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Elizabeth Neal

Author

Elizabeth Neal, a woman of unwavering strength and optimism, has faced life's challenges with determination and a sense of humor. Diagnosed with MS in 1991, she endured misdiagnosis and hostility in the RAAF. Despite constant fatigue, dizziness, and falls, she found joy in her marriage, motherhood and pursuit of higher education.


Through it all, Elizabeth's resilience continues to shine exploring various treatments and exercise routines to manage her condition. She discovered the empowering benefits of pole dancing and even ventured into stand-up comedy to embrace life fully.


Tragedy struck in 2020 when her beloved son Valentine passed away unexpectedly. Amidst the grief, Elizabeth remains hopeful, seeking a cure for MS while cherishing her son's memories.


With an unwavering spirit, Elizabeth faces each day with optimism, refusing to let MS define her. Her determination, support from friends and family, and love for life inspire those around her.




 


BOOKS CO-AUTHORED BY ELIZABETH



WHISPERS OF RESILIENCE: OUR STORIES OF MULTIPLE SCLEROSIS


Whispers of Resilience: Our MS Stories brings together 26 poignant tales from Australia, each sharing a unique journey with Multiple Sclerosis. Through personal accounts, the book unravels the intricate realities of MS, giving a human touch to the condition. Each story becomes a beacon of resilience, contributing to an inspiring collective portrait of hope and fortitude. The authors hail from diverse backgrounds, transforming their shared condition into a wellspring of courage. These resilient voices convey a powerful message: "We are more than our diagnosis." Inviting readers into their world, they reveal not just the challenges of MS, but also the extraordinary strength and resilience it invokes. In the Pages of this book, you'll find stories of courage, resilience and hope from individuals touched by Multiple Sclerosis (MS). As we delve into the lives of these brave souls, we are reminded of the immense challenges that MS presents and the impact it has on those living with the condition, and their loved ones it is with a profound sense of purpose that we have chosen to give back to the MS community. With every copy, sold 25% of the proceeds will be dedicated to MS research. Our commitment is to fold to raise awareness about a mess, and its far-reaching effects and to contribute to the scientific advancements that one day lead us to a cure!


MS is a disease that can strike at any stage of life. Its symptoms are unpredictable, and diverse from numbers and tingling to fatigue and mobility issues. The challenges faced by those with MS are varied as the people themselves. It affects their ability to work study, and engage in everyday activities, taking a toll on physical, emotional and mental well-being. Our collective efforts matter by purchasing this book, you become a part of something bigger, a community of compassion and determination together we can make strides in MS research, supporting the scientist and clinicians tightly working to improve the lives of those affected by this condition join us on this journey, a journey of giving back spreading awareness and inspiring changes. Together we can make a lasting impact on the lives of those living with MS and their families.  


Featuring Authors: Emma Archer,  Diane Barclay,  Leanne Boothroyd,  Allyson Brown,  Amanda Campbell,  Don Campillie,  Angharad Candlin,  Nina Crumpton,  Lillian Cuba, Colleen Daniels,  Laura Di Lulio,  Kim Eagle,  Jayne England,  Penelope Gemmell, Candice Graham,  Robyn Hart,  Justine Martin,  Stacey Metcalf,  Elizabeth Nea,l  Kristi Paschalidis,  Clare Reilly,  Tanya Rountree,  Kerrie Worsfield, Lachlan Terry,  John Van De Putt, Beth Wurcker.


Order your copy here.




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Elizabeth Neal
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