NKF Blog
Seeing someone you love go through kidney failure can be incredibly scary and frustrating. You may...
Ansara Piebenga is the parent of a child kidney transplant recipient. Elizabeth Fortune has spent...
By Mary Baliker, NKF Kidney Advocacy Committee Co-Chair
As a person living with kidney disease...
In March 2020, Patrick Gee, a former dialysis patient and five-year kidney transplant recipient,...
Adjusting to fluid restrictions can be difficult, but with the right support and mindset, we know...
On Wednesday, August 3, 2022, the Senate Finance Committee held a hearing, “A System in Need...
Reading your comprehensive metabolic panel (CMP) results doesn’t have to be intimidating....
Picture a gamer: you might see a young teen with color-changing lights in the back. Maybe a college...
Your loved one’s personality is as unique as their healthcare needs. By learning about their...
The summer heat can make it more difficult to adhere to your fluid and food restrictions, but...
National Kidney Foundation patient advocates played an integral role in The Scientific Registry of...
40%-50%of people with kidney disease experience hyperkalemia or high potassium. A healthcare...
Raise your hand if you've ever spent hours reading through lists of medical conditions after...
Jumping out of planes and diving with sharks - Corey Zaretsky has always had an adventurous side....
A surprise diagnosis of focal segmental glomerulosclerosis and stage 5 kidney disease flipped Jason...
Finding a living donor can sound scary and overwhelming. Where do you start and what are the best...
Take a stroll down any aisle at a grocery or convenience store, and you'll find a wide variety of...
4th of July means it’s time to break out the grill, bake some pie, and get ready to watch stunning...
