duchenne

What does it do?

  • Association founded in 2008 thanks to the initiative of a group of families with children affected by Duchenne and Becker muscular dystrophy.
  • It works towards finding a cure or treatment for these diseases.
  • The Association promotes and funds clinical research, psychosocial care services, awareness campaigns and educational programmes.

What countries does it work in?

  • Currently in Spain, through families with children affected by these diseases.

Other information of interest

  • Since 2012, the foundation has raised more than €1,000,000 for research.

Choose how you want to collaborate with
Duchenne

Apply for your card Transfer to NGO

 

 


Solidario

Collaborate

with the solidarity causes that concern you using the Solidarity Card or Transfer.

 

Just choose the NGO or foundation you prefer and the amount to donate.

Find out more