Hutchinson-Gilford Progeria Syndrome, or Progeria, is a rare, genetic condition that appears in children as the effects of accelerated aging. Progeria is caused by a mutation of the gene LMNA. Prior to April, 2003, the cause of Progeria was unknown. Children with Progeria die at an average age of thirteen to heart disease. Progeria was first described in the late 1800’s by Dr. Jonathan Hutchinson and Dr. Hastings Gilford.
A cure for any ailment can only come about through extensive efforts and studies. Funding for these studies is extremely costly. For this reason, education is key to finding a cure for these children. A cure for Progeria will likely also help millions of adults who suffer from heart disease and stroke as part of a natural aging process.
The Progeria Research Foundation is located in Peabody, MA. They have now located 54 children in 30 countries living with Progeria. However, researchers believe there are statistically another 150 children living undiagnosed, or not identified by the Foundation, with Progeria in the world. I have seen their volunteers work first hand at raising money and spending their time working to raise money to cure Progeria. Please give to the Progeria Research Foundation.
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