What can I do?

[Youssif]

I am a pkd patient . Want to know more about it .

[ramana42]

I suggest you join the group for Kidney disease,which is dedicated to problems like yours.That would be more appropriate,in my opinion.

[YollyD_NKF]

You can find more information on PKD at:kidney.org/atoz/content/pol...

[TaffyTwoshoes27]

I would look for groups on Facebook too.

[KidneyCoach NKF 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

[Youssif in reply to KidneyCoach]

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.