Pulmonary Hypertension Association CEO Matt Granato will join leaders of other rare disease groups April 26 to educate the European Parliament about pulmonary hypertension (PH).

The event will be live in front of parliament, but it will be broadcast on Facebook Live. The meeting will include discussions on:

  • PH, rare diseases and EU policies.
  • Patient empowerment.
  • Treatment access.
  • Clinical research and innovation.
  • Screening and awareness.
  • Psychosocial support.

The event begins at 4 a.m. EDT in the United States, so the PH community in the Americas may want to watch the recording afterward.