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Margarete Cassalina

Nationally Recognized Speaker & Author of Beyond Breathing <meta name="description" content="" />

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CF

Personal Journey · August 28, 2017

Margarete Cassalina’s interview about her latest book, ‘See You at Sunset’

iUniverse author Margarete Cassalina tells us about her second book, See You at Sunset, a story based on real-life experience with cystic fibrosis. Margarete Cassalina Talks About 'See You at Sunset' Please briefly describe your book . . . When people started asking me what my second …

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April 12, 2017

Cystic Fibrosis Great Strides Walk-Poughkeepsie, NY

Want to change a life on a Sunday morning? Want to make someone breathe easier and add more tomorrows for those fighting CYSTIC FIBROSIS? What Is CYSTIC FIBROSIS? CURRENTLY THERE IS NO CURE WHAT CAN YOU DO?? Use your lungs and take a walk for those who can’t and COME JOIN …

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March 30, 2017

CF Foundation’s 2017 Volunteer Leadership Conference, Dallas, TX

Margarete Cassalina, author of the memoir, Beyond Breathing , will be joining other dedicated volunteers for 2017 Cystic Fibrosis Foundation's National Volunteer Leadership Conference in Dallas, TX. April 7th - April 8th More information regarding VLC:  The Cystic Fibrosis Foundation …

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March 12, 2017

CF Education Day: Grand Rapids, MI

Margarete Cassalina, the author of the memoir, Beyond Breathing , will be speaking at Spectrum Health's CF Education Day in Grand Rapids, MI   Date: Saturday, March 25, 2017 Place: Frederik Meijer Gardens More information to follow or contact: Jessica Bustraan, LMSW Medical …

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Personal Journey · November 12, 2016

When Cystic Fibrosis parents get together, love is there.

When CF parents get together, love is there. It doesn't take long in a room full of cystic fibrosis parents to see love. I was honored to be asked to speak to a group of CF parents in Salt Lake City Thursday night. I expected a small group but the room was filled to capacity with me being …

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Margarete Cassalina is a motivational speaker, award-winning author, and national advocate for the Cystic Fibrosis Foundation. Read More…

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