Support. Friendship. Hope.

Living with a rare disease can sometimes feel lonely. But you are not alone. PHA has a strong network of local support groups and an active online community. By reaching out to people who've been there, you will find fast PHriends who offer support, information and hope for the future. You can connect with the community however you prefer, whether that's on the web, on the phone, or in face-to-face support group meetings.

Walking for a cure at Baltimore Orioles Stadium
Walking for a cure at Baltimore Orioles Stadium

       

Connect

Online

  • Discussion Board
    Share information and support on PHA's popular discussion board.
  • Email Groups
    Stay in touch with PHers via email in the general community group, special interest groups such as parents or young adults, groups to share tips on getting involved in advocacy and awareness, or networking groups for leaders and medical professionals.
  • Online Support Group Chats
    Attend daily online support group chat meetings.
  • PHA Teens Social Network
    Connect with other teen PHers on a social network just for you! PHA Teens is a private network for teens ages 13-18 living with PH.
  • Patient and Caregiver Mentor Program
    Email with an experienced patient or caregiver who can help you find the information and support you're looking for.
  • RareConnect Community
    Share experiences and ask questions on these international online community groups for pulmonary hypertension and other rare diseases. Translations are available.

Telephone Support Groups

Local Support Groups

Find a support group near you and find information on your group's website.

Patient-to-Patient Support Line

Ask questions and receive support from other patients who have been there.

Stories

Our Journeys

Read about other PH community members' journeys with PH and share your own.

 

Follow Us On

    

 

PHA Launches Telephone Support Group for Patients

Have a hard time making it to a support group meeting? No problem. PHA is bringing the support group to YOU — straight to your home — via a telephone support group. Email Supportgroups@
PHAssociation.org
to participate.

Medical Professionals

PHA has two membership networks for medical professionals.

Learn more

Find a Support Group Near You

From the Community

Generation Hope Blog

Generation Hope, PHA’s community for young adults, now has a blog! Read about Jenny and friends, who tackle all the adventures of life as 20- and 30-somethings while living with PH.

Visit the blog

Become a Member

When you join PHA, the membership base expands, and we can do much more, much sooner, to fight PH.

View membership benefits

Email Updates

Stay informed about current research, events, and more.

Sign up

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.