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PH Support Groups provide SUPPORT, EDUCATION, and most of all HOPE for patients and caregivers.
If you are in the area we encourage you to join us!
For questions and to be added to the official email list, please send a quick message to LivingWithPH@gmail.com. Feel free to also contact us, if you would like to be a speaker or sponsor a meeting.
Meetings on held a Saturday afternoon during the spring and fall.
(must be signed in)
Go to "Leader Site Admin" on bottom of above navigation to post updates, or Sign In if you're not already.
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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.
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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.