by PKD Foundation Staff | Mar 13, 2018 | Education
At the PKD Foundation, we strive to give all types of patient experiences a voice in the community. Recently, an almost un-heard of story came to us from our Orlando Chapter Education Coordinator Brittnee Boyd, and we reached out her to learn more about her story: My...
by PKD Foundation Staff | Mar 9, 2018 | Education
At the PKD Foundation, we honor various and unique patient perspectives to show the broad scope of experience that PKD patients face with this disease. This includes the reality of dialysis, which can go undiscussed in our community in comparison to kidney...
by PKD Foundation Staff | Mar 6, 2018 | Staying Healthy
Between March being National Kidney Month, National Nutrition Month and the start of spring, there has never been a better time to get on the right track with your eating habits! Check out these tips to “spring clean” your kidney diet: 1) Eat fresh, unprocessed foods,...
by PKD Foundation Staff | Mar 1, 2018 | Awareness
March is National Kidney Month! Join us as we raise awareness for PKD. The more who know about PKD, the more resources we can dedicate to finding treatments and a cure. Here’s how you can get involved and help spread the word: Update your profile picture....
by PKD Foundation Staff | Feb 28, 2018 | ARPKD, Voices of PKD
Published on February 28, 2018 | Today, on Rare Disease Day, we give voice to millions of people worldwide living with rare diseases through education and advocacy. Autosomal recessive polycystic kidney disease (ARPKD), a rare form of PKD, affects 1 in 25,000...
