Sickle Cell Disease Association of America, Inc.

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The Sickle Cell Disease Association of America (SCDAA) serves as the nation's headquarters for sickle cell disease support and advocacy & the search for a cure. The Official Facebook Page of the National Sickle Cell Disease Association of America, Inc. To advocate for people affected by sickle cell conditions and empower community-based organizations to maximize quality of life and raise public consciousness while advancing the search for a universal cure.

ICO

237175985

Facebook

20000

X (Twitter)

5126

Traffic

1029151

Address: 7240 Parkway Dr Suite 180, HanoverWeb: Sign in to see organisation websiteFacebook: sicklecellcampaignX (Twitter): SCDAAorgRevenue: 1104795ICO: 237175985

Home - Sickle Cell Disease Association of America Inc. Rare Disease Day Help Us Raise 20K this Month to Support Our Mission. MARAC Statement ASH Report on Exercise and SCT Crisis Report Editas Medicine Announces Strategic Transition SCDAA Statement on Recent Natural Disasters SCDAA Statement CMS Cell and Gene Therapy Access Model SCDAA Statement Know Your Rights in the ER 50 Years Forward Join us as we look to the next 50 years of hope awareness and progress. Spring CHW Training Learn the skills you need to serve the sickle cell community with this signature training opportunity. SCDAA and MedicAlert Pilot Program The Mental Health and Wellness Campaign Learn the tools you need to manage your mental health as a sickle cell warrior.

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News about from their social media (Facebook and X).

Christine

Sending lots of support to the SCDAA and everyone fighting against sickle cell disease! Let's continue to raise awareness and work towards a cure together! 💚 #SickleCellWarriors

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Katherine

What strategies can we implement to increase awareness and advocacy for sickle cell disease during Rare Disease Day?

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Goldie

So inspired by the SCDAA and their incredible efforts! Every dollar counts—let's hit that $20K goal this month! Together, we can make a difference! 🙌❤️ #SupportSCDAA

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Christine

How can community-based organizations better support mental health initiatives for individuals living with sickle cell disease?

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