For more than twenty years, the village of Hawarden and the surrounding North Wales community have come together in support of NA research, thanks to the remarkable dedication of Gill and Gordon Parry. Their tireless fundraising efforts,  inspired by the memory of their children, Sian, David, and Mark, have created a tradition of generosity that continues to uplift our community and strengthen our work.

The annual Hawarden Walk has long been at the heart of these efforts. Each spring, walkers gather on the Gladstone Estate to follow woodland trails, share memories, and raise vital funds for NA Advocacy and epilepsy research. Rain or shine, families, friends, children, and even dogs join in the walk. Over the years, this single tradition has raised tens of thousands of pounds and brought together people from near and far.

The Irvine family, including Alex, VPS13A diagnosed patient, joined the known Hawarden walk for many years. In 2013, Alex was carried with great care by friends of Mark and David for the two-mile Hawarden hike.

But the Parrys’ impact extends far beyond the walk. Their presence at village fairs, carnivals, craft markets, and Christmas events has become a familiar and welcome sight. From handmade crafts and brooch workshops to bustling sales tables and friendly cafés, Gill and Gordon and their friends have turned creativity and community spirit into meaningful support for NA research. Their efforts have often involved entire villages, with cyclists, walkers, church groups, and local choirs joining in to help raise awareness and funds.

One particularly memorable contribution came through music, when Gordon’s former choir director returned to Wales with the Andante Chamber Choir to perform a special concert in support of NA Advocacy. Events like these show how deeply the Parrys’ commitment has resonated with others, inspiring people across North Wales and beyond to lend their voices, talents, and time.

Across countless weekends, fairs, and sponsored challenges, Gill and Gordon have raised well over £100,000 for NA Advocacy and epilepsy research. Their work has supported scientific studies, helped families, and strengthened our ability to raise awareness of NA syndromes. They have kept the memory of their children alive through acts of kindness that continue to ripple outward.

We are profoundly grateful for everything Gill and Gordon have done, and continue to do, for our community. Their dedication reminds us that meaningful change often relies on steady acts of generosity. Their story shows what can happen when compassion becomes a lifelong commitment.

To everyone inspired by their example: thank you. Whether through a sponsored walk, a bake sale, a craft table, a coffee morning, or a simple conversation that spreads awareness, your efforts help us move closer to better understanding, better support, and better futures for those affected by NA syndromes.