Category: Advocacy

WE ASKED FOR YOUR HELP LAST WEEK AND YOU ROCKED IT! YOUR HELP IS NEEDED AGAIN – HTC FUNDING COULD BE IN JEOPARDY! President Trump sent Congress a

The House of Representatives will be voting this afternoon on the American Health Care Act (AHCA), the bill to repeal and replace the ACA. Final

More than three million Americans have a bleeding disorder—such as hemophilia, von Willebrand disease or rare factor deficiencies—which: prevents their blood from clotting normally; can

This information was provided by the National Hemophilia Foundation 2016 Red Tie Challenge - https://www.thunderclap.it/projects/38113-2016-red-tie-challenge   LET’S MAKE HISTORY! JOIN NHF’S THUNDERCLAP TODAY SO WE CAN REACH 500,000

State Advocacy Please join us on Tuesday, May 17, 2016, for Harrisburg Day. This is the single most important day for bleeding disorders in Pennsylvania each

WPCNHF is partnering with the La Roche College Film Club to create our very own Hemophilia Walk Video and we want you to be a

WASHINGTON, Feb. 25, 2016 /PRNewswire-USNewswire/ -- The halls of Congress were the setting for the launch of the Red Tie Challenge, a new movement created by

We're so proud of the campers of Camp Hot-to-Clot for the great job they did in creating this PSA which won third place at NACCHO

Congratulations to Nikole Scappe for winning the Ryan White Youth Award! The Ryan White Youth Award is presented to a young person who has helped educate

Von Willy Who? By: Tracy Simon Sethman We discovered that our son had Von Willebrand Disease because of routine blood work to check his liver function due