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PHA Europe works together with its members to enhance awareness of pulmonary hypertension across Europe, promote optimal standards of care for people living with the disease, ensure the availability of all approved treatments, and encourage research for new medicines and therapies.
PHA Europe is active in many different areas which include the dissemination of information (newsletters and updates), awareness raising (Rare Disease Day and previous campaigns), advocacy (Call to Action) and patient empowerment (annual meetings, support programs).
Projects & Activities
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Giuliana, Italy
I wish for the tulips I planted yesterday to flower and that I’ll be so busy planning my wedding that I’ll forget about PH!
Giuseppe, Switzerland
Healthy people have a lot of dreams. Sick people have only one.
Radu, Romania
I dream to still be around to see my 18 year old son become an architect.
Nina, Switzerland
I want to be cured and have a pony.
Tuulia, Finland
I hope to live a good life in spite of illness and that one day there will be a cure.
Jennifer, USA
I hope to feel better and to train to be a nurse.
Jana, Slovakia
I am on a waiting list for lung transplantation and hope that the operation will take place in the next 6 months.
Marion, France
I dream to be able to dance and party ! Walk in the mountains… and swim !
Patrik, Sweden
My dream is that a cure will be found for my son and for everybody else who suffers from PH.
