Rally for Medical Research Capitol Hill Day
Here's a selection of information from patients & professionals to better understand Idiopathic Pulmonary Fibrosis.
Where: Washington DC, USA, your home or office
When: on 18 September 2013
Join the PULMONARY FIBROSIS ADVOCATES, the Pulmonary Fibrosis Foundation and 55 other patient and
research advocacy organizations (as of July 11th) for a Day of Action in Washington DC.
If you would like more information on this new advocacy opportunity, write or give the PFA a call.
YOU DO NOT NEED TO TRAVEL TO WASHINGTON DC TO PARTICIPATE!
You can organize an e-mail campaign or a letter-writing or phone calling campaign from your home or office.