PKS Kids

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Hope and help for those touched by Pallister-Killian Syndrome PKS is a rare tetrasomy of 12p. Visit www.pkskids.com for more information. To educate the medical community and promote research to ensure the early diagnosis of children with Pallister-Killian Syndrome, and to provide emotional, medical and other resources and support to familie of children with Pallister-Killian Sydrome.

ICO

205653043

Facebook

2300

X (Twitter)

83

Address

Green Bay

Address: P O Box 12211, Green BayWeb: Sign in to see organisation websiteFacebook: pkskidsX (Twitter): PKSKidsRevenue: 24504ICO: 205653043

HOME | PKSkids | Non-Profit HOME ABOUT US ABOUT PKS EVENTS FOR FAMILIES NEWS SUPPORT CONTACT More Education Awareness Support Our Goal Vision Commitment Register Help Make Change Volunteer Participate or Donate Latest News Showing their love PKS Clinics at CHOP PKS Kids Live 2021 has been postponed RESEARCH OPPORTUNITY. CHOP is doing a prenatal PKS study. A hero is an ordinary individual who finds the strength to persevere and endure in spite of overwhelming obstacles. Christopher Reeve SupportUs Education Awareness Support PKS Kids provides hope and help to families.

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News about from their social media (Facebook and X).

David

How can we better support families affected by PKS in accessing specialized healthcare and resources?

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PKS Kids

If you are in the Chicago area, I highly recommend checking out Abilities Expo. Check out the website for other expos around the country. https://www.

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Evelyn

What are some effective strategies that NGOs can use to raise awareness about rare conditions like Pallister-Killian Syndrome in local communities?

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Alan

You're doing an amazing job raising awareness and supporting families affected by PKS! Every effort makes a difference in the lives of those touched by this condition. ❤️

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Nicole

So proud to support PKS Kids! Together, we can provide hope and resources to families navigating this journey. Keep up the fantastic work! 🌟

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