Hello, and welcome to my blog. My name is Shona, and I’m here to share my personal journey with kidney disease—a path that’s been filled with challenges, learning, and unexpected moments of gratitude. I was diagnosed with IgA Nephropathy (a rare kidney disease) in 2018, and life was turned upside down almost overnight. Suddenly, routine became filled with doctors’ appointments, blood tests, and an endless stream of new medical terms to understand.
As my condition progressed, I faced the daunting reality of dialysis. The thought of depending on peritoneal dialysis to do what my kidneys no longer could was overwhelming at first. However, through determination, support from loved ones, and the resilience I discovered within myself, I learned how to adapt and live fully even with dialysis as part of my daily routine.
This blog is my space to document the highs and lows, offer practical advice, and hopefully inspire others who are on a similar journey. Whether you’re newly diagnosed, preparing for dialysis, or supporting someone with kidney disease, I hope you’ll find comfort and encouragement in my story. Thank you for stopping by, and please feel free to reach out or share your own experiences—I believe we’re stronger together.
IgAN & Me 