This website and It’s Rare For Me project is organised and funded by
Chiesi Global Rare Diseases

This website and It’s Rare For Me project is organised and funded by Chiesi Global Rare Diseases

This website and It’s Rare For Me project is organised and funded by Chiesi Global Rare Diseases

NEVER GIVE UP!

Natasha

“High school, that was the hardest part of my life… but what kept me going were my goals.”

Diagnosed with beta thalassemia as a baby, Natasha has always been a strong child with a constant eagerness to learn and show what she could do. That determination has guided her through life: despite facing stigma in high school due to frequent medical absences, she responded by achieving the highest marks. Today, she is actively involved in the Thalassemia Movement, a local patients’ association where she both finds and offers the understanding and support essential to navigating life with the condition.​

DISEASE

Beta thalassaemia

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