Breathing Room: The Art of Living with Cystic Fibrosis

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Organ Donor Awareness!

Breathing Room has lots in store for the year. If you would like to share your personal stories, news items or poetry with us, please contact: us at: info at thebreathingroom.org.

Stories, Poems and opinions of participants are their own, and not necessarily those of the Breathing Room organization.

Please visit cfmessageboard.com to connect with members of the CF community online.

Breathing Room
facilitates candid and open communication between adults with Cystic Fibrosis, supports the development of a community of adults with CF and provides education and insight for families, caregivers, and medical professionals who impact our lives.

Shaping Our Choices

We take a look at how Cystic Fibrosis has shaped other choices (career and family spring to mind).

photo from Caregivers' Collection

Through the Looking Glass

An ongoing multimedia project showcasing the emotional journey traveled by adults living with this genetic disease.
Image index
Featured Image Hidden Agenda
"Me discovering the giant tailpipes in the sky,
spewing coal ash in my air so we can feel cozy indoors.
My audience can't see my core motivation,"

Featured story
My Three Teachers
by Walter M. Robinson, MD
One of the most important lessons I learned during my medical training was to remember the difference between disease and illness.
Go there | Story index | Poetry index

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