This week on Take a Pain Check, we’re joined by Ela Murray, a university student who has been living with Central Nervous System Vasculitis which an invisible, life-altering condition since childhood.Symptomatic at just 8 years old and diagnosed at 16 during the height of COVID, Ela shares what it was really like navigating years of uncertainty, MRIs, a brain biopsy, steroids, seizures, and university life while still finding her voice as a young advocate.In this episode, we talk about:• Delayed diagnosis and navigating complex medical systems• The impact of steroids on body image, confidence, and mental health• Living next to a hospital while trying to experience “normal” university life• Finding purpose through advocacy and youth representation• What it means to show up vulnerably on stage and in everyday lifeThis episode is a reminder that young patients deserve to be heard, believed, and supported both medically and emotionally. Watch now, share with someone who needs to hear this, and join us in prioritizing youth voices in healthcare.Donate to Take a Pain Check Today: ⁠https://www.gofundme.com/f/takeapainc...Vasculitis Canada: https://vasculitis.ca/Our socials:

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Your pain might not mean damage and that could change everything. In this episode of Take a Pain Check, we sit down with Vanessa Blackstone, Executive Director of the Pain Psychology Center, to talk about Pain Reprocessing Therapy (PRT) — a science-backed approach helping people move beyond “just managing” chronic pain. We break down how the brain can learn pain, why fear keeps symptoms stuck, and how safety, language, and emotional trust can unlock real recovery. If you’ve been told your pain is permanent, this conversation may completely change how you see your body.

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What happens when both a mother and daughter are diagnosed with psoriatic arthritis?In today’s episode, we sit down with USPORTS basketball athlete, advocate, and STEM Without Limits scholar, McKinley Penninga, and her mom Lisa Penninga, to talk about navigating life as a family living with the same chronic illness.Diagnosed years apart, McKinley and Lisa share:- how psoriatic arthritis shaped their mother-daughter bond- the early signs Lisa saw in McKinley based on her own lived experience- what it was like recognizing symptoms she personally knew all too well- how both supported each other through flare days, school challenges, and identity changesMcKinley opens up about staying in basketball, balancing varsity-level training with chronic pain, and proving that invisible illness doesn’t define your athletic ability. Lisa shares the parent perspective while managing her own health needs — something rarely talked about in chronic illness stories. Together, they discuss advocacy, youth voice in healthcare, the STEM Without Limits Scholarship, and how their shared experiences are shaping the healthcare provider McKinley hopes to become.Donate to Take a Pain Check Today: ⁠https://www.gofundme.com/f/takeapainc...Our socials:https://www.takeapaincheck.com/https://www.instagram.com/takeapaincheck_/ https://www.tiktok.com/@takeapaincheckhttps://ca.linkedin.com/company/take-a-pain-checkhttps://www.youtube.com/@takeapaincheckhttps://www.facebook.com/TakeaPainCheckhttps://www.x.com/takeapaincheckDon't forget to like, comment, and subscribe for more episodes.