PKD Foundation
PKDFoundation's Channel
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16 videos
PKD and Dialysis
7 months ago
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5 videos
PKD and Nutrition
7 months ago
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20 videos
PKD and Pain
7 months ago
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29 videos
PKD and Kidney Transplants
9 months ago
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13 videos
About ARPKD
9 months ago
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14 videos
PKD Research
11 months ago
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28 videos
PKD and Pregnancy
1 year ago
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20 videos
PKD and PLD
1 year ago
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7 videos
Living with PKD
1 year ago
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9 videos
PKD Stops with Me
1 year ago
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8 videos
About PKD
1 year ago
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2 videos
PKD Related Health Issues
1 year ago
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1 videos
Walk for PKD
2 years ago
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PKDFoundation
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Profile
 
Channel Views:
11,196
Total Upload Views:
120,521
Age:
31
Joined:
Jul 21, 2009
Latest Activity:
1 month ago
Subscribers:
191
Website:
http://www.pkdcure.org
About Me:
 
The PKD Foundation is the only organization, worldwide, dedicated to promoting research to find a cure for polycystic kidney disease (PKD) and improving the care and treatment of those it affects.
Country:
United States
Recent Activity  
PKDFoundation uploaded a new video (1 month ago)
Presented by Benjamin Cowley, MD, Professor of Medicine and the Chief of...   more
 
 
PKDFoundation uploaded a new video (5 months ago)
Many parents don't know what the future holds when they have a child dia...   more
 
 
PKDFoundation uploaded a new video (7 months ago)
PKD Foundation tips and tactics for using social media
 
 
PKDFoundation uploaded a new video (8 months ago)
This inspirational interview with living kidney donor Melissa Blevins an...   more
 
 
PKDFoundation uploaded a new video (8 months ago)
 
Channel Comments
757mauri (11 months ago)
i'm italian and i have pkd, please help us and watch the Italian site of AIRP. Thanks for your generosity-
Swamivision349 (1 year ago)
im 14 months post transplant thanks to my sister

good energy to all my fellow suffers
Endlessfantasy (1 year ago)
thank you for all that you do! I wish with all my heart we would find a cure soon!... my father died from pkd at 34 ...and now my husband I find out has pkd really weird why all the men in my life all have this disease...I got tested and I don't have it.. but it's like I do because my loved ones have it.. it's been really hard..THANK U AGAIN for your SUPPORT<3
Lima547 (1 year ago)
Thank you very much for the channel! I'm a Brazilian living in the UK and unfortunately I have PKD. I think if we help each other exchanging info, donating money for research and supporting campaigns we can change our future!
tula97 (2 years ago)
tx for channel
MADDPOETTDYER (2 years ago)
Hi I'm Scott from the Philadelphia Chapter!!!!!!!!
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