Living with PKD During COVID-19
Published May 12, 2020 | In these unprecedented times, families across the globe are adapting their way of life to stay safe and healthy. Living with PKD during the COVID-19 pandemic can be even more challenging. Whether you're a transplant recipient, currently on...
About
The PKD Foundation Blog is contributed to by PKD Foundation staff and members of our incredible community. Focused on bringing you important PKD and Foundation updates, our blogs cover advocacy initiatives; awareness events; education for patients, caregivers, and health care professionals; and updates from and for our researchers.
Advocacy
Awareness
Education
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The Hands of Time
My eyes scanned the crowd of people with great speed and excitement. As the doors of each incoming tram opened, I grew more anxious to see my parents’ faces in person. It had been more than seven...
My Caregiver of the Year
There is not one word that could adequately describe how wonderful my dear husband Noah is and how much I love and appreciate him. When allowed 300 words by The American Kidney Fund to nominate...
11 Years Strong
I looked over at Noah and asked, “Do you want to know if it is a boy or a girl?” The ultrasound technician and Noah and I giggled, as we were well aware that was not why I was getting an...
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When we deal with chronic health issues it is easy to acquire tunnel vision. Our peripheral vision is lost andRead More -
“So, you’re all good now?” I have heard this comment countless times from individuals after they hear that I receivedRead More
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My PKD and health challenges have led me down paths I would have never imagined: both good and bad. AsRead More
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My eyes scanned the crowd of people with great speed and excitement. As the doors of each incoming tram opened,Read More
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There is not one word that could adequately describe how wonderful my dear husband Noah is and how much IRead More
