Back to top

Isaac Fraser

Isaac's mom became concerned that something was wrong when, as a baby, he was not reaching typical developmental milestones.

At eight-months-old, Isaac was referred to the IWK where he was diagnosed with a rare form of congenital muscular dystrophy – a neuromuscular disease that impacts every muscle in his body.

Isaac Fraser, IWK Patient

The IWK is a big part of our lives. We’d be lost without them.

~Sarah MacKinnon, Isaac’s mom

Thanks to the incredibly generosity of donors, Isaac has access to leading-edge equipment and the expertise of IWK care teams – all working together to help him live a fulfilling life.

Watch Isaac's story

 

Share this Story with Others!

 
 
Zaccari, IWK Patient

Zaccari

Born with a rare and life-threatening kidney disease, Zaccari needed a kidney transplant to survive. In February 2018, his mom received the call that would save her…

Alyssa Rose, IWK Patient

Alyssa Rose

After experiencing frequent headaches and blurry vision, Alyssa was diagnosed with a tumour on her brain stem that required a complex surgery.