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Our two boys, Conor and Dean are living with Duchenne Muscular Dystrophy (DMD) – a rare, muscle wasting condition for which there is no cure.

Their diagnosis means that their muscles don’t work the same as other children’s; and gradually they will be unable to do many of the things they love, such as running, dancing and wrestling.

Although the boys’ condition is life-limiting – we want to remove as many barriers as we can for them, by providing the range of equipment and level of care that they will need to perform ordinary tasks each day of their lives. 

The boys will require power wheelchairs, profile beds, a mobility vehicle and ultimately, an adapted family home – with lifts and ceiling hoists- to cater for their growing needs.

If you can, please be part of our journey and support our cause through the link below.

Every single donation will be gratefully received and will help us to build a future for Conor and Dean.

Buíochas mór ó chroí,

Karen and Jamie

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