Meet Leatha.

I know how valuable it can be to have someone to talk with who has walked a similar road.

My kidney journey began in 2010, when I was diagnosed with IgA nephropathy and interstitial lung disease shortly after losing my mother. Just four months later, after trying to become pregnant for three years, I unexpectedly learned I was expecting. Because of my kidney and lung disease, the pregnancy was considered extremely high-risk, but my family and I made it through together.

For many years, my kidney disease remained relatively stable. Then, in 2025, my kidney function declined rapidly, and I eventually began peritoneal dialysis. I spent 12 hours each night connected to dialysis while continuing to work, attend my kids’ football games and band competitions, and stay present for the people I love.

My family was an incredible source of strength throughout that time. My younger sister was even approved to participate as a living donor through paired exchange.

I also found support through ReMend. My mentor, Dom, gave me something different from what my medical team and family could provide: the perspective of someone who understood the questions, uncertainty, and everyday realities of living with kidney disease and dialysis. He patiently answered my many questions, encouraged me, and made a lasting impact on my journey.

On April 12, 2026, after eight months on dialysis, I received the call that a deceased donor kidney was available for me. I received my transplant and, just three months later, returned to work at a San Diego nonprofit.

Now I want to give back the same kind of support that was given to me. I know how valuable it can be to have someone to talk with who has walked a similar road. I hope my experience can help others feel more informed, encouraged, and less alone as they navigate kidney disease, dialysis, and transplantation.