In the summer of 2024, our youngest son, Maksym, was diagnosed with a rare genetic condition – Duchenne muscular dystrophy (DMD).

Unfortunately, the trials for our family did not end there. The doctors explained that DMD only affects boys, so they suggested we have our older son, Vladyslav, who is now 12 years old, tested as well.

At the time when we had already opened a charitable fundraiser for Maksym, Vlad was also undergoing all the necessary examinations. When the results came back, we were stunned – Vladyslav was diagnosed with the same mutation, the same disease. Duchenne muscular dystrophy has been affecting him since he was two years old, and although the disease is progressing more slowly, doctors cannot predict its future course.

Our family finds itself in an incredibly difficult situation. We are fighting for both of our sons, and we desperately need the support of each and every one of you. Please help us save our children. Every contribution, repost, or sharing of our story is a chance for a future for our sons. Thank you to everyone who is standing by us!