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Welcome to Jack's Kids

The heart of Jack’s Kids is to ease the financial burden to families dealing with serious childhood illnesses and/or serious disabilities so they can focus on wrapping their family in the love and attention they need.

Kids Stories

Read the stories of Jack's Kids below

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Nicholas was born on May 20, 1996 with Oromandibular Limb hypogenesis syndrome, or Hanhart syndrome.
On June 29, 2012, we received the news that Simon was diagnosed with adrenoleukodystrophy, or ALD. ALD is a rare genetic disorder (affecting one in 21,000 males) characterized by the inability of the body to break down “very long chain fatty acids” (VLCFA). In the cerebral variety of ALD (which Simon has), VLCFA ...
Emily’s diagnoses includes cerebral palsy, global developmental delays, myoclonic astatic epilepsy, apraxia, sensory processing disorder, and re-flux.
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Upcoming Fundraisers

Here are some events where you can make a difference.

Volunteer Registration

Why we need your help?
We are a 501(c)(3) organization that is made entirely of volunteers that open their hearts to help local families in their time of need.

HOPE & RELIEF FOR LOCAL FAMILIES

WE WANT TO HELP AS MANY AS WE CAN

YOUR SUPPORT WILL BRING INSIPRATION

GIVE BACK TO THE COMMUNITY

Thank you for your continued support.