Wednesday, May 28, 2014
Journalism vs. Creative Writing
When our teacher, (who was very talented, by the way), explained the age old story about what the audience wants to hear, dog bites man is passe...not interesting. On the other hand man bites dog, now THAT'S a story.
I personally would rather not read about ANYBODY getting bitten, If it were left to me, crime reporting would only happen in our police offices across the nation.
A creative writer might describe a sunny day in this method. "The sun shone brilliantly, reflecting off a crystalline lake. A journalist might say, "The sun shone, the lake was pretty. Not a brilliant comparison on my part but a relatively accurate one.
Use of hyperbole in journalistic writing is forbidden. My sweet church going, God loving Mama once said to me when caught in an obvious fabrication of the truth, "If I told the story exactly how it happened who would want to listen?" Who indeed? She passed on to me the desire to add to a story, not delete. In fact, I have been given a wonderful skill set. The ability to make a SHORT story, LONG. I quickly realized that if hyperbole was forbidden, I was in the wrong place.
Newspapers are threatened to go the way of the Stegosaurus. No more crisp words folded neatly on paper. We will gain our news via the internet. Gone will be our newsy youngsters, out earning a living by tossing a newspaper accurately on your porch.
Can you imagine what chaos would reign in our newspapers if creative types like me were given free rein as reporters? Suddenly stories that could be adequately covered in 100 words or less would spring into novelettes. There might even be mini-series in print. There would be MORE paper used in the paper. My consumption of paper might cause environmentalists to rise in protest.
Envision this writer's report. "Man bites dog. There was a report printed last week that dead pets were showing up on doorsteps all over town. The creatures are basically zombie's. They are inherently evil. A man was bitten by his evil zombie pet, and he in return bit his pet. Madness may be ensuing."
I will let you guess as to the identification of the aforementioned imaginary newspaper article. What about this delivery? "Joyfully she gazed into the man's eyes. She had finally found her life's love. He was not handsome. He was not brilliant. He was hers. That was all she wanted."
To sum up this rambling post, the journalistic class taught me a few principles that I recall profoundly. One of these is the cut-off paragraph. That is the very last word on the subject that is not necessarily important and can be "cut-off" if needed to provide space for other articles. Of course, the discretion would belong to your editor. He alone would decide...
Wednesday, May 21, 2014
Dictionary Walking?
One of my roommates gave me a quote that they had found that said, "People who strive to be walking dictionaries need to remember that reference books are never taken out!" lol I love that quote.
Not long after I met my hubby he confessed in chagrin to me that as a child he read the dictionary routinely. He ADORED words, and the origins of speech. I was a freelance typist as well as a secretary in the Brigham Young University Theater Office. Typing a screenplay that Nyle wrote, I fell in love with the man. My reasoning was that anyone who could write with such joy, such passion, HAD to be a man with the gifts I was looking for in a husband. I was ever so correct in that impression.
In High School I took a lot of remedial classes. I am NOT proud to admit that I learned they were easier than regular classes and therefore signed up for them. No ACCELERATED courses for me!
In my remedial English class my teacher asked me, "WHY are you in this remedial class? You should be in my advanced class. You are intelligent, and a gifted writer. You need to challenge yourself."
Well I DIDN'T sign up for any ACT classes. Yet she gave me the courage, and self-awareness that I needed to do more writing. Through the years I still hear her voice encouraging me to do more, and try harder!
One of the lessons that I learned in her class that I still adore was a lesson about how Greek and Latin Roots were involved in the formation of our language. It was ever so exciting to me to learn that "man" referred to hands. In other words when we discussed MANUAL labor, we were referring to labor that you performed with the use of your hands.
Knowing even a few of these "roots" helps to unlock the mysteries of language meaning, even if you have no access to a dictionary. Thank you Mrs. Beatty for those gifts that you introduced me too.
Hyperbole is a tool of language that I engage. I don't see a nice blue sky, or a white cloud. I see an azure sky, blue as the water of the Caribbean. The clouds are puffy, fluffy, floating gently on a tender breeze. Hyperbole is an exaggerated expression of words. Nice is simply not nice enough for me. These are my routine words for nice, wondrous, grand, great, exceptional, splendid, etc. etc. etc.
Today, look at the world around you and see if you can explain it to yourself with new ideas. Instead of thinking the grass is green. Maybe you can say, "Green began in the center of each blade of grass. As spring progressed, and water nourished, the green moved outwards. Green expanded until the contagion of the color filled the lawn." Don't worry about grammar...don't worry about ridicule from others. Just open your mind and your ideas. Create newness in the world around you.
If you have access to a child, whether it be yours, a child you teach, a grandchild, or the neighbor's child, take them for a walk. Listen to their expressions about the world. Their curiosity about the world around them is precious. It can uplift and enlarge our spirits and help us to remember the importance that this life bears.
For those who are blessed with more mathematical intelligence, there is a science that converts words to numbers. My husband loved this class. Quantificational Symbolic Logic was the name of the class. He would come home and explain to me how to use these ideas to turn words into numbers. That was, unfortunately for me, a road that I could NOT travel. My brain simply refused to understand anything having to do with these ideas.
Isn't it marvelous to focus on the strengths of each and everyone of our brains? There are strengths in all our minds. The trick is to find those strengths and utilize them.
Well enough of words, and images. It's time for me to rest my mental faculties, and use my physical ones for awhile. Exercise, here I come! :)
Thursday, May 15, 2014
Fear/Faith?
As a baby I was diagnosed with severe allergy asthma...and a miserable immune system, almost non-existent.
Our church group became involved with our family needs. The Doctor had told Mama and Papa that they could NEVER lay me down in a crib. He demonstrated, (OK LET GO OF THAT HELD BREATH), by wrapping me in a blanket. I tried to get out of that blanket but my oxygenation dipped to the level where my lips were turning blue.
He said, "You can NOT lay this infant down...at all. Somebody must hold her at all times!" So our church group came in and helped hold me around the clock. Mama and Papa still did not get much sleep worrying if I was going to quit breathing.
As I grew older, (which I'm convinced happened because my parents were so pro-active in getting help for me, AND because they just wrapped me up in love and prayer) I would often awaken in the night gasping for air. NOW you may understand why I had you hold your breath. That may have been hard for you as an adult. Try to envision a small child gasping, struggling to even get enough oxygen to speak, to be able to call for my parents to come and help me.
There were many nocturnal trips to the ER for oxygen. That was all they could do for asthma in the late 1950's. The medicos told Mama and Papa that small children will not let them place a face mask over their faces to get oxygen. Imagine their surprise when I grasped that mask with all my might and would NOT let go! (Again if you did the little exercise I suggested you may have a small understanding of what it's like to be oxygen starved).
On our journey the Doctor's explained to my parent's that it was critical for them to NEVER show fear. They explained that if I became fearful I could choke to death before they could receive medicinal assistance.
To this moment I wonder HOW? As a parent now myself I struggle with hiding MY fears to protect THEM from fear. If your child is in medical danger, how do you restrain showing your fears. Fear IS a natural defense mechanism. It exists to help us protect ourselves from harm.
Mama and Papa's ability to face the unknown with faith, faith that God was with them, faith that I would be protected from harm, and faith in a future where my health would become stable, blessed me. Their strength and faith over time became my own.
Can faith and fear co-exist in the same mind? Not really. When fear finds focus in your thoughts, it chases faith away.
Those years of struggle, were filled with powerful master classes on faith. I remember hearing my Mama say to me, (after a night of illness, and breathlessness), "Listen sweetie, the birdies are singing. We have made it through the night into a brand new day." I still rejoice when I hear the birdies sing their joy at a new day.
I remember my Papa (who was working a full-time job, and then volunteering as chaplain at Chino Men's Correctional Center), stumbling into my room dizzy with sleeplessness. He would pray and put his hands on my head. I learned that his faith, and my Mama's faith combined had vivid power. It was not just a benign concept of belief.
For those who do not align themselves with organized religion I would remind you that faith is a valid principle for every person on earth. Whether you are Taoist, Buddhist, or LDS, or whether you do not ascribe to any type of religious organization, you still need faith as a power to move through life. It takes faith to know that the sun will rise again, faith to face the death of a loved one. you need faith in your own potential and faith in the power of love amongst family and friends.
The Beatles sang, "All you need is love." I disagree to an extent. Love IS powerful. Still it takes faith to believe in an untried relationship. It takes faith to feel love. You simply can not have love without faith. Today in your minds you can change the Beatle's powerful lyric, "All You Need is Faith." That is what I'll sing today!
Monday, May 12, 2014
Fibromyalgia - ALL IN YOUR HEAD?
I have heard about every sort of homeopathic, alleopathic, naturopathic "cure" for it. One woman said that taking baths with Epsom salts 15 minutes a day for two weeks would cure Fibromyalgia. It did help with the generalized overall pain, but it did NOT cure the overall symptoms and causes of the disease.
I have lived with Fibromyalgia since 1991. I received a double diagnosis. I was 34 and I was diagnosed with Breast Cancer, AND Fibromyaliga. Two lumpectomies, and 25 radiation treatments, and I have been in remission from Breast Cancer for 22 years plus. I am ever so grateful that my Breast Cancer has been in remission for all this time.
I wish that my Fibromyalgia would go into remission and stay there! One of the first things that I learned about Fibromyalgia is that there is no cure. Once you have this disease, you will battle with it for the rest of your life.
I am still very grateful for one of my sister-in laws who sent me a wonderful resource book shortly after my diagnosis. She, unfortunately, was diagnosed with this disease before me. Bright, and studious she had done research to find this wonderful book written by two medical doctor's who both have Fibromyalgia. I would love to share it with you...but that was over two decades ago, and I don't know where that book is any more. (I could probably find it if I was given a week to look).
Even better than having the book was the knowledge that I didn't just have to give up living, and let this disease be in charge of me. I have done years worth of research. Some of the things that I initially learned about Fibromyalgia have later shown to be false.
Still there are even pain specialists who do not understand this disease, what triggers it, if there are hereditary factors involved, do exercise and diet play a role, etc. etc. I actually had a pain specialist tell me, (less than 5 years ago), that Fibromyalgia was a "Throw away diagnosis." That means that he didn't even think it was a valid condition. Forgive me but I secretly wished him a temporary case of Fibromyalgia. I would love to have seen his response when he had this "Throw Away" condition.
LIFE LESSONS THAT HAVE HELPED ME
1. YOU MUST be your own advocate. Many people are able to continue working while they manage their medical condition with the help of a combination of western medicine, exercise, and alternative medicine such as acupuncture, massage therapy, etc. If a well meaning clinician tells you that you aren't feeling what you know you ARE...don't believe them...believe yourself! Do research, find sources that can back up your needs.
2. Learn everything that you can about this condition. Knowledge IS power.
3. If you have done all in your power and your condition simply makes working impossible, apply for disability. I was told that nobody ever is accepted for disability with the diagnosis of Fibromyalgia. I received approval the very first time I applied. I was very clear in listing the details of my job description, and then one by one I listed the physical challenges that made those details impossible. If you are not able to wage the battle on your own for whatever reason, get an attorney. Legal clinics will often take a case pro bono (free) to give their students valuable experience.
4. Find a support group, or create your own. It's critical to have someone that you can call to say, "I feel really lousy!" Or someone that YOU can lift and help teach meaningful ways to face this disease. Being able to help others cope with Fibromyalgia helps me to affirm that there is a purpose for living with this syndrome. Being ill can make you feel extremely isolated. Don't quit living, just find new ways of doing things.
This sounds weird, and I am NOT a masochist, but this miserable condition has given me some powerful gifts. I have learned lots about empathy, and about what really matters in life. I have learned that it IS possible to find joy even when you may be stuck in bed for a while. I have also learned that "chair aerobics" are better than no movement at all. I have made many friends that I wouldn't have met otherwise. It's remarkable to me how many amazing people that I've met that do not let this disease define them, but neither are they ashamed that it IS a part of who they are.
If anyone reads my post and has questions or comments I would be very happy to answer them. Fibromyalgia is NOT curable, but it is also not terminal. You CAN have a positive quality of life, even when faced with a "New normal."
Releasing my Inner Hispanic
When we moved to Colton, California we bought a lovely home at the end of a culdesac. It was slightly run down, but my hard working parents soon had it looking lived in and loved. Each and every one of our neighbors was Hispanic.
My two best friends were identical twins named Rosemarie and Toni. I adored visiting them at their home. Their Madre was amazing! One moment she was embracing a child and giving them love in Espanol, the next she was correcting another child with her eyes flashing in a righteous call to repentance.
I adored the Spanish language. It seemed so much more musical, fluid to me than English. In English language we were taught to make each separate word crisp and clean. Diction and enunciation were an early part of our education. In Spanish the words blended together so that the speaker sounded like they were singing as much as speaking.
The adobe homes of my neighborhood were usually quite brightly colored. Next to each other the house colors were orange, red, purple, turquoise, yellow, every single amazing color. There was no attempt to make these homes blend in to the landscaping around them. The homes were bold in jeweled colors. My adoration for brilliant color began there.
I learned that California had many names that were Hispanic because the area used to belong to Mexico. In other words, if you immigrated into the area, the governmental body, the rules and regulations were all Mexican.
I have absolutely NO intention of discussing the controversial topic of illegal immigration in America. I wish this post to be about the humanitarian issues, not the political ones.
I was ever so sad when our family moved to Utah. So boring, everyone was the same skin color, same language, and same religion....dull...dull...dull I HATED the state with all that was in my six year old soul for an entire year, and then gradually I began to "Bloom where I was planted."
Decades later a lovely young woman from Tampico, Mexico married the man who lived across the street from us. She was lovely, enthusiastic, and ever so caring. I felt like that the very first time I met her I had discovered a friend. She was such a gift in my life.
She and I danced to Zumba one day. She told me laughingly that I had an inner Mexican! I loved the concept. What she meant by that was that I respond positively to music with a Latin beat. This is absolutely true. When I exercise with "Just Dance," I always score the best on Latin songs.
Cinco de Mayo always remind me of my gratitude to grow up mostly Hispanic. The food of Mexico fills not only my stomach, but my soul as well. The clothing are comfortable, and often colorful. Give me a Mariachi band any day to wear out the souls of my dancing shoes!
The countries that comprise those of the Hispanic group are not free from troubles. Mexico is so sadly in constant flux due to the drug cartels. Yet the people do their best to keep putting one foot in front of the other, doing their best to keep living a positive life in spite of the negativity they often face.
How about today? Do you feel your "Inner Mexican," calling you to dance, sing, or eat delicious food?
Is Mexico free of problems?
Tuesday, April 29, 2014
Valleys and Hilltops
My life could easily be compared to a hike in the mountains. As a young woman I ADORED hiking in the Utah mountains. The trails would be steep, uphill, labored breathing, and then suddenly, there was a valley, a lovely portion of the trail when I could trek along with no effort.
This analogy has always closely paralleled my life experience. I was born severely allergic to pretty much every substance and food in this world. I had no immune system to speak of. There were no antihistamines, very few antibiotics. We had frequent trips to good old Mount Baldy in Southern California. For whatever reason up there my breathing would clear, stabilize.
Sometimes when I was seriously oxygen starved our neighbors would let me use their oxygen. Oxygen was very expensive, and Mr. Bench needed it for his emphysema. Day or middle of the night they would willing, lovingly, offer me the breath of life.
Many times it was necessary to take me to the ER. The chronic inflammation of my lungs triggered many bronchial infections. A hospital was NOT a frightening place to me. It was a place of sanctuary. A place where I KNEW that they would give me oxygen. Sometimes, when I had a really bad infection they would put me in an oxygen tent. That was so soothing to me, the sound of the oxygen flowing, and my breathing leveling out. There was no tortured, aching attempts just to draw breath in and out of my tiny body.
My medical expenses kept us in constant medical debt. My
parents constantly juggled and struggled with finances, and living with a child always on the edge of a short slide into death.
Mama told me about one hospital visit. She was exhausted. She had spent several nights by my side, watching over me. I was never left alone in the hospital. My medical condition was so fragile that Mama was terrified that I would become oxygen starved and die before anyone noticed.
Sleep deprived, worried sick about me, and frazzled from constant medical debt Mama was reluctant as she went into the financial office to make payment arrangements. She simply could not imagine how they could squeeze one more payment plan into their harshly squeezed budget.
The clerk looked at my list of expenses and said, "Mrs. Cheney do you think you could afford to pay $10.00 a month?"
Mama, the lady who hates to show emotion in front of others broke down and cried. She simply was overwhelmed with the kindness and understanding that this clerk showed. $10.00 was worth a lot more in 1958 than it is now, but it still was do-able.
Most people would define this life experience as all hill, labored, tortured climbing. These experiences were absolutely challenging to me, to my family who are friends, and my friends who are family. It actually was a constant challenge and struggle. Was it ALL hard, miserable climbing? As an infant it was determined that any time I was put in a crib, or swaddled in a blanket tightly it would trigger an asthma attack. A few times I was so oxygen starved that my lips, and skin turned blue.
On one visit to my doctor he wrapped me tightly in a receiving blanket. Quickly I began to wheeze. The doctor quickly unwrapped me and said, "If you leave her in a crib or bassinet she could develop a serious asthma attack. She could become oxygen starved and die. Or it could cause serious brain damage for her to become oxygen starved. You need to hold her, all the time. She can never be laid down...ever!"
Mama and Papa were overwhelmed. How is it possible to live life while constantly holding a seriously ill baby? Our Church Family rallied around us with love. They set up a schedule for around the clock holding of one seriously ill baby, me.
Let's review our facts. I was desperately ill. My parents and I faced the almost certain knowledge that I would not live very long. Doctors from the Mayo clinic came to Los Angeles. Mama and Papa took me to be evaluated. After a thorough examination they told mama and papa, "Your daughter is the most seriously allergic/sensitive child that we've ever seen."
Some of the many doctor's that my parents took me to said, "She won't live very long. Don't get too attached, it will be too hard on you when she dies." As a mother I can attest that I simply would not be capable of caring 24/7 for a desperately ill child without becoming bonded, attached with love. This was most definitely true of my parents.
The good doctors gave Mama a list that was three pages long, single spaced, things that she MUST do to keep me alive. I have a brother 10 years older than I am, and a sister 6 years older than I am. This "list" of "must do" also impacted them as they were conscripted into assisting mama and papa.
It's all sounding dire and grim don't you think? Yet you would be wrong. The daily, nightly battle to keep me oxygenated and alive pulled us together as a family. It was necessary for us to work together to confront my health challenges.
I remember fond memories of my brother sitting in our recliner holding me when I was struggling to breath. I remember him reading to me when I was bed bound.
My sister was not too thrilled initially when I joined the family. She had the spotlight for six wonderful years and she was loathe to give it up to a sick small sister. In spite of that she held me, sang to me, and shared an awful version of chicken pox with me. This form turns the pox water blisters into boils....ever so painful....ever so hard to get rid of! Yet my beloved sis was loving towards me even when she herself was so sick and miserable.
One day I walked into the kitchen (I was about 3 at the time) and there on the table was the most amazing cake. It was a lamb, completely with fluffy wool. (The fluffy was flakes of coconut). A couple were there to bring the cake. I did not realize in that brief meet and greet experience that these two beloved people, "The St. Charles," would become my second Mom and Dad.
Mary...she had sons, no daughters. So she adopted me, and adopted our family. Mary had a secret life that she did NOT like to share. Her husband was a mean drunk. He seemed to be a charming, loving person when he was not drunk. Mary lived with Dr. Jekyll and Mr. Hyde for a very long time. In spite of these trials (I remember noticing once that she had lots of bruises all over her arms and legs, but didn't understand why) she blessed our lives with laughter, and endless quantities of love.
Mama made certain that my life was not ALL about doctors, ER's, shots, pills, and other medical scenarios. If I had an appointment that involved tough things like shots, blood tests, or other medical unpleasantries afterwards we went to a cafeteria for lunch, or window shopping, or to the park.
Papa would come home from work exhausted. He always made time for me. I would sit on his lap and comb his hair. We would have a snack together and he would tell me about his day.
I knew that our lives were HARD! We were not in denial, ignoring the hard, and living in a happy bubble. Aware of the hard we made the conscious choice, over, and over, to THRIVE, not merely to SURVIVE. Is that even possible? Is it possible that life can hold great joy, and cherished experiences in the middle of sorrow, and struggle?
To be clear, I'm not speaking about abnormal sorts of behavior like sadism, or masochism. It is NEVER healthy to learn to ENJOY either your own pain and sorrow or someone else's. That is NOT what I'm referring to.
I'm speaking of becoming aware and grateful for joy and blessing in the middle of rough and challenging. Blessings such as the friends that became family as they moved forward to serve us. Feelings of closeness as a family as we pulled together continued to bless our family unit when my health became less critical due to the discovery of modern medicines.
Sunday, April 27, 2014
Just Who Was Rescued...You Decide
My 8 year old and 11 year old daughters were with me. My husband was back in Oregon blessing the quiet of our home as he studied the law. Keeping two small children quiet in a humble cottage was simply impossible for any length of time. So off to Utah we went to see our beloved Mom and Grandma.
The first day we arrived I couldn't seem to tear my eyes away from the kitten on the porch. She could not stand. It seemed as though she might have a broken leg. When Mama would put food on the porch she would wait until all the other cats had eaten their fill, and then slowly, painfully, she would drag herself to what was left.
My daughters could not bear the sight of another creature suffering. My husband and I had been rescuing cats since we first married. The girls had seen that example. The oldest came to me, "Mama, we have our vacation money that we earned. We'll give you all of the money if you will take the kitten to the vet."
I tried to argue but it was halfhearted at best. How could I ignore this creature's need? So to the vet we went. The little feral kitten was so sick that she didn't even resist when we put her in a carrier to go to the vet.
The vet told us that she had been in a fight. Her right front leg had become abcessed (an infection that usually is limited to the site of the wound). In her case (for we found out that the little creature was a girl) the infection had spread to her entire system. She was deathly ill. Left untreated she would have soon died.
I asked my Mother permission to let me bring the kitten into the house. I knew that if I started to give her antibiotics, and she started to feel better, our feral kitten would be gone. She would relapse, die, and the entire attempt at rescue would be for nothing.
Mama did not believe in having indoor pets, but graciously she agreed to let the kitty stay in our bathroom. We gave the kitten food, water, and a kitty box. We gave her a soft blanket to sleep on, and Katty Kaliko (our oldest daughter named her) went from feral to family.
The first night I stumbled into the dark bathroom. I didn't even turn the light on, (I had grown up in that house). Sleep clumsy I stumbled into the bathroom cat existence completely forgotten. Suddenly I was greeted by the warmest, loveliest purring that I had ever heard. It was vibrant, and every couple of minutes a chirping was part of the purr.
Her grateful purring started when anyone walked into the bathroom. It was amazing to me. She was FERAL, meaning wild, and wanting NOTHING to do with humanity. How did she know that we were trying to save her life? Giving her bitter, gag awful antibiotics didn't seem to cause her a minute's resistance. She would suck the nasty stuff up like it was catnip. Even when her health improved she didn't become vicious. She never clawed us, or bit us.
When our vacation was done we were flying home to Portland. We could not afford to purchase a seat for our kitty. The airline policy was that if you took an animal in a carrier under the seat, you had to pay the price of a seat. I understand the rule. Imagine a nervous cat in a noisy airplane urinating or defecating. The plane would become nasty quickly.
As life would have it, my sister was traveling to the Oregon Coast the following weekend. So she brought Katty Kaliko to us. Quickly, the tiny kitten adapted to our life. Nyle, my husband, used a motorized scooter due to mobility issues. We would plop her in the basket, and off we would go for a walk (me), ride (Katty and Nyle).
Our youngest girl began using Katty as a doll. She dressed her in all the most elegant of doll clothes. Then she would put her in a stroller made for dollies and wheel her about the house, and up and down the street in front of our house. This continued for about a year. Finally one day Katty was finished with playing house. She fussed and growled when Sarah tried to dress her, and then she ran away. That was it...KATTY WAS DONE!
For sixteen years she faithfully acted as family confidant (she's excellent at keeping secrets), guru of chill, (nobody can teach you how to chill effectively better than a cat), and filled our home with unlimited quantities of her musical purr.
We were very surprised to learn that this little kitty with the magnificent purring capabilities meowed like the worst scratchy, rusty, door hinge you can imagine. She had the purr of Heaven and the meow from Hades!
When my husband died at 54 and I moved into an apartment, living alone for the first time in my life, our little kitty slept faithfully by my side. When I would awaken crying in the middle of the night, Katty would purr, and then lovingly wash my face with her teeny, tiny, tongue. (That felt like I was being sanded by the smallest sandpaper imaginable).
So imagine our families sorrow at learning that sixteen year old Katty has a tumor in her bladder. If she were a human they would remove the tumorous bladder and give her a urostomy. She would then have a teeny, tiny, little bag on her side where the urine would travel instead of her bladder. Katty is NOT a human, she's much nicer than many, many humans.
Modern science can clone animals...why don't they learn how to make our pets live longer instead!! At 16 our kitty is the equivalent of a 98 year old human. We all know that death is an inevitable part of life. That realization does not seem to make it easier when our loved ones both human and animal die.
Especially when we have to make the excruciating decision to euthanize our pet rather than letting their suffering go on, and on, and on.
TOMORROW! We are taking Katty to the Vet. They will do an ultrasound of her bladder and tell us exactly what they are able to visualize. Then it will be our turn to make a decision. At least I have the comfort of knowing that when it IS Katty's time to pass away, there will be my husband's loving arms waiting to welcome her. Yet oh how we will miss her!