Hello Everyone!

As some of you may or may not know our son, Hariton (2 years old), was diagnosed with Phelan McDermid Syndrome (PMS) or 22q13 Deletion Syndrome almost a year ago. It is an extremely rare genetic condition that is caused by a mutation of the SHANK3 gene or a deletion (in Hariton's case) of genetic material that causes many different but related symptoms. Some of these symptoms include hypotonia (low or weak muscle tone), absent to severely delayed speech; most do not acquire functional language, moderate to profound developmental delay and about 75% have been diagnosed with an autism spectrum disorder, as well as many other chronic medical conditions.There is currently no cure or treatment specifically for PMS, but we know how to manage many of the symptoms and researchers are working diligently to improve our knowledge of PMS and to find drugs and therapies that can help people affected by PMS. In spite of these medical, developmental, and behavioral conditions, people with PMS tend to be laid back, easily amused and often have a sweet and loving disposition as our little Hariton has for sure. :-)

In honor of Hariton and all those affected by PMS, please consider donating to this amazing cause which goes directly to the Phelan McDermid Foundation. Let's try to help researchers find a cure and the foundation to be able to give families the opportunity to come together and support each other. Please help us to reach our goal! 

From our hearts to yours. Thank you!

Nick, Megan, Kalli and Hariton Parashos