Founded in 1990, The Chromosome 18 Registry & Research Society is a registered 501(c)(3) non-profit, tax-exempt public charity dedicated to making chromosome 18 conditions the first treatable chromosome abnormalities. We count within our membership thousands of parents, siblings, extended family and friends, businesses, and affected individuals. Registry membership is open to any interested person.
Our work is supported by private donations from members, foundations and charitable organizations, businesses, and others interested in supporting our mission. We use these contributions and gifts to invest in both people and science; supporting our members through education and a sense of community while also focusing squarely on impactful clinical research that will lead to healthier, happier, and more independent lives for those affected and their families.
Are you looking for an easy way to help support the Registry and our mission? Shop on Amazon Smile and a portion of your order total will be donated to us by Amazon!
We began our relationship with the Rock ‘n’ Roll Marathon Series in 2014 and have since raised over $45,000 to fund Registry services and research. Please check out our event page for more information on our upcoming races. We hope you can join us.
Our 23rd Annual Family Conference will be held from July 10th to July 13th, 2016 at the San Antonio Marriott Riverwalk in San Antonio, TX. We hope that you can join us for what will surely be an exciting and informative experience!
Join our Canadian families in celebrating a day a fun by the pool.
We are excited to share the story of one of the many wonderful families of The Chromosome 18 Registry & Research Society. The Morgan family rallied their community around Ben, who has Tetrasomy 18p.