Top Tweets for #SCDPolicyForum
The SCDC is excited to join community members and advocates at the 2026 #SCDPolicyForum, hosted by @SickCells and the @SCCConsortium.
🗓️ March 17–18, 2026 | Virtual
Register: https://t.co/XXl7FtX5t9
#SickleCellDisease #Advocacy #SickleCellAwareness
🎯 That’s a Wrap! 🎯
The 2025 SCD Policy Forum has officially come to a close, and what an impactful two days it has been! Here’s to the power of advocacy, unity, and making our voices heard! 💬💪
#SCDPolicyForum #AdvocacyInAction #SickleCellAwareness
Today is Day 1 of the SCD Policy Forum. We start at 11AM ET to learn about the federal priorities for the sickle cell disease community and prepare for Day 2's Virtual Hill Day. Stay hydrated and see you soon! #SCDPolicyForum #FundSickleCell #SickCells #SC3
Tomorrow marks the SCD Policy Forum, Today is the final day to register for Day 1, which commences tomorrow. We look forward to seeing you all there.
#scdpolicyforum #sicklecellawareness
🔗 https://t.co/huBptNIIFk
Happy Monday! We are pleased to announce a robust lineup of speakers for the 2024 SCD Policy Forum. See you tomorrow! #SCDPolicyForum #FundSickleCell #SickCells #SC3
Learn more about the forum: https://t.co/mRIYRzJAC9
The SCD Policy Forum is approaching fast on March 19th and 20th! Reserve your spot before Monday by signing up using the link provided.
🔗https://t.co/cYE68NSAWC
Join us for essential insights on amplifying the voices of the sickle cell community to legislators.
#SCDPolicyforum
Our third federal priority will support SCD HRSA programs.
Federal ask #3 Appropriate S15 Million for Programs under the HRSA Sickle Cell Disease Treatment Act.
Learn more at the following link: https://t.co/mRIYRzJAC9
#scd #warriors #scdpolicyforum
I'm encouraged to see the support from physicians, caregivers, and other organizations. Today's National Sickle Cell Disease Policy Forum is a step in the right direction to improve the future for families impacted by #sicklecelldisease.
#SCDPolicyForum
We're thrilled about the #SCDPolicyForum.
Policy Efforts to Promote Comprehensive Care for #SickleCellDisease, the panelists are:
🩸@DrewChicago from @ChildrensNatl
🩸Georgenè Glass from @DreamsiCkleKids
🩸@DrTitiFasipe from @TexasChildrens
🩸Stephanie Kaplan of @ASH_hematology
#SickleCellDisease is a #chronicdisease, but it's not being treated as such right now. A chronic disease includes the medical aspects as well as the quality of life aspects- @DrTitiFasipe. This is why #ComprehensiveCare is such a HUGE NEED for #SickleCellWarriors!
#SCDPolicyForum
We're thrilled about the #SCDPolicyForum.
Policy Efforts to Promote Comprehensive Care for #SickleCellDisease, the panelists are:
🩸@DrewChicago from @ChildrensNatl
🩸Georgenè Glass from @DreamsiCkleKids
🩸@DrTitiFasipe from @TexasChildrens
🩸Stephanie Kaplan of @ASH_hematology
Now listening to the #SCDPolicyForum, Panel: "Policy Efforts to Promote Comprehensive Care for #SCD". Happy to hear from @DrewChicago of @ChildrensNatl, Georgenè Glass of @DreamsiCkleKids, @DrTitiFasipe of @TexasChildrens & Stephanie Kaplan of @ASH_hematology!🙌🏿❤️
#SickleCell
#SCDPolicyForum 2day, I'll be meeting w/legislators my very 1st time!😬 Thankful 2 @SickCells 4 showing us how it's done & 4 mentors like Kevin Wake 2 help newbies like me! Also gonna use some of my @patientsrising AMC lessons & tips too!🤞🏿🙏🏿
#FundSickleCell
#SickleCellLifeMemej
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