On Saturday June 2, the Third Taylor's Wish Race 2 Cure PH will take place in Tay's memory in Anaheim, California.  The event is ...

This blog is about a shift that is dangerous – and unnecessary – for our country.  It offers a story and a call to action from the America...

Last night, PHA was pleased to receive the National Organization for Rare Disorders’ Abbey S. Meyers Leadership Award for 2012. Here...

As a community grows, it develops traditions and opportunities. The First World PH Day – celebrated on May 5, 2012 – offered both of ...

For the past year or so, the ISeek Cultural Center in China has been using film to tell PH patient stories.  This weekend Yue, a Chinese h...

In 2010, Juan Fuertes and Irene Delgado of the Asociación Nacional de Hipertensión Pulmonar (ANHP) began a quest. They believed that i...

A few weeks ago, I wrote a blog titled Pediatric research: the power of one...and a half . It told the story of Steve Van Wormer and his t...