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Children's Interstitial Lung Disease - ChILD Foundation

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chILD News

Join the chILD Foundation and the Boston Children’s Hospital for a Lung Family Reunion

The Lung Family Reunion is both fun and educational weekend for children, siblings, and families affected by Children’s Interstitial Lung Disease (chILD). chILD specialists and clinicians will be leading informative presentations and engaging discussions. Families will have an opportunity to learn about these complex diseases, while socializing in a fun and welcoming with others on similar journeys.

chILD Foundation Nominates Joe McMonigle as Chairperson

The chILD Foundation is excited to announce that Joe McMonigle as the new Chairperson of the Board. Joe has served in several capacities on the board, including member, treasurer, and vice-chair, over the course of several years. Joe brings a strong, family centered vision to the board. Stay tuned for more updates!

November 28th is Giving Tuesday!

Every year the chILD Foundation participates in Giving Tuesday. This global day of giving recognizes the important roles that non-profit foundations, like the chILD Foundation, play in improving society. We also want this day to recognize those that make our Foundation and the important work we do possible, our donors! Please consider giving to give a child a breath of hope!

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The chILD Foundation establishes Scientific Advisory Committee

chILD Foundation board chairman Aaron Knobloch has announced the formation of a Scientific Advisory Committee (SAC) consisting of leading physicians and researchers focusing on chILD disorders. The committee will help guide the board regarding research priorities as well as how to document and share research findings.

Join us September 16th for a NY chILD Family Event

Hosted at NYU Winthrop Research and Academic Center on Long Island, this special event will provide valuable information for families coping with chILD. Check-in begins at 8:00 am and the program runs to 2:30 pm. It will include such topics as: chILD conditions and history, updates on research and treatment, national registry and the chILDRN Research Network, living with chILD, and family care tips.

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