birth to a baby boy. She named him Rickey. Before his birth, Lametra had no idea that…

    sickle-cell-foundation-of-arizona
    SCFA_Coach September 25, 2023
    0 Comments

    Real Stories from People Living with Sickle Cell Disease: Aaron Nicole

    Aaron’s Story Aaron Nicole Washington is 25 years old and a sophomore in the Georgia Tech Excel Program, a program that gives people with developmental…

    sickle-cell-foundation-of-arizona
    SCFA_Coach September 25, 2023
    0 Comments

    Real Stories from People Living with Sickle Cell Disease: Mimi

    Mimi’s Story Sickle cell disease (SCD) is an inherited blood disorder that can cause pain, anemia, infection, and other serious health problems. Although the exact number of…

    sickle-cell-foundation-of-arizona
    SCFA_Coach September 25, 2023
    0 Comments

    Real Stories from People Living with Sickle Cell Disease: Rae Blaylark

    Rae’s Story Rae Blaylark is the founder and Executive Director of the Sickle Cell Foundation of Minnesota; a certified community health worker; a certified hemoglobinopathy…

    sickle-cell-foundation-of-arizona
    SCFA_Coach September 25, 2023
    0 Comments

    Real Stories from People Living with Sickle Cell Disease: Shantá Robertson

    Shantá’s Story Print Shantá and her family. From left, Ryan, Khari, Derek, Shantá, and Mikaili. Shantá and her husband Derek are the parents of three…

    sickle-cell-foundation-of-arizona
    SCFA_Coach September 25, 2023
    0 Comments

    Recent Posts

    • Celebrating Community, Advocacy, and Innovation in Sickle Cell Disease Care
    • A Medical Minute Introducing Sickle Cell Disease with Dr. Rob
    • SCFA CELEBRATES SEPTEMBER NATIONAL SICKLE CELL AWARENESS MONTH 
    • SFCA Celebrates September as SCD Awareness Month with Both Presidential and Arizona Governor Proclamations
    • A Collaborative Surveillance Initiative for Sickle Cell Disease Awareness in Arizona
    © 2025 - The 360° SCD Hub™ brand, app and community is owned and operated by the Sickle Cell Foundation of Arizona a 501c3 non-profit from a grant funded by the Health and Human Services Administration. Special thanks to The Force for Health® Network, gamifying the sport of healthy global citizenship, for co-development and hosting the site and app.
    Real Stories from People Living with Sickle Cell Disease: Shantá Robertson

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