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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Life is coming up roses
I love when an idea unfolds organically, with serendipitous surprises along the way that lead one to believe it was all meant to be. This is what happened with my 15-year kidney transplant...
Tips for caring for yourself during hospital stays
One of the first things I love to do when I’m home for the night is put on my comfy clothes. There is something so nice about being cozy in your own home. Our homes are our safe places—with...
Celebrate life
A couple weeks ago, on the evening of August 12, my husband Noah and I were sitting in beach chairs along the shore of Lake Tahoe. We were watching the sun set behind the Sierra Mountains with...
A letter from a transplant recipient to her donor
Dear Sally, Many of us only get one chance at life. A chance to grow up, dream big, find our purpose and fulfill it. Looking back, when I was a teenager, I did not have many dreams or plans for...
Caring for the caregiver
I believe health issues become harder to face as we age. As children, we don’t analyze and worry about things the same way we do as adults. When growing older, the focal point we have on...
A good day
When you live with chronic health issues, the definition of a good day can be much simpler than what most people think. I have also learned that we cross paths with people for a reason. There are...
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There are experiences and tragedies which we endure and can’t ever forget, but I believe it is important to findRead More
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Our diet and how we approach nutrition changes as we age, especially as a PKD patient. When we’re younger, weRead More
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I look at PKD as a family disease. For those of us who are not victims of a spontaneous mutationRead More
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I love when an idea unfolds organically, with serendipitous surprises along the way that lead one to believe it wasRead More
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One of the first things I love to do when I’m home for the night is put on my comfyRead More
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A couple weeks ago, on the evening of August 12, my husband Noah and I were sitting in beach chairsRead More
