By Kim Maring | Manager
We are just a few days away from the beginning of our next family conference. Four hundred family members from around the world - as far away as Switzerland and Australia - will be joining us to hear the latest news in dup15q syndrome research and treatment. Your support is what makes conferences like these possible. Thank you!
This year we also have opportunities for those with dup15q syndrome to participate in research studies from UCLA, Geisinger, FaceBase and Coriell Genetic Cell Repository. Bringing the researchers to the families saves the inconvenience and expense of travel.
Our science meeting is also happening adjecent to the family meeting. This gives families the chance to meet those that have dedicated their careers to advancing the science and treatment of chromosome 15q duplications. We are so greatful for the work that they do everyday!
A special thanks to all of you for your generous donations. For more than 20 years, Dup15q Alliance has worked tirelessly to improve the lives of those affected by dup15q syndrome. We couldn't do it without you!!
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