There are lots of simple ways to register. Or maybe you need to check if you are already registered.
Find out how to and what happens afterwards.
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Charlene was just 20 when she tragically died from Cystic Fibrosis. A lung disease which severely limits the lives of hundreds of young people in Northern Ireland every year.
Many with Cystic Fibrosis are not expected to live beyond their 40’s, unless they receive a lung transplant.
There are lots of simple ways to register. Or maybe you need to check if you are already registered.
Find out how to and what happens afterwards.
Charlene’s Project started in 2010 because a girl limited by so much refused to be defined by what she could not do. One decade later Charlene’s Project continues to work creating better futures for thousands of children around the world.