Welcome to the PHA Europe Website
This website is for anyone who suffers from Pulmonary Hypertension (PH) as well as their friends and family. Here you will find information about the condition, as well about the PHA Europe organisation.
PHA Europe’s Facebook
PVRI Symposium Report 2025
I recently attended the PVRI Drug Discovery & Development Symposium 2025 in Amsterdam, held 16–17
ERS Prevention Summit 2025
The ERS Presidential Summit on Prevention, held in Dublin in June 2025, gathered leading voices
Report on the EPF Annual General Meeting 2025
The European Patients’ Forum (EPF) is an independent, non-profit umbrella organisation representing 78 patient organisations
One of our main goals is to spread the information about PH to facilitate early diagnosis. It also helps for the wider community to better understand the difficulties PH patients are living with in their everyday life.
We participate in a great number of projects, partnerships, working groups and various task forces with the aim of ensuring better quality of life for the patients, best treatment and ultimately a cure for PH.
The stronger the patient organizations are, the more they can help the patients on local level. PHA Europe has various initiatives to help their members become mature.
In partnership with our valued sponsors we provide educational materials, useful resources and various tools. These programs provides up-to-date information, and serve as a tool during local negotiations and campaigns.
About PH
Pulmonary hypertension (PH) is the broad, inclusive name for a group of several chronic diseases that affect the lungs and the heart.
Send Donation
There are many ways you can get involved and help us improve awareness of pulmonary hypertension.
