episode 5: complications and mental health

In this episode, I sit down with Gerald Major, he's the President of the Canadian Spondylitis Association (CSA). He provides an overview of the findings of a recent CSA survey titled, Addressing Comorbidities of Spondyloarthritis Through Patient Organization Partnerships, that indicates the vast number of patients who experience mental health issues and other medical complications... Continue Reading →

podcast episode 4: coping and staying positive

In this episode I speak with my new friend, Victoria Elliot Gibson, a fellow patient and health professional. We chat about ruts, staying positive, coping and not letting your illness define you. Victoria has had some pretty intense years of psoriatic arthritis and associated autoimmune complications, and somehow manages to be an amazing role model... Continue Reading →

podcast episode 3: first symptom stories

In this episode I chat with Jennifer Boyle from Patient Partners in Arthritis. We share our 'first symptom' stories, what psoriatic arthritis feels like for us and she tells me about a new Psoriatic Arthritis Guidebook; Answers and Practical Advice she developed with the Canadian Spondylitis Association. I was excited to sit and chat with... Continue Reading →

wait, what is psoriatic arthritis?

Big words, stats and long winded explanations are easy to come by when googling a medical condition. Let's strip all that away and just quickly touch on what psoriatic arthritis (PsA) is at a basic level. my armour that decided to attack Sorry, I'm getting ahead of myself. An autoimmune disease simply put, is when your immune... Continue Reading →

welcome

When you think of arthritis you don’t think of a twenty-something hopping off her road bike at the end of a 40km ride; that’s ok, it’s not what I pictured either, until it was me. This blog gives my perspective living with an invisible illness, psoriatic arthritis.

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