Independent Book Reviewer Nicole Galloway – Miller

Meet Nicole Galloway – Miller. Nicole is an independent, online, book reviewer.

So what initially interested you in doing book reviews? How long have you been a reviewer?

I started my book review blog as an assignment for my Master’s in Fine Arts Program at Seton Hill UniversityNichole Gallawayy. It is a low-residency program. In place of class discussions, students are required to write a review blog post. In addition, students comment on the blog entries. I’ve only been reviewing books since last January, but I’ve been reading and writing my entire life.   

When conducting a review, what elements stand out for you?

Every book is different, so my reviews tend to evaluate a wide variety of writing techniques. I love experimental formats and creative figurative language. I also enjoy books that present the world in new and different ways.

What’s the most recent book that you’ve reviewed? Did you find it interesting?

My most recent review was historical fiction, Like Mayflies in a Stream by Shauna Roberts. I loved it. It’s part of the archeology series published by Hadley Rille Books. http://www.hadleyrillebooks.com/archseries.html I highly recommend them.

What type of books do you read for personal enjoyment?

Anything I can get my hands on. I am big believer in reading a wide variety of different genres, styles and authors. I read several books at a time. Currently, I am reading Casual Vacancy by J.K. Rowling, The Night Circus by Erin Morgenstern, Railsea by China Miéville and Extremely Loud and Incredibly Close by Jonathan Safran Foer.Nichole Gallaway.jpg II

When reading reviews of a book that you’ve already rated, what‘s your reaction if the reviewer gives an opposite take from yours?

I love to read reviews expressing different opinions. Different reviewers tend to notice different things and every reader brings their personal experiences to their interpretation. I’m not a big fan of particularly negative reviews. It’s good to strike a balance between the good and the bad. Criticism can be helpful when it is presented in a respectful and professional manner.

I’ve read your reviews and you have a nice command of the English language. Tell us a bit about your background.  Do you feel as though schooling or hands –on learning benefited you the most?

I’ve always loved words and language. When I come across a new word during my reading, I have to look it up. I have two dictionary/thesaurus apps on my i Pad and smart-phone. These are the greatest inventions and save a lot of time.

I have an autism spectrum disorder and communication is challenging for me. Writing is how I express myself and how I learn about the world. I use a person’s word choice during conversation as replacement for nonverbal cues, since I cannot process things like body language and facial expressions. The words a person chooses and how he or she constructs phrases, and sentences is more than an objective statement about what is going on – they communicate intention, personality and emotion. This carries over into how I read. I’m a slow reader, who reads one word at a time.

Have you ever had a confrontation from someone, who disagreed with one of your reviews? What positive input have you had?

Authors tend to appreciate my reviews. I strive for a balance between positive and negative criticism while being objective and fair. Several people have expressed that my reviews teach them a lot about different writing techniques. I wish I could say that everyone loves my reviews, but that isn’t the case. I’ve been accused of being dishonest when writing reviews, because I choose to keep personal emotions out of my reviews. If I don’t care for a book, I maintain a professional attitude, state specific examples and reasons. I would never disrespect an author.

If a reader would like to have their book reviewed, what advice can you give them on finding individuals to help them?

Some social networks are a great place to find people to review your novels. There are some great Facebook pages and LinkedIn groups. It never hurts to ask someone. Don’t be afraid to contact a blogger who you respect. I love hearing from authors who would like me to review their books. It makes me feel like I’m posting quality work.

When you’re not reviewing, what does your life look like?

I read and write. Even if I wasn’t a reviewer or pursuing a degree, I would still read and write every chance I got. Video games are too stimulating for me, and I can’t stand commercials, so I watch shows, movies and documentaries on Hulu and Netflix from time to time. This weekend, I just finished watching the second season of The Walking Dead (originally aired on AMC). I love listening to music and walking through cemeteries – I find them peaceful.  

I appreciate you joining us today, Nicole! You’ve giving us a bit of insight, into the mind of a book reviewer. I wish you all the very best.

If you are interested in getting your book reviewed, please visit Nicole’s website where you can read her book review policy:  http://nrgalloway24.wordpress.com/book-review-policy/

Email: gallowaymiller@gmail.com

Twitter: @GallowayMill

LinkedIn Profile: http://www.linkedin.com/pub/nicole-galloway-miller/47/397/638 

Facebook author page: https://www.facebook.com/NicoleReneeGalloway

Facebook: https://www.facebook.com/people/Nicole-Galloway-Miller/100000217063148

Book Review blog: http://nrgalloway24.wordpress.com/

An Autistic Blogs about Autism: http://nrgallowaymiller24.wordpress.com/

Jackie Aitchinson’s Herculean Journey – Flourishing with Ankylosing Spondylitis

When I was a teenager, I begin having lots of aches and pains. The doctors labeled them as, “growing pains”. After having constant pain in spine I went from physician to physician yet, they could find nothing wrong, and they basically said it was all in my head.  My general practitioner believed there was a problem so kept sending me to different hospitals, different specialists.  Eventually I was diagnosed with Ankylosing Spodylitis, a painful, progressive, extreme form of inflammatory arthritis.  However by the time I received the correct diagnosis, my x-ray showed I had severe damage and needed fusion in my spine.  I was told the doctors had not been looking for AS, for it is generally a mans,’ medical problem!

It was the early 1970’s. By this time I was married and in my early 20’s. One of the things I was told was that my spine was not strong enough to carry children. For the next few years, I was continually taking painkillers and had several stays in hospitals with major flare ups.  The consultant at the Northern Hospital in Edinburgh, viewed my drugs. He expressed his concern and disgust that – a)I had never been referred to the hospital before, and b) that I had never been on anti inflammatory medications.  After Naporsyn was prescribed, the pain was held under control. Unfortunately, I spent undesired time in the hospital.

The next major event in my life occurred a few years later on New Years Eve. I decided I was not going to drink alcohol, as my friend were simply going around  to visit the neighbors in the wee village, we lived. While walking about, I slipped on the ice and was carried home by two drunk men. Fortunately, one was a fireman so knew how to carry me safely.  The next morning my general doctor, called and immediately insisted I got to hospital.  As it turned out, upon falling,  I had smashed a vertebrae. It was contained so no danger, so I insisted on going home, even though it was very painful. I was informed by my doctor that if I had been drunk, I would probably have been far more relaxed and therefore, would not have done much more damage to my spine.

The next incident that followed, involved one of my eyes left. My eye looked strange so I went to see my general doctor.  He found nothing, however two days later, he arrived at my door and insisted I go to the Alexandra Eye Pavilion in Edinburgh,   where I ended up staying for a week.  After reading up about AS, he  spotted a connection between my eye irritation and the disease.  I had developed iritis  and since it had not been treated promptly, it had become worse. I needed injections administered directly into my eyeball, for drops did not work. From then on I had iritis on average 3-4 times at least every year, as eventually, both eyes were effected.  Each time, I detected a flare, I went straight to the eye hospital, for I learned my lesson from the first incident. Thankfully, I only had two additional hospital stays due to my iritis  I got to be so good at recognizing the signs of the condition that, I ended up in a few arguments with nursing staff who told me there was no sign of iritis. After I insisted on seeing my doctor, he would confirm that indeed my eye was infected.  In over 30 years, I have only misdiagnosed myself once!  The doctors should by now read the bloody notes from previous appointments and listen to me! I am reactive to steroid eye drops, for it can cause the pressure to build up in my eye.  This pressure can turn into glaucoma. On one occasion I actually lost sight completely in one eye for a few hours and was rushed to eye hospital. The doctors were rushing around and accidentally gave me pills plus an eye injection. This combination made the pressure in my eye soar. My eyes are now very sensitive to light and I have lost some peripheral vision in one of my eyes and will most likely need surgery for this problem. I go to the eye hospital every few months for check ups.

A few years later,  someone pulled away a chair that I was about to sit on it.  I fell hard and the next day I was in great pain.   The doctor insisted it was a flare up of AS,or a bad bruise. (For I was not screaming and crying when I saw him) I told him it wasn’t, for I know my body.  However when I went to see my rheumatologist. He took one look at my face as I walked in, and sent me immediately to x-ray which turned out to be break number two.  The third time was five years ago as I bent down to pick up a bit fluff on the floor, I heard a crack. Same old same old. I pulled a muscle, torn ligament etc.. So my doctor sent me to a physiotherapist. It was an interesting journey crouched in the back of a taxi, for you have no idea the number of potholes in Edinburgh!! Anyway the physiotherapist sent me home as they refused to touch me, as I was in so much pain. They made arrangements for an x-ray, and insisted that they would need to come to me until they were satisfied with my situation, so I would not need to travel.   They found that I have osteoporosis.  This bone condition, combined with the AS, means I have to be very careful of falling over etc.

In December 1999 they my rheumatologist decided to operate on my back as I was becoming very badly bent over. This meant opening me up from shoulder to bum, breaking the spine in a couple of places, placing metal rods at each side of the spine and inserting hooks to pull everything into alignment. The operation was on a Tuesday and they put me in a plaster body cast on the Friday. (It should have been longer before applying the plaster, but it was coming up to Christmas and the holidays and they hurried the procedure along.  It was the worst thing ever!  If you can imagine, I could only sit up being held by several people and I was in extreme pain and experienced dizziness. The nurses placed a huge amount padding all around me.  It went from under arms, up to my throat, and then down to my hips.  I was given morphine injections whenever I wanted one. Then there was the scaffolding. I was carried over and laid on this structure, with pipes running under my knees and under arms. There were material bonded around my neck pulling my head into place and the same ones on my feet so my back was being pulled straight. When they finished the plastering, I was carried back and sat up as they had to make sure the plaster wouldn’t be too high to choke me, or too low to hurt me when sitting. Then laid me down on a trolley and sent to x-ray to make sure everything was in the right place. I was then put on a morphine drip and was in hospital for a month.

I had to learn to walk, to get washed without wetting the plaster etc.. After a few weeks had to go back to hospital for there was a black discharge, leaking out the bottom of the plaster, which my mum noticed when she was bathing me.   It turns out it was an infection because the plaster went on too early. The plaster  was taken off for less than a week and I had to say on the bed, in the wee room and couldn’t be moved. No further problems, but I had two further changes of plaster, each one a little lighter than the last, over a 10 month period. After all this, I was fitted with leather and metal strap-on body brace.  This switch was bliss, as I could take it off at night and when I bathed.  I needed to wear the brace for a year.

I began to suffer from extreme fatigue and when I saw my doctor, he sent me to the Western General Hospital in Edinburgh for tests. There they carried out my first endoscopy, to see what is going on in stomach. It was found I had a hiatus hernia and lots of lesions in my stomach due to taking the anti-inflammatory drugs over such a long time. Blood tests also found I have an under-active thyroid.   The thyroid and AS both have the same side effect – fatigue. I describe my continual exhaustion like, “Walking through water, all the time.” They also discovered that I had a lot of irritation in my stomach and colon due to the years taking anti inflammatory drugs, and that I was anemic. Again, this produced even more fatigue. So I was limited to taking, which really are ineffective for me.

A few years ago I read about a very new injection which had been used for similar conditions, called Enbrel.   I qualified to be given the medication so started with initially twice weekly self injection. The dosage was then doubled, so I could receive it once a week.  However the anemia was becoming a problem and I needed to be rushed several time to the emergency room for blood transfusions. The average blood count is 120-150 for a woman. At one point mine count was 50. My doctor gets excited of my count is in 3 figures!! Despite several endoscopes, colonoscopies and a camera pill evaluation, there was no obvious reason for the ongoing severe anemia.  It was determined that it is just attributed to my AS.

So daily I take painkillers, injections, thyroid pills, hernia pills, iron pills, calcium pills, osteoporosis pills and eye drops. I get a shopping bag full with each prescription, luckily as I don’t pay for any prescriptions!

There has been the almost inevitable depression at times, mixed with loss of confidence caused by the way I look.  At times I have the feeling of being such a nuisance when out with friends, for I can’t walk far for long.  I don’t want to go out much for I always need to have a seat before long, so I longer have a social life. What I do enjoy is having friends over for visits. This too can be difficult, as I worry that I can’t manage to have my home as nicely as I’d like it to be.  My true  friends will understand my limitations.

The AS was also a contributing factor to the breakdown of my marriage. It is a very difficult condition for a patients’ partner to understand.  This is even more challenging when ones partner is young and active, as in my case.  Work life was also very difficult due to the constant medical struggles, and after the association I worked for merged with another,  they moved offices.  This meant hours of travel each way with three change of buses.  After three years of working with AS, I simply knew I couldn’t go on any longer and one day just got up and went home. My HR manager and my GP were very helpful and guided me through it all.  Thankfully, I signed off sick for a year which meant I could claim early retirement on health grounds. I remember going to see my GP with trepidation. After explaining the situation to him, he quietly said, “I can’t believe it has taken you so long to get to this point”.    He told me he admired my determination to work, and didn’t have any idea how I had managed to go on for so long. Well that was it, several boxes of tissues later we got organized. Again I think I was especially touched at this rare moment for AS patients are so used to people not really getting it.  We feel we have to defend ourselves from being considered lazy. Presently, I don’t get the old age pension as I am too young, and I could not have been able to do it with out the support of my partner an my mother.

I had major surgery last year, as I was finding it more and more difficult to breathe. I was taken off Enbrel while they investigated my chest/lungs. What they found was my entire stomach and part of my colon had moved through the hernia into my chest cavity and were squashing my lungs.  This happened because of my bent back.  The surgeon opened me up hip to hip in order to pull everything back into place and then stitch my stomach to the abdomen wall, so this will not happen again! Unfortunately while in for this procedure, I caught MRSA  and a throat infection.  I was also told they found my hernia did not close, as they couldn’t get me flat enough, so after all that still have a hiatus hernia!.

Another problem which has manifested itself this last year or so has been a twitch at my left eye, which became stronger and eventually moved down my face. This caused my lip to become a bit twisted up, looking as if I’ve had a stroke.  I was given Botox, several times but did nothing to really help. My doc suggested an MRI to see why this was happening. It was all arranged that I go in to have the scan of my head, however as the table part is very hard and flat so, It was too painful to lay on it.  So I must wait for them to come up with a better way of diagnosing this problem.

I got back on Enbrel in January, however I have been disappointed with the results.  It’s as though it’s not as effective as it used to be. I have also noticed my hands are very painful now, with the knuckles swelling, and some morning they are completely numb. The doctors are thinking perhaps it is carpel tunnel and my knees are also in pain while I am walking. Feet, ankles, and sciatic nerve are all in pain too.  My neck is bent very badly for I have to strain to look up the whole time I am walking.  This is very uncomfortable, as you can imagine.

My eyes have been much better lately, in respect of my iritis. Leaving work has been helpful in this way, as I am not on the computer all day long like I use to be.  Less stress from my job has also improved the situation, I believe.   I am also using two different very mild steroid drops in both eyes continually, as a maintenance program.

These are the “highlights” of the last forty years of my life. There are too many to go over each one of them for their have been many over the years .These days the depression is more disabling, partly because just so tired of it all and partly because in all honesty, I don’t have much of a life. As I said earlier, no social life in the evenings, too much is involved when planning transportation.  I am always  concerned if I will be guaranteed a seat.  I don’t think it’s fair to make plans with a friend and then  call off at the last-minute.  During the day,  my friends all work and my partner now works nights.  Even when I have visitors over, we have to be very quiet for my partner sleeps during the day.

I go out as often as weather allows usually with my Mum, as I am not too confident on my own any more. I think the effect of years of living with a chronic disease, is often thought of in terms of the effect on the body alone.  It also  equally affects the mind, family,  and friends of those living with the disease. Ones life becomes AS, as it controls every aspect of your person. People treat you differently than those who are healthy and it affects every decision you make.

I would like to make known that having joined various groups pertaining to AS, and by starting my own for group for AS’ Peeps, has been the best thing ever. I’ve met so many fabulous out there, who are a pleasure to know. These people are from all over the world. All  have a generous spirit.  They are the ones who listen to my concerns and support me.  We all exchange ideas, treatments, hopes and dreams, My life is much richer for these new friends even though I shall probably never meet them. But the big thing, the HUGE thing, is they all know,understand and accept everything you have to say because they LIVE IT.  I wish social media, would have around in the olden days when I started on this journey, for it would have detracted from the loneliness and isolation.

What a joy there has been in the new friendships made, because of this horrible condition! That has been one of the major factors in me getting more involved and active in spreading information about AS. When I hear all the different stories, (and many similar conditions), the huge delays in diagnosis I can understand what these patients are going through.  Some were diagnosed late, which allows the disease to do severe damage before any treatment has been given. This delay also allows the mental wounds to fester.  Those that don’t understand have hinted that we are simply seeking attention or have a mental illness. In my case if it was not for my doctor who doggedly kept sending me to specialist after specialist, until the final x-rays showed a very damaged spine.

About Ankylosing Spondylitis

The disease usually starts in ones teenage years and early 20’s.  Men are three times more likely to get AS than females. The disease usually starts with lower back, and early morning stiffness. It can also affect most joints, eyes, heart, liver etc as well.  Many people with AS take NSAID’s (non steroid anti inflammatory drugs).  The inflammation causes the pain. However in recent years, the treatment is a mix of these type of medication with muscle relaxants.  Other medications that are used are the newer biologics in the form of injections or infusions. These suppress the immune system and so stop the inflammation.

There are periods of extreme activity known as flares, which can last any amount of time.  There are periods of quiet, but usually the pain is somewhere in between.  AS causes the bones, in particular the vertebrae, to fuse together, which restrict movement.  (So some can end up like me, which is very bent over.) Patients frequently need fusing in the neck area. The other main symptom of the disease is severe fatigue. This can be a real problem as people can look well and so appear to be lazy! One day you can be severe pain, the next fine, but very tired. This again, is what people find hard to understand about AS. One doesn’t get ill, get treated and get well. Every one is different, and there is no way of knowing how you will progress, so the priority is to get pain management in place that works for you, and try to stay as mobile as possible.

I have now put on too much weight due to going a long time with little exercise. It is difficult to exercise with my breathing problems, recent surgery and the fact that it is winter here. I am hoping to get out and active soon and start a healthy diet. Hopefully this should help me shed some of the excess weight. The only exercise I am allowed to do is to walk. Having a fused spine and neck coupled with osteoporosis, this is the safest activity for me. I am not even allowed a massage!

A friend once told me my appearance, told the world, what kind of day I was having. When I am having a good day, I wear normal make up, all neat and tidy. Everything is in place – full face, hair, nails, jewelery and I wear a scarf.  If I am having a very bad day,  I represent myself in full camouflage mode! Do you know what? She was right!!”

I feel optimistic that with all the work being done to investigate the disease. The AS community is bringing much information to the attention of people interested and doctors, the new medication available, that those who have recently been diagnosed and those who will be will have a brighter future than those of us from all those whose journey started all those years ago. There is certainly much more support and information out there to enable them to be able to investigate and learn so they can make informed decisions.
Information from The National Ankylosing Spondylitis Society

– Ankylosing Spondylitis (AS) is a painful, progressive form of inflammatory arthritis.

– It mainly affects the spine but can also affect other joints, tendons and ligaments.

– Ankylosing means fusing together. Spondylitis means inflammation of the vertebrae. Both words come from the Greek language. Ankylosing Spondylitis describes the condition where some or all of the joints and bones of the spine fuse together.

– Entire fusing of the spine is unusual. Many people will only have partial fusion, sometimes limited to the pelvic bones.

– Other areas such as the heart, lungs and bowels can also be involved with AS.

– Inflammation occurs at the site where certain ligaments or tendons attach to the bone. This area of the body is known as, enthesis.

– The inflammation is followed by some erosion of the bone at the site of the attachment. This is known as, enthesopathy.

– As the inflammation subsides, a healing process takes place and new bone develops. Movement becomes restricted where bone replaces the elastic tissue of ligaments or tendons.

 – Continued inflammatory leads to further bone formation and the individual bones which make up your backbone (vertebrae) can fuse together.

– The pelvis is most commonly affected first. The lower back, chest wall and neck may also become involved at different times.

AS is a very variable condition. Some people with AS have virtually no symptoms whereas others suffer more severely. AS tends to affect men, women and children in slightly different ways. In men, the most commonly affected areas in men are the pelvis and spine. Other joints which may be involved are the chest wall, hips, shoulders and feet.  In women, the involvement of the spine tends to be less severe. The most commonly affected areas are the pelvis, hips, knees, wrists and ankles.

As a devoted advocate to informing others of the dangers of AS, she writes for various chronic illness blogs:

Masquerade of Words ( Spondylitis Blog Carnival) masqueradeofwords.wordpress.comA group committed to spreading information about the disease. This way the variations of the disease can be clearly seen.  This blog also educates friends and family of the many facets of AS.

AS Peeps and AS Standing Tall Together and  Thinking out Loud – jackie-aitchison.blogspot.com – Jackie created these groups to exchange ideas and offer support to those with the disease.

She is also a very active book reviewer.  For a book review, you can find her at Book Reviews by Jackie feline9-bookreviewsbyjackie.blogspot.com.

Valentinno: Poet and Screenwriter


Carla: Tell us a bit about yourself and your pen name.

Valentinno: To my family and friend I’m Kevin Brian Wright (but to my international following, I’m best known as Valentinno.)– A romantic poet, letter writer, renaissance thinker, and author of the critically acclaimed book, ” A Romantic’s Passion: The Tenth Muse”.

In this business a pen name, book cover, even the title of a book can affect how your book will sell. So being that I am a romantic poet my birth name “Kevin Brian Wright” sounded more corporate to me. Perhaps it would fit better for someone writing a book on finance.  It wasn’t very marketable for someone writing romance. But the name Valentinno being a variant of valentine which also means, romance, true love, heart, etc., was perfect in every sense of that word for me.

Carla: How did you make the transition from screenwriting to books? 

Valentinno: You’re absolutely right I am a screenwriter and that was my main focus, but I wore many other hats in the film industry as well. I was an award-winning action and fight director, I choreographed stunt, fight sequences and starred in over eight films. But the thing I most enjoyed was writing the scenes and watching them come to life on-screen.

After writing screenplays for so long I wanted to pursue other creative avenues. At the same time I was working on several collections of romantic prose and I wanted to tell my love story to the world. So I basically took a very long vacation and decided to concentrate on just my poetry, and so I published my first bestselling book in Europe in 2006.  I guess being a screenwriter will always be in my blood because, it seems I’m back from that vacation. Today I have two feature screenplays written with my business partner, Christina Sampson.  One is an action science fiction film named, “Vooshaday” and the other is an action movie entitled, “Organized Crime Bureau.”

Carla: You’re incredible popular in Europe and your latest book, “A Romantic’s Passion: The Tenth Muse”, that was released in January, has already sold out in France and Germany.  What element of originality do you feel fuels your popularity?

Valentinno: January 25th 2011 my book was published and by the 28th it sold out in Germany and France. Since then,”A Romantic’s Passion”, has been getting a lot of media attention. I have been doing radio tours, appeared on talk shows, been on the front cover of numerous newspapers, and have done many interviews, etc. It has been very exciting.

As for how I feel, I really go by what the reader feels because they are your true critics.  According to my readers my popularity stems from the old world romantic style and my elaborate imagery.

“O’ beauty, her endearing armor, that meets my elated glance,

My dear warrior! The courier of Saint Cupid’s almighty bow,

Where I have only pressed my lips against the cheek where

Rests love’s fair kiss and passion kindles those votive rays,

But a lover’s bliss, that blessed day!

When that seraph light retained my soul upon her

Flowering face and the tender tones of her sweet accents.”


Carla: Name the most unusual place you’ve found inspirations for your writings.

Valentinno: Honestly I don’t have to be inspired; I can just sit down at any time, pick up a pen and just write. Maybe because I write about my true life romantic experience, so the muse, emotions and visions are already the reality of my mind.

Carla: You’ve used photography in your latest book to coincide with your poems. 

Valentinno: I used photographs in my book so readers can not only read the love story through words but visualize the romance through photos. I wanted to give the audience something different.

Carla: A line of poetry that changed your way of thinking.

Valentinno: I don’t think a line of poetry could change my way of thinking, but writing, “A Romantic’s Passions”, opened my eyes and mind to many new things. Even though I’m an expert on the subject I am still just a student of the world and love will always be the greatest teacher.

Carla: What was it like writing for the Queen of England?  Was the process a bit intimidating?

Valentinno: I was honored and very excited to write for Queen Elizabeth II. The poem in which I wrote was entitled, “O’ Blessed Nightingale.” It’s now displayed in her private estate, in Balmorals Castle.

Regardless of how high-profile someone is you have to look at them like every other reader. You can’t get intimidated or you won’t give your best work. So I sat down behind my computer and wrote the poem like I would for anyone else. Weeks later I received a letter by royal mail telling me how much she loved the poem, it’s presentation etc.

Carla: When you’re not writing, what’s your favorite thing to do to unwind?

Valentinno: I always like to unwind with a good run or walk, or a couple of hours in the gym.

Carla: What did you have for dinner tonight?

Valentinno: Chicken stuffed with crab meat and asparagus

Carla: Your most beloved coffeehouse?

Valentinno: Tea and Sympathy; because I’m a tea drinker.

Carla: Favorite romantic vacation destination?

Valentinno: Venice, Italy

Carla:  Cats or Dogs?   Cats

Thank you Valentinno!  I wish you much success, in your future endeavors.

While he now writes full-time, Valentinno has more than 27 years of award – winning writing experience. He has received 60 international literary awards in less than 5 years, including a nomination for the Dickinson Award from the Poetry Society of America, and was inducted into the “Who’s Who of Poets.” Valentinno also won best manuscript at the Christopher Newport University’s annual writers conference, as well as composed poetry for Queen Elizabeth II. Valentinno is a consummate writer and his excellence in his craft has earned him international fame. He is no emerging romance writer. He has already earned worldwide recognition for the finest embodiment of the art of poetry, thus ranking him among the greatest old world romantic poets.     

To purchase Valentinnos’ books:

http://www.valentinno.webs.com

http://www.bn.com

http://www.amazon.com

RA Warrrior Review

I just received a wonderful review from the famous,”RA Warrior” (Kelly Young).    If you’re interested, check it out on my links. I’m hoping to interview her soon.   Her research on Rheumatoid Arthritis is unmatched.  She is amazing!!!

Another Place at the Table

Just wrapped up reading the gem,”Another Place at the Table.”  by Kathy Harrison.   The writer dictates the rewarding and unfair facts learned from fostering nearly one hundred children.   Upfront and tastefully done, this book captures the selfless lifestyle of a Massachusetts couple.  They were named Massachusetts, Foster parents of the Year and in 2002, they received the Goldie Foster Award.   In a society that rarely credits, let alone acknowledges the positive impact of foster parents, it’s refreshing that this couple gained recognition.  Her background in early childhood education primed her to springboard, into the role of a foster parent.   (Although many unforseen episodes were not conveniently stated in the mandatory courses taught by the local agency.)  While parenting three biological sons, The Harrisons adopted three of their foster girls.

Overwhelmed with emotion, I honestly had to pull away from the book on a few occasions.   Imagery of pain, abuse and abandonment filled the pages.   Leap frogging from story to story Kathy’s gave just the right amount of substance to simulate a  blindfolded rollercoaster ride of jubilation and gut wrenching fear.

In the end, multiple children benefited from a caring stable environment and three blessed girls found a permanent loving home. Yes Virgina, the modern-day hero does exist.