We are thrilled to celebrate Awareness Day with our 17q12 crew on July 12th! The 17q12 community has a lot to celebrate. The 17q12 Patient Registry launched in April 2024. The 17q12 Foundation continues to grow and has welcomed new families and individuals worldwide. We are looking forward to more opportunities to connect through our virtual meet-ups, the 17q12 Near You program, and hopefully an in-person conference in 2026. This year's fundraising goal will go towards making a much-needed conference possible. We will continue to push for more research and advocate for individuals with 17q12 duplication or deletion syndrome. As our community grows we appreciate all the continued support from family, friends, medical professionals, and the rare community. Thank you for supporting individuals with a chromosome 17q12 syndrome! 100% of profits will support the 17q12 Foundation. Learn more at chromo17q12.org