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It’s finally here! The GANSID Congress begins tomorrow!
Our first in-person Congress brings together presenters, experts & participants from around the world for 3 days of learning, connection & collaboration.
Tag @iblooddisorders in your Congress moments!
#GANSIDCongress2026
We’re officially underway at the #GANSIDCongress2026! 🌍We can’t wait to see what the rest of the weekend brings!
Attending the Congress? We’d love to see it through your eyes! Please send or tag @iblooddisorders in any photos and videos you capture throughout the weekend.
We’re officially underway at the #GANSIDCongress2026! 🌍
We can’t wait to see what the rest of the weekend brings.
Attending the Congress? We’d love to see it through your eyes! Please send or tag @iblooddisorders in any photos and videos you capture throughout the weekend.
1 week left to recognize #WIBD!
1) Use Toolkit : tinyurl.com/WIBD2026
2) Share your #WIBDStory: tinyurl.com/GANSIDWIBDStory
3) Advocate to governments: tinyurl.com/WIBDLetterSample
Send your photos, videos, and events/activities to [email protected] by October 31.
We are honoured to share another #WIBDStory from Melody, an advocate of SCD who shares a recent experience with a vaso-occlusive crisis.
Please read their message, show your support, and share your own story:
🔗 tinyurl.com/GANSIDWIBDStory
#WIBDStory #TieRedFlexArm #SickleCell
Today, we are recognizing #FanconiAnemia in honour of World Inherited Blood Disorders Month!
Explore GANSID’s World Inherited Blood Disorders Toolkit for resources to support awareness and advocacy:
🔗 tinyurl.com/GANSIDWIBDS2026
#WIBDMonth #InheritedBloodDisorders #WIBD
Only 3 Days Until the 4th International GANSID Congress for Sickle Cell & Other Inherited Blood Disorders!
We are honoured to announce that Sree Damodar Raja Narasimha will officially open the Congress.
We look forward to welcoming you to Hyderabad!
#GANSIDCongress2026
Red represents the strength, resilience & hope of people living with inherited blood disorders.
Take 20 seconds to join the #WIBD Tie Red, Flex Arm Campaign!
💪 Tie red, flex, share & tag @ibloodisorders!
Every share helps raise awareness. ❤️
#InheritedBloodDisorders
Yesterday was WIBD Day, but you can still advocate today!⏱️Got 20 seconds? Make them count!
📥 Download FREE WIBD campaign materials: tinyurl.com/WIBD2026
📲 Share with your network
🏷️ Tag @ibloodisorders!
One download. More awareness. 🌍
#WIBD #InheritedBloodDisorders
In honour of #WIBDDay, Lincy shares her message of resilience, challenging stigma, and amplifying silenced voices. ❤️
Read her message, show your support, and share your own story: 🔗 tinyurl.com/GANSIDWIBDStory
#WIBDStory #TieRedFlexArm #SickleCellDisease
Today is World Inherited Blood Disorders Day — October 18.
Take action:
📩 Write to your government
📸 Join #TieRedFlexArm and tag @IBloodDisorders
🔹 Access the WIBD Toolkit: tinyurl.com/WIBD2026
🔹 Share your #WIBDStory: tinyurl.com/GANSIDWIBDStory
#InheritedBloodDisorders
Celebrate World Inherited Blood Disorders Day- October 18 with Us - mailchi.mp/inheritedblooddis…
In honour of #WIBDDay, Gloria shares her message of resilience, challenging stigma, and amplifying silenced voices. ❤️
Read her message, show your support, and share your own story: 🔗 tinyurl.com/GANSIDWIBDStory
#WIBDStory #TieRedFlexArm #SickleCellDisease
Tomorrow is World Inherited Blood Disorders Day - Help Us Amplify Voices Globally!
Use our free WIBD Toolkit: 🔗 tinyurl.com/WIBD2026
Share your Tie Red Flex Arm x #WIBDStory: 🔗 tinyurl.com/GANSIDWIBDStory
Advocate for official Oct 18 recognition: 🔗 tinyurl.com/WIBDLetterSample
Why advocate for #WIBD2026?
Your voice can improve care and support for people living with inherited blood disorders.
Toolkit: tinyurl.com/WIBD2026
#WIBDStory: tinyurl.com/GANSIDWIBDStory
Register for tomorrow's global webinar! tinyurl.com/WIBDWebinar2026
#InheritedBloodDisorders
How are you recognizing #WIBDDay?
Share your events, toolkit posts, #WIBDStory, advocacy letters, Tie Red, Flex Arm photos, or other contributions!
📩 Email photos, videos, links & a brief description to [email protected] or tag @iblooddisorders in posts!
⏱️ Turn awareness into action in 60 seconds! Choose a message about #WIBD2026 and share it. Every voice makes an impact! 💙
Toolkit: tinyurl.com/WIBD2026
Join our GLOBAL WIBD Webinar! tinyurl.com/WIBDWebinar2026
Share your story: tinyurl.com/GANSIDWIBDStory
#InheritedBloodDisorders
How much do you really know about sickle cell disease? Visit our page for the Sickle Cell Myth vs Fact Quiz.
📖 WIBD Toolkit: tinyurl.com/GANSIDWIBDS2026
🎙️ WIBD Webinar: tinyurl.com/WIBDWebinar2026
🔴 Share your #WIBDStory: tinyurl.com/GANSIDWIBDStory
#WIBD #SickleCellDisease #WIBDStory
How much do you really know about sickle cell disease?
Test yourself with our Sickle Cell Myth vs Fact Quiz!
📖 FREE Toolkit: tinyurl.com/GANSIDWIBDS2026
🎙️ WIBD Webinar: tinyurl.com/WIBDWebinar2026
🔴 Share your #WIBDStory: tinyurl.com/GANSIDWIBDStory
#WIBD #SickleCellDisease #WIBDStory
