Craig Ramseyer is a PKD patient and transplant recipient. He has been a supporter of the PKD Foundation for more than 15 years and is excited to join the PKD Foundation Board in July. I have four children, ranging from […]
I never pictured myself on a national disease foundation board. A local non-profit in San Francisco, perhaps, but never this! I am living with PKD and it runs in my family. We first got involved with the PKD Foundation nearly […]
Perhaps you’ve wondered this – I used to before I became a Board member. Why does it seem sometimes like we aren’t making progress toward curing this disease? And what does the board have to do with this – what […]