In The News
Check out the articles and press on Jack’s Miracle Mission Foundation.
NJ parents launch mission to find treatment for child’s fatal disease
NJ parents launch mission to find treatment for child’s fatal disease.
Jack’s Miracle Mission ✨
This month, we’re sharing the story of one incredibly special family — the Drurys — and their brave little boy, Jack. 💙
How Celebs Are Supporting 2-Year-Old Boy After Rare Diagnosis
After Tim and Kelsey Drury’s son Jack, 2, was diagnosed with Infantile Neuroaxonal Dystrophy (INAD), they launched Jack’s Miracle Mission to raise awareness and were met with overwhelming support.
Race against time: ‘Jack’s Miracle Mission’ aims to support children with progressive disease
Race against time: ‘Jack’s Miracle Mission’ aims to support children with progressive disease
Jack’s Miracle Mission to Find a Treatment for Terminal Genetic Disorder, INAD
After Jack Drury was born prematurely, he participated in therapies to help him meet his developmental milestones. Jack thrived at first, but after he turned 2 in June, his development slowed.
Big pharma won’t help, so these N.J. families are finding a cure for their kids’ disease themselves
After Jack Drury was born prematurely, he participated in therapies to help him meet his developmental milestones. Jack thrived at first, but after he turned 2 in June, his development slowed.
Their Son Could Die by Age 10 Without a Cure for His Rare Disease. They're Fundraising Against the Clock.
After Jack Drury was born prematurely, he participated in therapies to help him meet his developmental milestones. Jack thrived at first, but after he turned 2 in June, his development slowed.
Our baby was totally healthy until 8 months…
In New Jersey, a grassroots group is racing to launch the first clinical trial for a gene therapy that could give Jack — and others like him — a fighting chance.
2-year-old NJ boy in need of 'miracle' treatment: How to help
Jack Drury has been diagnosed with infantile neuroaxonal dystrophy (INAD), which causes progressive loss of motor and cognitive skills, according to the National Institute of Neurological Disorders and Stroke. Sight and speech loss are common, and there is no known cure.
Jack’s Miracle Mission was created to deliver hope and support families in the their fight against Infantile Neuroaxonal Dystrophy (INAD), a rare and devastating neurological disease. Created on behalf of our two-year-old boy from New Jersey named Jack, our mission is to raise the funds needed to make a potentially life-changing gene therapy treatment possible, not just for Jack, but for every child living with this illness. Through compassion, community, and relentless hope, we believe that together, we can turn what feels impossible into a miracle.
Today, our single mission is clear, support the INADCure Foundation fully fund the first-ever gene therapy trial, a treatment that could finally slow or stop this heartbreaking illness.
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