Your dialysis social worker is a key member of your health care team, providing you with emotional support, connecting you to helpful resources and more. Learn about how they help you fight kidney disease in our Webinar recap: Ask a social worker blog post. READ MORE >>

In our work to increase kidney transplants through living organ donation, we’ve met inspirational allies in state legislatures around the country. In 2019, we worked to introduce legislation to protect living donors in 14 states—and nine of those passed the legislation! READ MORE >>

What does a second chance mean to you? For kidney patients like Miles, Ken and Alysia, a second chance means the ability to live life on their own terms. READ MORE >>

People with kidney disease are at higher risk for foodborne illnesses. As we head into Thanksgiving, our guest blog post from @FoodSafety.gov shares four simple steps that can help protect you and your family from foodborne illness this holiday season. READ MORE >>

Izzy is four years old, loves the dog park and is a certified people-magnet. But she means so much more to her owner Tony, who inherited her from his late friend, Jay. READ MORE >>

Did you know that keeping a healthy weight after a kidney transplant is just as important as keeping a healthy weight before transplant? If you missed our webinar on managing weight both pre- and post-transplant, catch up on the highlights in our webinar recap blog post. READ MORE >>

One way to fight kidney disease is through watching what you eat. Making easy changes to common Hispanic foods can give a healthy boost to recipes the whole family enjoys. Learn more about Kidney-friendly Hispanic food for people with diabetes on our blog. READ MORE >>

Historically, racial and ethnic minorities (referred to here as minorities) are underrepresented in clinical trials. This is unfortunate because kidney disease disproportionately impacts African Americans and Hispanics. READ MORE >>

My name is Beth Nalker, and I’m fortunate to call myself Henry’s mother. When Henry was diagnosed at age five with progressive kidney disease by doctors at Walter Reed National Military Medical Center, my husband and I learned that our family had begun a lifelong journey involving Henry’s kidneys. READ MORE >>

My name is Henry Nalker and I was born with a rare disorder called Joubert syndrome, which is a neurological disorder that can also involve kidney, retina and/or liver disease. At age five, my family and I found out that I have a progressive form of kidney disease genetically linked to my Joubert syndrome. READ MORE >>

People often call living organ donors heroes, but I wasn’t looking to wear a superhero cape. Instead, I wanted to give my friend another chance at life. READ MORE >>

Learning you have kidney disease often leaves people with many questions. Dr. Delphine Tuot, an experienced nephrologist, answered questions about kidney disease from the AKF community. READ MORE >>