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 …
Speaker
Rose to Runway-Stamford, CT
Margarete Cassalina, author of the memoir, Beyond Breathing and See You at Sunset will be honoring Katy Starck-Monte with the Spirit of Courage Award at the 2017 Rose to Runway charity event benefiting cystic fibrosis. About Rose to Runway Rose to …
Cystic Fibrosis Scientific Update-NYC
Margarete Cassalina to Speak at the 2017 Scientific Update for Cystic Fibrosis Margarete Cassalina, author of the memoir, Beyond Breathing and See You at Sunset will be speaking at: 2017 Scientific Update regarding #GivingTuesday To RSVP or to learn about …
Cystic Fibrosis Scientific Update-NYC
Margarete Cassalina, author of the memoir, Beyond Breathing and See You at Sunset will be speaking at: 2017 Scientific Update regarding #GivingTuesday To RSVP or to learn about the live stream, please contact: Shara Swift …
Guest Speaker at Vertex Pharmaceuticals, Boston, MA
Margarete Cassalina, the author of the memoir, Beyond Breathing , will be speaking at Vertex Pharmaceuticals in Boston, MA on April 27, 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 …
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 …
Recap, Reset, Rename
4 hours 600 people 2 million dollars all for Cystic Fibrosis research. Thursday night was our last CF event of the year. We left on a high note and a fist full of cash for the CF cure. I left the evening with hope for the future, a couple of roses, and a York Peppermint …