My Mother's Interview

Video links of my mom's interview describing her experience with PKD and her kidney transplant were lost so I uploaded them new to YouTube.
Part One: PKD and the Florine family The first diagnosis, the loss of her mother and the impact on her brothers and sisters
Part Two: Pat is diagnosed with PKD Being tested before having kids, dealing with the diagnosis, the tendency towards denial and the unbelievable comments of a medical student
Part Three: Dialysis then a transplant Dialysis experience, the transplant list, the donor and others who benefited, the donor was a perfect match “it was as though he were like my son”
Part Four: Eight years after A list of goals written in hope of a kidney transplant, what she’s accomplished, she monitors her health and volunteers for organ transplant awareness
Part Five: Work with the blind and visually impaired Pat worked to develop mobility skills for visually impaired adults, she describes the work and the clients
Part Six: For PKD research and organ donation We hope to raise PKD awareness, what PKD Foundation can do, the need for more Americans to become organ donors