Goalkeeper Andrew Lonergan and his wife Jennifer, whose two-year-old daughter suffers from a rare genetic disorder, are planning a summer of fundraising.

Millie Lonergan suffers from phenylketonuria (PKU), a recessive genetic disorder which, if left untreated, can affect brain development leading to mental retardation and seizures.

There is no cure for PKU, but experts say it is one of the few genetic diseases that can be controlled by diet and careful monitoring by specialists.

The Preston North End keeper said: "Millie was diagnosed with PKU at only a few weeks old during a routine blood test.

"At home we take Millie's blood once a week to check her levels are stable. She attends hospital every three months for a developmental check which includes a general health check, measuring and weighing, plus dietary advice."

"Jennifer and I want to repay the Willink Biochemical Genetics Unit at the Royal Manchester Children's Hospital for providing constant support for Millie."

The couple intend to raise awareness of metabolic disorders by raising money for the GEM Appeal (Genetics, Enzymes, Metabolism), which supports the Willink Unit.

Jennifer will take part in the Great Manchester Run 2009.

Andrew added: "We are truly grateful for all the help and support we receive and want to give something back.

"That is why we want to raise money and awareness for the GEM Appeal, so they can help many more children in the future."

You can help this fund-raising bid by visiting www.sponsorjen.com or www.justgiving.com/lonergan.

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