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Pulmonary Arterial Hypertension (PAH) Community Survey

As we step into a new year, we’re excited to strengthen our connection with our incredible #phaware community—Patients, Care Partners, Medical Experts, and Global Thought Leaders. Your voice matters, and we want to hear from you!

How can we better support, engage, and advocate for our Rare Disease Community? By sharing your thoughts through this quick survey, you can help us tailor our efforts to meet your needs and amplify our collective impact.
1.What is your connection to the Pulmonary Hypertension Community?
2.If you are a Patient, what WHO Group Classification has your Care Team assigned or diagnosed you with? (Check all that apply)
3.If you are a Patient, what other conditions has your Care Team discussed with you?
4.If you are a Patient, how long have you been diagnosed?
5.Where do you live?
6.Have you ever participated in a Clinical Trial?
7.Are you interested in participating in a Clinical Trials?
8.Where do you go to get information on Pulmonary Hypertension? (Check all that apply)
9.In which ways do you connect with Phaware?
10.Do you participate in Support Groups?
11.How do you use Facebook (or online) Support Groups?
12.Why do you attend in-person Support Groups?