Support for Ola

Ola fundraising image

Bartosz has been with NCPS for nearly ten years and his daughter Ola suffers with a genetic disease, where she is missing one gene from her skin filaggrin. This is responsible for the protein barrier against bacteria and viruses and also moistursing the skin; without the gene it means that Ola’s skin is constantly dry. In addition to this problem, Ola has many different allergies and she was diagnosed with pancreas and liver dysfunction.

NCPS staff and Directors are proud to have raised €1,700 to help with the cost of Ola’s medical expenses.

 


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