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Pulmonary Hypertension Awareness Month comes to an end!

With the support of the community and partner organizations from coast to coast, we’ve reached so many people. One more way we’re reaching more people every day is through the #Heart2CurePH campaign. The #Heart2CurePH PSA is running in Times Square from Nov. 15 through December, raising awareness for a disease for which awareness can be a matter of life or death.

Visit http://aheartcures.org/ for more info on PH and what you can do to stay connected and involved year-round!


Caring Voice CoalitionCaring Voice Coalition (CVC) to Re-open PH Assistance Fund this Week

Caring Voice Coalition (CVC) tells PHA that at 9 a.m. ET on Thursday, Dec. 8, it will reopen its 2017 PH patient financial assistance fund for a limited number of applicants. Last week, PHA reported that CVC had reached its application limit for 2017. People who received application codes in a letter sent to them from CVC and have not been able to apply for assistance are encouraged to do so using those codes when they apply on Dec. 8.

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Make a Gift TodayMake an Investment in Hope This Holiday Season

The Pulmonary Hypertension Association (PHA) is a community-based nonprofit that relies on donations to fund many programs, including the nation’s largest PH patient and caregiver support group network, lifesaving early diagnosis awareness and education programs, medical education, specialty care resources, and research to find ways to prevent and cure PH. Make a difference with a gift to PHA today.

Donate Today

PHA NewsConnect with the Latest News, Events and Updates

Join a news network dedicated to bringing you the latest in pulmonary hypertension research, news, events, resources, education and more. PHA News is a weekly newsletter and publication of the Pulmonary Hypertension Association (PHA), and a trusted source for patients, families, caregivers, healthcare professionals and supporters.

Stay Connected

Group at CapitolPHA Urges Support for PH Senate Bill

U.S. Senator Bob Casey (D-PA) recently introduced the Pulmonary Hyprtension Research and Diagnosis Act (S. 3361), giving new hope to people living with PH. Pushed by PH patients, caregivers, family members and healthcare professionals, a similar House bill (HR 3520), introduced by Rep. Kevin Brady (R-TX) and Rep. Lois Capps (D-CA), is gaining bipartisan momentum with 57 co-sponsors.

Read more at PHA News


Watch my Music Video - Breathless not Hopeless

 
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NORD

The National Organization for Rare Disorders (NORD) awarded PHA the Abbey S. Meyers Leadership Award in 2012 for outstanding service to PHA members in advocacy, education and other key areas.