"I sometimes maybe exaggerate a little too much how well I'm doing when I'm not really, just to give people the permission to engage. You wouldn't know that
I can barely brush my teeth anymore."

After Rick Zwiep's diagnosis in August of 2022, he was quick to become a loud and proud part of the ALS community, spreading awareness about the disease at every possible turn. Today, Rick sits on the board of directors for ALS Action Canada, where he leads a community support group to uplift his fellow pALS. Rick is also part of the ALS Super Fund's advisory council, providing his patient input as to how donated funds should be allocated across the country. Join us for a conversation of science, research, accessibility, support, and what it means to be a patient-led organization.

For more information on ALS Action Canada and the ALS Super Fund, visit https://www.alssuperfund.ca/

To view the ALS Super Fund 2024-2025 Impact Report, visit https://drive.google.com/file/d/12U8As6IIAoubCv-Ih-e2bpy9IRKifS0T/view

For more information on Everything ALS webinars, visit https://www.everythingals.org/

For more information on Eric Brunner’s project, Flickering Souls: Illuminating ALS, visit ericbrunnerart.com

For more information on the ALS Therapy Development Institute, visit als.net

For more information on Brooke Eby’s project, ALSTogether, visit alstogether.org

For more information on the Northeast ALS Alliance, visit neals.org

For more information on ALS, please visit the ALS Canada website at https://als.ca/

Episode Transcript

"When you're caring for somebody living with ALS, it's going to be tough. You can't imagine it. You can't explain it. But being there for the person after they're gone, it'll mean the world to you."

Lea Storry, believe it or not, tells stories for a living. An accomplished writer, journalist, and CALI graduate, Lea’s life was profoundly shaped by her experiences with ALS through the diagnoses of her mother, Shela, and her close friend, Pauline. Those experiences led her to create Speaking ALS: An Anthology, a collaborative writing project that amplifies the untold stories of the ALS community. Join us for a conversation spanning grief, love, science, accessibility, support, and the power of storytelling through Speaking ALS.

To support Speaking ALS: An Anthology, visit ourfamilylines.ca/speakingals

For more information on the Carey Me Fund, visit vrhfoundation.ca/carey-me

For more information on the International ALS/MND Symposium, visit https://www.als-mnd.org/

For more information on ALS, please visit the ALS Canada website at https://als.ca/

Episode Transcript

"In one sentence, our lives were turned upside down."

Andrew Dundas was diagnosed with ALS in December, 2022. Today, he's an official ALS Canada Community Ambassador, an author, and a fierce accessibility advocate who has dedicated his life to inspiring the community around him. Join us as we delve into the details of Andrew's lifelong journey of turning lemons into lemonade!

To join Andrew's Virtual Mobility Challenge, visit https://alslemonade.org/

To read Andrew's blog, visit https://myalschallenge.com/

For more information on the TIME program, visit https://abilitiescentre.org/home

For more information on the Rotary Club of Whitby-Sunrise, visit https://www.rotarywhitbysunrise.com/

For more information on ALS, visit https://als.ca/

A big thank you to Nathalie Picard for providing the music for today's land acknowledgement. We encourage you to check out more of her music here.

Episode Transcript