When Linda Crabtree was growing up in a small Canadian city in the early '40s, the future for a little kid with a disability didn't look too promising. Seventy-five years later she writes about her forays into education, journalism, running a charity, publishing, art, antiques, designing a house and her travels. The emotional undercurrents of love, the question of children, marriage, alcoholism, divorce, marriage again and great loss are explored. And then there's her love of dogs. It has been a roller-coaster of a ride and this passionate, entrepreneurial woman has kept plugging away all the while dealing with an inherited neuromuscular condition called Charcot-Marie-Tooth (CMT) disease, named after three doctors, that has slowly progressed over the years to take away her ability to walk and is now robbing her of the use of her hands. The recipient of 28 awards, medals and honours, Linda is proud to be a Member of the Order of Canada and the Order of Ontario and has been in Canada's Who's Who for the past 20 years. Find out why. Excerpt: " ...With $15 for paper and envelopes and a few postage stamps, I typed letters to editors of all of the newspapers in Canada, telling them that I had a rare disease with a strange name, knew no one else with it, and was looking for information and people to share our concerns and triumphs. My letters were published in newspapers across the country and within a few weeks I had received so many letters from people also diagnosed with CMT, or suspecting they had it, and wanting information that I knew I was onto something. My curiosity was piqued. How many people with CMT were out there? Now I had a real challenge. How many could I find? I went back to the library and photocopied all the addresses for the newspapers in the United States. Those letters went out and, before I knew it, I had more than 350 replies from people all wanting to know more. Trouble was, I didn't have more to give them. We'd have to learn from each other. And there was no way I could type 350 individual letters in reply. I had to figure out a way to answer them all at the same time. Personal computers were a rare commodity at that time. The solution to my dilemma turned out to be a mass mailing and in the summer of 1984 the CMT Newsletter was born. It wasn't much - only eight pages, the columns typed, cut out and pasted down and then everything photocopied - but it was something."

Walk A Mile In My Braces is a journey through the experience of challenge as taught by the young. 75 youth who all experience Charcot Marie Tooth Disease (CMT) share their joys, their struggles, and the wisdom they have learned by walking through life with challenge. Prepare to be inspired by all that these young authors share with regards to their scars, lessons learned, and gifts received by rising to their challenge.

Arlene knows what it's like to be different. But in her quest to become the youngest student government officer in Greenwood Elementary history, she finally realizes the value in embracing differences.

Welcome to the world of Charcot Marie Tooth (CMT) disease, a rare, progressive and hereditary neurological condition. Author Dawn Johnson takes readers through the physical challenges-the toll on the body, passing the disease on to her son, numerous surgeries, and ongoing treatments. She addresses the emotional toll as well, weighing in on the societal issues of bullying, lack of CMT awareness, giving back and paying it forward. Most of all, Dawn's spiritual journey is inspirational. As a wife, mother, daughter, co-worker and friend, she shares a raw and courageous view of coping, while trusting God's plan for her life.

For a woman of reproductive age, any medical appointment is a pre-conception visit and an opportunity to address pre-existing conditions that affect pregnancy and the maternal-fetal dyad. However, many neurologic conditions are rarely seen in pregnancy, and limited experience and knowledge may prevent the team from developing a shared approach to these complex conditions during pregnancy. Neurological Diseases and Pregnancy: A Coordinated Care Model for Best Management brings together experts across the disciplines of maternal fetal medicine, neurology, obstetrics, family planning, genetics, anesthesia, psychiatry, neurosurgery, and lactation to provide a multi-disciplinary, comprehensive, protocol-driven guide on best care for patients with neurologic disease before, during and after pregnancy. Each chapter provides a detailed care map on each unique disorder, and discusses the use of neurological medications during pregnancy and in lactation. Through this multi-disciplinary approach clinicians can navigate the complexities of preconception and pregnancy care, and help to optimize outcomes for the mother-infant dyad. Beyond pregnancy care, this volume further serves as a resource on best care for the life-course of women affected by neurologic disease including pre-pregnancy planning, genetic counseling, contraception, and sexuality in neurologic disease, as well as post-partum depression and menopausal neurologic changes.

The Model Rules of Professional Conduct provides an up-to-date resource for information on legal ethics. Federal, state and local courts in all jurisdictions look to the Rules for guidance in solving lawyer malpractice cases, disciplinary actions, disqualification issues, sanctions questions and much more. In this volume, black-letter Rules of Professional Conduct are followed by numbered Comments that explain each Rule's purpose and provide suggestions for its practical application. The Rules will help you identify proper conduct in a variety of given situations, review those instances where discretionary action is possible, and define the nature of the relationship between you and your clients, colleagues and the courts.

We live in a world of noise where everyone is so quick to speak. When we slow down and give someone our full attention, we offer them a safe place to be fully heard and accepted. Hear’s the Thing is a story about what is possible when someone is brave enough to listen to others… and, ultimately, themselves without judgement. For Cody Alan, one of country music’s most famous on-air radio and TV personalities, listening to other people has always been a crucial part of his role. It was by fostering his ability to hear others that he discovered the person he most needed to listen to was himself. Listening ultimately led him on a journey of self-discovery where he found the courage to come out as gay, the openness to question spiritually, and the strength to explore a new definition of parenting and family. In his debut memoir, Hear’s the Thing, Cody shares some of the many lessons he’s learned along the way such as: How to actively listen with empathy and without judgment Why a willingness to “let people in” better equips you to receive from others How genuine attentiveness can help you build healthier and deeper relationships The art of listening is often lost but Cody’s story will inspire you to hear that inner voice that is leading you to a deeper connection with yourself and the people around you.