Adam's Life Moments
Step into Adam’s world – his everyday moments, his quiet battles, and his radiant smile.
Through these videos, you’ll meet a little boy living with Duchenne muscular dystrophy. Despite the challenges, Adam’s days are filled with love, courage, and a joy that shines through even the toughest moments.
You’ll see how Adam and his family face this rare disease – from daily routines to treatments – and how they hold on to hope while finding beauty in the little things. These snapshots of his life are touching reminders of strength, resilience, and the power of standing together.
💙 If Adam’s story touches your heart, please share it and help us support him on his journey to a brighter, healthier future.
9-year-old boy from Transcarpathia, Adam Major, is suffering from Duchenne muscular dystrophy. A tremendous wave of support has formed to help his recovery / TV2 Mokka, a Hungarian TV morning program (March 15, 2025)
Ádám continues to fight Duchenne muscular dystrophy with unwavering determination; the report shows the changes of the past months and the treatments still needed. / TV2 Mokka, a Hungarian TV morning program (October 16, 2025)
Duchenne & Adam Video Stories – See What We See!
This page was created to share the small but deeply meaningful moments that shape Adam’s everyday life — moments that are both heartwarming and thought-provoking. Through the videos, we get a glimpse into what life is like with Duchenne muscular dystrophy, the challenges a young boy with a muscle disorder faces, and how each small step becomes a true victory.
This is not only a story of healing — it is also a story of hope. The strength of the family, the power of medical care, and the support of a united community all come together to help give Adam the chance for a fuller, happier childhood.
The “United for Adam” Foundation dedicates every donation to Adam’s medical treatments, therapies, and the improvement of his quality of life. By sharing the family’s journey and Adam’s videos, we hope to inspire and bring hope to others facing similar challenges.
Be a part of this journey! Support Adam so that his childhood can be about more than illness — let it be filled with play, growth, and love. Because every child deserves that.
Videos About Duchenne Muscular Dystrophy
Duchenne muscular dystrophy is a rare genetic disorder that causes progressive muscle weakness. In this section, you’ll find various videos that offer insight into the nature of the disease, the appearance of its symptoms, as well as current research and treatment options.
The Natural History of DMD (Duchenne Muscular Dystrophy)
Tests and Outcomes - DMD (Duchenne Muscular Dystrophy)
Duchenne Muscular Dystrophy (DMD): Gene Therapy and How Muscle Responds
The videos above help us understand what it means to live with Duchenne muscular dystrophy — a condition that turns everyday life into a significant challenge. The diagnosis can often be shocking, but knowledge, early detection, and continuous medical supervision can make a meaningful difference in managing the disease. New and promising treatment options — such as gene therapy — offer hope to many families who fight every day for their children.
These videos not only inform but also provide support to those affected and help raise awareness in society. Every share, every bit of interest, and every act of support matters — because together, we can do more for the children facing this difficult, yet not hopeless, battle.
🎗️ Thank you for taking the time to learn about us. Every bit of attention, support, and sharing brings us closer to giving Adam and others like him a chance at a fuller, happier life. 💙
