CEO, GANSID delivers the World Inherited Blood Disorders Day message
Global Action Network for Sickle Cell & Other Inherited Blood Disorders
Non-profit Organizations
Dover, DE 465 followers
Amplifying the Impact of the Global Inherited Blood Disorders Community Together.
About us
The Global Action Network of Sickle Cell & Other Inherited Blood Disorders will enable the advancement of shared priorities within the benign inherited blood disorders (IBDs) community through unified and coordinated data-driven advocacy. As a collective, we will improve the health outcomes of people affected by benign inherited blood disorders (BIBDs) regardless of where they live in the world. We will strive towards equitable access to care by connecting regions, nations, localities, partners, and people to effectively advocate for and improve care infrastructures for All people living with benign inherited blood disorders
- Website
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https://inheritedblooddisorders.world/
External link for Global Action Network for Sickle Cell & Other Inherited Blood Disorders
- Industry
- Non-profit Organizations
- Company size
- 2-10 employees
- Headquarters
- Dover, DE
- Type
- Nonprofit
- Founded
- 2022
- Specialties
- Advocacy, Training, Mentorship, Regional Network, Cross-disease initiatives, and Capacity building
Locations
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Primary
8 The Green
Suite 4000
Dover, DE 19901, US
Employees at Global Action Network for Sickle Cell & Other Inherited Blood Disorders
Updates
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Join the Congress Now! Don’t miss Mrs. Tunji Ajayi's insightful updates on critical issues in advocacy, research, care, and treatment. Stay informed on the latest developments and strategies that are shaping the future of these important areas. #GANSIDCongress2024
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🌟 GANSID Congress 2024 Registration is CLOSING TOMORROW 5th Nov. 🔗 Secure your spot now: https://lnkd.in/gHrN5VX9 You have few hours left to register. Here is a video from our congress last year showing the similar goals of all our members of the inherited blood disorders community. Register NOW to secure your spot at the two-day virtual #GANSIDCongress24 slated for Nov 8-9. We promise an inspiring gathering that unites healthcare providers, others clinicians, patients, families, educators, advocates, researchers, and industry partners. Together, we’ll share knowledge, foster collaboration, and advance care and treatment for inherited blood disorders. #GANSIDCongress2024
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🌟6 Days to GO! GANSID Congress 2024 Registration closes soon but we still have your spot available till November 5th 🔗 Register here: https://lnkd.in/gHrN5VX9 Register today to secure your attendance at the two-day virtual #GANSIDCongress24 slated for Nov 8-9. There is something for everyone. ✨ Don’t miss your chance to be part of this transformative event- #GANSIDCongress2024
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🌍✨ Get ready to take your patient organization to the next level. 👉 Register now: https://lnkd.in/gHrN5VX9 Join us for our **Regional Capacity Building Workshop on Strategic Plan Development** tailored for patient organizations in Europe, Africa, Asia-Pacific, and the Middle East! 🌏 It is virtual event on Nov 9 at the GANSID Congress 2024! It promises to empower professionals with the skills and knowledge needed to make a real impact in the field of inherited blood disorders. 🕔 Join us from 5:30 AM - 6:30 AM EST for an hour of transformative insights and collaboration. 🗓️ Remember, registration closes on November 1st—don’t miss out on this opportunity to improve your leadership skills! #GANSIDCongress2024
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🌍✨ Get ready to take your patient organization to the next level Join us for our **Regional Capacity Building Workshop on Strategic Plan Development** tailored for patient organizations in North America, Latin America & Europe. 👉 Register now: https://lnkd.in/gHrN5VX9 🌏 It is virtual event on Nov 8 at the GANSID Congress 2024! It promises to empower professionals with the skills and knowledge needed to make a real impact in the field of inherited blood disorders. 🕔 Join us from 2:00PM - 3:00PM EST for an hour of transformative insights and collaboration. 🗓️ Remember, registration closes on November 1st—don’t miss out on this opportunity to improve your leadership skills! #GANSIDCongress2024
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🚀 Ready to be inspired? 👉 Register now: https://lnkd.in/gHrN5VX9 🌟 Meet our incredible lineup of speakers at GANSID Congress 2024! From groundbreaking researchers to passionate advocates, these voices are shaping the future of inherited blood disorders. Join us on Nov 8-9 for cutting-edge insights and transformative discussions that will elevate our community. 🗓️ Don’t wait—registration closes on November 1st! Let’s learn, connect, and innovate together! #GANSIDCongress2024
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🌟 GANSID Congress 2024 Registration closes soon but we still have your spot available! 🔗 Secure your spot now: https://lnkd.in/gHrN5VX9 Register today to secure your attendance at the two-day virtual #GANSIDCongress24 slated for Nov 8-9. We promise an inspiring gathering that unites healthcare providers, others clinicians, patients, families, educators, advocates, researchers, and industry partners. Together, we’ll share knowledge, foster collaboration, and advance care and treatment for inherited blood disorders. ✨ Don’t miss your chance to be part of this transformative event—registration closes on November 1st! #GANSIDCongress2024 University of Toronto Hamilton Health Sciences
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🌟 Excited to announce Dr. Durhane Wong-Rieger, PhD, as a key speaker at our upcoming event. Nov 8-9, 2024! Join us as she shares her expertise on "Working Together: Building An Interconnected Alliance to Advance Inherited Blood Disorders." Let’s collaborate for a brighter future in healthcare! 💉✨ 👉 Register now: https://lnkd.in/gHrN5VX9 #GANSIDCongress2024 Allianz Asia Pacific Canadian Organization for Rare Disorders
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🌍❤️ A heartfelt THANK YOU to everyone who participated in #WorldInheritedBloodDisorders Day on October 18th! Your engagement and support helped raise awareness and foster a sense of community. Together, we’re making a difference! Let’s continue to stand for those affected by inherited blood disorders. Engage @Iblooddisorders #WIBDsDay #GANSID #WorldInheritedBloodDisordersDay