My Story
Hi, I’m Trish! At 20, I had an acute lupus flare that was controlled but left me with kidney function at 32 eGFR. Life carried on as usual for the next 15 years, with regular three-month doctor’s visits to monitor my kidneys. Like many of you, I eventually caught COVID-19, which led to my need for a transplant. On December 13th, I received a live, planned kidney donation—just in time for Christmas. I feel incredibly blessed to have such a generous donor and an amazing support system of family and friends. This truly feels like a fresh start and an opportunity to pursue my passions.
I know many people are still waiting for a transplant or are on dialysis, and I don’t take my transplant for granted. My thoughts are with all of you still on that journey.
A friend once told me, “You won’t realize how sick you were until after the transplant,” and I can’t believe how right she was. Since my transplant, I’ve already noticed a huge energy boost, I’m mentally clearer, and I’m excited to get back to my passions—traveling, hiking, and swimming. It’s amazing how much better I feel!
The journey wasn’t always easy—there were plenty of tears (more than I care to admit), moments of fear, excitement, and many highs and lows. Along the way, I encountered a few surprises—like how swollen my tummy would be for the first six weeks after surgery, how much your loved ones go through (sometimes more than you, since you’re at least on medication), and how quickly the doctors want you up and moving—sitting or standing—right after surgery!
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