Join GANSID’s November Journal Club!
Explore the clinical spectrum of hereditary hemorrhagic telangiectasia with Dr. Deepa Anantha Laxmi N.V., featuring data from the CHORUS registry.
📅 Nov 26 | 🕘 9–10 AM EST
💻 Virtual | Zoom
🔗 tinyurl.com/JournalClubNov…
#JournalClub
Explore the clinical spectrum of hereditary hemorrhagic telangiectasia with Dr. Deepa Anantha Laxmi N.V., featuring data from the CHORUS registry.
📅 Nov 26 | 🕘 9–10 AM EST
💻 Virtual | Zoom
🔗 tinyurl.com/JournalClubNov…
#JournalClub
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Your voice matters! GANSID invites patients and caregivers to share their perspectives on barriers to clinical trial participation in inherited blood disorders.
Anonymous, voluntary & just 3–5 minutes.
Take the survey: tinyurl.com/clinicaltrialp…
#PatientExperience #ClinicalTrials
Anonymous, voluntary & just 3–5 minutes.
Take the survey: tinyurl.com/clinicaltrialp…
#PatientExperience #ClinicalTrials
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GANSID retweeted
A valuable learning and networking experience at #GANSIDCongress2026, Hyderabad
The SCF team connected with international delegates, NGOs and healthcare professionals working on inherited blood disorders.
Proud to see our Advisor Dr. Tarun Sahu presented at Gansid 2026
The SCF team connected with international delegates, NGOs and healthcare professionals working on inherited blood disorders.
Proud to see our Advisor Dr. Tarun Sahu presented at Gansid 2026
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Are you a clinician? We want to hear from you! 🌍
GANSID is exploring challenges in clinical trial participation worldwide. Share your insights in this 5-minute survey:
🩺 High-income countries: tinyurl.com/clinicaltrialH…
🩺 Low- & middle-income countries: tinyurl.com/clinicaltrialM…
GANSID is exploring challenges in clinical trial participation worldwide. Share your insights in this 5-minute survey:
🩺 High-income countries: tinyurl.com/clinicaltrialH…
🩺 Low- & middle-income countries: tinyurl.com/clinicaltrialM…
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CALL FOR MENTORS
GANSID is seeking experienced healthcare providers to support physicians serving the Hereditary Blood Disorders community worldwide through mentorship.
Become a GANSID Mentor: tinyurl.com/GANSIDMentor
#HealthcareProviders #Hematology #InheritedBloodDisorders
GANSID is seeking experienced healthcare providers to support physicians serving the Hereditary Blood Disorders community worldwide through mentorship.
Become a GANSID Mentor: tinyurl.com/GANSIDMentor
#HealthcareProviders #Hematology #InheritedBloodDisorders
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GANSID is now on TikTok! 🎉
tiktok.com/@inheritedbloo…
Follow us @inheritedblooddisorders to watch videos on Congress, GANSID events, and be part of the global inherited blood disorders conversation!
#GANSID #GlobalHealth #Hematology #SickleCellDisease #inheritedblooddisorders
tiktok.com/@inheritedbloo…
Follow us @inheritedblooddisorders to watch videos on Congress, GANSID events, and be part of the global inherited blood disorders conversation!
#GANSID #GlobalHealth #Hematology #SickleCellDisease #inheritedblooddisorders
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Thank You for Making GANSID Congress 2026 a Success! - mailchi.mp/inheritedblood…
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Join GANSID’s November Journal Club!
Explore the clinical spectrum of hereditary hemorrhagic telangiectasia with Dr. Deepa Anantha Laxmi N.V., featuring data from the CHORUS registry.
📅 Nov 26 | 🕘 9–10 AM EST
💻 Virtual | Zoom
🔗 tinyurl.com/JournalClubNov…
#Research #HHT
Explore the clinical spectrum of hereditary hemorrhagic telangiectasia with Dr. Deepa Anantha Laxmi N.V., featuring data from the CHORUS registry.
📅 Nov 26 | 🕘 9–10 AM EST
💻 Virtual | Zoom
🔗 tinyurl.com/JournalClubNov…
#Research #HHT
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We are honoured to share another #WIBDStory - Kasia shares her and her family's experiences with hereditary spherocytosis.
Please read her message, show your support, and share your own story: 🔗 tinyurl.com/GANSIDWIBDStory
Toolkit: tinyurl.com/WIBD2026
#HereditarySpherocytosis
Please read her message, show your support, and share your own story: 🔗 tinyurl.com/GANSIDWIBDStory
Toolkit: tinyurl.com/WIBD2026
#HereditarySpherocytosis
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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.
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.
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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 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.
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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/WIBDLetterSamp…
Send your photos, videos, and events/activities to media@inheritedblooddisorders.world by October 31.
1) Use Toolkit : tinyurl.com/WIBD2026
2) Share your #WIBDStory: tinyurl.com/GANSIDWIBDStory
3) Advocate to governments: tinyurl.com/WIBDLetterSamp…
Send your photos, videos, and events/activities to media@inheritedblooddisorders.world by October 31.
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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
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
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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
Please read their message, show your support, and share your own story:
🔗 tinyurl.com/GANSIDWIBDStory
#WIBDStory #TieRedFlexArm #SickleCell
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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
Explore GANSID’s World Inherited Blood Disorders Toolkit for resources to support awareness and advocacy:
🔗 tinyurl.com/GANSIDWIBDS2026
#WIBDMonth #InheritedBloodDisorders #WIBD
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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
We are honoured to announce that Sree Damodar Raja Narasimha will officially open the Congress.
We look forward to welcoming you to Hyderabad!
#GANSIDCongress2026
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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
Take 20 seconds to join the #WIBD Tie Red, Flex Arm Campaign!
💪 Tie red, flex, share & tag @ibloodisorders!
Every share helps raise awareness. ❤️
#InheritedBloodDisorders
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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
📥 Download FREE WIBD campaign materials: tinyurl.com/WIBD2026
📲 Share with your network
🏷️ Tag @ibloodisorders!
One download. More awareness. 🌍
#WIBD #InheritedBloodDisorders
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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
Read her message, show your support, and share your own story: 🔗 tinyurl.com/GANSIDWIBDStory
#WIBDStory #TieRedFlexArm #SickleCellDisease
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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
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
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