Sickle Cell Disease Association of America-MI

❤️ THANK YOU, MICHIGAN! 🗳️

Thanks to our supporters, families, advocates and especially our Sickle Cell Warriors who made their voices heard at the ballot box!

Advocacy continues, we remain committed to ensuring our community is SEEN, HEARD, and REPRESENTED! #SickleCellMatters

🗳️ TODAY IS THE DAY! Whether you’re a first-time voter, just turned 18, or a longtime voter, your voice matters! Our communities, healthcare and future deserve representation. Make your voice count! ❤️ #YourVoteMatters #SickleCellMatters #ElectionDay2026

🗳️ 5 DAYS UNTIL ELECTION DAY! Nov. 3 is approaching. Our voices matter in decisions affecting healthcare, treatment, research & community services. 💗 Make your plan to vote and check early-voting locations at Michigan.gov/Vote.

#SickleCellMatters #YourVoteMatters

Registration is NOW OPEN!

Join the Sickle Cell Community Consortium @SCCConsortium for Warrior Con 2026! 🎉

July 22–26 in LA for advocacy, education, wellness, research, and community.

Theme: Legacy in Action: The Next Move
📍 Sheraton Gateway Los Angeles

#WarriorCon2026

💚❤️💛 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-…