Voices of PKD is a collection of stories, testimonies, photos and videos that tell the story of PKD through the eyes of the PKD community.
You can help give a voice to a widely unknown disease by sharing your story. Your experiences can paint a more powerful picture of what it’s like to live with PKD.
If I can raise awareness and tell the story of PKD on television, I will do it. I want to engage the viewers and reach those affected by PKD.
Having PKD had a lot to do with me auditioning. I didn't want to waste a day. I don't want to let any time go.
My hope is for treatments to be available for the younger members of my family with PKD. I am committed to the fight to end PKD and this is why I support the PKD Foundation.
I want to connect with others who have the disease so we can work together to find a cure.
When you have a lifelong disease, you have to decide how you are going to let it affect you. I could wallow in self pity, but why? It's my one life. I'm not going to waste a moment.