When our wonderful daughter Rebecca Zoe was diagnosed with Spinal Muscular Atrophy (SMA), we were completely lost…for months we kept thinking what to do and how to tackle everything. Then, thanks to a few friends, we decided to create an association to raise funds for Research, the best we could
do.

We would also like to help those who felt and unfortunately will feel lost, will feel pain and anger when something like this happens.

We would also like to let people understand which problems a disabled person and his/her family should tackle in every day life.

Many people tell us that we are strong. We believe that strength is a natural process when the future of our children is at stake. It is normal to struggle.

When the going gets tough, the toughs get going.Impossible is nothing!!!

Elena Muserra

Luca De Luca