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 …
Margarete’s Blog
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 …
See You at Sunset
Buy SEE YOU AT SUNSET on Amazon People have been asking what my soon to be released 2nd book, See You at Sunset, is all about. See You At Sunset: Elevator Pitch "If hospital rooms could talk, what would they say? If true love really could last for eternity, how would you know? What if a 13 …
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 …
Where Do You Come From?
I travel a lot. It’s almost inevitable when I’m somewhere, in some state, at some new place that I get asked, “Where do you come from?” I smile and tell them, “New York.” Their response is usually, “Yeah, I can tell by your accent.” I laugh, and say in an fake exaggerated Sopranos-Italian …
The Gift of LOVE…it’s a one size fits all. (The annual ‘Beyond Breathing’ book give-away)
Back by popular demand... Read below and see how YOU can receive a FREE signed copy of BEYOND BREATHING The Gift of LOVE...it's a one size fits all. In today's world we hear so much about the negative; the greed and contempt, the wars and fighting among one another, the …
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 …
05/18/2014 — Cystic Fibrosis Great Strides Walk-Plattsburgh
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?? Join us and use your lungs and take a walk for those who can’t and COME JOIN US! Check-in: 12:00 PM Walk: 1:00 …
