Save Laurinha

#SAVELaurinha.

Laurinha is 9 months old and at 7 months she was diagnosed with a very rare disease called SMA (spinal muscular atrophy).

The cure is the most expensive treatment in
the world. Her parents are simple workers like
you and are desperate to get the highest
amount possible to buy the medicines that cost around 2 million dollars.

Every help is welcome.

THINK! what if it was your son?

If you want to know more about the disease. 

Visit:
https://www.mda.org/disease/spinal-muscular-atrophy