In September of 2023 my dad Brice Morin aka White Owl, was diagnosed with ALS. May 1st 2026 He peacfully passed away with his girls by his side one week after his 65th birthday. Brice is deeply missed by all his friends and family. Help us raise money to make a diifernce to to current and future familes who are suffering with this terrible diease.

We would also like to acknowledge his partner Nicole for all her love and care. She poured her entire soul into looking after our dad through his journey and I'm sure he wouldn't have survived as long as he did with out her by his side ! THANK YOU NICOLE !!!! We love you ! 

This summer I will be participating in the Walk to End ALS. Now more than ever, the ALS community needs our support to provide hope and help to families affected by ALS/MND. That’s why I’m joining thousands of others, a part of a passionate and motivated community to “walk” in celebration of hope and a world free of ALS, also known as Lou Gehrig’s Disease. Please consider supporting me and donating towards this important cause.

Your support will help to:

• create a better day-to-day reality for people and families living with ALS by providing community-based support throughout Manitoba as well as necessary medical equipment like wheelchairs, liftchairs, mobility aids and other items that increase safety in the home, at no cost to those who need them.
• further scientific progress by investing in the ALS Canada Research Program, which funds promising ALS research. This program provides peer-reviewed grants to researchers whose work has the greatest potential to advance the field of ALS. There’s been more progress made in ALS research in the last five years than over the last century – we need to keep building on this momentum.

Join me in making a difference. Please consider donating to my fundraising page as we work towards a world free of ALS/MND.

Your support is needed now more than ever - we are stronger together!