Ciara MorinSep 153 minI Opted to See a New Nephrologist and Our Initial Conversation Changed EverythingOne year ago, I asked my nephrologist to refer me to someone else... and it's not at all what you're thinking. There was never a problem....
Ciara MorinFeb 110 minThe Truth About Tolvaptan: a PKD Patient PerspectiveShedding light on my personal experience with Tolvaptan & sharing some of the truths I think all patients deserve to know.
Ciara MorinNov 7, 20223 minPain & PKD: The Invisible TruthI want to shed light on the truth by speaking about the everyday challenges that aren't often discussed by medical professionals.
Ciara MorinOct 31, 20224 minA Message to My Younger Self as Someone with PKDIf it was possible to go back in time, I'd have a lot to say to my younger self. As a teenager, I was diagnosed with Polycystic Kidney...
Ciara MorinJul 26, 20223 minHow to Use Your Voice For Change: Raising Awareness For PKDThe helpful people around us who aren't aware of what we're up against, can't support us (yet). So, how can we give a voice to this disease?
Ciara MorinJul 6, 20222 minSupplements & PKD: Are They Safe?I often get asked "what sort of supplements do you recommend for PKD?" or "is this supplement safe for PKD?" The inspiration for this...
Ciara MorinJun 23, 20223 minMy PKD Life: Finding Empowerment & Purpose Through NutritionLife with a chronic illness has its challenges, but it has also opened my eyes to a purposeful & more empowered way of living.