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As part of its mission to promote awareness regarding 22q11.2 deletion syndrome, The 22q Family Foundation strives to provide timely content from credible sources through channels that include but are not limited to this website. All content is made available for information purposes only. The Foundation gives no assurance or warranty, nor makes any endorsement or other representation, as to the accuracy, completeness, or validity of such content. Each person accessing this site is responsible for making his/her own assessment of the information provided.
It was a simple question, really. One that Carson Rehm was prepared for. A man standing at the Hunt of a Lifetime booth at this year's Great American Outdoor Show in Harrisburg asked Carson, "If you could hunt anywhere in the world, for anything, what
Natera Inc. "The Next Generation of Prenatal Testing" and the International 22q11.2 Foundation today announced that they have entered into an exclusive partnership to raise awareness about 22q11.2 deletion syndrome and the importance of early diagnosis.
Being a military family can be filled with many surprises, challenges, and opportunities. Part of the military life is moving every few years or more frequently. This can be a bit more challenging when there’s a child in the family who has a disability.
Sacramento-area youth in the early stages of serious mental illness can receive a new smartphone app that helps them detect early warning signs of psychosis, through a one-year, $588,000 grant to the UC Davis Early Diagnosis and Preventive Treatment (EDAP
As well as working for Skillset, she volunteers as president of the VCFS 22q11 Foundation (www.vcfs22q.org.au) and is a member of Rare Voices Australia – Australia’s national organisation advocating for those who live with a rare disease.
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