Tag Archives: biography

A Migraine in the Light by Tony Peluso (Book Spotlight)

Tony Peluso began having migraines as a child but developed headaches every day in the year 2000, which have persisted to the present day. Living a life in and out of hospitals since he was a teenager. It is a life so surreal it is hard to imagine, and words are the only thing that can illuminate the invisible curse of chronic migraines, a disease for which the only diagnostic tool for any doctor will only ever be the patient’s voice. His disability covers the first quarter of the 21st century, and with it a unique Odyssey of failures, challenges, and changes in healthcare. It is a book that took him 14 years to write and is a path that has led him to a philosophy he calls The White Tower.

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Meet the Author

I’m 39 and I’ve been disabled with chronic migraines for 24 years. My disability started at 15 when the pain became daily. After a decade of daily headaches, I began writing and it took 14 years to finish. The disease is invisible and complex, and the only diagnostic tool is a patient’s voice.

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LIAM: The Boy Who Saw the World Upside Down by R. Janet Walraven (Book Review)

What does a teacher do with a teenage student who can’t seem to read, write, speak, or want to mix in with others? What does a parent do when their child is continually bullied throughout elementary school without teachers or administrators seeming to care? Where is a safe place for students with challenges that no one seems to understand?

This is a true story. When Liam came to my classroom, I knew something was off. What was I supposed to do with this student who was extremely withdrawn? I didn’t know, but I knew I had to find out ̶ a challenge that I could not ignore. This book isn’t only about bullying, though there was plenty of that. It’s about a boy who needed help to allow his potential to surface. If you are a teacher, a parent, or anyone who has witnessed, or have themselves experienced this, you need this book. LIAM will give you hope.

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I received a complimentary copy of this book from Reedsy Discovery. I voluntarily chose to read and post an honest review.

 

There was a time when anyone who didn’t catch on at the same pace as others were labeled “retarded.” R. Janet Walraven notes thanks to former President Obama passing Rosa’s Law, “mental retardation” and “mentally retarded” were replaced with “intellectual disability” and “individual with an intellectual disability.” Unfortunately, this change in federal law did not replace the use of these terms in state law. The author also states in chapter eight, “In 1975, President Gerald Ford signed a law guaranteeing that every child with a disability would get Free and Appropriate Public Education (FAPE). This is supposed to be included in the Individualized Education Programs, IEP’s, that special education teachers write. From there, they have options of working with the child onsite, sending them away for therapy, …or waiting for litigation.” R. Janet Walraven states that many teachers look the other way at a child’s apparent struggles because they lack support in costs and help from the administration. LIAM: The Boy Who Saw the World Upside Down is a prime example of when the administrator fails a teacher, fails to support the students and makes doing a teacher’s job harder than necessary. 

Thirteen-year-old Liam has made a move from public to private school. His parents made a choice, not out of a need for better education. No, they are transferring him because they feel he’s unsafe in public school. Ms. J, the 8th-grade teacher at the private school, has a full class, but the principal, Mr. Chadwick, doesn’t care. That’s a recurring theme with him. He doesn’t care about the students’ safety, best interests, or helping the faculty. He abuses his power on several occasions. 

Ms. J. could’ve been like Liam’s other teachers and accepted Liam as “mentally retarded” and let him float by. Liam’s parents, even Liam, accepted the label. Since Ms. J didn’t have proper special education training, the parents and Liam wouldn’t have faulted her. However, Ms. J was different from the other teachers. She thought Liam was mislabeled. She saw his intelligence, his potential. Ms. J stood up to the principal. She put her foot down when the bullies chants shredded Liam’s confidence. She sought outside help for Liam and even drove him to his sessions at Hope Clinic. 

Hope Clinic properly diagnosed Liam, and he was not “retarded.” Liam has visual perception dysfunction. The book explains it in length, but (basically) Liam’s brain wasn’t computing what his eyes saw. He needed special glasses and exercises to retrain the brain. Thanks to Ms. J and her cousins, Liam never missed an appointment. Liam could afford specialized care thanks to his parents selling their home and moving into a trailer. I was angry to see the colossal sacrifice his parents had to make but also touched by their display of love. 

LIAM: The Boy Who Saw the World Upside Down was FULL of emotions. I wanted to cry when the boys tore him down with their chants. I wanted to cry again at his graduation. My heart nearly burst when Willow asked Liam to join her in Jump Rope for Heart and the school newspaper. I cheered Liam when he repeatedly showed the world they were wrong about him. 

I’ve worked in mainstream and special education classrooms. I’ve seen how people treat students that need extra help. Basically, I’ve run into my share of Mr. Chadwick’s. However, I also had the great pleasure of working with teachers who resemble Ms. J. They go the extra mile and then a thousand more. 

Ms. J didn’t know to teach Liam (at first), but she didn’t give up on him. Students like Liam are highly intelligent. They only need to discover a way to show it. It could be reading glasses. It could be having questions read to them. I know teachers are overwhelmed, overworked, and underpaid, but this story is a prime example of what can happen when teachers, administrators, and parents work together. 

I encourage educators and parents of children with intellectual disabilities to read this book. It’s inspirational. It’s heart-warming. It’s worthy of five stars! 

Be sure and look at the bonus material at the back of the book. Meet “Liam” and his best friend “Willow.” See where they are now. View writing samples from Liam. Also, check out appendix C: Characteristics of Dyslexia.

 

Heart Rating System:
1 (lowest) and 5 (highest) 
Score: ❤❤❤

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Meet the Author

 

R. Janet Walraven, Silver Award Winner (Readers’ Favorite International Book Awards) has written historical romance, a teacher-mentor book, children’s book, & historical fiction. She lives in New Mexico with her companion, Mal, her best critic & support. She loves to read, write, garden and travel.

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Unseen Arms: A Story about Cancer, Crisis, and Being Carried by Faith by Evelyn & Wayne Hausknecht (Book Spotlight)

 
Patient and Caregiver: the main characters in a drama that started in 2007 and is still unfolding for Evelyn and Wayne Hausknecht. In 2007, Evelyn was diagnosed with an aggressive, recurrent type of non-Hodgkin’s T-cell lymphoma. Although in Unseen Arms Evelyn and Wayne are as medically accurate as their memories and blog allow, the greatest purpose here is to tell the story from a patient’s and caregiver’s perspectives.

Recently, while having an in-depth conversation with a lung doctor when Evelyn was in the hospital with pneumonia, Evelyn was thanked by the doctor for what she and Wayne were doing. She was in awe of his excitement for the book. The doctor saw the need for future patients to learn from experienced patients. Evelyn and Wayne were peer volunteers for the Leukemia & Lymphoma Society for years. The goal of that program was the same: an experienced caregiver and patient walk beside a person entering the transplant program to make their path smoother. Even though each diagnosis and circumstance is different, every patient has the same questions, fears, and needs. The greatest need is for someone understanding to talk to. When Evelyn was diagnosed, it was easy to find medical information, but caregiver and patient perspectives were limited.

​Evelyn and Wayne had three purposes for writing this book. One was to give God the Glory for His faithfulness during this process. The second was to give hope to the patients and caregivers of today and the future. The third was to give some limited insights into the stem cell transplant process. The medical part of this process is rapidly changing, but the patients and caregivers still have the same needs.

 
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Meet the Author: 
Evelyn and Wayne Hausknecht

 
Evelyn and Wayne Hausknecht have spent most of their careers in education. Evelyn has taught different subjects and ages in public and Christian schools. Wayne, a wood engineer, helped build the largest sawmill in Brazil and has managed mills in Michigan and North Carolina. They both enjoy motorcycle riding and rode their Harley Davidson Road King to Glacier National Park in 2006. Recently, they traded their motorcycle for a Model A truck and now enjoy going to car shows. They have two married children and six grandchildren and reside in Harrisonburg, Virginia.
 
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Travels With Maurice: An Outrageous Adventure in Europe, 1968 by Gary Orleck (Book Spotlight)

TRAVELS WITH MAURICE by Gary Orleck

 
“‘Travels with Maurice is a gem of a book that just sneaks up on you with its greatness. While the title makes you think it’s a travelogue or road trip book (and we’ve all read enough of these), Travels is so much more.” – Michael Berman
 

 
Book Description:

“Every Women Wanted to Be with Him Every Man Wanted to Be Him”― Gary Orleck

A simple “thank you” led to the trip of a lifetime, along with an unbreakable friendship of two opposites. See them come of age while rubbing elbows with the rich and famous like the Shah and Queen of Iran, The Who, Paul McCartney, Brigitte Bardot, and even Shirley Temple Black. An unbelievable story, yet it’s true because nobody could make this story up. Find out things the rich and famous do not want you to know.

 
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Meet the Author: 

Author Gary Orleck

​I grew up in Lincoln, R.I. which is a blue-collar town, went To Babson University School of Business, and graduated with a BSBA in 1966. I worked my way around the USA for six months.

Two years later, I traveled with the son of the richest man in the world – covering 19,988 miles, twelve countries, and ten weeks.

Then, I went to work at Broadway Tire Inc. Twenty years later, I bought the business. I then owned and operated it for thirty more years before retiring in 2016!

In Between, I met and married my wife Ronna and had two beautiful children, and now I have five grandchildren!

The love of travel remained with me, and I’ve been fortunate enough to have visited 75 countries – each in a unique style – all my own way, using much of which I learned in my travels with Maurice in 1968. 

 
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Cerebral Palsy: ‘A Story’ Finding the Calm After the Storm by Ilana Estelle (Book Review)

 
Living with cerebral palsy is enormously difficult. But what if you never knew you had it? This is the incredible story of Ilana Estelle.

Born the second of premature twins, from a young age Ilana knew she was different, but for all the wrong reasons. A child of the 60s, Ilana experienced first-hand the way that disability was so often brushed under the carpet and not spoken about. Her constant physical and mental struggles made her feel isolated, alone, frustrated, and misunderstood… it took 46 years for her to find out why.

Part memoir, part motivational guide, Cerebral Palsy: A Story is Ilana’s open and honest journey from an angry, confused child, knowing something was wrong, but not knowing what, to the ‘real’ her – a courageous woman using her experiences and lessons to create inspiring messages about mental and physical health, positivity, resilience and change. 

 
 
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I received a complimentary copy of this book from iRead Book Tours. I voluntarily chose to read and post an honest review.
 
 
Cerebral Palsy: A Story: Finding the Calm After the Storm informed me about 11 secondary conditions connected to CP (cerebral palsy). The memoir also gave me facts that escaped me until now. For example, 800,000 individuals have CP, and 10,000 people are born with it each year. Ilana Estelle also explained how the brain is affected in those with cerebral palsy. There are physical limitations. People also face emotional and mental roadblocks. 


She went in-depth on how emotional stress can affect a CP’s immunity. A positive attitude, surrounding yourself with positive people is vital for a CP person’s overall health. Ilana Estelle gave examples of how to achieve a happy mind, cope with stress, and live a healthier life. 


There were many sections in Cerebral Palsy: A Story: Finding the Calm that could apply to those not living with CP: foods to maintain good high blood pressure, foods that alleviate arthritis pain, and parenting tips. At times, these areas seemed to deter away from the topic at hand—cerebral palsy. While I appreciate the extra health tips and her parenting advice, I wanted more about her journey in life with CP. 


Ilana Estelle discussed the misdiagnosis at the age of 2 (2.5). She spoke of the lack of family support  (often) and felt guilty and depressed about failing in life. She also emphasized what she learned in the process. 

  • know your limitations
  • ask for help
  • gain knowledge about your condition

To parents, she stressed having a sit-down and make sure all siblings are aware that people with CP need patience, understanding, compassion, and assistance. 


While Ilana Estelle has struggled in life and will as she continues her journey in this world, I’m pleased to see she’s not bitter or angry over what’s occurred in the past. She’s working hard to achieve a happy mind. Peaceful soul. 


You can’t change the past, but your actions today can pave the road for a better tomorrow. 

 
 
Heart Rating System:
1 (lowest) and 5 (highest) 
Score: 
 
 
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Meet the Author:
Picture

 
Ilana was born with a disability she didn’t know she had until the age of 46, when through her medical notes she discovered she had been diagnosed with cerebral palsy at the age of 2.

That discovery turned out to be a unique and life-changing experience that has forced Ilana to stand back and look at her life experiences differently. On her late diagnosis, Ilana set up her website The CP Diary and uses her experiences to explore her emotional and physical health, with an inspiring message advocating resilience and change.

Ilana likes to spend her days writing and blogging about anything that contributes to her health and well being. She is an animal advocate and is passionate about environmental issues. When she is not writing to tending to her blog, Ilana enjoys days out exploring the Yorkshire countryside. Ilana lives with her husband and their much-loved cat, in Yorkshire. Her grown up son and daughter both live in London.

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