Your Health is Your Choice with Sara Troy and her guest Sherri Scott, on air from August 29th
Everyone should be encouraged to learn how the body can naturally detox, and regenerate on its own, if we provide the information, tools (nutrition, energy/frequency) and guidance. I was diagnosed with stage IV breast cancer in 2016 with meets to liver, spleen and lower lung lobe. I was told my prognosis was grim, to prepare for leaving this earth. The fear tactic was utilized to try to convince me to go in for full right breast and partial left breast mastectomy with anticipation of follow-up with chemo or radiation and reconstructive surgeries. It all sounded overwhelming to me. I have managed my MS for almost 10 years with nutrition, lifestyle management and herbs however this was more intense. My hubby reminded me that “I Had this”. I wasn’t so confident.
As a Holistic Nutritionist, I figured nutrition, life style management would be enough – I just needed to be very strict. It wasn’t enough. I spent many hours searching for answers, solutions. I knew energy to the cell was key.
I had, just prior to my diagnosis, purchased a frequency system that I thought it might be a good time to learn how to use it! So I did. I have not looked back! I use frequency every day for myself, my friends and family, even my pets.
This was my introduction to frequencies. I have not looked back. I now help others around the world tap into their own boy’s natural regenerative abilities utilizing nutrition and frequency. The latest frequency is the most outstanding! Terahertz frequencies are amazing. There is plenty of research out there on it and it is definitely worthwhile to look into!
I am a holistic nutritionist, Cellular detoxification & regeneration Specialist. I provide the tools, information an guidance to those who wish to ulitize the body’s natural ability to return to optimal health with as little interference as possible.
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Why readers love a literary thriller that draws from magical realism, 1990s rock ‘n’ roll, myth, and romantic suspense
Why her book centers around a spiritual war that’s been fought for thousands of years
How the research she did to create her musician characters led her to study music, form a band, and tour around the USA
Why the book is set in the early 1990s – before the Internet, cell phones, or 24/7 streaming
Whether practicing criminal defense law later influenced her decision to release the book, which explores themes surrounding the law
Why she chose to leave a hard-won tenure-track position teaching British literature to write fiction
The Maenad’s God explores a variety of thorny topics:
Alienation. Why some people are cynical and ‘done with society’
The nature of divinity; creativity as a way into some kind of higher reality; imagination as a sacred space
How creativity is an art of rebellion – and a healing force
The degree to which reality and fantasy inform each other
Whether creating a private world is a subversive act against a toxic culture
“Michalson’s prose, as narrated by the loquacious Pete, is by turns wisecracking and obsessive. . .. Even so, Pete’s quest takes him in unexpected occult directions, opening up an intricate world of ecstasy and paranoia. … the novel’s angst and atmosphere-both authentically ’90s-make for a strangely alluring reading experience. An engaging, snaking, and spirit-tinged murder tale about obsession and control.” —Kirkus Reviews“
TheMaenad’s God receives 5 stars and the ‘Highly Recommended’ award of excellence.” —The Historical Fiction Company Chosen by Independent Book Review as one of the best books of 2022, Karen Michalson’s fourth novel, The Maenad’s God, is the story of a war that’s been fought for thousands of years, the war between the ancient arts of music, poetry, and love; and the equally ancient forces of artistic envy, oppressive law, and authoritarian religion. Boston 1992. Alienated FBI agent Pete Morrow discovers a murder and becomes obsessed with Jade McClellan, a mysterious mafia-backed rock musician. Tough-guy Morrow has never been in love before—but Jade is almost magical, creating a private imaginary world from his songs and stories that rapidly become the only thing Morrow values in his otherwise empty life. Unfortunately, Morrow is investigating the mafia family that is investing in Jade’s musical career. Being open about their relationship could get both of them killed.
Michalson, who has taught nineteenth-century British literature, performed across the USA with her rock band, Point of Ares, and runs a criminal defense practice, is uniquely suited to write this book. “If you like hard boiled gritty realism with an edge of surrealism – you will like this book,” promises the author. “If you like rock band fiction, stories about the mafia and the music business, or ever engaged in any kind of creative pursuit, you will like this book. If you like romantic suspense, particularly if it involves complex multi-dimensional characters whose conflicts with society extend beyond their relationship, you will like this book.” “The Maenad’s God is never the same book twice: flowing from intrigue to mysticism, romance to mythology, Karen Michalson weaves an epic and constantly surprising narrative.” —IndieReader “The Maenad’s God deserves attention. . . . it also deserves the highest rating, for it seems to me a work of substance and original thinking.” —Reedsy“ . . . gripping, satisfying, and impossible to put down even after you’ve finished it.” —Readers’ Favorite
Karen Michalson has assumed many identities – criminal defense attorney, scholar and teacher of nineteenth-century British literature, and progressive rock band performer. All her experiences find a home in her writings as an award-winning, critically acclaimed author. She has written four novels, including The Maenad’s God, which was selected by Independent Book Review as one of the best novels 2022 and by IndieReader as one of the Best Reviewed Books of March 2023. It also received a 5-Star Highly Recommended Award of Excellence from The Historical Fiction Company and a Literary Titan Gold Book Award (2022). Her earlier novels form the Enemy Glory Trilogy: Enemy Glory, Hecate’s Glory, and The King’s Glory. Enemy Glory, the first book of the trilogy, was one of the books that received the most votes for the Locus Award for Best First Novel. It was chosen for Locus’s Recommended Reading List of Best First Novels. Michalson’s first book, a non-fiction work, Victorian Fantasy Literature’s Literary Battles with Church and Empire, examines the non-literary and non-aesthetic reasons underlying the bias in favor of realism in forming the traditional literary canon of nineteenth-century British fiction. Her books have been favorably reviewed by Clarion Foreword, Kirkus Reviews, Publishers Weekly, Independent Book Review, Literary Titan, Blue Ink Review, and numerous others. Michalson practiced criminal law for a decade. She left the law profession a little over four years ago to return to her full-time novel-writiPh.D.full-timeBefore. Prior to what she calls her “detour into law,” she wrote novels, formed a progressive rock band, Point of Ares (she plays bass guitar), and ran a small record label-distributor (Arula Records). Point of Ares released four CDs, two of which are concept albums based on her Enemy Glory books. The band received airplay in the USA, Canada, Mexico, Belgium, Brazil, and Italy and what she calls “embarrassingly kind reviews.” Before rocking out on music and fiction writing, she began her literary career as an assistant professor of English at the University of Connecticut. She holds a PhD in English (British literature) from the University of Massachusetts and a JD from Western New England University School of Law. She lives in New England.
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Your Health is Your Choice with Sara Troy and her guest Mikki Gaffen Stone, on air from August 29th
I would like to shed some light on the topic of often invisible chronic pain conditions such as hypermobile type Ehler’s-Danlos Syndrome. It is said to be a rare condition, but I call bullspit on that. It is rarely diagnosed and that is another thing altogether.
Ehlers-Danlos Syndrome (EDS) is a hereditary condition that affects the skin and the mobility of joints due to abnormal collagen synthesis, an important component of connective tissue; the latter is abundant in the skin, joints and vessels, to which it gives strength and elasticity. Although it develops in childhood, the diagnosis is only reached in later years. The condition takes many different forms that vary in severity, so the clinical manifestations vary widely. Ehlers- Danlos syndrome diagnosis is based on physical examination, through observation of how the patient moves, and the doctor’s analysis of his/her medical history. Usually, a rheumatologist or a physiotherapist establishes the diagnosis rather than a general medical practitioner.
Ehler’s Danlos Syndrome brings with it many, many challenges. One of those challenges is that people with this condition often ‘look well’. This can lead to some unpleasant public scenes where someone tries to shame a person with EDS for using mobility aids for example. The judgment and lack of support can, and all too often does, extend all the way to medical gaslighting.
Born in England, I am a lifelong learner and nomad. Having lived in eight countries to date, I consider myself to be a Global citizen – where I come from is a story, not a place. Home is wherever I am, right now. And we are moving soon I work with people. Meeting them where they are and guiding them to exactly where they want to be. We make big changes and small ones. Whatever is needed. I do so while working with my own chronic condition of Eheler’s – Danlos Syndrome, hypermobile type. I believe my own experience with pain enables me to understand others on a level that you only ‘get’ if you experience it yourself.
More on the difference between fibromyalgia and E.D.S, HERE
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Mental Health Awareness with Sara Troy and her guest Deborah L. Staunton, on air from August 29th
Disruptive mood dysregulation disorder (DMDD) is a condition in which children or adolescents experience ongoing irritability, anger, and frequent, intense temper outbursts. The symptoms of DMDD go beyond a “bad mood.” DMDD symptoms are severe.
I am the daughter of a mentally ill alcoholic father and the mother of a mentally ill daughter. At that time it was a brand new diagnosis, very little was known about it and there were no resources for parents. Now that she is 18, her diagnoses have changed and while they are still challenging, I have insight and clarity that I didn’t have then. Sharing my experience and what I learned from it can help parents who are on that difficult journey with their own kids. It can save them some heartache and provide validation and support. Mental illness still has a lot of stigma associated with it and removing that stigma is an important step in supporting those who suffer from it and those who love them.
Deborah L. Staunton was raised by a mentally ill father and is raising a mentally ill daughter. She came to motherhood late after enduring four miscarriages and despite having an extensive background in Early Childhood Education, has had an extremely difficult journey in raising two neurodivergent children. Writing has been Deborah’s lifeline and her passion since childhood and has kept her grounded when her life was unravelling.
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Sara’s View of Life with Sara Troy, on air from August 29th
As the last warm rays of summer start to mellow, they cast long shadows, heralding the approach of autumn. It’s always a bit melancholic when summer draws to an end, but fall, with its russet hues and crisp air, brings its own sense of purpose. It reminds me of turning pages in a book, which is apt because I’m about to dive deep into two significant writing projects.
The first is deeply personal – My Life’s Reflections. Penning down a lifetime of experiences, choices, moments of joy and sorrow is no small feat. It requires introspection, vulnerability, and sheer honesty. I need to encapsulate all that I’ve felt, seen, and done. While it’s daunting, I also believe it’s going to be therapeutic, allowing me to see patterns, learnings, and maybe even offer others some insights from my journey.
Then there’s the ‘Our Forgotten Children’ anthology. This is not merely a project; it embodies a movement. It’s a collection of tales from individuals who have actively worked with children, shedding light on the pressing need to transform the surroundings we nurture our children in. Each chapter is a testament—a voice, a story, an appeal, even an anthem of hope. These narratives highlight the inherent flaws in our systems and emphasize actionable ways to reform them, ensuring the well-being of both parents and children. By strengthening their bonds and fortifying their spirits, we can hope for a brighter future. Having Krystal Hille Publishing on board for the editing instills a sense of calm within me. Their esteemed reputation and meticulous approach guarantee that every tale will be treated with utmost respect and refinement. Yet, the road ahead is long – there’s the challenge of raising funds, streamlining coordination, and overseeing production. And the clock is ticking, with only four weeks at my disposal, to get all the chapters over to Krystal and raise that money to produce it.
The urgency isn’t just about the change in season; it’s also personal. The UK is calling me back. Family ties, with near death experiences with aging siblings, the need to see them is strong, as it has been 4 years since. The pandemic has been a formidable barrier, keeping me oceans apart from loved ones. This upcoming trip is about reconnection, healing, and maybe even finding some semblance of direction for the future in hand. But before that, the tasks at hand loom large. The next four weeks are going to be intense, filled with late-night writing sessions, brainstorming, and possibly copious amounts of coffee. But there’s a intense excitement too. The kind you feel when you’re on the brink of something profound. As the leaves turn golden and begin to fall, I’m reminded of the impermanence of it all and the importance of making every moment count.
All of our shows/interviews are done by donation, if you enjoyed this show please support us here with either a one-time donation or subscribe and support, thank you..
I work with people. Meeting them where they are and guiding them to exactly where they want to be. We make big changes and small ones. Whatever is needed. I do so while working with my own chronic condition of Eheler’s – Danlos Syndrome, hypermobile type. I believe my own experience with pain enables me to understand others on a level that you only ‘get’ if you experience it yourself.
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