The Adventures of Miss Messy Suzie McGoo and The Cuff Cough Crew

The Adventures of Miss Messy Suzie McGoo and The Cuff Cough Crew

Author: Nicholas Kelly

Publisher: Define Your Success LLC

Published: 2021-04-06

Total Pages: 47

ISBN-13: 173615950X

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Meet Miss Messy Suzie McGoo, a delightful little girl who lives for adventure. Follow her as she embarks on her latest adventure – a trip through the jungle – where she and you will meet beautiful animals, see fantastic sights, and learn a thing or two about her and just how extraordinary and brave she is. This book will delight parents and children alike and will teach both about what it’s like to live and thrive with cystic fibrosis and the special lung therapy that makes her life easier and helps her remain healthy and strong. Subject matter •This book is designed to teach children with Cystic Fibrosis how to complete the lung therapy, the "Huff Cough". We have renamed it the "Cuff" Cough as the "C" alliteration more easily achieves the desired results, without in person training. Theme• A lighthearted and whimsical book, designed to act as an educational tool, while also helping normalize having to complete lung therapy. Target audience• Families affected by Cystic Fibrosis and Children age 5 -10 Main characters' names for children's books• Miss Messy Suzie McGoo Problem it will solve or lesson it will teach• The “Cuff Cough” lung therapy


The Adventures of Miss Messy Suzie Mcgoo and Her Respiratory Zoo

The Adventures of Miss Messy Suzie Mcgoo and Her Respiratory Zoo

Author: Nicholas Kelly

Publisher:

Published: 2023-08-31

Total Pages: 0

ISBN-13: 9781736159552

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After the amazing trip through the jungle, Miss Messy Suzie McGoo is ready to invite you and the cuff cough crew to her secret magical tea party! This time, the awesome Mama McGoo is helping her, and so are the four wise animals. Suzie would love it if you could join her for a tea party full of surprises, while you discover the great secret of AHDA together!Whimsical and educational both, this book will show children and their parents it's perfectly possible to have fun and thrive with cystic fibrosis, teach them how respiratory medications (Albuterol, hypertonic solution, Dornase, and antibiotics} help Suzie live a fulfilling life and show them the exact order to take them in, in a way they will easily remember.


Having Cystic Fibrosis Is A Lot Like Being A Superhero

Having Cystic Fibrosis Is A Lot Like Being A Superhero

Author: Kelsey M Finn

Publisher:

Published: 2020-07-02

Total Pages: 28

ISBN-13:

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This book tells the story of Jack, a boy who has a genetic condition called Cystic Fibrosis, and his Cystic Fibrosis Superpowers. Cystic Fibrosis affects approximately 1 in every 2,500 people of European ancestry, and also affects people of other ancestries, but less frequently. This book is intended to serve as a way to communicate with children about Cystic Fibrosis, to embrace and foster acceptance of the human condition, and help children understand what Cystic Fibrosis means for themselves or someone they know who is affected by Cystic Fibrosis.


Breath from Salt

Breath from Salt

Author: Bijal P. Trivedi

Publisher: BenBella Books

Published: 2020-09-08

Total Pages: 744

ISBN-13: 1948836629

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Recommended by Bill Gates and included in GatesNotes "Elaborating on the science as well as the business behind the fight against cystic fibrosis, Trivedi captures the emotions of the families, doctors, and scientists involved in the clinical trials and their 'weeping with joy' as new drugs are approved, and shows how cystic fibrosis, once a 'death sentence,' became, for many, a manageable condition. This is a rewarding and challenging work." —Publishers Weekly Cystic fibrosis was once a mysterious disease that killed infants and children. Now it could be the key to healing millions with genetic diseases of every type—from Alzheimer's and Parkinson's to diabetes and sickle cell anemia. In 1974, Joey O'Donnell was born with strange symptoms. His insatiable appetite, incessant vomiting, and a relentless cough—which shook his tiny, fragile body and made it difficult to draw breath—confounded doctors and caused his parents agonizing, sleepless nights. After six sickly months, his salty skin provided the critical clue: he was one of thousands of Americans with cystic fibrosis, an inherited lung disorder that would most likely kill him before his first birthday. The gene and mutation responsible for CF were found in 1989—discoveries that promised to lead to a cure for kids like Joey. But treatments unexpectedly failed and CF was deemed incurable. It was only after the Cystic Fibrosis Foundation, a grassroots organization founded by parents, formed an unprecedented partnership with a fledgling biotech company that transformative leaps in drug development were harnessed to produce groundbreaking new treatments: pills that could fix the crippled protein at the root of this deadly disease. From science writer Bijal P. Trivedi, Breath from Salt chronicles the riveting saga of cystic fibrosis, from its ancient origins to its identification in the dank autopsy room of a hospital basement, and from the CF gene's celebrated status as one of the first human disease genes ever discovered to the groundbreaking targeted genetic therapies that now promise to cure it. Told from the perspectives of the patients, families, physicians, scientists, and philanthropists fighting on the front lines, Breath from Salt is a remarkable story of unlikely scientific and medical firsts, of setbacks and successes, and of people who refused to give up hope—and a fascinating peek into the future of genetics and medicine.


Mallory's 65 Roses

Mallory's 65 Roses

Author: Diane Shader Smith

Publisher:

Published: 1997-01-01

Total Pages: 24

ISBN-13: 9780970035301

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Mallory explains how she and her family cope with her cystic fibrosis, a disease of the lungs, that is sometimes more easily pronounced as "65 roses."


Taking Cystic Fibrosis to School

Taking Cystic Fibrosis to School

Author: Cynthia S. Henry

Publisher: Jayjo Books

Published: 2000

Total Pages: 0

ISBN-13: 9781891383090

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Illustrations and simple text help children learn what cystic fibrosis is and how it is dealt with.


Sticky Icky Booger Bugs

Sticky Icky Booger Bugs

Author: Sherry Frith

Publisher: Archway Publishing

Published: 2013-07-31

Total Pages: 32

ISBN-13: 1480800821

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There are 30,000 children each year diagnosed and battling cystic fibrosis. There is no cure for this progressive disease. Sticky Icky Booger Bugs is the tale of a boy’s battle with cystic fibrosis as he attempts to avoid the hospital. Kory is just like any other child. He loves recess, playing soccer and exploring his neighborhood with his best friend. With every puff, cough, and sneeze, Kory keeps the sticky icky booger bugs away so he can have fun every day!


Grandma Has Huntington's Disease, and It's Okay

Grandma Has Huntington's Disease, and It's Okay

Author: Kelsey M Finn

Publisher: Independently Published

Published: 2020-07-02

Total Pages: 28

ISBN-13:

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This book tells the story of a grandmother who has Huntington's disease, a genetic condition, from the perspective of her grandson, Leo. Huntington's Disease affects 5 to 7 people in every 100,000 people of European ancestry, and also affects people of some other ancestries but less frequently. This book is intended to serve as a way to communicate with children about Huntington's Disease, and help children understand what it means for them and their family member affected by Huntington's Disease.


Diary of a CF Kid

Diary of a CF Kid

Author: Tim Sweeney

Publisher: Independently Published

Published: 2021-04-19

Total Pages: 225

ISBN-13:

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Are you a CF kid? You're not alone! When Tim Sweeney was (much) younger, he wished he had a book like this to help him navigate the ups and downs of having cystic fibrosis. Tim was born with cystic fibrosis at a time when there wasn't a lot known about it. Throughout Tim's life, he has faced challenge after challenge and never gave up. As a result, Tim has learned all of the tools he uses to be a CF Warrior everyday. Tools such as exercise, good eating habits, compliance with breathing treatments and medications, and having the right mindset. Just like a superhero, Tim relies on his family, friends, and doctors to help, but he also relies on himself. In Diary of a CF Kid, Tim teaches the life lessons he's learned, such as trust, self-esteem, integrity, courage, and many others, to help be a CF Warrior who is winning daily battles. Tim's mission in life is to live with health and happiness. Living with CF has many challenges and it helps to be inspired by someone who has seen every stage of CF including 3 life saving surgeries (and even managed to run a marathon less than year after his double lung transplant). Tim has been a personal trainer for over 20 years with a wife and 3 boys. Let's face it, a lot of kids find reading too boring and not as exciting as an iPad. Diary of a CF Kid is told in the entertaining Diary of a Wimpy Kid style with funny sketches and stories that will make you laugh, engage, be inspired, and learn. Tim's diary also brings to life important topics for a CF kid. Each diary entry focuses on a new value with examples that include historical figures such as Helen Keller, the Wright Brothers, Gandhi, Nelson Mandela, and many others. Tim also uses his own experiences to teach valuable lessons that have made a huge impact on his life. Learning from such real life heroes will inspire CF kids to live a life with health and happiness. This book is for a CF Kid. It is also for the parents of a CF kid who want to know how their kid experiences the world. How do CF kids perceive CF? What are the fears and hopes of a CF kid? What are some of the values that are important for a CF kid to practice daily? Perfect as a bedtime story, neatly divided into small sections, Diary of a CF Kid is a one of kind book for CF Kids.