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Matteo's Mob | Fighting Cystic Fibrosis HELP MATTEO FIND A CURE FOR CYSTIC FIBROSIS. CLICK ON THE SQUARES TO THE LEFT. Good luck everyone and thanks for your support. Mobsters on the Move Scholarship The Matteos Mob Foundation is not only committed to raising money for Cystic Fibrosis research but also keeping those living with CF active so they can live their best life.
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Organisations from Matteos Mob Foundation
1. Greater St Louis Data Professionals Association
Connect with other people who love the same things you do.
2. Catholic Healthcare International
CHI has a formal Collaboration Agreement with Padre Pio's Home for the Relief of Suffering, the Vatican-owned hospital in Italy, to replicate it in the USA, with a Medical School.
3. Rockwood Parent Teacher Organization Council
Rockwood is St.
4. Rockwood Parent Teacher Organization Council
Rockwood is St.
Kids Central helps create brighter futures for children and families in Citrus, Hernando, Lake, Marion, and Sumter Counties (Circuit 5) and Central Florida.
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Cure SMA is dedicated to the treatment and cure of spinal muscular atrophy (SMA).
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LIVEFIT WITH LUPUS is dedicated to raising awareness of autoimmune diseases and over-coming life's challenges by living a fit and healthy lifestyle.
Since 2015, DHF has raised nearly $15 million and has funded 67 cutting-edge research studies that are changing the future of digestive health.
Similar Organisations Worldwide
Organisations in the world similar to Matteos Mob Foundation.
HEARTLANDS CYSTIC FIBROSIS CENTRE (uk)
The West Midlands Adult Cystic Fibrosis Centre/Heartlands Cystic Fibrosis Centre, Ward 26, Heartlan.
CF Warriors is a charity focused on promoting sport and exercise to help people with cystic fibrosis to be as fit and healthy as possible.
To provide the education, support and services that empower people in the cystic fibrosis community.
Cure4CF Foundation Limited (au)
Raising funds to find a cure for cystic fibrosis.
Interesting nearby
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Raising awareness and funding for Wolfram Syndrome research, an ultra rare disease.
Encouraging, empowering, & educating those living with Li-Fraumeni Syndrome (LFS) and genetic cancer.
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