I am a pkd patient . Want to know more about it .
What can I do? : I am a pkd patient . Want to... - Kidney Disease
What can I do?
Written by
Youssif
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5 Replies
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I suggest you join the group for Kidney disease,which is dedicated to problems like yours.That would be more appropriate,in my opinion.
You can find more information on PKD at:kidney.org/atoz/content/pol...
I would look for groups on Facebook too.
KidneyCoachNKF Ambassador
Go to pkdcure.org which is the National Organization for Polycystic Kidney Disease. It took my grandmother, father, 2 sisters, 2 brothers and I have it myself. I'm happy to answer any questions you may have. It does impact many people without them even knowing it. Many have it but never have any symptoms. Blessings
I have 2 brothers arrived to last stage then got a kidney transplants. Few year later I will be in same situation. Really I am so worry about it.
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