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The Pulmonary Hypertension Association (PHA) is a community-based nonprofit that brings together over 16,000 pulmonary hypertension (PH) patients, caregivers, family members and healthcare professionals. We work every day to end isolation, provide education, involve our constituents in everything we do, and find a PH cure.

Our mission is to extend and improve the lives of those affected by PH. Our vision is a world without PH, empowered by hope.

You can make a difference for people living with PH by fundraising in support of our mission and vision. PHA provides tools and resources to make fundraising easy!

Fundraise Online

Fundraise online iconA fundraising page with your story is a great way to help friends, family and co-workers understand what it means to live with PH and why early and accurate diagnosis matters, and it gives them a way to offer their support. Creating a personal fundraising webpage can be done anytime! It's simple and doesn't require technical knowledge. Since PHA began using personal fundraising pages, community members have raised more than $200,000. Get started creating your page by selecting the "Fundraise" button on PHA's Crowdrise website.


Organize an Event

Party iconFrom a small house party to a fun walk or gala, you can choose the right size event for your community and needs. Workplace or special occasion fundraisers (such as on a birthday or anniversary) are also good ways to educate your community about pulmonary hypertension and enable them to support a cause close to your heart. Some employers will even match an employee's charitable contributions — check with a human resources representative about your company’s policies.


Ready to start?

PHA has a network of volunteer mentors and a full-time staff member dedicated to helping you make your fundraising efforts a success. Connect with us to get support on setting up your Crowdrise page, brainstorm event ideas, learn about free fundraising resources and find answers to all your questions.


Call: 301-565-3004 x765


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The information provided on the PHA website is provided for general information only. It is not intended as legal, medical or other professional advice, and should not be relied upon as a substitute for consultations with qualified professionals who are familiar with your individual needs. PHA does not endorse or recommend any commercial products or services.

801 Roeder Road, Ste. 1000, Silver Spring, MD 20910   Patient-to-Patient Support Line: 1-800-748-7274
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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.