Lachlan Terry

Lachlan Terry led a vibrant, active life until the unsettling prospect of being confined to a wheelchair emerged. In his 42 years, he had avoided debilitating injuries, relying on a mix of good luck and management. The gradual and unexpected onset of his condition hindered job opportunities and even mundane tasks like picking up a coin.

The question "Why me?" lingered, but Lachlan learned to accept life's unpredictable nature during 13 years of uncertainty, misdiagnoses, and hurdles. His upbringing on an outback station instilled a pragmatic outlook, and he embraced the idea of playing the hand he was dealt.

Despite his undiagnosed condition, Lachlan remained mobile, using a walking frame or electric mobility scooter, covering an impressive 5,500 kilometers in a year. He remained devoted to various roles as a Scouts Australia leader, radio DJ, home barber, traveler, photographer, and Art Leasing business entrepreneur. Grateful for opportunities, he eagerly shared his story, embracing the power of politeness and gratitude that had always guided him. Determined and resilient, Lachlan Terry showed the world the strength to seize every chance life offers.

BOOKS CO-AUTHORED BY LACHLAN

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 Sculac, Lachlan Terry,  John Van De Putt, Beth Wurcker.

Order your copy here.