Our daughter Tynlee was diagnosed with a rare genetic syndrome called GATAD2B-associated neurodevelopment disorder (GAND). After 10 years of many doctor visits and no answers and many prayers, the good Lord gave us Tynlee's diagnosis. We are so grateful to have a small but mighty community surrounding this rare disorder. We want to bring more awareness to this rare disease and to hopefully help another family a long the way. As of right now, there is no cure, and we are raising money for more research opportunities and to be able to join this amazing community for their annual conference this summer. If you feel called to donate we are so grateful for your generosity. Most of all, we ask for prayers for our daughter Tynlee, along with the other 224 children currently with this diagnosis and their families.
This volunteer-run nonprofit charity is the only organization in the world with a mission to support the GAND community and to fund GAND research. HHFG's mission means so much to my family, and we hope you will partner with us and make a rare impact today!
GATAD2B-associated neurodevelopmental disorder (GAND) is a rare genetic syndrome currently identified in approximately 225 individuals worldwide. This small but growing community needs your help. Please join us in supporting the mission of Helping Hands for GAND by making a donation today! Thank you so much for your support!
Tynlee Jacks and Family
On February 28, we hope you'll join us in observing World Rare Disease Day. This is the perfect time of year to show your support for rare groups, such as the GAND community! To date, GATAD2B-associated neurodevelopmental disorder (GAND) has been identified in approximately 230 individuals worldwide. More than 90% of them are children. Despite being such a small group, in 2021, we welcomed over 40 newly identified cases into our community.
Helping Hands for GAND was established in 2015 with a mission to support individuals and families affected by GAND, to increase awareness, and to work toward research and treatment opportunities to enrich the lives of those with this rare genetic condition. Since then, we've accomplished a lot, including hosting 4 conferences and facilitating $140,000 in research grants for GAND studies, including another $40,000 grant from HHFG in 2021. Please partner with us to continue supporting this important work. This year, we're counting on your help to host another conference, launch our patient registry, continue supporting GAND research, and much more.
To make a lasting impact, we need donors like you to support our efforts. We also need fundraisers like you to set up your own fundraising page for this campaign and share with your family, friends, and co-workers. You can even captain your own fundraising team! Share your story! Tell us how GAND has impacted you or your loved ones. Help us raise awareness and support for this rare disorder while funding research which can give us new insights into our children's challenges!
Please set up your personal campaign page today. It's fast and simple! To show our appreciation, we will send 5 silicone awareness bands to everyone who joins the campaign and shares their personal fundraising page to social media. In order to receive your bands, be sure your post is made public and tag Helping Hands for GAND (@GATAD2B). Wristbands will be shipped in late March.
Our TOP fundraiser will receive a coupon code for FREE registration to the 2022 GAND Gathering & Scientific Conference for their immediate family. 2nd place will receive a coupon code for one free adult registration ($75 value) to this year's Gathering. 3rd place will receive one free GAND shirt from our Bonfire store.
What are you waiting for? Get started on your personal campaign now! Let's work together to make a rare impact for the GAND community!