About lscotthoughts

This blog was born after I turned 50, with a little nudging from my family. I write from the heart, focusing mainly on Romance, inspired by my husband of 24 years. However, I also write to inspire, to create smiles, laughter or an uplifting moment to move forward in life. Humor is a big part of who I am. I love to laugh and I love those who make laugh. And lastly, you'll find some tears along your journey here. Life is not all smiles, but it's getting through the trials with the love of our family and friends that is most important. I appreciate you stopping by and I hope you enjoyed and found something you resonated with...Lauren

KC

While sitting in this memory
my eyes begin to water

as my mind wanders through
the road together we traveled

but as tears fall, their love washes
over all that was unraveled

leaving a smile on my face
knowing his love and humor

will always leave a trace
for this moment and into my future

While sitting in this memory
I hold deeply in my heart

what once was of the man
whose presence I miss

Lauren Scott © 2015
(written for a friend)

“Finding a Balance” is available!

Dear Family and Friends,

My book, “Finding a Balance” is now available on my publisher’s site, Xlibris,
Amazon and Barnes & Noble. The links are below if you’d like to order a copy
and I want to thank you all in advance for your support to my writing, but most importantly, to the awareness of my daughter’s disease, PSC, and to becoming an organ donor.

More information is found on my prior blog post: http://lscotthoughts.com/2015/01/12/working-on-finding-a-balance/

BOOK COVER FINAL 1.26.15

http://bookstore.xlibris.com/Products/SKU-000756814/Finding-a-Balance.aspx

http://www.amazon.com/s/ref=nb_sb_noss?url=search-alias%3Daps&field-keywords=Finding+a+Balance+Lauren+Scott

http://www.barnesandnoble.com/w/finding-a-balance-lauren-scott/1121084225?ean=9781503528000

ALL PROCEEDS WILL BE DONATED TO THE CHRIS KLUG FOUNDATION, which is dedicated to promoting lifesaving donation and improving the quality of life for donors, donor families, organ transplant candidates and recipients.

chris klug foundation(chrisklugfoundation.org)

Please also feel free to visit my Published Work Page
on the tab 
beneath my header.

Much love to You All! Lauren ♥

Tanglewood

 

saddle shoes

I would walk downstairs
for breakfast and Morton,
the parrot, would greet me
in his feathery way and
I would wish him the same.

I had a friend who was a boy
but it wasn’t what you think.
We were only five years old
and at the time, it was a
friendship to behold.

Our neighborhood mascot was
Sam, the frog and he
was the size of a football.
He wasn’t as fun as a dog
but when we moved I missed him.

Mom made me a frog
I could keep forever

(out of red corduroy and beans).

These are some things I recall
since five years old was eons ago.
Fourth of July was fun with Dad
setting off amazing fireworks
in the sky for my youthful eyes.

On the first day of kindergarten
I stepped up into the big, yellow
school bus, wearing a plaid jumper
and black and white saddle shoes
with excitement and no sign of the blues.

A memory that sticks with a frown
is my short, pixie haircut
I had to wear around town!

Lauren Scott © 2015
Photo: Google images
(A little bit of fun but sorry, no pics of the haircut!)
:)

One Kiss

I stare at this
blank page,
white as the
blanketed ground
in winter’s staging

Where are the syllables
I crave to create a
mixture of magic?

I fear they have traveled
to faraway places,
across desert dunes
and boundless oceans,

and might not return
so that I may tell him
(again)
how he’s irreplaceable

Instead
I’ll just kiss him
and steady myself
in the arms of a man
who is satisfied
with my simple
existence

Lauren Scott © 2015

Working on “Finding a Balance”

Dear Friends,

I am embarking on a new adventure and this is an introduction. My second poetry book, “Finding a Balance” is almost ready for publication and it’s nice to not be such a novice the second time around. This book isn’t just about sharing more poems I have written. It’s not only about me. It holds a deeper meaning; the new adventure part. The proceeds will be donated to an organization for a purpose close to my heart and my family’s. I’ll begin, though, with a back story…

Part I:
After three years of abdominal pain and ongoing tests, on October 4, 2012, our daughter, Stephanie, was diagnosed with Primary Schlerosing Cholangitis (PSC). She was 21 years old. Her doctor was the head of the Gastroenterology department and was extremely competent. He didn’t beat around the bush. He told us this wasn’t good. Below is a brief description:

Primary sclerosing cholangitis (PSC) is a very rare condition where the bile ducts inside and outside the liver become inflamed, leading to scarring, narrowing and blocked ducts, potentially causing a build-up of bile in the liver, and in some cases cirrhosis. Patients with PSC are at a high risk of developing liver cancer. Symptoms begin gradually with abdominal pain and itchiness and include worsening fatigue and, later, jaundice. Liver transplantation is the only cure for prolonged life. This is usually needed within 10 years of the diagnosis, but each patient’s case is different. 

I’ll try to keep the drama at bay, but I’m sure you can imagine our reaction. Our daughter doesn’t drink or do drugs so there is nothing she did to provoke this diagnosis, which is why it’s called an auto immune disease. This was a shock to our entire family. My husband and I had many emotional moments, wishing we could take her place. We were paralyzed of doing anything that didn’t need doing for the rest of that year, except for the necessity of living. We asked God why…why Steph? She has a heart of gold and is simply a nice, caring individual. Many have asked these same questions and there are still blanks waiting to be filled.

Since 2012, she has had symptom flare ups with several ER visits, but otherwise, on the outside, she’s beautiful and looks perfectly healthy. The doctor told her to live life to its fullest. That was his profound advice. She has a stellar attitude. She lives in the HERE AND NOW and there is no other option. She is due to graduate this year with a Bachelor’s Degree and has been busy with school, friends, her boyfriend and of course, family, with no time to sulk. She is human, though. She has broken down at times, but I think, as her parents, our score is higher.

So…I’m telling you this not for sympathy but to bring awareness to this horrible, slow progressing, life threatening disease and most importantly, the need for organ donors.  

Part II:

All proceeds from my book will go to The Chris Klug Foundation (www.chrisklugfoundation.org), also found on Facebook.
Chris (born November 18, 1972) is a professional alpine snowboarder. After receiving a liver transplant in 2000 to treat PSC, he went on to compete in the 2002 Winter Olympics in Salt Lake City, winning a bronze medal in the Parallel Giant Slalom. This was the first and so far only time a transplantee had competed in the Olympics. He also won a bronze medal and lit the torch at the 2002 National Kidney Foundation U.S. Transplant Games. In 2004, Chris released a book called To the Edge and Back: My Story from Organ Transplant Survivor to Olympic Snowboarder. (Wonderful book of inspiration and hope)

chris klug foundation

Below is an overview and mission of his Foundation:

Founded in 2003 by liver transplant recipient and Olympic snowboarder Chris Klug, The Chris Klug Foundation is dedicated to promoting lifesaving donation and improving the quality of life for donors, donor families, organ transplant candidates and recipients.
CKF is passionate about sharing the message of donation, and educating people on the impact one person can have on the lives of so many others. Over one hundred and ten thousand people are currently on waiting lists for solid organ transplants across the U.S.A. CKF is devoted to making a difference to those waiting for a second chance. We are also there to help promote the message of organ donation.
Working with young people across the nation, CKF provides campaign materials and information for “Donor Dudes” chapters in high schools and college campuses. People everywhere are touched by organ donation and transplants, and we want to get the message to everyone.

The publication for my book will be at the end of this month or beginning of February. I’ll do a separate post when it’s available and again, I’m very excited for this new collection to have a greater, deeper purpose.
Our life now is about “Finding a Balance” between PSC and all the good things!

Someday Stephanie will need a liver transplant so becoming an organ donor is an unselfish way of giving another soul a second chance. 

Thanks so much for reading and I wish you all Happiness and Good Health!
If you’re so inclined, prayers and positive thoughts
for Stephanie will be greatly appreciated.

Lauren
♥ ♥ ♥

Crystal Ball

 

crystal ball

Imagine the future visible through a magic globe,
what is it you would wish to know?

Would peace of mind follow the facts
or would your mind be less relaxed?

Long awaited answers would fill in the blanks;
no more wondering, but would you give thanks?

Learning the future and after all is said
could strip your days of joy, filling you with dread

So living in the here and now might just be the best
instead of venturing into this mysterious quest

Lauren Scott © 2015
Google image

I don’t think I’m the only one whose mind wanders into the future,
especially in the beginning of a new year,
so this is just something fun (or not) to think about.
But for now, I’ll just take each day as it comes
and enjoy the anticipation!

:)