My name is Augustin, I'm 9 years old, and I was diagnosed with Duchenne muscular dystrophy at age 4. Duchenne muscular dystrophy (DMD) is a genetic disorder that causes progressive muscle weakness and wasting. It is the most severe type of muscular dystrophy, primarily affecting boys and characterized by a deficiency of the protein dystrophin, essential for muscle health. Symptoms usually appear around age 4. Duchenne muscular dystrophy weakens my entire body day by day. Loss of gait: Most boys require a wheelchair by age 9. Generalized weakness: Muscle weakness extends to the arms, neck, and other muscles. Scoliosis and contractures: Weakening of the back muscles can cause a curvature of the spine, and stiffness of the joints (especially in the ankles, knees, and hips) can limit movement. Adults Cardiomyopathy: The heart muscle weakens, causing heart failure and is the leading cause of death. There is currently no cure, only treatments. It is very important that I receive my therapies to prolong my life and improve my quality of life. Currently, my medical team is at the Neuromuscular Hospital of Rochester. I have an incredible team of doctors in all specialties. Duchenne muscular dystrophy affects the entire body. My parents have worked since I was 4 years old to provide me with everything I need for my condition and to ensure I always have access to my medical devices and therapies. I would like a power wheelchair to be more independent and not tire out. As a family, we appreciate every prayer for our son, who is truly a wonderful and courageous boy. And thank you for every donation. The funds raised will be used for my treatments and therapies, and for my power wheelchair. Thank you for your support.