The association ELEONORA’S DREAM is the fruit of a simple idea, an innate need, a temptation which is humanly difficult to resist:
“Turn a tragic experience into something good and useful for others”
Eleonora left us after only 52 days of life due to a rare genetic disease called Spinal Muscular Atrophy (SMA).
We, her family, like to think that what we had to face and live through together was not in vain.
It is our to endow her brief life with greater dignity and meaning by helping others, that is to say other children and other families looking for simple and concrete support.
