Get Involved … Feel Better

Race Against PH 2009 participantsPHA believes that every person whose life has been touched by pulmonary hypertension has the right to fight back as much or as little as their health and interest allow. PHA has the obligation to build programs that make that possible.

PHA’s above philosophy is brought to life in everything we do. We offer almost limitless opportunities for patients and their family members to get involved with PHA in ways that are most meaningful to them. 

Advocate. If your passion is to help ensure that Members of Congress know why legislation that positively impacts the lives of PH patients is so important — from research to public awareness and more — we have countless tools, tips and tricks for you! 

Raise awareness. Touch another’s life by educating your community or by sharing your story with the media. Spreading the word about pulmonary hypertension might just help someone you don’t even know achieve an early diagnosis.

Fundraise. PHA provides programs that so many have come to depend on with the support of our community. Our fundraising programs offer you the chance to get involved, raise awareness and support a wide range of services for our community.

Fight the cause online. The Internet can be a powerful tool in the fight against PH. Online tools make it easy for you to raise awareness and funds for PH — all from the comfort of your computer chair.

Volunteer. It’s a rare volunteer who doesn’t say they get back more than they give through volunteerism. Whether you want to help out from time-to-time or lead a support group on an ongoing basis, we can help you put your time and talent to good use.

Early Diagnosis Campaign

Somtimes It's PH
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Why Get Involved?

From members of our community

This lobbying business has been really good for me. It has brought a sense of purpose back into my life. I’m getting excited about waking up in the morning again.

 — Patient & Advocate Charlotte McCabe

Even here in my small-town, rural area there are plenty of opportunities to keep spreading the word … if I can even help just one more person, that’s all I hope for.

 — Patient & Awareness-raiser Theresa Stah

I went on PHA’s website and looked at the online fundraising program and thought, ‘I can do this.’ People wanted to help and I wanted to give them a way.

 — Web of Friends fundraiser Tony Lahnston

Working with the support group gives me a sense of still being useful. It is rewarding to know that what you have done is helping someone else.

 — Patient & Support Group Leader Cindy Pickle

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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.

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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.