Donate to Action 4 Arvin here.
Action 4 Arvin
Nothing can prepare you to hear such devastating news it felt like our hearts had been ripped out. It takes away all the dreams you have for your child and you start grieving for the life that they should have. Arvin looks like any other normal healthy child but on the inside his muscles are wasting away, no parent should ever have to see their own child die or waste away before their eyes. It’s been a struggle to come to terms with the diagnosis and what the future holds for Arvin but we are strong, resilient and willing to fight for Arvin. Currently there is no cure for DMD and treatments like steroids are used to delay the progression, but this comes at the price of side-effects. The cure is getting closer and closer with rapid advances in the medical science and recent breakthroughs in gene therapy for the first time there is some light at the end of a very dark tunnel. However, the boys need it now for a chance to live a healthier and longer life, it’s a race against time and we need to act now. Our mission is to raise awareness and as much money as possible to fund research in order to find a cure for this cruel disease. Help us reach our goal and eliminate Duchenne. Support us: Donate to Action 4 Arvin here.