Ambassador

  • TALKING ABOUT PROGRESSION
  • Getting ahead of ADPKD
  • FROM DENIAL TO DEFIANCE
  • LOOKING AT ADPKD DIFFERENTLY
  • IT’S ALL RELATIVE
  • FROM DIAGNOSIS TO TREATMENT
  • TAKING A STAND
  • HOPE FOR THE FUTURE

Hear from the first generation at risk of rapidly progressing autosomal dominant polycystic kidney disease (ADPKD) with a treatment to call their own.

JYNARQUE is a prescription medicine used to slow kidney function decline in adults who are at risk for rapidly progressing ADPKD.

Real patients share their stories.

Talk to your doctor to see if JYNARQUE is right for you.

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WE ARE GEN 

Real patients share their stories.

Talk to your doctor to see if JYNARQUE is right for you.

TALKING ABOUT PROGRESSION

Knowing what my mom went through, I thought there has to be more to my ADPKD.

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Getting ahead of ADPKD

If I met someone that was at risk for rapidly progressing ADPKD, I would strongly encourage them to begin seeing a nephrologist, and not to wait.

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FROM DENIAL TO DEFIANCE

Because I was in denial for so long, now I want to take charge of my disease. I want to help others and spread awareness. 

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LOOKING AT ADPKD DIFFERENTLY

For many people, ADPKD is a slowly progressing disease, but it doesn't stop progressing on its own.

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IT’S ALL RELATIVE

The history of ADPKD in my family goes back a few generations. There wasn’t much discussion and people didn’t talk about it.

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FROM DIAGNOSIS TO TREATMENT

My doctor said, “Let’s do an ultrasound.” And that’s when they found all of the cysts on my kidneys.

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TAKING A STAND

The treatment means hope for me. It also means that people are investing time and money looking at this disease and finding ways of addressing it.

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HOPE FOR THE FUTURE

JYNARQUE popped on my radar the first day that I met my new nephrologist.

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MORE TO COME

There are more patients with a risk of rapidly progressing ADPKD who want to share their stories. Visit our sign-up page for updates and more information.