Education, genetic counseling, advocacy, follow-up laboratory testing, case management, events, medical referrals, summer camp, and more.

Joined May 2016
363 Photos and videos
💚❤️💛 Sickle Cell Warriors, Families & Supporters 💛❤️💚 Join us in Ypsilanti! 🎁 Pre-register for a FREE T-shirt while supplies last! Register here: eventbrite.com/e/sickle-cell…
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Sickle Cell Disease Association of America-MI retweeted
May 23
Effective May 20, 2026 at 11:59 PM Eastern Daylight Time (EDT), CDC initiated public health entry screening for travelers arriving from the Democratic Republic of the Congo (DRC), South Sudan, and Uganda. Effective May 22, 2026 at 11:59 PM EDT, operations have expanded to include Hartsfield-Jackson Atlanta International Airport (ATL). CDC’s Port Health Protection system operates 24 hours a day, 7 days a week, 365 days a year to support these and other public health response activities at U.S. ports of entry. Public health entry screening serves as an important part of CDC’s layered prevention approach. In combination with existing public health measures already in place to identify symptomatic travelers, these efforts help slow and reduce the potential spread of disease into the United States. Travelers who have been in the DRC, South Sudan, or Uganda within 21 days prior to arriving in the United States will be escorted to a designated airport screening area. There, travelers will answer public health screening questions and may undergo additional assessment as needed. cdc.gov/media/newsroom/relea…
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Sickle Cell Disease Association of America-MI retweeted
Sickle Cell Disease is not just pain. It's chronic fatigue, anemia, vision problems, and a higher risk of infections. This complex condition affects the entire body. Awareness sicklecellmidwest.org
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🚨 Calling for blood donors! Join us June 19 in Detroit for the One Dove sponsored blood drive benefiting SCDAA Michigan Chapter. 🩸 Save lives 🎁 Donor incentives available Register today using sponsor code: OneDove #DonateBlood #HelpFillTheNeed #SCDAAMI #SCDAA #OneDove #SCD
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Calling all sickle cell warriors, families, and caregivers. Join the Pediatric Sickle Cell Improvement Program (P-SCIP) and help improve care for children. May 12 | 9:30 AM–1:30 PM ✔️ $200 compensation childcare meals 📲 Call or text 734-323-8732 to register .
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🚗 Drive With a Purpose, Michigan! Get your Sickle Cell Awareness License Plate today. ✔️ Only $35 tabs ✔️ Supports SCDAA-MI programs ✔️ Personalization available 📞 Call SCDAA-MI or your local MI Secretary of State office Help us by purchasing plates! #SCDAAMI #Michigan
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Black History Month Spotlight In 1910, Dr. James B. Herrick documented the first recognized case of #sicklecelldisease after examining Walter Clement Noel, a dental student from Grenada. BHM reminds us: ✊🏾 Health equity is civil rights. Awareness saves lives. #BHM
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Rebecca Lee Crumpler made history in 1864 as the first African American woman to earn an M.D. She cared for freed slaves after the Civil War and later published one of the first medical books by a Black author in 1883, focused on women’s and children’s health. A true pioneer!
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Happy #BlackHistoryMonth! ✨ 2026 marks 100 years of national Black history commemorations. From Dr. Carter G. Woodson’s Negro History Week to today’s month long celebration of Black excellence, resilience, impact and black leadership in healthcare & SCD advocacy. #SCDAAMI #SCDAA
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💙🤍 Happy Founders’ Day to Phi Beta Sigma Fraternity, Inc. 112 years of Culture For Service & Service For Humanity. Honoring the Sigmas’ legacy of sickle cell advocacy and saluting Nu Alpha Sigma, Xi Beta Sigma & Pi Rho Sigma for serving Michigan’s community. #PBS1914 #detroit
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Looking for a powerful way to support the sickle cell community? Michigan’s Sickle Cell Awareness License Plate is now available—collectible or for driving with purpose. ❤️‍🩹 🎥 Dr. Shurney explains why: youtu.be/qFKXPmn1Sjw Gift idea 🎁 Info: SOS site
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The SCDAAMI is most thankful today for the strength and resilience of all our sickle cell warriors, caregivers and families affected by Sickle Cell Disease. Our hope is that you will remain healthy and happy, this holiday season. #SCDAAMI #SickleCellWarriors #Michigan #SCD
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Sickle Cell Disease Association of America-MI retweeted
Happening today at 12 PM EST. We are covering a very important topic during the Summit. Join the plenary Caregiver Empowerment and Advocacy with Demitrea Kelley and learn how caregiver voices influence real policy change. You can still register at scdcaregivers.org.
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💜 Caregivers, it’s your time. Join us November 13–16 for the 5th Annual Virtual Sickle Cell Caregiver Summit. A weekend of connection, healing, and love.
👉🏽 Register now at scdcaregivers.org#SCDCaregiverSummit2025 #CaregiverLove #CommunityStrong
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What an incredible week in Chicago! 💪🏾❤️ The 53rd Annual National Convention brought together warriors, advocates, clinicians & researchers from across the nation — all united to advance sickle cell care & awareness. @SCDAAorg #SickleCellAwareness #SickleCellStrong #SCDAAMI #SCD
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The SCDAA-MI team showed up in FULL FORCE — learning, sharing, and representing Michigan with passion & pride! 🙌🏾 We’re bringing the energy, insight & inspiration back home to continue the mission. ❤️💪🏾 #SCDAAMI #SickleCellStrong #SCDAA53
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From powerful workshops & inspiring lectures to vital networking and new research updates — this year’s theme, “Empowerment: Forging Ahead with Strength and Courage,” truly came to life. 🌟 #SCDAA53 #Empowerment #CommunityInAction
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🩸THANK YOU! 🩸 To our Warriors, caregivers, families, friends, sponsors, donors, walkers, DJ, Detroit City Council Pres. Pro-Tem James Tate, DPD, State of MI & Lt. Gov @garlin — we couldn’t do it without you! Special thanks to @CBSDetroit @wxyzdetroit and @Local4News
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👟✨ Have you registered yet, fam? We’re only 2 days away from the 2025 Sickle Cell Matters! Awareness Walk! 📅 Sat. Sept. 13 | 9 AM–1 PM 📍 Charles H. Wright Museum, Detroit This year we make HISTORY: Don’t miss it 👉 scdaami.org #SickleCellMatters #Detroit
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