Information from the Coalition for Pulmonary Fibrosis

Below is news from the wonderful people from The Coalition for Pulmonary Fibrosis. Check out their newsletter full of information as well as information about the American Thoracic Society's (ATS) conference in May. This is the conference that I have been asked to give a formal speech on my disease, Hypersensitivity Pneumonitis.

Check out all the sites below:

Also, please join us for these these UPCOMING EVENTS: 
San Francisco, CA–Friday May 18^th The ATS Public Advisory Roundtable and the CPF are pleased to invite you to the Patient & Family “Meet the Expert” Forum and “Quality of Life” Presentations. For more info. and to rsvp, please click here:http://www.coalitionforpf.org/cpf_events_detailes.php?id=552.


Daughters of PF Member Meetings A chance to meet and talk with CPF staff and other daughters about the program, your ideas, and how the CPF can help you.
New York, NY - Saturday May12^th http://www.coalitionforpf.org/cpf_events_detailes.php?id=550
San Francisco, CA - Friday May 18^th http://www.coalitionforpf.org/cpf_events_detailes.php?id=551

Save the Date: September proclaimed National Pulmonary Fibrosis Awareness Month:http://www.coalitionforpf.org/cpf_news_detailes.php?id=549 Watch for news of how you can be a part of this month of activity around PF.


Click here for other Upcoming Events: http://www.coalitionforpf.org/cpf_events.php