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...
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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.
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Positivity – Knowledge – Determination
“This is one of the best diseases to have as it is slow progressing and you should not be affected until your late 40’s to early 50’s,” said my pediatric nephrologist. I vividly remember sitting...
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Last July, I learned that the Renal Support Network was having its 9th Annual Essay Contest. The theme was “WhatRead More -
Positivity, the “P” in my PKD! The power of positive thinking has no limits! Every morning when we wake up,Read More
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At the end of every PKD Educational Seminar I have attended, there was always one question that broke my heart.Read More
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“This is one of the best diseases to have as it is slow progressing and you should not be affectedRead More