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Ms. Butcher worked as a Lab Technician in various hospitals and laboratories until she was stricken with the serious autoimmune/neuroimmune disease Chronic Fatigue Syndrome. She is an avid cook when she feels up to it, and in 2005 she published a small cookbook. In 2008, she was inducted into World Wide Who's Who in Executives, Professionals and Entrepreneurs, formerly Cambridge.She was made a Platinum Member in 2009. In 2013, she was selected as VIP of the Year and as the Top Female Executive of the Year in 2013 by the same organization. In 2014, she was selected as Top Female Executive for Life by World Wide. In November 2014, She was selected as the Top Ranked U. S. Executive by the National Council of American Executives. She was asked to write an article for Living well Magazine about life with the disease and her hometown news paper the Elgin Courier News did a full page article for the Sunday edition of the paper. Ms. Butcher was also interviewed for a feature article in Pro~files Magazine for sometime early in 2016. Ms. Butcher lives in her hometown of Elgin, Il. Her website is:http://:beckiesbutcher.com. A Clarion Review follows: My Battle with Chronic Fatigue Syndrome Reviewed by Kristine Morris May 29, 2014 Butcher’s encouraging tone helps people find meaning in life during a debilitating illness. It was 2007, and forty-three-year-old Beckie Butcher thought she was dying. Something was dreadfully wrong. Every joint and muscle in her body ached; her brain and vision had fogged over. She was unable to get out of bed except to eat and use the restroom, and she couldn’t carry on a coherent conversation. When she was finally diagnosed with Chronic Fatigue Syndrome (CFS), an autoimmune disease, she was devastated. In My Battle with Chronic Fatigue Syndrome, Butcher shares the intimate and moving story of how the disease impacted her life and led to personal and spiritual transformation. Butcher had worked as a lab technician, but had made plans to follow her dreams and open her own catering business until CFS struck her life. Although warned by a support group, she was completely taken by surprise when the person she least expected to leave her did just that. “It was worse than a death for me,” she writes, “because it wasn’t a death at all. It was a conscious decision made of this person’s own free will.” Butcher’s hope is that, by sharing her experiences, she can offer hope to others who are frightened, angry, and feel that they are alone as they deal with the ravages of CFS. Christians especially will find her story encouraging, as it was through hearing of God’s ability to turn her suffering to good and believing that, no matter what difficulties she was facing, God was always with her, that she found the strength to go on. Ultimately, she found a chiropractic treatment that improved her condition, and she shares this information in her book. Butcher’s “Five Questions to Ask God” are designed to help Christians find meaning and purpose in their lives even when they are downed by a debilitating illness, and her “Five Questions to Ask Family and Friends” can help those who are ill and their loved ones build bridges of mutual cooperation, shared faith, and honesty. Especially helpful are her pointed examples of what not to say to someone who is ill—the well-worn clichés that are more likely to provoke irritation and anger than to provide comfort. Conversational in tone and generally well written, the book nonetheless has errors, including the frequently incorrect placement of quotation marks (“While I was doing’ ok,’”) and apostrophes (“Gods’ promise); a few sentences could be improved, such as “after twenty years of helping others, I was helpless to myself.” The cover design, while obviously well-intentioned, is a bit dark and murky, leaving the relevant features somewhat obscured. The back cover matter, with its words of praise for the book, is clear and inviting, and the author has supplied an attractive photo that enhances the brief biographical statement. The table of contents and copyright pages are clear and informative, and the book’s design and layout are pleasing and easy on the eye. The author has succeeded in providing information, hope, and encouragement to those who suffer from CFS. She shows how it is possible, even when faced with a devastating illness, to grow in understanding, tolerance, and faith. Disclosure: This article is not an endorsement, but a review. The author of this book provided free copies of the book and paid a small fee to have his/her book reviewed by a professional reviewer. Foreword Reviews and Clarion Review make no guarantee that the author will receive a positive review. Foreword Magazine, Inc. is disclosing this in accordance with the Federal Trade Commission’s 16 CFR, Part 255. Review by Kristine Morris.
I hope to find buyers for my book as well as an agent so I may spread the word as well as build patience and tolerance for the seriously misunderstood disease Chronic Fatigue Syndrome.I am also looking for opportunities to give presentations on the subject. Here is a link to a Clarion review of my book.https://www. forewordreviews.com/reviews/my-battle-with-chronic-fatigue-syndrome/

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