Global Action Network for Sickle Cell & Other Inherited Blood Disorders

Global Action Network for Sickle Cell & Other Inherited Blood Disorders The GANSID serves the inherited blood disorders community.
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🧬 Speaker Spotlight: Dr. Ravindra Kumar from IndiaJoin Dr. Kumar, Scientist D at the ICMR–National Institute for Tribal ...
09/04/2026

🧬 Speaker Spotlight: Dr. Ravindra Kumar from India

Join Dr. Kumar, Scientist D at the ICMR–National Institute for Tribal Health Research, as he shares his expertise during "Disparities in Access to Lifelong Care for Thalassemia: A Global Lens" at .

A leading expert in genetics and molecular hematology—and a thalassemia warrior himself—Dr. Kumar has dedicated more than a decade to advancing research in thalassemia and sickle cell disease. With over 130 scientific publications, including work in Nature Medicine, and key contributions to India's National Sickle Cell Anemia Elimination Mission 2047, his work continues to shape equitable care and research worldwide.

📅 23–25 October 2026
đź“Ť Hyderabad, India
đź”— Register: https://tinyurl.com/GANSIDCongress2026

Whether you're a hematologist, researcher, clinician, policymaker, or patient advocate, don't miss this opportunity to learn from one of the field's leading voices.

From Innovation to Implementation: Bridging Science and Access 🩸Take a look at the GANSID Congress 2026 Program at a Gla...
09/03/2026

From Innovation to Implementation: Bridging Science and Access 🩸

Take a look at the GANSID Congress 2026 Program at a Glance! Explore three days of cutting-edge science, emerging therapies, clinical insights, and conversations focused on bridging the gap between innovation and access in inherited blood disorders.

Don't miss out! Register now: https://tinyurl.com/GANSIDCongress2026

📅 October 23–25, 2026
đź“Ť Hyderabad International Conference Centre, India

Join experts, researchers, clinicians, and advocates from around the world as we work toward a future where innovation reaches every patient.

Hello everyone!We have many exciting opportunities to be featured at the 4th Annual GANSID Congress 2026, taking place i...
09/03/2026

Hello everyone!

We have many exciting opportunities to be featured at the 4th Annual GANSID Congress 2026, taking place in Hyderabad, India on October 23-25, 2026. Please visit this link for all opportunities to share with your colleagues and network: https://tinyurl.com/CongressOpportunities

a) Through the Lens - Photography Exhibition (GLOBAL) - Due September 18 https://tinyurl.com/CongressExhibition

b) Knowledge on Display - Research Publications (GLOBAL) - Due September 18 https://tinyurl.com/KnowledgeDisplay

c) Young Investigators & Medical Fellows Programme (INDIA ONLY) - Abstracts - Due September 18 https://tinyurl.com/CongressIndiaAbstract

d) Partner with GANSID Congress (GLOBAL)
https://inheritedblooddisorders.world/congress-2026/contact-us-2

e) Register for GANSID Congress Today! (GLOBAL) https://tinyurl.com/GANSIDCongress2026

The GANSID Young Investigator & Medical Fellow Programme offers postgraduate residents, medical fellows, and young inves...
09/03/2026

The GANSID Young Investigator & Medical Fellow Programme offers postgraduate residents, medical fellows, and young investigators across India the opportunity to present their research at GANSID Congress 2026 in Hyderabad.

In collaboration with AIIMS New Delhi and NIMS

Connect with leading experts from around the world, exchange ideas with fellow researchers, build valuable professional networks, and contribute to advancing research and care in inherited blood disorders.

Submit your abstract by September 18, 2026:
https://tinyurl.com/CongressIndiaAbstract

📅 October 23–25, 2026
đź“Ť Hyderabad, India

🌍 Are you ready to expand your impact in hereditary blood disorder care?Join the GANSID Mentorship Program and connect w...
09/03/2026

🌍 Are you ready to expand your impact in hereditary blood disorder care?

Join the GANSID Mentorship Program and connect with physicians around the world to exchange knowledge, share experiences, and grow together.

Whether you’re an experienced physician looking to mentor the next generation of clinicians, or a physician seeking to strengthen your expertise in conditions like Sickle Cell Disease, Thalassemia, Hemophilia, and more — this program is for you.

Through 6 months of mentorship, you’ll:
• Connect with global peers
• Share and gain clinical insights
• Build lasting professional relationships
• Contribute to improving patient care worldwide
Apply today as a Mentor or Mentee:
đź”— Mentor: https://tinyurl.com/GANSIDMentor
đź”— Mentee: https://tinyurl.com/GANSIDMentee

Bring your work to Knowledge on Display at GANSID Congress 2026! We invite faculty, delegates, researchers, and patient ...
09/02/2026

Bring your work to Knowledge on Display at GANSID Congress 2026! We invite faculty, delegates, researchers, and patient advocates to showcase their authored or co-authored publications and resources.

We’re looking for contributions across:

🔬 Academic & Clinical Literature — from textbooks and clinical resources to peer-reviewed publications and educational materials.

📊 Research & Data — including clinical research, real-world evidence, registries, and reports highlighting inherited blood disorders.

🤝 Patient Advocacy, Care, & Lived Experience — including books, patient education resources, community stories, and innovations in care.

Submit Your Requestby September 18: https://tinyurl.com/KnowledgeDisplay
📍 Hyderabad | October 23–25, 2026

Your Photograph Could Be Featured at GANSID Congress!The GANSID Inherited Blood Disorders Photography Exhibition 2026 – ...
09/01/2026

Your Photograph Could Be Featured at GANSID Congress!

The GANSID Inherited Blood Disorders Photography Exhibition 2026 – People’s Choice Gallery invites registered clinicians, researchers, patients, and advocates to share original photographs that capture the science, experiences, and communities behind inherited blood disorders.

📸 Submit your photograph: https://tinyurl.com/CongressExhibition

Choose from three categories:

a) The Microscopic Canvas — Science & Clinical
b) Faces of Resilience — Human Experience
c) Advocacy in Action — Community & Care

🏆 Two winning photographs will be selected by Congress delegates for the prestigious People’s Choice Best Inherited Blood Disorders Photography Award and recognized during the closing ceremony.

đź“… Deadline: September 18, 2026
đź“· Maximum 2 submissions per delegate

Partner with GANSID Congress 2026 and connect with a global community advancing the future of inherited blood disorder c...
09/01/2026

Partner with GANSID Congress 2026 and connect with a global community advancing the future of inherited blood disorder care.

The 4th GANSID Congress brings together clinicians, researchers, healthcare professionals, patient organizations, policymakers, and industry leaders from across the world.

Why partner with GANSID?
• Showcase your therapies, diagnostics, technologies, and innovations
• Connect with global experts, key opinion leaders, and decision-makers
• Strengthen your organization’s visibility and presence within the field
• Demonstrate your commitment to advancing patient care
• Support scientific education, collaboration, and knowledge exchange

Partnership opportunities include: Industry Symposia, Exhibition Booths, Presentation Theatres, Networking Opportunities, Congress Program Advertising, and Industry Meeting Spaces.

đź“© Interested in partnering with GANSID? Scan the QR code to request the GANSID Congress Exhibition & Industry Symposium Prospectus and explore opportunities to collaborate.

🌍 Calling All Clinicians! Help Us Advance the Future of Clinical ResearchGANSID is conducting a global survey to better ...
08/31/2026

🌍 Calling All Clinicians! Help Us Advance the Future of Clinical Research

GANSID is conducting a global survey to better understand the challenges clinicians face with clinical trial participation in their regions.

Your experience and insights are essential to identifying barriers, improving research accessibility, and strengthening the future of clinical research worldwide.

đź©ş Clinicians practicing in high-income countries:
Complete the survey here: http://tinyurl.com/clinicaltrialHIC

đź©ş Clinicians practicing in low- and middle-income countries:
Complete the survey here: https://tinyurl.com/clinicaltrialMIC

⏱️ The survey takes just 5 minutes to complete. Your perspective can help shape more inclusive and accessible clinical research.

🧬 Moderator Spotlight: Mr. Chandrakant Agarwal from IndiaJoin Mr. Chandrakant Agarwal, President of the TSCS (Thalassemi...
08/28/2026

🧬 Moderator Spotlight: Mr. Chandrakant Agarwal from India

Join Mr. Chandrakant Agarwal, President of the TSCS (Thalassemia and Sickle Cell Society), Hyderabad, as he moderates "Disparities in Access to Lifelong Care for Thalassemia: A Global Lens" at .

A respected industrialist, philanthropist, and advocate, Mr. Agarwal has dedicated decades to advancing care for individuals living with thalassemia and sickle cell disease. Under his leadership, TSCS has grown into one of the world's largest NGOs delivering comprehensive, free care while championing voluntary blood donation, prevention initiatives, and global partnerships.

đź“Ť Hyderabad, India
📅 October 23–25, 2026

Register today: https://tinyurl.com/GANSIDCongress2026

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