BEGIN:VCALENDAR
VERSION:2.0
PRODID:-//ALS Society of Alberta - ECPv6.15.18//NONSGML v1.0//EN
CALSCALE:GREGORIAN
METHOD:PUBLISH
X-ORIGINAL-URL:https://www.alsab.ca
X-WR-CALDESC:Events for ALS Society of Alberta
REFRESH-INTERVAL;VALUE=DURATION:PT1H
X-Robots-Tag:noindex
X-PUBLISHED-TTL:PT1H
BEGIN:VTIMEZONE
TZID:UTC
BEGIN:STANDARD
TZOFFSETFROM:+0000
TZOFFSETTO:+0000
TZNAME:UTC
DTSTART:20250101T000000
END:STANDARD
END:VTIMEZONE
BEGIN:VEVENT
DTSTART;TZID=UTC:20260613T000000
DTEND;TZID=UTC:20260613T235959
DTSTAMP:20260404T083635
CREATED:20260117T022857Z
LAST-MODIFIED:20260401T214718Z
UID:10000007-1781308800-1781395199@www.alsab.ca
SUMMARY:Side by Side for ALS Edmonton
DESCRIPTION:Time TBA\n\n\n\n\nRundle Park Family Centre \n\n\n\nThe ALS Society of Alberta is excited to introduce a new name and look for our walk and run events across Alberta! Side by Side for ALS is inspired by Betty’s legacy (of “Betty’s Run”) and driven by hope. \n\n\n\nWe call on communities across Alberta to strengthen every connection and create lasting impact in the fight against ALS. \n\n\n\nFull event details will be available will be available soon. We can’t wait to see you there. \n\n\n\n\n\n\n\n\n\n\n\n\n\n\n  \n     Registration is Now Open\n  \n\n\n\n\n\n\n\n\n  \n\n  Hi\, I’m Kenneth Shock. My journey to an ALS diagnosis was basically a choose-your-own-adventure book where every path led to “tripping over nothing” or “talking like I gargled gravel.” I wrote it off for years as “moving too fast” (spoiler: the floor disagreed) or “just tired” (my voice had other plans). Officially\, I got the PLS (Primary Lateral Sclerosis) label in June 2023\, and then in January 2024\, they upgraded me to an ALS diagnosis. Think of it as going from bronze to platinum status…except the perks are terrible. \n\n  Here’s the deal: ALS has stolen a bunch of things from me: balance\, a normal-sounding voice\, and the ability to look cool while falling. But it will NEVER take away my sense of humor. Or my terrible dad jokes. Why don’t skeletons fight each other? They don’t have the guts… and apparently neither do my legs anymore! \n\n  I’ve decided to stop focusing on what’s leaving and start focusing on what’s still here: making new memories\, laughing until my abs hurt (which they still can\, thank you very much)\, and squeezing every ounce of joy out of life. This role isn’t about standing on a pedestal; it’s about standing side by side with every person living with ALS\, every caregiver powering through another tough day\, every family member holding on tight\, and every friend\, neighbour\, and stranger who says\, “I’m in this fight with you.” \n\n  None of this would be possible without the incredible\, unwavering support of my wife\, who’s been my rock\, my cheerleader\, and my best laugh partner through every stumble and silly moment\, and my amazing family and friends who lift me up (literally and figuratively) every single day. I’m also deeply grateful for the ALS Society of Alberta\, whose tireless work provides the equipment\, resources\, support groups\, and hope that make the hard days bearable and the good days even brighter.  \n\n   ALS is a tough opponent. It sneaks in. It tries to steal strength\, speech\, movement\, the everyday things I used to take for granted. But here’s the thing: I will never let any disease dictate my spirit. My motto is “laugh into the darkness.” I laugh because laughter is medicine\, the kind no prescription can match. I laugh at the ridiculous moments that sneak in amid the hard ones. I laugh because every chuckle is a tiny rebellion\, a spark that says\, “ALS\, you don’t get to win today.” \n\n  This year\, I want you to walk in remembrance and in hope\, because every step we take together lights up the darkness just a little more. I want you to walk for better treatments\, for a cure on the horizon\, for equipment that gives dignity back\, for support that lets families breathe easier. I want you to walk because research is advancing\, stories are being shared\, and a community like this one is unstoppable. \n\n\n\n\nI’m honoured to be Edmonton’s 2026 Side by Side for ALS Ambassador because I want to prove that even with ALS trying to slow me down\, I can still live fast\, laugh loud\, and walk together\, maybe with a walker\, maybe with a cane\, but definitely with a smile. \n\n\n\nCome join me at Side by Side for ALS on June 13\, 2026\, at Rundle Park Family Centre in Edmonton. Every step counts\, every laugh helps\, and I promise at least one more dad joke. Let’s show ALS who’s boss… or at least who’s got the better punchlines. \n\n\n\nALS doesn’t get the last word. We do.
URL:https://www.alsab.ca/event/side-by-side-for-als-edmonton/
LOCATION:Rundle Park Family Centre\, 2903 - 113 Ave NW\, Edmonton\, Alberta
CATEGORIES:Key Event,Side by Side
ATTACH;FMTTYPE=image/jpeg:https://www.alsab.ca/wp-content/uploads/2026/01/IMG_1108.jpg
END:VEVENT
END:VCALENDAR