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Austria-Be-Be Azienda Directories
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Azienda News:
- KidneyLuv Interviews Kidney Advocate Uncle Jim Myers
Under the guidance of Dr Hellman, I learned that PKD was hereditary and had no cure, but the growth of the cysts could be slowed and controlled by high blood pressure medication and a renal diet
- James “Uncle Jim” Myers | Chronic Disease Coalition
I am an ESRD PKD patient I was lucky enough to have a transplant on April 27th, 2016 I write to you today to tell you my story, as well as, my experiences with polycystic kidney disease
- James Myers: Kidney Advocate - The Hope
I am an Ambassador for the American Kidney Fund, AAKP, the Polycystic Kidney Disease Foundation, the Dialysis Patient Citizens, the Renal Support Network, the National Kidney Foundation of Indiana, More Than Just Your Kidneys and Waitlist Zero
- Polycystic Kidney Disease (PKD) and Me: Living with a Genetic . . .
Learn how Charlotte Smith, a mother, equestrian, and adventurer, overcame polycystic kidney disease (PKD)
- Starting a family when you have polycystic kidney disease . . .
With expert care, many individuals with polycystic kidney disease (PKD) successfully start families Because PKD is a genetic condition, steps can be taken to reduce the risk of passing it on to children
- Los Angeles - Polycystic kidney disease | PKD treatment . . .
Walk for PKD - Your Way! offers you the freedom to choose – how, when, and where you Walk for PKD Participate as an individual or a team of loved ones, select a date and decide how you are going to Walk for PKD Your Way
- Walk for PKD | PKD Foundation
The Walk for PKD is the largest polycystic kidney disease (PKD) fundraising and awareness event that is held coast to coast Walk events will take place nationwide in September and October, with donations fueling critical research and improving the lives of those affected by PKD
- Taking a stand to change family history - Polycystic kidney . . .
For Candi Zitzka, her family's burden has been the debilitating disease of polycystic kidney disease (PKD) When Candi started seeing family members affected by the disease, she took matters into her own hands and decided to give an incredible gift: her kidney
- Voices of PKD - Polycystic kidney disease | PKD treatment . . .
Voices of PKD is a collection of stories, testimonies, photos and videos that tell the story of PKD through the eyes of the PKD community You can help give a voice to a widely unknown disease by sharing your story
- Delilah Rivera - Polycystic kidney disease | PKD treatment . . .
I walk for polycystic kidney disease (PKD) because it’s profoundly affected my family I walk for my dad, my cousins (Wanda and Nana), and my uncle (Junior), all of whom have battled the challenges of this disease
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