How the Monaco-based Only Project Association aims to defeat muscular dystrophy

Formerly known as the Monegasque Association Against Muscular Dystrophy, the Only Project Foundation brought together the cream of international research at the Monte-Carlo Bay on 16 and 17 April 2026. At the heart of these meetings: the induction of the first recipients of the ‘Pioneers’ Grant’. A major new milestone for this organisation, which has now become a key global player in the quest for a treatment for Duchenne muscular dystrophy.

The history of Only Project is rooted in resilience. Founded in 2001 by two Monegasque families faced with the diagnosis of their children with muscular dystrophy, the association immediately set itself an ambitious goal: to make a substantial and international contribution to medical research.

Luc Pettavino, president of the association and father of Paul (who died as a result of the disease), sums up this philosophy with a quote that inspires him every day: 

“The best way to predict the future is to create it.”

Refusing to accept fate, the founders were able to capitalise on the Principality’s unique environment to bring people together.

Today, the organisation is evolving. To reflect its influence, which extends far beyond the borders of the French-speaking world, it has adopted the name ‘Only Project’.

This change of identity underscores its core mission: to act across the globe, from the United States to the Netherlands, via South Africa, to support the most promising researchers.