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Cowboy & Wills: A Love Story by Monica Holloway

Book Review by Zinta Aistars

 

·         Hardcover: 288 pages

·         Publisher: Simon Spotlight Entertainment (October 6, 2009)

·         Price: $24.00

·         ISBN-10: 1416595031

·         ISBN-13: 978-1416595038

 

To set the parameters of my review: I know next to nothing about autism. My knowledge of this disorder is limited to the anecdotal, the various news items and studies that pass across our daily consciousness, this and that about autism being over diagnosed, that it may be caused by something in our food, or by various childhood vaccinations, and other such. I won’t claim to hold strong opinions on any of this, as it has not been an area of research or particular interest to me. I have a couple of casual acquaintances with autistic children, both highly functional, and that’s it—that’s all I’ve got.

For this very reason—because I know so little about this diagnosis which children today alarmingly often seem to have attached to them—I took on reading Monica Holloway’s Cowboy & Wills: A Love Story with particular interest. I wondered if autism might be something like ADHD, another diagnosis that seems difficult to make. Indeed, my own son was diagnosed with it at one point in his childhood and early teen years, only to have the next doctor cry “balderdash!” and the next one reverse that and the next one reverse that again. I eventually agreed with the balderdash opinion. He does not, never did, have ADHD. Nor did he have any other number of diagnoses that various doctors with an alphabet soup of credentials behind their names make. He was a teenager growing up without a father in a single-parent home, and so he acted out his anger and confusion and fear of abandonment. He grew up, gained maturity and understanding, and stopped acting out. End of story. So is this epidemic of autism anything like that? I don’t know, don’t claim to know, but my curiosity was piqued.

I was quickly drawn into Monica’s story about her young son, Wills.

“Wills Price is exceptional.

“If you happen to meet him walking down our street, you’d see a lanky boy in red baggy sweatpants. His thick black eyelashes frame enormous, cornflower blue eyes and he has freckles that march across the top of his tiny turned-up nose. When he lets loose with a belly laugh, his dimples deepen and he throws his head back while twisting the front of his shirt. He prefers wearing stripes—T-shirts, and turtlenecks mostly. He’s very particular about this. There have to be stripes.”

As a mother, I was already smiling. My son is a big man now, with great heart and great shoulders, carrying his own world upon them, but how well I remember that sweet little face then, those moments of shining brightness, the up-turned nose and freckles, the childish chortle that would remind me, in my adult world, how to laugh.

So Monica Holloway quickly became my friend. My distant alter ego, struggling with parenting and its myriad challenges. The particulars didn’t matter. What mattered to me as a reader was that I recognized a mother who loves her child with every fiber of her being, and would do anything but anything for him, even the toughest task of all—step back and let him occasionally take a fall on his own. I won’t say that all her parenting skills were perfect. Who am I to know? There is no manual, only heart required, lots of it and always open. Holloway has that. And in her self-effacing style of telling the story of Wills and his golden retriever pup, Cowboy, she was touchingly willing to put her own shortcomings out there for public scrutiny. Her writing style reminded me a little of the popular author Elizabeth Gilbert (Eat, Pray, Love and Committed), juxtaposing serious medical concerns (in Gilbert’s case, the seriousness of the pain of a marital breakup) with delicious moments of humor. After all, sometimes life hurts so much all you can do is laugh and get on with it.

Using animals as therapy may not have initially been Holloway’s intent, but as most mothers do, she operates by instinct. When Wills has a particularly bad day—sobbing when his classroom of peers are too loud, too fast, too bustling with a confusion of activity, for instance—Holloway makes a detour to the pet store. She brings home guinea pigs, hamsters, fish, rabbits, hermit crabs, turtles, in short, a menagerie of critters to soothe and amuse her son. And it works. Any pet owner will tell you, and the medical profession, too, that our pets can relax rattled nerves, lower blood pressure, and alleviate a sense of isolation. It is not unusual to hear about animals opening up humans to functionality when other humans fail to do so. Buying the boy a puppy seems a natural progression on the animal chain of pets.

While I may question Holloway’s decision to be very close-mouthed with others about her son’s autistic spectrum disorder, and by doing so isolating herself and her family from social support and no doubt other avenues of help and advice, I will not judge her for it. I have not raised her son; she has not raised mine. Every individual is different, and if I have learned to trust anything, it is a mother’s loving instinct on raising her child. I trust that instinct even over medical professionals. I have had reason to do so. Perhaps she does, too. Wills, after all, is highly functioning, and really quite bright. The words that come out of this babe’s mouth gave me quite a few occasions for my own belly laugh in reading about his young life. There is no quibble with the boy’s high level of intelligence and wit!

So there is Cowboy, the other great personality in this story, the furry charmer. Cowboy is actually a girl dog, and she arrives with a medical issue of her own—canine lupus. Another thing I did not know: dogs, too, can get lupus. When Holloway first brought the puppy home from a pet store, even as she knew that buying dogs from pet stores isn’t always a good idea (puppy mill sources), she did not know about the lupus, only that the pup seemed infected with something. Cowboy did live about two and a half years, and charmed years they were. The Holloway family falls in love with her and she with them, but no one more so than Wills. The photographs alone in the book are enough to make one’s heart toasty warm: the boy and the dog curled up together in deep sleep, romping in play, snuggling. Where humans have fallen short in easing the boy’s discomfort in adjusting to the world around him, the dog nudges him beyond his comfort zone and inspires him to go beyond his earlier limits.

The Holloways spend a great deal of time and money on their son, and it is a blessing that they apparently are able to do so—maxing out credit cards, dipping into and emptying accounts, while taking Wills to a laundry list of specialists and therapists, even hiring someone to “shadow” him in school while he adjusts, a school they actually hired a headhunter to locate after Wills was rejected at a dozen others because of his disability. Not all parents have such means, but lucky are those who have them to use. We all do whatever we can for our children, and then some. Nothing can carry us through like the unconditional love of a good mother.

Love carries us through even when we have to deal with a very painful loss: Cowboy eventually succumbs to his lupus. Still a young dog, she dies, and having gone through that, too—the loss of a much loved pet that stayed true when not all humans would or do—I understand the grief the entire Holloway family feels. Yet the wonders Cowboy was able to accomplish for Wills live on. He is much more social, much more comfortable in his daily routine, because of those two plus years with Cowboy as constant companion.

This is a tender love story—between mother and son, between boy and dog. It tugs at the heart in all the right ways and by all the right strings, with laughter and tears, surprise and delight, frustration and grief. Whatever the particulars of how any one family chooses to deal with their problems, one thing rings true. Everyone needs a safe place in life in order to thrive. A place where we know ourselves loved for who we are, and are always encouraged to be more.

 

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Sleeping with Cats: A Memoir by Marge Piercy

Book Review by Zinta Aistars

 

·         Paperback: 368 pages

·         Publisher: Harper Perennial, 2002

·         Price: $14.95

·         ISBN-10: 0060936045

·         ISBN-13: 978-0060936044

 

An honest writer will admit that everything that he or she writes, down to a grocery list, is in some form autobiography, revealing the author's sense of life, core values, interests. The art of literary expression, like any art, is a self-portrait, and the higher the level of quality, the truer we have been to ourselves. When a book reads flat or false, suspect a lie.

When Marge Piercy writes—and she writes like nobody’s business, having to date published 17 novels and 17 collections of poetry—she comes to life on the page. Piercy is the perfect illustration of a writer’s words shaping the self-portrait, because it makes no difference what genre or style she chooses, she rings true. Poetry or prose, fiction, nonfiction, science fiction, no doubt even that grocery list, show facets of the author. Reading this memoir, Sleeping with Cats, confirms that accuracy, adding layers of understanding to her creative work, for here we see her characters at their birthing place, in the lifelines of Piercy herself.

Piercy was born in the mid 1930s in Detroit, Michigan. Her ethnic background is Jewish and Lithuanian, but it is the former that roots most deeply in her. Her father was a hard-hearted man, an often abusive husband and father, never letting her forget he would have much preferred a son. Their relationship moved between cool and cold, their most successful conversations “about the Tigers and the weather.” In his entire lifetime, Piercy's father never read any of his daughter's books.

Her mother was a submissive woman who made a career of repressing dreams while trying, as emotionally battered women do, to please the husband that would not be pleased. Yet she knew her feminine powers and used them like weapons or tools of survival, while they were not enough to save her own dwindling spirit (and perhaps contributed to its brokenness). She seemed to resent the unbreakable spirit in her daughter, who observed as a girl her mother around other men:

“Half the men we dealt with were convinced she was crazy about them, but she mostly felt contempt. They were marks. She had a job to do and she did it. She was obsessed with my father, not with any of these men about whom she had a rich vocabulary of Yiddish insults which she muttered to me after each encounter.”

It was a tough childhood of gangs and early sex, with boys as well as other girls, of a pregnancy at age 17 that Piercy had to abort herself, nearly bleeding to death in the process. She never would have children, never wanted them. She learned about life through the hardest knocks, losing a young girlfriend turned prostitute to a heroin overdose (“I understood why she had let her pimp get her hooked: it numbed her.”), and having her fingers broken by her angry father, and always knowing herself different, an outsider—yet somehow never really doubting her own worth. She made being different work for her. These were the makings of a young woman who would become one of America’s strongest feminist voices.

Piercy is educated at University of Michigan in Ann Arbor, Michigan. She wins scholarships. She earns top grades. She is self-sufficient in all things. Piercy is smart and she knows it, and she uses her mind with equal prowess to using her sexuality, enjoying both, lavishing easily in the pleasures each provide. Swearing to never marry (“Marriage… seemed to me a kind of death for a woman, in which she lost not only her will and her power but even her name. I was determined never to marry…”), she marries early, and marries three times. Piercy makes no saint of herself here, nor does she demonize her husbands or lovers. They come to one another with faults, give love best they know how, leave with a few scars left behind but also gifts and valuable lessons.

Piercy’s second marriage is open, like it or not, at her husband’s insistence. She comes to accept her husband’s affairs, focusing on her own interests and literary pursuits. Eventually, she takes a lover of her own. It is the 60s, a time of hippies and communal living and making love not war, and Piercy embraces this period of exploration. It works for her. Never becoming a mother, she becomes instead something of a communal mother, the woman at the center of the group, cooking and caring and cleaning for all, maintaining a kind of sanity and order to things. There is something about Piercy that is both rule breaker and order maker, the center of the storm and the anchor in chaos. Her husband’s affairs work only when the other women show her due respect and, preferably, friendship—often a closer one with Piercy than with her husband, the shared lover.

Writing and cats are the thread that binds a life that moves from Detroit to Chicago to New York to San Francisco to Paris to Cape Cod, with a few detours between. Piercy is determined to succeed at her art, and she maintains a disciplined pace at creating novels and other works even when nothing sells, or when it does and gets no notice. Piercy has a steely will and the persistence to carry it through. Her marriages succeed, it seems, when they give her the solid ground on which to set up her writing desk. Her second husband gives her five years to succeed, and she sets to work with determination. If it takes her longer than that, no matter, she shrugs off rejection and keeps writing.

Piercy meets her third husband while married to her second, and while one relationship unravels, the third takes on strength. Ira Wood is also a writer, and the two in some ways seem very different, including their 14 year difference (he is the younger), but are soul mates in the ways that matter. Of her relationship choices, Piercy writes: “I do not love primarily with my eyes. I have had lovers who were gorgeous and lovers who were plain, who were skinny and neurasthenic, who were bulky and overweight. I have cared far more for how each of them treated me than for my eyes’ pleasure.” Piercy speaks for most women in this, with women choosing partners who bring substance to a relationship as of primary importance, and she finds this in her third marriage, a partner with whom she can talk and talk and talk endlessly, argue and debate and discuss, and enjoy a companionship rich in all aspects of intimacy.

Memory is faulty and relative, Piercy writes in her memoir, but hers always rings sound with a story that does not show its heroine in always the kindest light. What gives her voice such strength, after all, is that she is honest in her portrayal of self, and so, of all her characters, admitting to faults and mistakes, not shying away from moments of truth. We see the outsider, we see the survivor, we see the woman who will never be ashamed or apologetic of her appetite for life.

At the conclusion of each chapter is one of Piercy’s poems, adding another layer of insight to her experience. Many times, these poetic interludes are our chance to look the deepest into Piercy’s psyche and heart. And if we ever doubt that this woman of determination and smarts and steely survival skills lacks a more conventional feminine softness, we can be assured it is there. We see it for those allowed into her closest circle—her cats. She loves fully her felines, her heart breaks at their loss, and she nurtures and nourishes and pampers like a true earth mother. Her observations of their personality quirks and antics and changing moods are often the most delightful sections of her writing. She loves and is loved unconditionally by her cats, and as living things do, here is where she comes most alive.

Concluding her memoir, for those who have already read some of Piercy’s works, and understanding her background gives a reader much greater understanding of the characters in her many, many books. We see the faces of Piercy, of her husbands and lovers, her parents, her friends, and yes, her cats. They appear in all her books, and so we see, this memoir is only one of her many memoirs, each one a stunningly honest and open look at what makes a woman a woman, how she expresses herself in freedom, how she loves and lets go and lives to love again—her men, her cats, her work, her homes, her world.

 

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Who Says I Can’t: A Two-Time Cancer-Surviving Amputee and Entrepreneur Who Fought Back, Survived and Thrived by Jothy Rosenberg

Book Review by Zinta Aistars

 

Paperback: 239 pages

Publisher: Bascom Hill Books (February 1, 2010)

Price: $14.95

ISBN-10: 193545613X

ISBN-13: 978-1935456131

If you tell Jothy Rosenberg there is something you think he can’t do, chances are better than good that is just the thing he will do.  Chances are even greater he will leave you in the dust while doing it, too.  He’s like that. He’s probably always been like that, but what has really strengthened Jothy’s perseverance to take on life at full throttle, meet and beat every challenge he encounters, has been his experience of being a two-time cancer survivor.

Who Says I Can’t is Jothy’s memoir, published in 2010 by Bascom Hill Books. It is the story of “a two-time cancer surviving amputee and entrepreneur who fought back, survived and thrived.” Jothy is an above-the-knee amputee with two-fifths of his lung removed, both due to cancer while still in his teens. He considers “considering” a dirty word (as in, “You’re good, considering you are missing a leg!”). Jothy does what he does perhaps in some aspects because of his physical challenges, but he achieves excellence that can be measured against any able-bodied person. A math major at Kalamazoo College, he went on to earn a PhD in computer science at Duke University, authored two technical books, founded six high tech companies. He has also participated in the Pan-Massachusetts Challenge bike-a-thon (supporting Dana-Farber Cancer Institute) seven times; has completed the swim from Alcatraz to San Francisco as part of a fundraiser to support Boston Healthcare for the Homeless 16 times; and has participated in countless other fundraising sports activities. He now lives in Newton, Massachusetts, with his wife Carole, and is the father of three children, grandfather of one. Writing a book to inspire others with his story is just one more item added to his long list of achievements.

“The book is about hearing the words, ‘You have zero chance of survival,’ at the age of 19,” Jothy says. “After already having lost one leg and one lung to cancer, as well as an extensive course of chemotherapy, it is about what all of that does to you. More importantly, the book is about how one goes about fighting back, recovering and thriving in the face of all that adversity.”

Jothy lost his right leg to osteogenic sarcoma at age 16; his cancerous left lung was removed while he was a student at Kalamazoo College. Born in California, Jothy grew up in the Detroit area, the son of two physicians. His brother, Michael, was a Kalamazoo College graduate (1975), so he knew the college well.

“I wanted a school that was smaller than my high school and far enough away that I would not feel pressured to come home too often, yet I still wanted to be within a reasonable driving distance. I applied for early decision to Kalamazoo; I was not the slightest bit interested in any other school.” (Page 39, Who Says I Can’t.)

At the time of Jothy’s dark diagnosis, chemotherapy was a new and experimental treatment. For the 10 months that Jothy underwent the tortuous process of chemotherapy ( he still feels nauseous when he remembers it), his professors at Kalamazoo College worked with him to keep him up to date with his college assignments. Professor Thomas Jefferson Smith was especially influential in young Jothy’s life, and after jumping from one major to another, he settled on math in great part due to Professor Smith’s caring attention.

“You have to keep in mind that this was before we had the convenience of computers and e-mail,” Jothy says. “My professors brought my course work to my hospital bedside, often written out by hand.”

Jothy writes about his years at Kalamazoo College in his memoir—and all that came after. He says he was inspired to do so, in fact, because of an earlier article that appeared in the Spring 2006 issue of LuxEsto. It got him thinking that he had a story to tell and that there might be others who might benefit from reading it.

“As a 16-year-old lying in a hospital bed with one leg gone, with a mind on fire with anguish about how I might live a normal life, and then as a 19-year-old with one lung trying to recover from chemotherapy and deal with a death sentence, I felt on my own. I was looking for inspiration, guidance, motivation—anything. I wrote this book because I want to help anyone facing a disability or serious life trauma deal with it better and faster than I did. Considering it took me 30 years to figure it out well enough to be able to write it down, I hope my experiences can shorten the learning curve for someone in a similar situation. “(Page 229)

Writing meant reliving. Jothy grasped how much it would have meant to him to hear the story of someone who had dealt with a similar blow and done well. A large part of what he had struggled with in those years, after all, was the feeling of being alone. Who to ask questions about learning to walk again? How to date when you might trip and fall on your face in front of a pretty girl? Without a role model or experienced advice, he did his best, and often, his best meant overachieving. If a two-legged person could do something, Jothy was going to outdo it. Even when it came to dating.

“I went on 40 dates in ten weeks when I was at Kalamazoo College,” he laughs. “Each one with a different girl.”

Not exactly the best way to develop a satisfying relationship. That’s the kind of advice Jothy could have used. Summing up his advice from the book, he says: “You are tougher and more resilient than you could ever have imagined. Fight back just one little victory after another. Set a modest goal for something you can do to regain your balance and sense of normalcy. Achieve that and set the next goal. Before you know it, you are strong and inspiring others.”

Jothy’s “small” victories outsize those that most of us will ever achieve. Completing the circle of receiving healing and now giving back to others, he regularly participates in AIDS fundraising bike rides from Boston to New York—a ride of a mere 375 miles. His bike is specially fitted to him, so that he can ride with one leg.  Jothy has become something of a celebrity participant, and his memoir recounts his grueling training, frustrations, and eventual victories.

“I have two main causes at this point,” he says. “I direct a lot of my fundraising efforts for Dana-Farber Cancer Institute in Boston. They were on the forefront of chemotherapy work in the mid-70s, and I am convinced it played a major role in my survival. I give them proceeds from the sale of this book and from the 192-mile Pan-Mass Challenge bike ride in which I participate every summer.”

Yet when Jothy is asked about his proudest achievement, it is not the physical challenges he has met, not the bike riding, long-distance swimming, or being an expert skier. It is not even the many business startups with which he has been involved over the years. “Without question, it is the fact that my kids like me and are proud of me. Like any father, I am insanely proud of them, too. We are truly good friends, and that is not something I take for granted.”

If the memoir is meant to give comfort and advice to those undergoing adversity or physical challenges, Jothy also hopes it gives those of us with limbs intact a better perspective on how to treat those who are different from ourselves. What he wants people to understand: “Don’t stare, and teach your kids not to stare,” he says. “But don’t ignore such people either. Feel free to ask a question. Just remember, we get lots of attention for being different, and that can be tiresome.“

Jothy wouldn’t call his early brush with death a blessing, challenging him to become a better man—although he believes it has in fact done that. “But I never sit around wishing it hadn’t happened. I can’t wish it away. It happened. So I make the very best of what I do have.”

“Everything becomes difficult with a bad leg. I can’t carry things. I can’t walk any distance for lunch with colleagues or to catch a cab. I walk very slowly and laboriously through airports. I worry about just walking down the hall to my boss’s office. It eats away at job effectiveness. It can affect how well I do my job, how likely a job promotion is, and therefore how much money I make. It affects my self-confidence in social relationships … Dealing with the superficiality of the disability is important for self-confidence. Dealing with the anatomic, physical, structural, mechanical aspects of the disability is just as important for success. With these daily challenges to self-confidence and self-esteem, the disabled person needs a constant outlet where they can excel, where they can overcompensate, where they can leave the temporarily able-bodied people in the dust.” (Page 228)

Along with insights into dealing with physical challenges, the book also provides an inside look at business startups. Jothy has been involved in starting, running or funding half a dozen startups. His memoir tells about the excitement of a new idea, the frustrations and danger zones of obtaining venture capital, the hard work of building a dream on a good idea, and then, at times, the heartbreak of having it swept out from under you.

Approaching his book promotion as he does everything else in life, Jothy is promoting it with everything in him. He has a Web site, whosaysicant.org, a fan page on the social networking site, Facebook, and he “tweets” regularly on Twitter as @jothmeister. He is currently on tour, giving talks and readings, signing books, and even trying to get a spot on Oprah’s talk show. Someone should tell him he can’t do it. And then stand back and watch what happens. 

 

 

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