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The Weston Basketball Association is proud to support the A-T Children’s Project and we welcome Rob Smarz and his family from Stratford CT to our event.  Rob is 23 years old and has A-T, but that has not slowed him down.  Rob loves to play video games, snow ski and snow tube, snowmobile, horseback ride, swim, ride his ATV, work out at the gym and listen to music. He has also para-sailed, white water rafted and parachuted out of a plane!
What is Ataxia-telangiectasia (A-T):
  • Is a rare genetic disease
  • Attacks in early childhood
  • One in 40,000-100,000 babies is born with A-T
  • Affects many body systems including the brain, lungs and immune system. As such, patients may suffer from symptoms like those seen in cerebral palsy, muscular dystrophy, and certain lung disorders. They are also much more likely to develop cancer, particularly immune-related cancers such as leukemia and lymphoma.
Who is affected with A-T:
  • Both boys and girls of all ethnic backgrounds are affected
  • Most children with A-T depend on a wheelchair by age 10
  • About 30 percent of children with A-T develop lethal cancers
  • About 70 percent of children with A-T have weakened immune systems
  • 100 percent of children with A-T experience relentless loss of muscle control due to brain cell death that affects their walking, speech, swallowing and reading
  • There is currently no cure for A-T and no way to slow the progression of the disease.
  • Parents of A-T children do not exhibit symptoms of the disease, but (usually unknowingly) carry a mutated gene that causes it. Each time two “A-T carriers” have a child together there is a 1 in 4 chance that child will have A-T.
  • Similarities between A-T and other major diseases suggest knowing more about A-T could lead to therapies for more common diseases such as cancer, Alzheimer’s and Parkinson’s.
About the A-T Children’s Project:
The A-T Children's Project is a nonprofit organization founded in 1993 by Florida parents with two sons who have ataxia-telangiectasia (A-T), a rare, fatal genetic disease that affects children. The A-T Children’s Project raises funds to support and coordinate first-rate biomedical research projects, scientific conferences and a clinical center aimed at finding a cure or life-improving therapies for A-T.
What the A-T Children’s Project does:
  • Encourages and supports laboratory research to accelerate the discovery of a cure or possible therapies for A-T by:
  • Awarding competitive research grants to top scientists using a peer-review board of scientific experts
  • Sponsoring workshops and symposia to encourage cooperation among laboratories and generate new research strategies
  • Working with Congress and the National Institutes of Health to encourage U.S. government funding of active research on A-T
  • Funds a multi-disciplinary, international center at Johns Hopkins Hospital in Baltimore, Maryland and supports a Cancer Center at St. Jude Children’s Medical Center in Memphis, Tennessee to focus solely on the clinical evaluation and treatment of patients with A-T.
  • Improves the accurate and timely diagnosis of A-T patients by increasing public awareness and educating physicians.
  • Maintains an international registry of A-T patients and tissue/cell banks to provide up-to-date clinical information and resources to researchers.
  • Provides emotional encouragement, guidance and hope to families impacted by A-T through telephone support, an internet forum and family conferences.
If you would like to donate directly to the A-T Children's Project click here.  To read more about the A-T Children’s Project click here.