A Legacy of Impact in the Fight to END PKD

For many years, the Montreal Chapter of the PKD Foundation of Canada has been a vibrant and determined community, raising awareness, research funds, and hope for those affected by polycystic kidney disease (PKD). From powerful educational forums to joyful community fundraising events, Montreal has played a key role in building momentum toward better care, treatments, and eventually a cure.

At the heart of it all is Luisa Miniaci-Di Leo, the long-time Chapter and Walk Coordinator. Her leadership and compassion have helped make Montreal a hub of connection, education, and action.

Following an investigation into another health issue, at the age of 34, I was diagnosed with polycystic kidney disease (PKD). As coordinator, I have used my knowledge and skills in order to raise awareness and research funds towards a cure. This has also allowed me to meet some amazing people facing the same battle. ~Luisa Miniaci-Di Leo

Over the years, the Montreal Chapter has hosted everything from fundraising galas to in-person learning sessions, with the Walk to END PKD in Montreal growing stronger each year. It has become not only a fundraiser, but a day of unity and recognition for families affected by PKD.

We have some high-caliber individuals doing research on PKD, and I sincerely believe that with their efforts, our future will improve. Our chapter understands the importance of pursuing research for and education on PKD, and we are continuously working to strengthen our community of supporters. ~Luisa Miniaci-Di Leo

As the chapter looks to the future, new educational and social events are in the works. Montreal continues to focus on community care, and on acknowledging every person living with or affected by PKD.