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It's nice when recognition for PHA comes from others who recognize the work this organization does. It's very special when that recognition comes from our own community. Recently, I got the following email message with the magic words, "Your supporters have spoken." » Read more
Learning that you have pulmonary hypertension or another life-altering disease can bring on many emotions. What do you do on a daily basis to help your emotional health? If you feel you are having trouble coping with a chronic illness, maintaining your emotional wellness or just want to see what others are doing to stay well, check out the following information. These nine fun tips are sure to brighten your life. » Read more
Need more information on communicating with others about PH, preparing for an emergency, recognizing the side effects of PH medicines or identifying and coping with depression? These are just a few of the topics that will be covered in PH Ready Caregivers, PHA’s new self-study curriculum for caregivers. Learn more and register today.
PHA has five cutting-edge research programs dedicated to exploring the causes and treatments for PH and contributing knowledge that will lead us to a cure. Your donation to PHA’s research program will be multiplied through PHA’s partnerships with renowned research organizations like the National Heart, Lung and Blood Institute (NHLBI), a branch of the National Institutes of Health. » Learn more and make a research contribution today
Space is still available for healthcare professionals who wish to attend our 2013 PH Professional Network Symposium, taking place Sept. 26-28, 2013. PHA is offering a reduced registration fee of $100 for the first 250 PH-treating healthcare professionals who register. Act now and don’t miss this opportunity to register at the reduced rate! » Register now
Research & Treatment News » Pulmonary Denervation Shows Promise for Resistant Pulmonary Hypertension
» Step Forward for Understanding Arterial Disease
» A Common Stem Cell for the Heart and Lungs Reveals Intricacies for Life on Land
» Test Your Medical Knowledge with the MKSAP Challenge: 38-Year-Old Woman with Fatigue and Dyspnea on Exertion
Updates From PHers Around the World » Generation Hope Blog: Celebrate Your Friends the Right Way This National Girlfriends Day
» People Stylewatch Magazine to Donate Portion of Proceeds to PHA
» Cancer Survivor and PH Patient Awaits Double Lung Transplant
» Desperate for Transplant, She's Still Glad Pa. Girl Got Lungs
» More News
CaregiversJuly 24, 20138:30 p.m. ET/5:30 p.m. PT
PatientsJuly 25, 20138 p.m. ET/5 p.m. PT
ParentsAugust 19, 201311 p.m. ET/8 p.m. PT
August 21, 20138 p.m. ET/5 p.m. PT
July 26, 2013O2 breathe "Under the Stars Lounge" with Brian Wilson and PHriendsHighland Park, Ill.
July 28, 2013Special Needs Night @ Intimidators Baseball StadiumKannapolis, N.C.
July 29, 20136th Annual Swing 4 the Cure: Wojo PH Golf ClassicAliso Viejo, Calif.
July 30, 2013PHA Classroom Webinar: Newly Diagnosed? What You Need to Knowonline
August 5, 2013"On Par to a Cure for PH" Golf ClassicSan Ramon, Calif.
» Go to the Events Calendar
Need more information? Contact PHANews@PHAssociation.orgPulmonary Hypertension Association 801 Roeder Road, Ste. 1000 Silver Spring, MD 20910Office: 301-565-3004 | Fax: 301-565-3994
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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.