Help Lara Sofia Fight Neurofibromatosis (NF1) 

Hello, my name is Ion Toma, and I’m a father reaching out with hope in my heart and a plea for support. 

My wife and I are raising funds for our beloved daughter, Lara Sofia, who has been diagnosed with neurofibromatosis type 1 (NF1)rare genetic disease , and behavior is like autism — a genetic condition that causes tumours to grow along the nerves throughout the body. This diagnosis has not only changed Lara’s life, but our entire family’s. 

Since her diagnosis, Lara has already faced serious health challenges, and her journey is far from over. As parents, it is heartbreaking to watch your child go through pain and uncertainty, knowing there is only so much you can do on your own. 

Lara is currently undergoing ongoing clinical treatment, which is essential for managing her condition and giving her the best possible chance at a healthier future. These treatments cost approximately £800 per month, and despite our best efforts, we are struggling to keep up with the financial burden. 

We are asking for your help during this incredibly difficult time. Every donation, no matter how small, will go directly towards covering Lara’s medical treatment and care. If you are unable to donate, simply sharing this page with others would mean so much to us and could make all the difference. 

Your kindness, generosity, and support give us strength and hope when we need it most. From the bottom of our hearts, thank you for standing with Lara and our family.

Denisa Nemeth

Anonymous

c paunoiu

Catalina Gonta

Valentin Barbus

DRAGOS CONSTANTIN Baltaretu

Alex Popa

Constantin Savin

Cosmin Miron

Victor Bodrug

Bledar Camaj

Viorel Ioanas

Petal Fernandes

Neurofibromatosis (NF1) rare genetic disease

Neurofibromatosis (NF1) rare genetic disease

Still £11,700 to go. Help us build momentum.