Federica Toffanin
Federica Toffanin is the mother of Lavinia, who was born with a very rare genetic lysosomal storage disease called Mucolipidosis 2. After Lavinia's passing in 2020, she and her partner have continued to advocate for the rights of children with chronic and incurable illnesses through their social media page 'In cammino per Lavinia'.
Global Media Ratings
Countries Mentioned
No country-level mention data available.
Interactive World Map
Each country's color is based on "Mentions" from the table above.
Recent Mentions
Italy:
Federica Toffanin is the mother of Lavinia, who was born with a very rare genetic disease.
7