Jayne England

Jayne is a self-employed businesswoman, married and a busy mother of two teenagers.

She trained and worked in the beauty industry for many years. 

Jayne was diagnosed with relapsing remitting MS in November 2009. She was 27 years of age at the time of her diagnosis, her children were aged just four and 18 months old at the time.

Since her diagnosis, Jayne has held roles with Multiple Sclerosis (MS) in Tasmania, been involved with the Tasmanian MS Community Engagement Council, including roles as Chair and Deputy Chair. She is a member of the consumer and community reference committee for the MS Research Flagship at the Menzies Institute for Medical Research.  Jayne is an active fundraiser and advocate for those living with MS.

Jayne has also tried and failed many MS disease modifying medications - and most recently undergone a Stem Cell Transplant with fantastic results.

BOOKS CO-AUTHORED BY JAYNE

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.