Let's Talk Special Needs - PKS Awareness Day
December 4th is Pallister Killian syndrome (PKS) Awareness Day. PKS is a rare genetic disorder with no known cause that fewer than 500 people have been diagnosed with worldwide. However, it’s believed there are many that go undiagnosed due to shortcomings in the current method of testing. Doctors believe there could be 2,000 cases in the United States alone. Traits of PKS include extremely weak muscle tone, distinct facial features, cognitive delays, visual and hearing impairments, seizures, and a high arched palate. Join Jane Lynn and Patti for a very special edition of “Let’s Talk Special Needs - PKS Awareness Day,” and meet the parents who started PKS Kids, a non-profit organization devoted to raising funds for research about PKS, for a candid discussion about their experiences and the importance of spreading the word about this mysterious genetic disorder.
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