First Steps: Q&A | PKD Foundation


First Steps You’ve been diagnosed, read up on the basics of PKD. Now it’s time to take those first steps towards becoming your own healthcare advocate. The following information has been developed to help you and your family feel more confident about the ins and outs of a PKD diagnosis.

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Common Questions

What questions should I ask when choosing a nephrologist or renal clinic for my healthcare?

How often should I see my nephrologist?

Is genetic testing available?

What are kidney function tests?

What do the numbers mean?

How frequently should my kidney function be checked?

Am I progressing if my creatinine is stable?

How will I know when I need a transplant or dialysis?

What are the signs of kidney failure?

How can I prolong my kidney health?

Why is blood pressure control important?

What is the best blood pressure medication?

How low should my blood pressure be?

What kind of medications should I avoid?

Can I exercise if I have PKD?

Are sports dangerous to my kidneys?

What are the best exercises for PKD patients?

Finished with this section? Learn more about Living with PKD. Or, return to the Learning Center.

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