About

We are a collective of patients, allied health professionals, doctors, lawyers, advocates, & researchers

(more committee bios coming soon)

barbara findlay

barbara findlay KC is a fat old white cisgender queer lawyer with ME and fibromyalgia, who has been an activist in Vancouver for five decades. She creates art about living with her disability. (oil painting by Rojina Farrokhnejad)

Amanda Kanuka

Amanda is a LifeLineBC mega worker bee and organizer with MLA letter writing campaign experience. She organized and helped lead BC-CLMF patient self directed virtual neuroplasticity practices, all while maintaining her decades of award winning Household CEO skillz. She has participated in all of Dr. Arseneau's offerings since 2014, having been sick on and off for 30+ years

Kate Holley

Kate Holley is a coordinator extraordinaire, bringing people and information together wherever they’re needed. With a background in communications, advocacy, and community building, she has become a unique asset to the LifeLineBC team. After developing disabling Long COVID symptoms, Kate experienced first-hand just how life-changing the BC-CLMF clinic’s support can be- it has saved her many times over. She is deeply passionate about fighting for its future so that thousands more like her can continue to access the life-saving, high-quality care they deserve.

Kayli Jamieson

Kayli (she/her) is a Long COVID Research Fellow at SFU’s Faculty of Health Sciences and a Communication Master’s student living with Long COVID & ME since Dec ‘21. She is also a science communicator and advocate.

Katy McLean

Since developing Long COVID & ME/CFS in 2020, Katy McLean (she/her) has been a patient advocate and research partner for post viral illness. Katy worked in urban planning before getting sick and remains very committed to community engagement, social justice and the arts. Katy has been a co-organizer with Millions Missing since 2024.

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