New Release: The Perfect Breasts by Cara Bertoia


I’m happy to welcome back author Cara Bertoia. Today, Cara is sharing her new release, The Perfect Breasts, a short story written for Breast Awareness Month.

Blurb

Hannah Clein will always remember the day she went to a department store with her mother to buy her first bra as her last best day, “B.C.” before the cancer. She considered herself an ordinary child who loved challah bread, reading, and her family – often in that order.

With a normal life in the rear-view mirror, we follow Hannah over three decades, as she navigates the tricky transition from girlhood to womanhood. All her life, she just wants to belong. Be normal.

In a tale that explores a women’s complicated relationships with her body, and the love of her life, we learn the psyche is a funny thing. What are the perfect breasts? And how does the loss of a loved one affect those left behind?

The Perfect Breasts mixes family lore with imagination in a compelling tale of loss, longing, and love.

I have published it on Amazon Kindle for breast cancer awareness month, and all the profits will be donated to cancer research.

Buy Links

Amazon US | Amazon CA | Amazon UK | Amazon AU

Editorial Reviews of The Perfect Breasts

Brilliantly written, The Perfect Breasts is a riveting tale that chronicles the lifelong impact that breast cancer has on every aspect of the lives of each member of the Clein family. Author Cara Bertoia has penned a tautly emotional plot driven by love, loss, trust, family ties, and the inner strength one must summon to face adversity created by both human fallibility and fate rather than turning away.

The story moves at a comfortable pace with flawed, but believable characters who drive the plot. Readers find themselves rooting for the protagonists from the beginning to the end of the story. The characters evoke strong emotions in readers right from page one. This reader found herself wanting to hug Hannah on one page and throttle her on the next.

The Perfect Breasts is a book that should be required reading for every woman because it does not soft-soap the emotional effect of a life-threatening disease and forces readers to face a hard truth: The ultimate symbol of femininity and womanhood can either be a source of great strength and pride or when lost, a weapon to destroy one’s faith in life and one’s self.

Reviewer: Susie Black author of The Holly Swimsuit Mystery Series

The Perfect Breasts is a heartfelt story about breast cancer and how it affects all of our lives. Because, yes, almost everyone knows someone who has been diagnosed with breast cancer.

In this story we follow, Hannah, a Jewish girl through three decades, from the death of her beloved mother from breast cancer to becoming a self-sufficient woman. Cancer itself becomes a character burrowing into Hannah’s psyche. Knowing oneself is difficult enough, but with this added fear, Hannah struggles to find happiness.

Cara Bertoia handles the issue with sensitivity and compassion. She takes us on Hannah’s journey. leaving us with hope and a promise for a good future. This is a story which should be read by everyone.

Reviewer: Janie Emaus author of Latkes for Santa Claus

Author Bio and Links

Cara Bertoia grew up in a strait-laced Southern family, but she was always fascinated with casinos. In her twenties on a summer hiatus from teaching in North Carolina, she drove to California and became a dealer at Caesars in Lake Tahoe. She discovered that after teaching high school, handling an unruly gambler was a piece of cake. Her mother highly disapproved of her working in a casino, “a place so bad it has ‘sin’ in the middle.”

Eventually, she succumbed to pressure from the family and returned east to take a hi-tech job in Boston. She also began working on her MFA in writing at Emerson. Her goal was to write the first realistic novel about casino life from the perspective of an experienced table games dealer. She is always amazed that normal and sometimes quite intelligent players become absolutely clueless in the casino. They repeat superstitious nonsense and no amount of logic can change their position, maybe her novel will.

While in Boston she was offered the opportunity to join Princess Cruises as a croupier. Jumping at the chance, she spent the next five years circling the globe. Sometimes life exceeds your dreams. She was awed by the wonders of Venice, the fjords of Norway, and the Northern Lights in St. Petersburg.

Cara returned from ships with a very special souvenir, her Scottish husband Ray. They went to work at the Spa Casino in Palm Springs, and now live in Hollywood, Florida, where she writes about her casino years while wistfully gazing out at the ocean.

She loves to connect with her readers. Please send her a picture with any or her work. She will post those pictures to social media.

TikTok | Blog | Twitter | Instagram | Goodreads | BookBub | Facebook | Email

HAPPY RELEASE DAY!

Book Blast: Voices of Cancer by Lynda Wolters

I’m happy to welcome author Lynda Wolters. Today, Lynda shares her new release, Voices of Cancer.

Blurb

“I don’t know what to say” and “I don’t know what to do” are common responses to a life-threatening diagnosis. Voices of Cancer is here to help.

Every cancer story is different, but there is one commonality: both patients and the people supporting them often struggle to properly articulate their wants and needs through particularly challenging and in many cases, uncharted territory. Lynda Wolters knows firsthand: she was diagnosed with stage 4 terminal mantle cell lymphoma in August of 2016.

Voices of Cancer offers a candid look into the world of a cancer patient, informed by Lynda’s own story and conversations had with dozens of patients weighing in on their needs, wants, and dislikes as they navigate the complex world of diagnosis, treatment, and beyond. With comprehensive and accessible insight from people who’ve been there, Voices of Cancer helps educate, dispel fears, and start positive conversations about what a cancer diagnosis truly means, while shining a light on how best to support a loved one on their own terms.

Excerpt

Cure Is a Four-Letter Word

Once you’ve had a cancer diagnosis, being “cured” may be an unreachable goal. And the fear never goes away.

“Remission is a lesson in guarded optimism rather than magical thinking,” is a line I read from a blog post by Steve Jacob, a consultant for Baylor, Scott & White Health, who was describing remission, and I appreciated it immediately.

The word “cure” is often misconstrued as “remission” and, conversely, remission is often thought to mean cure. Unfortunately, those words are mutually exclusive and can be painful when misunderstood or misused.

Remission is essentially classified as either partial or complete. At its truest level, it means there is no evidence of active cancer at the moment.

A cure, on the other hand, is defined as cancer never coming back again. That is a pretty lofty statement, since there is always a chance of relapse. Once diagnosed with cancer, being “cured” can really only be used if the person reaches their death without ever experiencing the cancer again. Therefore, “cure” is just too big a word for most of us to feel comfortable with.

As a patient who has been told there is no cure for her disease, the word remission feels like the heavens opened up and the angels sang; it really doesn’t get much better. Cure, however, feels like a pipe dream, out of reach and inconceivable. Regardless of how long a person has been in remission, we still hold our breath during checkups and hear the whisper in our head: “Is it back?”

Before becoming fluent in the language of cancer, I thought cure and remission were interchangeable. Now I realize that remission is the only dream we have and cure lives somewhere in fantasy land.

Many patients will go in and out of remission, some more than once during their journey, and each time they have to deal with the, “But weren’t you cured?” question from family and friends. Perhaps some of this responsibility for confusion lies with the patient, and we should use language that is less confusing and more accurate, such as No Evidence of Disease (NED); No Evidence of Active Disease (NEAD); and “dormant.” A non-patient cannot be expected to understand what a sting the word “cure” can have.

Amazon Buy Links

Ebook | Hard Copy | Audible

Author Bio and Links

Lynda was born and raised in a tiny farming community of 400 in northern Idaho. She worked on the family farm, with her first job being picking rocks out of the fields and ultimately graduating up the ladder to driving a grain truck and combine during harvest. Following high school, Lynda continued her education in Las Vegas before she moved back home to Idaho to raise her three sons.

Lynda still resides in Idaho with her husband and their peekapoo, Max.

Lynda has worked in the legal field for 30+ years and enjoys ballroom and swing dancing, horseback riding, kayaking, and river rafting. She has a heart for people and enjoys regularly volunteering. She spends the bulk of her spare time reading and writing.

Lynda was diagnosed with terminal stage 4 Mantle Cell Lymphoma (MCL) in August 2016. She touts herself as being a thriving warrior of the disease.

Lynda has completed two books of nonfiction: Voices of Cancer, released in October 2019, and Voices of LGBTQ+, released in August 2020.

The Placeholder, Lynda’s debut novel, was released in November 2022.

Lynda has published the following articles: Navigating the Workplace with Chemo Brain, February 23, 2020, Elephants and Tea. and When Masks Weren’t Popular, March 24, 2020, Patient Power. She has spoken on several podcasts, been a guest on a local talk show regarding Voices of Cancer, and given interviews for other outlets and print.

Jane Brody wrote up Voices of Cancer in the New York Times, her article entitled What to Say to Someone with Cancer, on January 13, 2020, with a follow-up on January 20, 2020, entitled, When Life Throws You a Curveball, Embrace the New Normal.

The Chinese translation rights of Voices of Cancer have been purchased by a grant to offer the book to medical students in Tawain.

Lynda donates Voices of Cancer books and a portion of its proceeds to Epic Experience, a nonprofit camp for adult survivors and thrivers of cancer located in Colorado.

Website | Facebook | Facebook Page | Instagram | Twitter

Giveaway

Lynda Wolters will be awarding a $25 Amazon/Barnes & Noble gift card to a randomly drawn winner via Rafflecopter during the tour. Find out more here.

Follow Lynda on the rest of her Goddess Fish tour here.

Lynda Wolters has crafted an emotional and powerful memoir filled with advice and anecdotes based on her cancer journey and conversations with dozens of patients. Having experienced my own bout with cancer, I found myself nodding, sighing, and sometimes tearing up as I turned the pages. I would love to have read this book while waiting for biopsy results, dealing with the side effects of chemo and radiation, and struggling to adapt to life after cancer. This memoir is an excellent companion for anyone diagnosed with cancer and an essential resource for caregivers, families, and friends.

What resonated…

“Cancer can change your body, and it can surely take your body away, but it can’t have your spirit.”

“Faith is in your control and fate is a matter of circumstance.”

“When you stop trying to get past your current state and accept where you are now, there is a sense of contentment, of understanding.”

“I have had to learn that I must stop gauging my abilities by the standards of previous (pre-cancer) me and must instead embrace the present me and my current capacity.”

“We choose our role models, but really we had to be our own best role model.”

Available for Pre-Order: 40 Life Changing Events

My essay, “Honoring My Inner Sloth,” appears in this anthology.

Blurb

In our constantly evolving world…

…where the unforeseen lies in wait.

Surprises abound.

In this latest anthology, 25 writers share events that have changed their lives. Some stories are tragic, others full of joy, but they all encapsulate the tenacity, resilience, and self-belief of the human spirit.

During these challenging times, with the world in turmoil, it is stimulating to learn from other people’s experiences.

What will you take away from these exceptional recollections that span the generations?

This fascinating compilation will encourage you to pause and reflect, with tales that offer much needed motivation and inspiration.

Get it now.

Excerpt (Honoring My Inner Sloth)

For too many years, I subscribed to the busy bee myth: Complete all given tasks and start on tomorrow’s To-Do List. That was my modus operandi for the first fifty years of my life. Or, more precisely, the first forty-nine years, seven months, and seven days.

All that changed with a diagnosis that came out of nowhere: Inflammatory Breast Cancer, Stage IIIB. To be truthful, my body had tried to communicate with me many years before the diagnosis. Persistent colds and bouts of bronchitis. Slow-healing bruises. Bone-crushing fatigue. Determined to soldier on without taking advantage of sick days or lazy weekends, I chose to ignore those whispers. But I knew all about them from the Oprah shows.

To this day, I get goosebumps when I recall those words of wisdom from television’s favorite teacher: “If you don’t pay attention to the whispers, it gets louder and louder. It’s like getting thumped inside the head like my grandmother used to do…You don’t pay attention to that, it’s like getting a brick upside your head. You don’t pay attention to that; the whole brick wall falls down.”

While I was in the thick of it with family and workplace stress, I didn’t realize—or chose not to realize—that those whispers were about to break a sound barrier.

Buy Links (ebook and paperback)

Amazon (CA) | Amazon (UK) | Amazon (US) | Amazon (AU)

Release Date: Sunday, December 12, 2021

Honoring My Inner Sloth

For too many years, I subscribed to the busy bee myth: Complete all given tasks and start on tomorrow’s To-Do List. That was my modus operandi for the first fifty years of my life. Or, more precisely, the first forty-nine years, seven months, and seven days.

All that changed with a diagnosis that came out of nowhere: Inflammatory Breast Cancer, Stage IIIB. To be truthful, my body had tried to communicate with me many years before the diagnosis. Persistent colds and bouts of bronchitis. Slow-healing bruises. Bone-crushing fatigue. Determined to soldier on without taking advantage of sick days or lazy weekends, I chose to ignore those whispers. But I knew all about them from the Oprah shows.

Continue reading on the 2021 Authors Showcase here.

On Becoming a Warrior

When Lynda Carter assumed the role of Diana Prince/Wonder Woman in the 1970s television series, I made a point of watching each program. Eyes glued to the screen, I waited with anticipation for the inevitable displays of Amazonian power. I especially liked watching Diana fling the magic lasso and use her golden belt and bracelets to deflect bullets.

She was the ultimate warrior, one that I hoped someday to emulate.

Alas, I was the ultimate non-athlete who shied away from athletic challenges and activities. In my workplace and interpersonal relationships, I preferred to adopt a non-confrontational stance that served me well (or appeared to serve me well) for almost five decades.

Continue reading on Brenda Whiteside’s blog.


Life is Good

On Wednesdays, I share posts, fables, songs, poems, quotations, TEDx Talks, cartoons, and books that have inspired and motivated me on my writing journey. I hope these posts will give writers, artists, and other creatives a mid-week boost.

During my cancer journey, I noticed one of the patients at the Juravinski Cancer Centre wearing a T-shirt with a grinning stick figure and the message: Life is Good. I asked about the T-shirt and learned that it was part of an apparel line launched by two enterprising young men in Massachusetts. Many cancer warriors throughout Canada and the United States wear these T-shirts during their treatments.

Here’s the inspiring story of Life is Good…

The story of Life is Good begins not with the company’s founding but in the childhood of Bert and John Jacobs. The youngest of six children, the two brothers grew up in Needham, Massachusetts, a suburb of Boston. Life in the Jacobs household was, by many people’s standards, hard. The second floor of their small home had no heat. Their dad had a temper. And they couldn’t always afford basic necessities. Their mom, Joan, joked that she bought them food they didn’t like so that it would last longer.

Despite all of this, Joan was a resilient and cheerful woman who focused on the positive. Every night at the dinner table, she asked all six children to share one good thing that happened to them that day. As the kids talked about finding a Rolling Stones CD at the dump, hearing a funny joke, or learning something cool in school, the energy of the room transformed. Everyone started laughing and smiling. Joan’s optimism lifted them up. “I like running out of money,” she would tell them, “because then I don’t have to worry about what I need to buy.” From her, the boys learned that joy comes form our mindset, not just your circumstances.

In 1989, when they were in their twenties, Bert and John started a business designing printed T-shirts, which they sold on the streets of Boston. They also traveled up and down the East Coast, selling the shirts door-to-door on college campuses, each time making barely enough money to fund the next road trip. They slept in their van, ate peanut butter and jelly sandwiches, and showered when they could.

On the road, they spent a lot of time talking. During one trip, they discussed the way the media inundates the culture with stories of murder, rape, war, and suffering day after day. Though bad things happen and it’s important to know about them, they agreed, the world is also full of good news. They thought of Joan and her ability to turn a light on in a dark room. They decided they wanted to promote her values in their work, to create a symbol that would serve as an antidote to the cynicism they saw in the culture–a superhero whose power was optimism.

John sketched a grinning stick figure on a T-shirt. He called the character Jake. When they got back to Boston, they threw a party and pinned the new T-shirt on a wall. Their friends loved it. One of them wrote on the wall next to the T-shirt, “This guy’s got life figured out,” with an arrow pointing to Jake.

Original Drawing of “Jake” from April 1994

The brothers distilled that phrase to three words: “Life is good.” Then, they printed the image of Jake and the phrase on forty-eight T-shirts. When they set up their stand on a sidewalk in Cambridge, they sold all of the shirts in less than an hour–a first for them. That was in 1994. At the time, they had $78 to their name. Today, they run a $100 million lifestyle brand.

As their business grew, they started receiving letters and emails from people who had faced and were facing difficult life circumstances, including cancer, the loss of a loved one, homelessness, and natural disasters. These people wrote about how moved they were by the Life is Good message, and how they had emerged from their adversity with a deeper appreciation of and gratitude for life.

In 2010, the company launched a non-profit arm called Life is Good Kids Foundation, devoted to children who are living with illnesses, violence, abuse, poverty, and other adversities.The primary program of the foundation is called Playmakers, an initiative that offers training and enrichment workshops to childcare providers like teacher, social workers, and hospital workers. Since its founding, the foundation has trained over 6,000 Playmakers who are working to improve the lives of over 120,000 kids each day. Each year, Life is Good donates 10 percent of its net profits to help kids in need.

Life is Good Website

Source: The Power of Meaning by Emily Esfahani Smith


Adding a Touch of Gold to Celery Soup

During chemotherapy, I found myself unable to tolerate a host of foods, among them coffee, meat, fish, cheese, tomatoes, onions, garlic, salad dressings, citrus fruits, and all cooked vegetables.

So, what could I eat?

Plain Eggo waffles without syrup, roasted chicken, white bread, some luncheon meats, white rice, apples, pears, carrots, and celery.

I was especially fond of celery, a preference that has remained in life abc (after breast cancer). I love munching on the stalks and tossing them into casseroles, stuffings, and soups. Almost every soup I make has at least one celery rib.

Last week, I decided to make celery the primary vegetable. While researching celery soups, I discovered that most of them included potatoes or cauliflower. The final results appeared a bit too pale and unappetizing for my taste. I experimented and came up with this golden alternative.

Ingredients

1 tablespoon of olive oil
1 medium onion, chopped
2 cloves of garlic, peeled and crushed
4 cups of fresh celery, chopped
2 cups of chicken or vegetable stock
1 cup of baby carrots, chopped
Handful of fresh parsley, roughly chopped (include stems)
1 cup water
1 tablespoon of lemon juice.
Salt and pepper (to taste)
Hemp hearts (optional)

Directions

1. In a large soup pot, heat the oil over medium heat. Add the onion and cook until soft.

2. Add garlic cloves and cook for a minute before adding celery, stock, carrots, water, and parsley. Increase the heat to medium-high and bring to a boil.

3. Lower the heat and simmer for about 30 minutes or until the celery and carrots are soft enough to be puréed.

4. Purée the soup in the pot using an immersion blender. Or remove the soup from the pot and purée in a blender.

5. Add lemon juice and salt and pepper (to taste).

6. Sprinkle hemp hearts into each individual bowl.

Makes 4 servings, about one cup each.

Buon appetito!

An Inspiring Passage for Cancer Warriors

On Wednesdays, I share posts, fables, songs, poems, quotations, TEDx Talks, cartoons, and books that have inspired and motivated me on my writing journey. I hope these posts will give writers, artists, and other creatives a mid-week boost.

Almost fifteen years have passed, but I can still recall feeling goosebumps as I read the following passage. It helped me survive and thrive during the most challenging season of my life.



Spotlight on Trixie Stilletto

I’m happy to welcome journalist and author Trixie Stilletto. Today, Trixie shares her inspiring journey and new release, Do Grave Harm.

Here’s Trixie!

I grew up in eastern Tennessee where storytelling is a huge part of everyday life. My dear departed husband used to say we were all experts at telling whoppers. And in a sense, he was right. Sunday afternoon was for family. The first question? What’s new?

If you stuck to the truth, it’d be a mighty boring story. So my family expounded more than a little. We didn’t consider it “lying” just making the story more entertaining. I never considered writing those stories down until I took a high school creative writing class. Though I excelled and my teacher urged me to continue, it wasn’t a “job.”

Fast-forward to college. I was on track to become a lawyer. Mostly for the money. While yawning through pre-law classes, I thought about where I’d be going drinking that night. A classmate suggested I take a journalism course.

I went to the “Intro to Newspapers” class the next day and I was hooked. (My mother lamented that day until she died.) My path was set. I spent the next twenty years working for different newspapers all over the eastern United States, meeting my husband, another journalist, along the way.

In my free time, I read. Voraciously. Yes, newspapers but also romance, mysteries, science fiction, anything. In 1988, I wrote my first romance novel. It was terrible. Life intervened. I was still working as a full-time journalist and on my books when I got my first publishing contract in 2001. I thought my life was set.

As often happens when we’re on one path, it veers away from where we think it should go. A series of deaths (both my parents and my husband), two moves, and finally a diagnosis changed me forever.

In 2014, my doctors discovered a small lump in my left breast. It was a particularly aggressive type of cancer called Her2+. Surgery, chemotherapy and radiation followed. I may never be completely free of this disease.

While undergoing my first treatment, I came up with the idea for my newest release, Do Grave Harm, and Jennifer Atkinson. Like me, she’s a cancer survivor. Unlike me, she’s plucky, determined and dedicated. I hope you’ll visit my website to learn more. There are links listed with this post to online retailers where it is on sale.

A percentage of all proceeds will be donated to metastatic breast cancer research. Each October, Breast Cancer Awareness month, 100% of the proceeds will be donated to these charities.

Blurb

“Helpless” and “vulnerable” aren’t normally part of freelance writer Jennifer Atkinson’s vocabulary. But there’s nothing normal about her regularly scheduled radiation treatment, especially when she discovers that while she was fighting claustrophobia inside the massive machine aimed at her breast, someone was murdering the technician at the controls.

As the gruesome scene plays over and over in her mind, small details that didn’t seem significant at the time start the wheels turning. Soon she’s asking more questions than she’s answering for the seriously attractive investigating officer, Blue Bald Falls Detective Ben Manteo.

Despite Ben’s warning she should keep her nose out of it, Jennifer can’t resist using her limited energy to pick up seemingly unrelated threads that, inevitably, begin to weave themselves into a narrative. A story of lies, deceit, and betrayal that someone will go to any length to make sure never gets told…

Excerpt

Something wasn’t right. I didn’t want to panic, but I was starting to feel claustrophobic. Having a two-ton radiation machine sitting only inches from your chest will do that to you, especially when it seems you’ve been forgotten.

You’re not truly alone, Jennifer, I reminded myself. There were dozens of people down the hall in the waiting room. And this was a hospital. People were constantly moving around, even though they kept the radiation section closed off.

Repeating these things and more didn’t help. At that moment, I felt abandoned, as if no one knew where I was.

“Excuse me,” I finally called, hoping the radiation technician who’d brought me in here would answer, reassuring me.

Robert. I picture his name tag in my mind. Raising my voice, I called again, “Robert?” Nada. The room was probably soundproof with the door shut.

Panic sped up my breathing as I stared at the machine. It hadn’t moved after my radiation treatment had ended. That was the problem.

In my mind, the six inches between me and it had shrunk to three. My arms were starting to go numb, as well as my feet and legs. No one was coming to help me. I had to do something. Now.

Moving while under the machine was kind of tricky. I was a large woman, and I’d never been dexterous on my back, much to my rat ex- husband’s lament, I guess.

I kicked my legs out of their rubber support and, after several tries, scooted my butt down the metal table. Then I did an ungainly slide, like I was slipping under a barbed-wire fence. Except this particular fence was the size of a VW Beetle, and it seemed to be inching closer to me with each passing second.

When I moved enough that my head and neck were no longer in the plastic mold that kept me still during treatment, I banged the back of my skull against the table. “Ow, ow, ow,” I muttered, inching my way farther down it until I cleared the machine.

Finally, my legs dangled off the end. I sat up, took my first relieved breath in eons, and waited for my head to stop spinning. Freedom! I looked around the room, and everything seemed normal. Walking over to the plastic chair to my left, I picked up my long-sleeved cotton jersey and put it on. Since I got topless for my treatment, most of the time I didn’t bother wearing a bra when I came here. It would be one more thing to take off.

I moved to the doors. They’re made of thick steel and tightly sealed. No wonder no one answered me. They wouldn’t have heard me even if I’d shouted. I pushed on one a bit, staggering under the unexpected weight. When it opened a scant few inches, I peered around the edge. I don’t know why I was acting like a guilty person, doing something or going somewhere I wasn’t supposed to.

I hid a giggle behind a cough. Jeez, Jennifer, get a grip. Something still wasn’t right. In fact, I felt an overwhelming sense that things were horribly wrong.

“Robert?” Still no answer, so I pushed the door open a little wider. Now I could see the second lab and computer station. It was as dark as it had been when I came into the radiation lab at the Blue Bald Falls Cancer Center no more than ten minutes ago. I opened the door wide enough and stepped into the bright lights of the hall.

Robert had his head down on the computer keyboard like he was napping. The scalpel sticking straight out from the side of his neck and the blood pooling on the table down to the floor told me sleep had nothing to do with it.

Buy Links

Amazon | Barnes & Noble | iBooks | KOBO

Bio

A southern girl, Trixie traveled north when she found the love of her life. Together, they enjoyed more than 20 years working as journalists. Now back home in Tennessee she’s writing stories that range from short hot romances with a kiss of humor to southern-flavored mysteries. She lives seven miles from the neighborhood where she grew up with two cats, an aging beagle and a host of characters waiting for her to tell their stories.

Get updates and win prizes by signing up for Trixie’s newsletter here.

Where to find Trixie…

Website | Facebook | Twitter

Find more information on Metastatic Breast Cancer Research here.


Living Vicariously Through My Protagonist

In the spring of 2001, I enrolled in the Career Development Practitioner Program at Conestoga College in nearby Kitchener, Ontario. After meeting with the course director, I sat down and meticulously planned the next seven years of my life.

I would continue teaching full-time during the day and take one online course each trimester. I even selected the order so that the more demanding courses would be taken during the summer months. Upon completion of the program, I would spend two summers interning in preparation for retirement and the launch of ReCareering, a counseling practice that would cater to boomers.

That was the fantasy.

The reality was very different.

Continue reading on Maggie King’s blog.