Behind this fiction story there is a very real cause.
Meet the Foundation
The foundation the PKU FOUNDATION and OTHER METABOLIC DISORDERS, is a non-profit entity recently founded in 2018 by a group of parents of the Catalan Association of Metabolics Hereditaris PKU/ATM Trastorns, with the aim of meeting the needs of people affected by inhered metabolic disorders.
With actions such as the release of the short film “ PKU: Protein Kills Us” we intend to publicize this disease and raise funds for our main objective: to finance the Home Phe Monitor that would allow real-time monitoring and, in this way, regulate the blood protein level of the people with PKU.
To facilitate a safe and transparent donation, we redirect you to the official website of the PKU Foundation, where you can help us easily.
What to you takes a few second it will be reflected in thousands of lives.
Contact Information
Tel. + 34 932 287 810 | E. info@fundacionpkuotm.org
We need to raise funds to develop the Home Phe Monitor
Learn the story of Candela, the girl who inspired «PKU: Protein Kills Us»
A project that, thanks to you, will help the financing of the Home Phe Monitor and that will change the life her and thousands of people.
