It's with a heavy heart that I share this news. Writing these words is incredibly difficult, but I know how important it is to share our story.
We recently learned that our little girl has polycystic kidney disease and tuberous sclerosis. Polycystic kidney disease (PKD) is a chronic, genetic disease causing the uncontrolled growth of cysts in the kidney, often leading to kidney failure. I won’t dive into too many more details here because, to be honest, it’s overwhelming and frightening, but over the past few months we've faced numerous doctor’s appointments, an ER visit by ambulance, and countless sleepless nights as we try to find the best way to help our sweet baby. It's been a challenge to maintain some sense of normalcy for our family, but I hold on to one certainty—God has a plan.
Unfortunately, there is no cure for PKD. So, I'm here to humbly ask that you please support me by donating or by registering for the Walk for PKD. A CURE is my finish line.
If you can't make it to Sacramento's Walk For PKD on Sept. 29th or if donating isn't possible (which is completely understandable), your prayers would mean the world to us. Thank you so much!
Sincerely,
Tiffany
My child is a #PKDWarrior! #WalkForPKD
