AAKP strives for change by promoting and celebrating the importance of kidney health for patients across the country. This blog will allow you to connect with experts, researchers, staff and volunteers surrounding our ongoing advocacy for healthy kidneys.
AAKP Ambassador, Chardae “Prima” Sanders knows the devastating effects of having high potassium. While on dialysis, Prima says that she did not watch her diet. She admits, “I was a chip eater! I would over-eat on chips. I also ate bananas as a comfort food. I never thought about the impact.”
Every morning when we awaken, our first thoughts are about how the Coronavirus is ravaging across America and the world. Each hour, more and more innocent people and their families are impacted. We also learn of the heroism of our brave first responders and selfless medical personnel. To gain strength, I think of my family and the lessons they learned from American history.
Dale Rogers is a two-time kidney transplant recipient. Like many other kidney patients Dale has struggled with high potassium (also known as hyperkalemia). Dale shares that high potassium became a huge problem for him when he was fasting and dieting, while on dialysis, in order to get to a health weight for receiving a kidney transplant.
March is National Kidney Month. It is a time where we raise awareness across the country about kidney diseases and the importance of kidney health. This March is drastically different as we are not only raising awareness of kidneys, but across the globe, united we are working to manage the implications of the Coronavirus (COVID-19).
World Kidney Day is observed annually on the 2nd Thursday in March. At the start of this holiday, 66 countries observed this date in 2006. Within two years, this number rose to 88. WKD is a joint initiative of the International Society of Nephrology and the International Federation of Kidney Foundations (IFKF).
As per the NORD (National Organization of Rare Disease) website: The main objective of Rare Disease Day is to raise awareness among the general public and decision-makers about rare diseases and their impact on patients’ lives.
