Genetic Research is the way


Donation is fundamental when Institutions are lacking.

We have decided to steer our forces towards an International Genetic Research which is Project MinE.

But donation is also very personal - it is you who decides where to put your money. That is why you are totally free whether or not to accept the suggestion to support Project MinE.

However, the reason behind this choice is that we do believe that researching across the DNA and sequencing the Genome is the key to unlock the knowledge we need in order to fix - once and for all - the MND/ALS in the world.

Below a brief description of the Project MinE and the link to its website: there you can find all the details, you can proceed with your donation and you can also start a campaign to raise money and spread awarness.

If you prefer, you can also Donate via crowdfunding: 100% of all donations will go directly to ProjectMinE to map and analyze DNA profiles.

Project MinE

International Groundbreaking Genetic MND/ALS Research

To understand the genetic basis of MND/ALS and to ultimately find a cure for this devastating, fatal neuromuscular disease, Project MinE aims to analyse the DNA of at least 15,000 ALS patients and 7,500 controls. The resulting 22,500 DNA profiles will be compared.

Project MinE is a patient-­driven groundbreaking genetic MND/ALS research.

The project is a worldwide collaboration between MND/ALS centres and foundations.

Make it yours!