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This March marks the 18th anniversary of the start of my writing the column “Life With A number of Sclerosis.” I started writing after a tough first few years of dwelling with my a number of sclerosis (MS) analysis. A lot has modified over that interval — together with how I write, what I write about, and the way these writings are delivered to you, my readers.
I’m completely satisfied to say that my latest guide has now been revealed by Coffeetown Press and will likely be out there to worldwide readers by Ingram.
It’s known as Residing Nicely With A number of Sclerosis, and I’d be remiss had been I to not name out the numerous efforts of a lady I name my “MS sister,” Emma Rogan, with whom I labored for almost two years to get the writing into its present format.
Whereas not written in a linear method, now we have organized it so. It’s been known as “one half primer, one half handbook, one half pocket translator, and 100% a necessary area information for navigating the challenges of dwelling with power sickness.” Humbling, certainly.
Much more humbling was that Tim Coetzee, PhD, chief advocacy, providers, and science officer for the Nationwide MS Society, wrote a stunning foreword to the guide.
An previous good friend as soon as stated, and it’s caught with me since, that “self-praise goes however little methods.” So I’ll let others communicate to that. It should be stated that I’m gobsmacked by the worldwide voices who’ve supplied up evaluations of the brand new guide.
What the Consultants Are Saying About My E book
“Pleasant, humorous, insightful, poignant, and compelling. Residing Nicely With A number of Sclerosis ought to be necessary studying for each affected person coping with any power well being situation and for the docs treating them.”
— Michelle Toshima, PhD, A number of Sclerosis Heart at Swedish Neuroscience Institute
“Trevis is daring, insightful, and delicate as he explores the taboo and sometimes uncared for topics that influence the survival of individuals dwelling with MS.”
— Barbara (Bobbie) Severson, ARNP-C
“An open, sincere, and actual account of life with MS. It’s confronting, uplifting, difficult, emotional and all issues in between. An excellent learn.”
— Trishna Bharadia, MS affected person advocate, MS Society UK
“Humorous, self-deprecating, pragmatic, and enlightened, Trevis offers a must-read account of taking part in the hand that MS has dealt him the very best he can.”
— Ava Battles, chief govt officer, A number of Sclerosis Society of Eire
“Trevis paints an image that provides readers an inside have a look at what it’s wish to reside and thrive with MS.”
— Pamela Valentine, PhD, president and chief govt officer, MS Society of Canada
“It’s like spending time along with your new heat, sensible, and humorous greatest good friend. You’ll really feel as if you might be hanging out whereas studying what it means to reside and love with a number of sclerosis.”
— Sara Loud, chief govt officer, Accelerated Remedy Mission
“A vivid diary of a private journey by a number of sclerosis. Whereas each journey is totally different, Trevis has managed to convey us into the shared expertise of individuals with power sickness.”
— Paola Zaratan, PhD, director of scientific analysis, Italian A number of Sclerosis Society
“You don’t must have MS to understand Trevis Gleason’s writings. Whereas he’s by no means lower than sincere in regards to the laborious elements, he additionally manages to maintain it mild and discover the humor in what he’s going by.”
— Ingrid Strauch, editor, On a regular basis Well being
“Trevis touches on the core themes which are on the coronary heart of communities of individuals dwelling with power circumstances: solidarity, company, data and schooling, discrimination and stigma.”
— Nicola Bedlington, former secretary normal, European Sufferers’ Discussion board
“The outline of a person life path that can provide folks dwelling with power sickness each braveness and hope.”
— Herbert Temmes, president, European A number of Sclerosis Platform
“This guide offers context and life to the phrases, to the questions, and to the fears that so many people dwelling with a power sickness are too afraid to talk of or too embarrassed to ask.”
“That is the guide that newly-diagnosed in addition to long-haul a number of sclerosis sufferers and their households ought to have on their bookshelves.”
— Meredith O’Brien, writer, Uncomfortably Numb: A Memoir
I’m Hoping It Can Assist You
I’m nearly embarrassed by such advance reward from an internationally distinguished checklist of authorities saying such good issues about this guide. I hope that you simply discover it useful to yourselves or your loved ones and buddies. I additionally thank all of you for therefore a few years of your feedback and help for Life With A number of Sclerosis.
Wishing you and your loved ones the very best of well being.
Cheers,
Trevis
My new guide, Residing Nicely With A number of Sclerosis, is now out there. Comply with me on the Life With MS Fb web page, and browse extra on Life With A number of Sclerosis.
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