#GANSID is seeking mentors to help enhance global Hereditary Blood Disorder care. Share your expertise and make a difference globally. Our mentorship program aims to build capacity among physicians. Want to make a difference in the HBD community? Apply: bit.ly/3uCktn1

As we approach #WorldHemophiliaDay on April 17, we stand in solidarity with WFH to advocate for equitable access for all. Show your support by updating your social media headers with the WHD2024 theme. bit.ly/3up6exA #TreatmentForAll #WHD2024 #hemophilia

Our latest Online #PedsPain Curriculum course module is designed to guide #HealthProfessionals in the effective and safe use of opioids for pediatric chronic pain management. Enroll now at bit.ly/4b43IAu Thank you @kidsinpain & Health Canada and PHAC! #ItDoesntHaveToHurt

Meet Hemophilia Advocates Philippines one of our member organizations in the Philippines that supports individuals affected by bleeding disorders. Watch their inspiring video to learn about their incredible work and journey. #hemophiliaawareness #hemophiliaadvocates youtube.com/watch?v=1ALEnf…

Calling all physicians around the world! Join GANSID's mentorship program for an enhanced understanding of hereditary blood disorders. Don’t miss this opportunity. Submit your application today! Apply here: inheritedblooddisorders.world/mentee-opportu…… #Mentorship #PhysicianTraining

Today, we honor International Thalassemia Day! It is a day dedicated to raising awareness, and offering support and hope to those affected by this genetic blood disorder. #ITD2024 #BeAwareShareCare #TreatmentForThal #TreatmentForAll

An enlightening event indeed! Happy to have been able to support it. GANSID Global Sickle Cell Disease Network

Please join me at the #HopeGala2024 on June 15 to raise vital funds for Sickle Cell Awareness Group of Ontario (SCAGO) to support families with sickle cell in Ontario. To purchase your ticket, visit sicklecellanemia.ca/hope-gala

Want to learn how to access and use the #WSCD toolkit? We've got you covered! Check out our latest video tutorial, where we walk you through the steps to get started with the toolkit. Click inheritedblooddisorders.world to access the WSCD toolkit. #WordSickleCellDay2024 #SickleCell

#DidYouKnow? Patients with sickle cell disease (SCD) often face chronic pain crises, impacting their quality of life. It's crucial for healthcare providers to explore beyond opioid therapy for better management. Learn more: inheritedblooddisorders.world/sickle-cell-di… #WorldSickleCellDay #GANSID

June 19 is #WorldSickleCellDay and I am reminded of the great support provided by Kirsty Duncan to the Canadian #SickleCell community over the years. You introduced me to Senator Jane Cordy who introduced the first #SickleCell bill to pass and receive royal assent. Thank you.

Thanks Senator Jane Cordy, Rudy Cuzzetto 🇨🇦🇺🇦 and Andrea Khanjin for helping to raise awareness and bring visibility to a disease categorized as a minority disease, and thereby largely neglected. The Canadian and Ontario #sicklecell communities are grateful to you! Sickle Cell Awareness Group of Ontario (SCAGO) CanHaem

Today is #WorldSickleCellDay! Let’s raise awareness, support research, and stand together as a community to support those affected by sickle cell disease. This is the message from the CEO Lanre Tunji-Ajayi. #SickleCellWarriors World Health Organization (WHO) United Nations Sickle Cell Awareness Group of Ontario (SCAGO) Sickle Cell 101 Sickle Cell Disease Coalition

Arrived in Bangkok for the 32nd Congress of the International Society on Thrombosis and Hemostasis (ISTH). The Global Action Network for Sickle Cell and Other Inherited Blood Disorders (GANSID) looks forward to participating at the #ISTH2024. Visit us at booth # 1611.

🌟 Meet Aariya, a young girl who shares her journey and tips for managing health and wellness with sickle cell disease. 💪 Aariya's journey is a testament to resilience and self-care. 💖 Share your tips and stories below! #GANSID #InheritedBloodDisorders #HealthTips

🗨️ We’re honoured to have Lanre Tunji-Ajayi on our panel at the 2024 Annual Pain Centre Conference. As a global patient advocate, her expertise in addressing disparities in #SickleCellDisease is not to be missed! Register today at cvent.me/Ym597q! #PedsPain #NPAW2024

Lanre Tunji-Ajayi, M.S.M, Chief Executive Officer, Global Action Network for Sickle Cell & Other Inherited Blood Disorder (GANSID) is joining us as a distinguished speaker at the 8th CSR Health Impact Awards! Join us on Friday, 2nd August 2024, at the Crowne Plaza Hotel, Okhla,

Honored to meet Shri Ramdas Athawale Ji, India's Minister of State for Social Justice & Empowerment today. The #GANSID will work with his office to optimize the lives of people with #inheritedblooddisorders in #India. Committed to working with governments for a lasting change!

📅 Save the Date! October 18 is #WorldInheritedBloodDisordersDay #WIBDsDay . Join #GANSID in raising awareness around inherited blood disorders. Together, we can make a difference! #WIBDsDay #InheritedBloodDisordersDay

Feel like giving? Help Sickle Cell Awareness Group of Ontario raise money for 2024 TCS Toronto Waterfront Marathon raceroster.com/events/2024/79… via Race Roster