Please Join us


October 2nd, 2014



For the Gala of Hope



We invite you to join us in what is sure to be a night full of memories, good times, and most importantly, hope.


Our dream is to live in a world were no mother will ever have to hear the words " your baby has Spinal Muscular Atrophy. There is no treatment and no cure”"

Please join us in our fight to raise awareness and help fund research.


Fiorenna and Jennifer

Help Us Find a Cure for Our Daughter


Spinal Muscular Atrophy (SMA)


As a parent, when your children are born you make silent promises to them. You promise to love them, care for them and always protect them. However, no matter how well you keep these promises, life can still be very uncertain. Aldo Israel, his wife Fiorenna, and their two precious daughters Mia and Bella are now facing the battle of their lives. Mia was only 2 and a half years old when she was diagnosed with SMA.

The Israels with their daughter Mia

Spinal Muscular Atrophy occurs in 1 out of every 6,000 children. There are currently no treatments or a cure. Aldo and his wife, Fiorenna, refuse to give up or lose hope. Mia is their little girl and they are going to do everything in their power to protect and take care of her. The Israel family is trying to raise as much awareness to this disease as possible. Awareness helps to raise more donations to help find new treatments or a cure! The Israel family is hosting "The Gala of Hope" for Mia on October 2nd, 2014 at Ferrari Maserati of Fort Lauderale.