About The little hercules foundation
The Little Hercules Foundation: Empowering Children with Duchenne Muscular Dystrophy
The Little Hercules Foundation is a non-profit organization that was founded by three moms who have sons living with Duchenne muscular dystrophy. This debilitating disease affects one in every 3,500 boys worldwide and is characterized by progressive muscle weakness and wasting. The foundation's mission is to raise funds to support groundbreaking research that will save this current generation of boys.
Duchenne muscular dystrophy (DMD) is caused by a genetic mutation that prevents the body from producing a protein called dystrophin, which helps keep muscle cells intact. Without this protein, muscles become weak and eventually stop working altogether. Boys with DMD typically lose the ability to walk by their early teens and often die from respiratory or cardiac failure in their twenties.
The Little Hercules Foundation recognizes the urgent need for effective treatments for DMD and has made it their goal to fund research that will lead to a cure. They work closely with leading scientists, researchers, and clinicians who are dedicated to finding new therapies for this devastating disease.
One of the ways they raise funds is through community events such as walks, runs, bike rides, auctions, and galas. These events not only help raise money but also bring together families affected by DMD as well as supporters who want to make a difference.
In addition to funding research projects directly related to DMD treatment options such as gene therapy or exon skipping technology; The Little Hercules Foundation also supports programs aimed at improving quality of life for children living with Duchenne muscular dystrophy such as physical therapy sessions or adaptive equipment purchases like wheelchairs or braces.
The foundation's efforts have already made an impact on the lives of many children living with DMD. They have funded several promising research projects including gene editing techniques using CRISPR-Cas9 technology which could potentially correct mutations in the dystrophin gene responsible for causing DMD.
The Little Hercules Foundation is committed to making a difference in the lives of children with DMD and their families. They believe that by working together, we can find a cure for this devastating disease and give hope to those affected by it.
In conclusion, The Little Hercules Foundation is an organization that is dedicated to raising funds for research aimed at finding a cure for Duchenne muscular dystrophy. Their efforts have already made an impact on the lives of many children living with DMD, and they continue to work tirelessly towards their goal of saving this current generation of boys. By supporting The Little Hercules Foundation, you can help make a difference in the lives of those affected by this debilitating disease.