"Without the ALS Society, I wouldn't have been able to stay at home as long as I could. It's always done on a family level. We are one big family - personal connection with the people, both family and staff. My sleep quality is very good with the bi-pap; it helped right off the bat. The moral and physical support is exceptional as well as support for the family. In the summer of 2015 I experienced shortness of breath and in May of 2016 I was diagnosed with ALS. I lived in Camrose with my wife Violet since 1993 until 2004. In 2004, we moved to Edmonton, then back to Camrose in 2012 where my wife was born and raised. I was born in Lausanne, Switzerland." - Henri Unverricht