Donate for Bruno
Together for Bruno:
Seven-year-old Heiner Bruno suffers from the incurable muscle disease Duchenne muscular dystrophy (DMD). To halt the rapid progression of the disease and enable him to live without a wheelchair, Bruno urgently needs a special gene therapy. This treatment is his only chance – but it costs approximately € 4.6 million.
Your donation can change his life
To make this life-changing therapy possible, every contribution counts. Please help us provide Bruno with the treatment he urgently needs – for a self-determined, happy life full of children's laughter, learning, and hope.
Donation account
Name: Cosplay Entertainment Austria
Bank name: BAWAG PSK
IBAN: AT41 1400 0272 1008 8577
BIC: BAWAATWW
Goal: € 4 million | 12,000 donations
Help us make this fundraising campaign a success! Make a one-time donation of € 1.000, € 500 or an amount of your choice — every contribution counts and makes a difference.
Donations € 1.000,-
Donations € 500,-
Donate desired amount
Bruno's story
Heiner Bruno is a cheerful boy born on October 11, 2016. In January 2024, he experienced severe muscle cramps in his leg – the subsequent genetic testing confirmed a diagnosis of Duchenne muscular dystrophy. Bruno is currently attending school enthusiastically, studying with great dedication and achieving excellent results – but time is running out.
About Duchenne muscular dystrophy
Duchenne muscular dystrophy (DMD) is a rare, congenital, and incurable muscle disease in which muscle cells are gradually replaced by fat and connective tissue. Affected children gradually lose their muscle strength, are usually wheelchair-bound from the age of 10, and later, their heart and respiratory muscles are also affected.
