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The PKS Support group is a wonderful, conclusive source of support and education for those who are diagnosed with Pallister Killian Mosaic syndrome or Mosaic tetrasomy 12 P. Formed on May7, 2003, it is the largest PKS online support group with almost 200 members worldwide. On the online group, we discuss medical information, pain management, medications, research, ask questions, vent our anger & fears, speak freely on the ups and downs of daily living, share our personal experiences and build lasting friendships. Help us support and educate and encourage those who are dealing with the challenges of a special needs child. Send us a message today with what you can do to assist our families. Areas needing assistance:
about PKS, this support group and educating the many agencies that deal with special needs kids.
Online donation (see PayPal button below) or mailed donations gladly accepted. All funds are used help pay for this web site and other sources needed to keep this site up and others operating in sound manner.
Researchers are needed, points of contact for services and other related information for our families
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We thank you in advance for your donation!
Sincerely, PKS Support Online
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