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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: The Green Family

    The Green Family Story “When AJ was born in 1992, there was a real lack of information and education about newborn screening and sickle cell…

    sickle-cell-foundation-of-arizona
    SCFA_Coach September 25, 2023
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    Real Stories from People Living with Sickle Cell Disease: Geno Atkins

    Geno’s Story “My story started when a young man met a young lady on the campus of Florida A&M University. On their first date he…

    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

    Real Stories from People Living with Sickle Cell Disease: Lance Jasper Jones

    Lance’s Story Lance Jasper Jones is 31 years old, is engaged to be married, is in graduate school pursuing a master’s degree in clinical psychology,…

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

    Real Stories from People Living with Sickle Cell Disease: Fatimah

    Fatimah’s Story When both parents have sickle cell trait (SCT), there is a 1 in 4 chance that each of their children will have sickle cell disease…

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

    Real Stories from People Living with Sickle Cell Disease: Joshua

    Joshua’s Story Joshua Adekunle is a high school senior who likes to play video games, draw, craft, and learn new things. He excels in school…

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

    Real Stories from People Living with Sickle Cell Disease: Dr. Alvarez

    Physician Perspective – Dr. Alvarez’s Story “When I have patients, I tell them that people with sickle cell trait (SCT) can have a normal lifespan and that…

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

    Real Stories from People Living with Sickle Cell Disease: Harry Williams Jr.

    Harry Williams Jr. is 44 years old, married, and a public health analyst and former adjunct professor. He also is a sickle cell warrior and…

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

    Real Stories from People Living with Sickle Cell Disease: Mikeia Green

    Mikeia Green’s Story “I knew there were a lot of things I could do to help myself stay healthy. I didn’t want to end up…

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

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