Welcome to our group's website! PHA support groups provide support, education and most of all hope. If you are in the area, we encourage you to join us.

The Fort Worth support group usually meets the second Tuesday of the month.  Please contact me at 817-528-9052 for more information.

Looking forward to seeing you there.

Leader Contact Information

Feel free to contact our group's leaders to share your story, ask questions and get connected with our group.

 View leader contact info

Upcoming Meetings and Events


Special Meeting of the PH Community and PHA Board in Dallas

Join us for a special meeting at the Omni Dallas, the location of PHA’s 12th International PH Conference and Scientific Sessions taking place in June 2016. This support group meeting is planned in conjunction with PHA’s Board Meeting, and members of the Board will stop by and meet with the group. We are providing a free Pulmonary Hypertension: A Patient’s Survival Guide, to the first 20 patients who RSVP to attend this free event!

WHY:  Learn about PHA’s Conference, how you can get involved and meet other patients. Get a FREE Pulmonary Hypertension: A Patient’s Survival Guide (to the first 20 patients who RSVP)

DATE:  Saturday, March 28, 2015, 12:30 p.m. – 3:30 p.m.

WHERE:  Omni Dallas Hotel, 555 S. Lamar, Dallas, TX 75202
In the Cedars Meeting Room, second floor via main escalators or elevators.

PARKING:  Hotel valet parking is free for patients and anyone in need of assistance.

RSVP:  We are providing lunch, so we need to know if you’re coming! 
RSVP by March 24 to Debbie Drell, PHA Senior Director, Volunteer Services, 240-485-0755,

Space is limited. Open to patients, caregivers, family, friends and supporters.

Refreshments are sponsored by PHA’s Support Group Central Fund, made possible by Platinum level sponsorships from Actelion Pharmaceuticals, Bayer Healthcare and United Therapeutics.

Valet parking and free Patient’s Survival Guides are sponsored by Reata Pharmaceuticals.


Read about it on our Blog:

Come meet with other patients and caregivers at our next support group meeting.


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Management of this Site: Each support group website is managed by the group's volunteer leader, usually a patient. If you find outdated contact information, old meeting information, or any content that requires attention from PHA, please send an email with the link to the group site to:
Medical Disclaimer: Medical information included in these pages, including in newsletters and to outside links, may not have been reviewed for accuracy and appropriateness by PHA. We encourage patients to discuss their healthcare with their doctors. We do not provide medical advice on personal health matters, which should be obtained directly from a physician. PHA cannot be responsible for web visitors' actions taken as a result of their interpretation of information contained on these pages.

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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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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.