Hi, my name is Amanda. I’m one of Kova’s moms. My family needs some help to get our son Kova his next kidney transplant.

Kova Jeffery Jemec was born March 31, 2020, with bilateral renal dysplasia due to a lower urinary tract obstruction. At two days old he had his first surgery to create an opening to help empty his bladder. Despite this surgery, his kidneys completely stopped working at 8 weeks old and he started daily dialysis. Kova spent the first 6.5 months of his life in the hospital. He went home at 6.5 months and did peritoneal dialysis at home nightly for 12 hours. Despite being on dialysis Kova did quite well at home for a year after his release from the hospital. However, dialysis is not a good long term solution for kids. Kids with end stage kidney disease have many complications including anemia, hypertension, trouble eating, fragile bones, and delayed growth.

Babies on dialysis have to get to 22 pounds to be eligible to get a kidney transplant. Kova hit that weight in August 2021 and started his work up for transplant. In February 2022, his first kidney transplant failed due to a clot. He spent 3 weeks in the hospital, got released for 2 days, and then his abdominal incision opened up and he had to have emergent surgery to close his abdomen. This led to another 3 week hospital stay. It was determined he can no longer do peritoneal dialysis at home due to the excess scar tissue in his abdomen. Currently Kova is doing hemodialysis 3 times a week at the hospital, which is approximately 90 minutes away. (We have no pediatric dialysis centers in Lakeland so we have to travel). We will be taking him to a larger, more experienced center for his next transplant- as recommended by his doctors. This center will be farther away. We are currently looking at Cincinnati, as they are one of the top children’s hospitals in the country. We are awaiting a date for the evaluation in Cincinnati currently (expected to be sometime in July). We have a potential living donor willing to donate her kidney to Kova, but there will be many upcoming expenses. (One of Kova's moms will be staying with him at the new transplant center, while the other stays and works. Kova is required to stay in the area for 6-12 months after surgery so that medication can be adjusted and he can be monitored for any complications. With only one income and two residences it will be costly. There will be travel expenses for our family and the living donor, as well.) We are so incredibly grateful for any amount you can contribute to help save our son! He is the sweetest, strongest little man ever.