2015 Walk for PKD

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The hardest thing to believe though is that as of today there are still no treatments and no cure for ARPKD and that 30% of babies born with this disease are still passing away at birth. That is why it is still so important that we are involved with the PKD Foundation and try to raise as much money as possible through the Walk for PKD. 

 
To learn more about the boys, to join our team, and to make a donation please go to:
 
No donation is ever too small. We are always so appreciative of all of the support we have been receiving since the boys diagnosis with ARPKD in April of 2006.
 
Besides donating feel free to come and walk with us if you can! We would love to have the biggest team there!!!!  And share our information with your friends and family to help us raise awareness of polycystic kidney disease.
 
Registration begins at 9 am on 10/25 at 
Hudson River Park, Pier 84
44th St. and 43rd St.
New York City, NY 10019 
 
Thank you again,
Matt and Michele
and our 3 P’s (Max, Nate, and Gabe)
INFO: michelehopekarl@gmail.com