Click here to go to my fundraiser page on PKD Foundation's website.

PKD runs in my family and has affected many of my immediate and extended family members. I too was diagnosed with PDK in the year 2010 and have seen my kidney function decrease consistently over the last few years. I was listed on the Transplant Waiting List in Aug 2019, the waiting period for my blood type is 5 to 6 years.

I've set up a fundraiser at the PKD Foundation. With this fundraiser, I hope to bring awareness about this genetic disease to my friends, family and to the general public.

I feel every dollar spent on research helps towards a goal of finding a cure for this disease, not just for me, but for the 12 million people worldwide affected by the disease, and their future generations. PKD foundation actively funds research for the disease and I setup my fundraiser so I can help contribute as much as I can towards it.

I hope you can help me achieve my goal of $2,000 by making a contribution today. Every small bit helps.

Thank you,
Bhavdeep.


Click here to go to my fundraiser page on PKD Foundation's website.

For more information on PKD Foundation - https://pkdcure.org/

For more information on the type of PKD I have - https://pkdcure.org/what-is-adpkd/

If you have any questions, please don't hesitate to contact me via email or Facebook or WhatsApp or the plain old phone call :)