Living with ALS is exhausting. Traveling with ALS is a tiredness beyond comprehension. Being the caregiver for someone with ALS who is exhausted and traveling is equivalent to cafeteria full of kindergarteners crying and helpless.
Insert: Dr Bronson Lester
In order for me to show up, interact with others, represent Her ALS Story and effectively participate in the symposium it takes all of the both of us. Fortunately many caregiver conference fees are waived, but we are still paying for two of most things: flights, meals, etc.
It feels great that we are supported by friends and family of our own, as well as the added support from sharing our story with your network. Bottom line: help me get this freeloading friend to Montreal so I can make him work and sing for his supper 😉
We love yall so much!
SunnyStrong 