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Wednesday, January 22, 2014

The Great Wolf Release Day

 The Great Wolf on Amazon

Abel’s been training for this day since the first day he found out he is a werewolf.  The Werewolf Olympics, in Kilkenny, Ireland, is where the big announcement will take place.  He will be stepping up as alpha, and what will mean for every pack throughout the world.  His faith is tested when his right hand man and bodyguard is up on murder charges.  Someone in the pack is a mole, will you guess who it is?  This action packed story will keep you on the edge of your seat to the very end.

Book one of The Legacy of Kilkenny Saga is available for Free on Amazon & I-books


 For sixteen years, my life has been normal. Piedsville, Oklahoma isn't the tourist mecca of the world, but it's where I live. It's my junior year and I've known everyone since Kindergarten, everyone except her, Pru Phelan. She walked into my English class, my heart stopped. I'd never heard the name Phelan before, so I Googled it and found Phelan means wolf. What I didn't know, she was a werewolf and soon my destiny would change.

This is the story about the prophecy of the Great Wolf and how it relates to me. I'm Abel Casey, and I am the Great Wolf.

The Legacy of Kilkenny is a young adult story about werewolves, friendship, family, and fear.


  I've thought of myself as a writer for as long as I can remember. Being a grown up with a grown up job and a family to raise, left me with little time to write. Everyone is grown up now, and I get to do something I want to do. My love of young adult books helped mold me into the paranormal writer I am today.

    The Legacy of Kilkenny Saga is near and dear to my heart.  When I started the series, my own son was a junior in high school and Abel has many of his characteristics.  Each character has a little of my daughter and son in them.  I wanted the series to be about friendship and family, two things that are important to me.  The first book really takes the reader on a journey with Abel as he matures.  By the time you get to The Great Wolf, you will see a transformed young man and the decisions how he handles the pressure of being a werewolf.  I hope you enjoy the Legacy books, 

  Thank you to all of the readers who have fallen for my wolf pack! 


Thursday, January 9, 2014

A Zebra Like Me - Amy Jones

Today is A Zebra Like Me's Book Birthday!


Maybelle Dawson longs for normalcy and belonging. Often misunderstood, she struggles with a rare disorder, labeling her a Medical Zebra.

Maybelle’s happiness and well-being threaten to slip through her fingers as she battles to take control of her life. She faces a never-ending battle on her journey to find love, courage and friendship in a world lacking acceptance.

With the guidance of her guardian angel, Maybelle finds her way out of emotional and physical isolation to discover lasting love and amazing friendships.

A Zebra Like Me is the story of one teenager’s battle with Ehlers-Danlos Syndrome, a disorder affecting one in five thousand people.


MY REVIEW OF A ZEBRA LIKE ME

This book is one of those books that all preteen and teens should read. It has a couple of lessons in the book that would serve both kids who are living with an illness and those who know a person with an illness. Maybelle thought she was a freak and people didn't like her. In all honesty, they didn't know her, not until she came out of her shell once she made a 'friend' Malach. It's hard to sympathize with a person who has an illness we don't 'see' on the outside. We're compassionate to a person in a cast or obvious sickness, but we forget about those who suffer in silence. I live with an illness that people can't 'see' and I don't run around telling everyone, so I understood Maybelle. I hope people will recognize the Maybelles in their life. The kid who walks a little slower, misses school, doesn't play sports, there's usually a reason why.

If you're looking for a 'clean' young adult book, this one is both clean and inspirational. If you like Christian Fiction, this book would fall in that category. I hope this book opens up conversations with parents and friends. Happy reading!

I was offered an ARC by the author for a fair and honest review. Rated Four Stars!



About the Author

Amy Maurer Jones has been happily married to her own version of Edward Cullen for sixteen years. She lives in the small town of Tabor City, North Carolina (close to the North and South Carolina shore) with her husband Kelly and their two beautiful children, Olivia and Keaton.

Amy loves reading and writing Young Adult because she finds young people inspiring. She appreciates how teens are able to look at the world with a fresh perspective and willingly open their minds to the endless possibilities that life has to offer. She particularly enjoys writing strong heroines who face problems head on, learn, grow and mature into the type of people who do the right thing.

When Amy isn't reading and writing, she teaches high school theater arts and dance. To say that Amy has a flare for all things creative would be an understatement, just don't ask her to assemble anything that requires instructions or sadly, you will be out of luck!


Favorite quote:
"You are unique, and if that is not fulfilled, then something has been lost." ~ Martha Graham

Links:
Website
Facebook
Amazon
Twitter

The Giveaway
A Zebra Like Me is a work of fiction but Ehlers-Danlos Syndrome and the message in this story are very real. I have EDS and I’ve learned to live with this disease. Sadly, much of my battle has been seeking compassion and finding acceptance from those who don’t understand it. My mission in publishing this book is two-fold.
1 – Awareness – I aim to educate people about Ehlers-Danlos Syndrome. I’m a teacher and through my teaching I’ve learned the best lessons are learned in unexpected ways. I hope my readers will gain a better understanding of this disease through the fictional world I created for Maybelle. There are people like her all over the world. Some EDS patients’ symptoms are less severe than Maybelle’s, some are worse. You may know someone with EDS and not even realize it.
2 – Self Empowerment – I want other people with EDS to know they are not alone. There are support groups and resources online that can help you learn how to cope with this disease. Don’t give up on a normal life. Learn how to avoid injuries and the external hazards that trigger your issues. Find hobbies that are safe, fun, and relieve stress. Surround yourself with positive people and avoid or tune out the people who can’t or won’t support you. Take care of yourself, physically, mentally, and emotionally.
Need Help? The Ehlers-Danlos National Foundation is just a click away.

Fast Facts about Ehlers-Danlos Syndrome
“Individuals with EDS have a defect in their connective tissue, the tissue that provides support to many body parts such as the skin, muscles and ligaments.”
The fragile skin and unstable joints found in EDS are the result of faulty collagen. Collagen is a protein, which acts as a “glue” in the body, adding strength and elasticity to connective tissue.”
“There are six major types of EDS, each classified according to their manifestations of signs and symptoms.”
“Clinical manifestations of EDS are most often joint and skin related and may include: joint hypermobility; loose/unstable joints prone to dislocation and/or subluxation; joint pain; early onset of osteoarthritis, fragile skin that tears or bruises easily, slow and poor wound healing and much more.”
“EDS can also be associated with rare and/or serious conditions such as tethered cord, cervical cranial instability, cranial settling, dural ectasia and chiari malformation.”
“In many cases those with EDS do not respond to local anesthetic properly or at all. This may mean complete failure of the anesthetic to freeze the intended area, a much lower amount of numbness, or a much shorter duration of effect.”
“EDS is an autosomal dominant genetic disorder (apart from types 6 and 7C) meaning if a parent has the disorder they have a 50/50 percent chance of passing it onto each child they have. Not everyone with EDS inherits the disorder from a parent. It is estimated that about half of those with EDS received it via what’s known as ‘spontaneous mutation’.”
“Currently EDS is estimated to occur in 1 out of every 5000 births worldwide, equally effecting men and women of every race and ethnicity.”
“Possible dental manifestations of EDS include a high palate, crowded teeth, gum disease and hypermobile tongue. Those with EDS are also more prone to cavities as well as weakness of both the enamel and tooth roots.”
“EDS can cause chronic debilitating pain throughout the entire body. Whether from chronic, repeated joint subluxations and dislocations or degenerative joint disease, this is often easily the most difficult aspect of daily life with EDS.”
“EDS can cause several gastrointestinal complications with one of the more serious being gastroparesis (partial paralysis of the stomach). This condition causes food to remain in the stomach for longer than normal, preventing the stomach from emptying entirely.”
“EDS carries many of the same and/or similar symptoms of several other genetic connective tissue disorders such as Marfan Syndrome and Loeys-Dietz Syndrome. It is not uncommon to have what appears to be a mix of more than one tissue disorder or for your diagnosis to change later in life from one to the other as more symptoms appear and more is learned about these conditions.”
“EDS can affect endless parts of the body, but has ‘variable expression,’ so each person is affected differently, even within the same family. While there are features that are frequently seen in many people with the disorder not all people will exhibit these features.”
“Connective tissue can surprisingly also be found in the bones and blood as well as being the glue that holds the body together inside and out. Collagen alone is found in tendons, ligaments, skin, the cornea, cartilage, bone, blood vessels, the gut, and intervertebral discs. All of this helps explain the endless possible complications and outcomes of EDS.”