I am raising money for National Society for Phenylketonuria because this cause is incredibly close to my heart.

My beautiful 5-year-old son, Oliver, was diagnosed with PKU (Phenylketonuria) shortly after he was born through the routine newborn screening test. PKU is a rare inherited condition that means Oliver's body cannot break down an amino acid called phenylalanine. Without careful management, it can build up in the body and cause serious, lifelong damage to the brain.

For Oliver, every single day revolves around his condition. He has to follow a very strict low-protein diet, carefully measure everything he eats, and take specialist protein substitutes to help him grow and stay healthy. Something as simple as grabbing a snack, going to a birthday party, eating out, or enjoying school events requires planning and preparation that most families never have to think about.

Despite these challenges, Oliver is a happy, funny (and very cheeky) little boy who takes everything in his stride. I couldn't be prouder of him.

I am raising money for the National Society for Phenylketonuria because they provide invaluable support to families like mine. They offer trusted information, practical advice, emotional support, and work tirelessly to raise awareness of PKU while campaigning for better treatments and a brighter future for everyone affected by the condition.

Every donation, no matter how big or small, will help the NSPKU continue supporting families, funding research, and giving hope to children like Oliver.

If you're able to donate, thank you from the bottom of my heart. If you can't donate, sharing the fundraiser would mean the world to me.

Together, we all can make a real difference for everyone living with PKU.

Thank you for supporting Oliver and the PKU community!

Emily