We aim to support individuals and families affected by GATAD2B gene variants, to increase awareness, and to work toward research and treatment opportunities.
Dare to be rare! Check out our new shirt campaign to raise awareness of GAND this #RareDiseaseDay. A portion of every sale goes to support HHFG. Choose from several shirt styles and colors to find the best fit for every member of your family: https://t.co/BtaTf5LKLI
Will you help us cross the finish line? Give to your favorite fundraiser's campaign or become a fundraiser yourself today! Let's finish GAND strong! Thank you for supporting HHFG! https://t.co/byFMbQGvLB
Join us THIS SATURDAY, September 27, for the 2025 GAND Online Conference! Your $15 registration fee gives you access to terrific speakers, fun games & prizes, big announcements, and community discussions.
View conference details and register today: https://t.co/BvNp8sZlkb
We are #GANDstrong! Thanks to our amazing community and supporters for helping us in our endeavor to support GAND families, raise awareness, and pursue research & treatment opportunities! Learn more about our mission: https://t.co/3DfO84CFFL
GAND families rock! More than 20 families have already registered for the 4th GAND Gathering and Scientific Conference…Early-Bird Registration ends tomorrow (April 30) – don’t miss out! We can’t wait to see you in Williamsburg! https://t.co/NmHibgjMky
Registration for the 2023 GAND Virtual Conference is now OPEN! Join us on #GANDawareness Day, September 16, to learn more about possible therapeutic approaches and GAND research. Visit our registration page for more information and stay #GANDstrong! https://t.co/4yHEEfX9LC
Thanks to everyone who joined us in raising #GANDawareness yesterday! You helped us reach thousands, and your posts are continuing to draw attention to this #RareDisease. If you missed out on yesterday's festivities, don't worry! It's always a good time to raise awareness!
We are proud to support current GAND research projects! Learn more and hear from our researchers by visiting our website. #GANDawareness#GATAD2B#GANDstrong#CareAboutRARE https://t.co/0NEMAWJcqZ
Did you know we have a YouTube channel? Learn more about GAND and the work of Helping Hands for GAND by following this link. Don't forget to subscribe! #GANDawareness#GATAD2B#GANDstrong#RareDisease https://t.co/LQiRCRe0Zd
If you've never heard of GATAD2B-associated neurodevelopmental disorder (GAND), you're not alone! This rare genetic syndrome was only first described in 2012. Since then, at least 168 individuals have been diagnosed. Learn more at: https://t.co/we0xiYQdlN #GANDawareness#GATAD2B
#Happybirthday to us! Helping Hands for GAND is 5 years old today! We are so grateful for the support that has made this work possible. With your help, we look forward to many more years serving this amazing population of patient families! #GANDstrong#GATAD2B#GANDAwareness
Our new #GANDawareness shirts are now available in multiple styles and colors! For every shirt you order, Helping Hands for GAND receives $10. Give a helping hand and look good doing it! #GATAD2B#GANDstrong#RareDisease https://t.co/085gqQuxED