Dads of Epilepsy
"The hardest part of being a parent is watching your child go through something really tough and not being able to fix it for them."
This year we are following up our mom stories with stories from a dad's perspective. A father's role is the protector of his family, so what is it like when he is at a loss as to how to protect his child from having seizures? Please take the time to read and share these heartfelt stories from dads of epilepsy.
Jim – Father of Jonathan
In November of 2012, my son Jonathan had the first seizure of his life at age 16. Up until this point, epilepsy and seizures were something that I knew about but not intimately like I was about to. Jonathan had three grand mal seizures within 2 weeks – all at school. Later when I did see him having a grand mal seizure, it left me feeling very sad, helpless and discouraged that I had no power to conquer this for him.
Barry – Father of Kate
Our daughter, Kate, was born perfectly healthy. As first time parents, we were delighted with our new family addition. For two and a half months we experienced what millions of young parents go through every day. Then, at the end of November 2012, we experienced Kate's first seizure.
Max – Father of Emily
For some reason, I never really paid attention to epilepsy. It always seemed to be someone else's concern as I didn't know anyone who had it, or at least I didn't think I knew anyone. It wasn't until my daughter, Emily Austin-Ward, was diagnosed with epilepsy in July of 2016 when she was 9 years old that I woke up to the world of life with epilepsy.
Don – Father of Katie
Flying over the Rocky Mountains yesterday made me think how small I feel in the big picture of life. When you think about the journey each of us makes, no one knows what the next day holds. And watching any of our children suffer is tough.
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