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Showing posts with label Conditions and Diseases. Show all posts
Showing posts with label Conditions and Diseases. Show all posts

Friday, June 7, 2013

DreaMS

by Kristie Salerno Kent

Kristie knew she wanted to be a star, even when she was just a little girl. Her mother encouraged her ambitions, and would pay along with Kristie's calling herself Wonder Woman.

Kristie went to college, worked hard, and studied the performing arts with diligence and exuberance. As she finished her formal education, she noticed an inconsistent weakness and unsteady walking. She prided herself on being able to hide this difference form those who might have encouraged her to see a doctor.

When her job became more challenging, her boss understood, and the entire staff was amenable to finding less difficult ways for her to continue working.

Despite her advancing weakness, Kristie is able to truly say that although the word DREAMS ends in MS, her dreams didn't. It's a delightful memoir of a talented young lady who realized goals she once thought would have to be sset aside. It's a realization that she shares with everyone.

This is a book you won't find at Amazon; it can be downloaded for free at Kristie's website, which is funded in part by one of the pharmaceuticals that markets medication for people with multiple sclerosis. Kristie has done a great deal of good as an advocate for people with multiple sclerosis, and for the public in gaining an awareness of what this chronic condition changes in a person's life, and in the lives around someone with MS.

Here's the link to find her website and download the book for free:
Dreams, the ebook

And, here's the link to hear a podcast and see a book trailer for the author's work
http://msstationbookclub.com/dreams/ 


Related articles

Wednesday, September 19, 2012

Reviewing by Indy Authors

I've received another Five Star review of my book, Multiple Sclerosis an Enigma. This is written by a fellow author, Philip Nork. Here's what he wrote:

Sept. 19, 2012

I just finished MultipleSclerosis, an Enigma by Terry Crawford Palardy and am sitting at my desk in a fog. This heart-felt memoir of a person diagnosed with MS and her battle to live a “normal” life has me re-thinking my own life.

The courage displayed, along with the confusion as to why, was portrayed brilliantly. As I read it, I felt like I was sitting with the author at a table or on a front porch, sharing a beverage, as she told me her story.

There were times I laughed and cried while in the pages of this book. It also took me back to the days when my grandparents were in the same situation … a different disease, but the same situations.

The author says, “Water doesn't try to choose a direction ... it just follows the water before it, rushing over the same rocks that were submerged in high water and exposed in drought last year, and ten years ago, and maybe fifty years ago. Nature is content to follow its established route. Only when man intervenes does the direction of the water have to change, finding and following new paths. Sometimes, the stream is strong enough to return to its own, natural path, to the dismay of those who had built in its original path.”

I take this to mean that nobody knows what is in store for them in this thing we call life. We can try to change the course of events by medicine or other things that the “professionals” prescribe, but the best things we can do is accept what fate delivers and deal with it in our own special way.

This book can help those diagnosed with diseases they don’t understand by letting them know they’re not alone. But at the same time, it can help those who are healthy by letting them into the “secret” life others may be in.

I am so glad I read this book.
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Wednesday, July 4, 2012

Reputable Medical Websites

We have the internet at our fingertips. We have a medical condition that we know is a topic of some websites. Which sites do we choose? Which sites do we trust? And do we share with our doctors what we find online?

Today's internet users have to take ownership of their responsibility in assessing their travels through informational sites. This obligation remains whether one is seeking medical information, historical data, or current event coverage. Every website has a webmaster, an editor or program director who selects what will be uploaded to their page(s). All have their own agendas.There are plenty of search engines available to help you find a plethora of sites dealing with the topic you are researching: Bing, Google, Yahoo, and more. Innumerable data bases exist, and consumers must learn how to create a library of trust.

What are the keys to unlocking this treasure house of information? Begin with the url (the web address) and start at the end: most will end with .com, .org, .net, .gov, .edu here in the United States. Students are taught early to expect a .com site to be one sponsored by someone with an agenda, true or not, and .net as being like a co-op of users with a common interest. Urls with the suffix .org are most often linked with organizations like museums or other private institutions that have a reputation to maintain. Those with.gov are government sponsored which, depending on one's political outlook, may be a positive or a negative. And I learned soon enough as a teacher leading young adolescents through research projects online that the suffix .edu can be widely variable: .edu may mean it is hosted by a college publishing highly qualified, scholarly articles, or it may be a classroom site hosted by an elementary school and showcasing third grade student compositions with factual errors, neatly typed.

Medical issues are also addressed in a wide range of sites, and so may be no more reliable than one patient's personal journal, complete with singular bias, or a site filled with many chatters sharing their experiences and differing amongst each other in their replies. These sites may be both confusing and misleading to a person recently diagnosed just trying to 'get a handle' on the terminology and stages of a condition. Other websites may be owned and thus influenced by the large pharmaceutical companies producing and marketing specific solutions at great expense toward greater profits. Most medical information sites will responsibly remind readers to always check with their own doctors before accepting any advice or practices sponsored by the site.

I've learned a great deal about multiple sclerosis by reading at the National Institute of Health's site. I've also learned a lot of vocabulary, and gained second hand knowledge of many medications, at the NMSS message boards; I'm careful, though, to remind myself that they are personal stories that differ widely in viewpoint and in credibility.

Many doctors don't want to hear what you've learned at a website, reputable or not. They may be offended that in reading there you are less dependent on their professional knowledge. Yet they haven't the time to spend educating you about your condition at the level of detail that you may wish to be educated. Nor do they expect you to take medical courses at a university. This lack of professional information sharing within a doctor's tight schedule is what leads to patient frustration and reaching out to the internet for further information.

There are new sites appearing almost every day on every medical condition. Doctors haven't the time nor the interest in screening those sites for their patients. But they may have experience and knowledge of some sites that they believe are reputable, and it doesn't hurt to ask for a list that you can turn to when the doctor is not available.

The articles below are sites that I have found trustworthy, and have shared at my Facebook page for others looking for online resources. But I, too, must ask you to always check with your own medical team before choosing to follow a practice learned online.

And I'll remind you to go to my online store, or CreateSpace, or Smashwords, for a 50% discount on my book, Multiple Sclerosis, an Enigma. The links will be listed below the related articles.
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Sunday, May 13, 2012

Two More Five Star Reviews of Multiple Sclerosis an Enigma!

I'm happy to share two more reviews of my book; these are posted by readers at Smashwords.com. I want to acknowledge the assistance I had from Lucinda Campbell, a formatter who helps writers trying to meet the demands of Smashwords' premium style. Thank you, Lucinda. Your work was noted and appreciated in one of the following reviews!



Review by: Cat Mahoney on May 08, 2012 : star star star star star
This story is a honest look inside the world of a multiple sclerosis patient and woman trying to adjust to the MonSter.It is a good beginner's guide about plotting through the world of auto immune diseases.

She is honest and refreshing sharing her thoughts with the readers and tells the pros and cons of this vague disease. She has a strong support system and knows how to advocate to the physicians for the treatment all ill individuals deserved.

I like the upbeat positive attitude she is developing along her journey to transform her life from a Type A personality to a mellow lady with I do not care attitude and lives for each day.

She was brave enough to put in the Almighty's hands and release herself from Western medication and looking for an better approach to deal with the symptoms of loss muscle and cognitive capabilities.

She explains how it affects her and her husband and the adjustments they made to learn how to dance and not be furious with a personal storm some of us experience everyday.

Kudos for sharing your experiences and trials with others who might of just received the news "You have MS". This is a good book to start to comes to terms with the diagnosis of any autoimmune condition.
(reviewed within a month of purchase) 
 
Review by: Dana Gagnon on April 27, 2012 : star star star star star
In "MS: An Enigma," author Terry Palardy takes a reader along with her through the process of her MS diagnosis. This book, however, is not just for MS patients and their families, and it’s not just a list of medical tests. Readers will relate to many of the author’s experiences: childhood memories, combining work days with family and illness responsibilities, and caring for aging parents. Terry’s writing style is easy to follow, and the book is well-edited. I read the ebook edition, and was happy to find the pages well-formatted.

From the first chapter of the book, Terry is completely transparent with her readers, inviting them to share the emotion and frustration of the moment. She also shares the support she receives from her husband, Rick. The author does not separate descriptions of the illness and treatment from her daily life, and instead tells a story.

In this book, it’s clear that a diagnosis is not an event with a date that can be marked on the calendar, but rather a series of moments that begin early in life. Terry begins with moments in her childhood, and her writing is engaging as she creates in herself and her family complete characters for us to follow. Rather than simply list medical tests she was subjected to, she tells the story of how the test impacted her work day and how the constant interruptions affected her emotions. A careful description of her MRI experience will encourage anyone about to go through the same test.

Terry ends her story with a treatment experiment, and I hope she revises the book at some point to include her results. As the author is about the same age as my own mom, I was also looking for her experiences telling grown-up kids about her diagnosis and their reactions—but perhaps that is a story for them to write.

True to her academic roots, Terry ends the book with a section of reliable resources readers can turn to for information about multiple sclerosis, along with a list of online forums readers can go to for a community of encouragement.
(reviewed within a month of purchase)
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Thursday, April 19, 2012

I'm offering a coupon for a Discounted Download  (April 19 through 25th) Here's the information you'll need:
 Multiple Sclerosis, an Enigma http://www.smashwords.com/books/view/152332
Your coupon code for 50% off is TC78K

The print version remains discounted at Create Space: here is the information you'll need for that:
and enter this discount code at the checkout: VXXURQMH

Please consider writing a review at Smashwords, Amazon, Goodreads or in an email to me - I would love to post the reviews here for others to read.
 Today's writing prompt: What five people would you invite to a dinner party, and why?

I have to expect that my immediate family (husband, daughter and companion, son and companion, and grandchildren) would already be at the table with me. And, we always set an extra place. So here are my six guests:
In that case, I would like to invite Hillary Clinton (accompanied by her husband, Bill), in order to thank her for her service to our country as Secretary  of State in such difficult  years.  
I would next want to invite Barack Obama and his wife, and two daughters. I would want to thank them for the decision to stay at the White House at great personal expense, and for the benefit their presence gives to the rest of America.
These six people are currently in the position to advocate for improved health care for all Americans, and are currently receiving top notch medical care for themselves. Their futures are assured by earned pensions, and their safety is in good hands with the secret service protection no matter where they are in the world. 
All six of them have every reason to want to sit together at the same table; I would love to have my family break bread and have a chance to talk freely with each of them.
As a teacher, I would want to engage the Obama daughters in a conversation about how they are developing their own social and political beliefs, and how the move to Washington may have affected those. My own grandchildren would no doubt have some comments to share about attending public high school in a state widely impacted by the economic decline.  

As a retired teacher whose pension was affected by a premature retirement caused by a diagnosis and treatment that weakened me both physically and emotionally, I would want both Hillary and Barack to hear my limited economic rewards for thirty years of dedicated, 'highly qualified' teaching. I would want my son to have a chance to explain to them that though he works more than forty hours through multiple positions as a highly skilled public servant he is not yet entitled to quality health insurance. I would want my daughter to have an opportunity to ask both of them how they are working to improve the long-term economic planning to benefit her children. I would want my husband to have a chance to point out that his years of unpaid elder care have limited his maximum earnings towards pension and social security benefits. 

I would like to give our dinner guests a healthy menu, one which would feature vegetables, grains, clear filtered water and fresh fruit for dessert. I would like to host this dinner during cold winter weather, using our wood stove to supplement the oil furnace that we really cannot afford to turn higher. While the stove would keep them comfortable, they would see that carrying in the wood and maintaining the fire and the area surrounding the stove would take energy and attention, more so than simply turning a thermostat higher. 

I would ask our guests to bow their head for a moment of silence, meditation or prayer, just as I did with my colleagues for thirty years of public education. And I would teach them the Pledge of Allegiance in American Sign Language, explaining the meaning so evidently attached to each word's sign. And then, after dinner, I would offer a simple grace expressing thankfulness for the healthy food and good company shared. 

And I would wish them all well.
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Saturday, April 7, 2012

Day 7 Health Awareness Writing Prompt: Write about What You Want Today.

See, I thought I was on track for securing what I want. I had gone to college because my guidance counselor saw potential in me. When I finished the two-year school, I headed into the work force, and then married, and began a family, which is what I'd wanted to do. And I was happy.

The economy, though, was crashing in the early seventies; gas was rationed to every other day purchasing, inflation was eating up what I could earn in my part time position in a department store that was seeing a slow down of purchasing, and I realized that the time had come to go back to college while it was still affordable and get that teaching degree that would let me take a stable position. That was the new want - I wanted to teach, and to work in a secure environment that would not be harmed by fluctuations in the stock market and in supply and demand. There would always be a demand for teachers, for there would always be students. And when I finally signed the teaching contract six years later, I was happy.

Our family continued to grow, first with a second child, and then with grandchildren. It grew and grew with cousins, and we often got together to share holidays. But then it began to shrink: our parents were aging and declining, and needing more help from us. When they had finished passing through the sadness of decline, and were laid to rest, I looked at where we were then, saw that I had managed to keep my job and my professional reputation intact, and saw that we still had each other, and I was happy.

When my own symptoms took me to the doctors' offices, and I learned that they believed I had multiple sclerosis, I decided to comply with the diagnosis and take the prescribed injections each night, rather than taking the less frequent interferons which could have interrupted my attendance at school. I stuck with that prescription for four and a half years, following it downward into a depression so deep that I needed additional doctors and prescriptions to help me out of it. When I finally exited that, I decided to go with my inner belief and stop the injections, as their side effects of depression and anxiety had already cost me my teaching position. With the guidance of family and friends, I got through the paperwork and secured a pension; it was less than it would have been had I been able to stay longer, but what happened had happened, and was irreversible. I once again took stock: I realized I had completed thirty years in the classrooms, believed I had done some good, and still had a happy marriage and so I could be happy about that.

So, what do I want today? I'd like to say I know what I want, and that I have a plan. Truth be told, I am happy with the way things evolved thus far. It would be nice to earn a little extra money to compensate for the shortfall in my pension, but in time, we will have some of the larger bills paid off: bills I took on believing I would have two more years of full salary to pay for them, but I haven't, and so we're tightening out belt until they are paid. I don't want for much, ever. My father told me years ago, when he retired, that we didn't have much, but we had enough. It is my mantra now. There isn't much left to want; I have it all. Peace, love, a home, food to eat, and a family with which to share my stories. It is enough.
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Thursday, April 5, 2012

Two more reviews, and Day 5 of the WEGO health prompt


Day 5: The Ekphrasis Post. Go to flickr.com and write a post inspired by the image... link it to your health focus ... post the image.

I found at that page Rodin's sculpture, The Farewell. and wrote what elicited this initial reaction/post from me:

I can't post the image, as it is noted "All rights reserved."  But I have linked it here for you:
 "The Farewell" by Rodin (sculpture)


The eyes appear to be looking to the left, indicating a memory. The hands seem to be repressing a spoken thought, remembering something that ought not be shared. It's a pensive pose, and one suggesting some confusion. The word "enigma" is titling the post of this image.

I use the word enigma in my book title, Multiple Sclerosis an Enigma. It is a diagnosis that leaves one with only unknowns, and regrets for having sought an answer but having found only more questions. I was my doctor's enigma, a patient with a great deal of clinical evidence of the disease but showing few visible symptoms, and no acceptance of what science pronounced as true.

I've often written in my journal of the losses brought to me with this diagnosis. My reaction to the treatment prescribed was negative, prompting unwanted feelings of present and future losses, beginning with the loss of energy (fatigue), organizational skills (depression related) and anxiety (also depression related.) These losses led to the loss of my career (public school teacher) and my self image (30 years of successful teaching and collegiality.) My loss of my classroom created a void in my social contacts, loss of my partners and their wit and wisdom. I might well have, at times, taken the pose of Rodin's sculpture.

So, to turn this post from negative to positive, I will offer you other reactions: those of readers of my book!

**********************************************************************

There are two more reviews posted at Amazon for Multiple Sclerosis an Enigma:


From "Hot Toddy", an author whose own book shares the story of an MS diagnosis and path:

As avid readers know, the quality of books in the literary landscape has changed, but Multiple Sclerosis, an Enigma by Author Terry Crawford Palardy renews our appreciation for the written word. Author Palardy skillfully composed a well-written book and conveyed a story of compassion and resilience for her respected readers.

As a former teacher herself, Author Palardy did not ask the reader to overlook typos, or disregard poor sentence structure. Instead, the book is a well-formatted, fluid glimpse into the sometimes challenging, always endearing family she so eloquently introduces to us.

We learn who the self-described author and her family are, not by what she says, but by what they do. She doesn't tell us within quotes, that she and her spouse love their parents instead she tells us that they visited them daily, sacrificed their own finances, yet continue to smile when visited by a memory of their now dearly departed parents. Her wonderful husband doesn't spout I love you's either, rather the author tells us that he carries her purse without hesitation. In addition, she doesn't 'tell' us that she's a dedicated teacher, but she tells the willful doctor that she's happy to see him...anytime outside of school hours. We experience the compassion and commitment that exists within this family from the deeds so proficiently, yet humbly described.

Yes, there is talk of doctors, diseases, diets and medications, but it's framed so very well in a magnificent family photo.

Multiple Sclerosis, an Enigma, is a story of unconditional love shared over decades between generations of two families joined by a marriage strengthened from reverence to their marital vows.

It's a worthy investment for the serious reader who will immediately share this title when asked, "Have you read any good books lately?"


From Faye, another friend who shares the diagnosis of MS: 

Amazing! As I read along, I felt I was walking right beside her. In the story you could see that she was sticking to her recollections of symptoms throughout her life starting at an early age. And as I stated to her, I wonder also, were her family members misdiagnosed and had MS as well. We will never know. I felt comfortable walking beside Terry through her journey as I felt she had my heart in hand. I admired her for many years, but now is "special" to me! Quite brave to share such intimate details along this struggle we all experience in the Dragon of MS.

I recommend to all with MS and friends/family of someone suffering from MS!

Beautiful Read!
*********************************************************************
For the month of April, I've renewed the discount at CreateSpace for Multiple Sclerosis an Enigma. To receive 35% off the regular price, go to this link:
and enter this discount code at the checkout: VXXURQMH
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Tuesday, April 3, 2012


Day Three Prompt: If you had a superpower, what would it be and how would you use it?

Hmmm ... a superpower. What would it be? What would I most like to have as a superpower? And if I did use it, would it benefit some without causing harm to others?


For example, mind-reading ... if I could read others' minds, recognizing truth vs lies, courage vs bravado, honesty vs deception ... what would I do with that knowledge? Would I make my power known publicly, as Superman did? Or would I hide my power from others to protect myself from those seeking power over others? Would I be so distracted by others' thoughts that I would lose awareness of my own? Or would I use that knowledge to try to intercede in conflicts about to be, in the optimistic belief that I could make a difference if only I knew what motivated the disagreements ... or would that intervention serve only to make things worse?


Or would I want a superpower that was physically beneficial? If I suddenly became invincibly strong, able to lift great weights, or dive to great depths, or climb mountains tirelessly, or run endlessly at great speeds... perhaps that strength would have value a hundred years ago, but technology today can help people do all of that virtually, communally, through immediate technological communications, explorations, and demonstrations.


Could I have a superpower that would make a difference in the world's political arena? If I were able to implant positive, peaceful motivations in world leaders' minds leading to the recognition that, regardless of geographic location or economic situations we ought to act as one united human race, protecting our planet from further devastation, pollution, and consumption? Would my priorities, my beliefs, my values and my humility and altruistic desires serve to better the human race's situation? Could I make the best decisions?


If I had a superpower in my brain, a creative discovery of the best way to grow enough crops in even the worst climates and soils, to help every area on earth become self-sustaining and not dependent, would it allow various cultures to retain their identities without retaining their legacies of hardship, starvation and disease? Could such a brain recognize and share natural disease treatments? Would the population then increase exponentially across the globe? How many years would the natural resources last? Would a super-powered brain be able to plan for that?


I'm not a super-powered being. I'm a rational American, one who has followed the rules, set goals, and worked toward them, accomplishing much along the way and learning to accept the shortfalls that come with life. I think often of the word Namaste ... translated by Mother Teresa to "I see God in every human being" and by the people of Hindu belief as "I recognize and bow to the divine in you, as you do in me."  If we all could accept that premise of life, what a beautiful race we could be, with the superpower of respect.


Related articles
For the month of April, I've renewed the discount at CreateSpace for Multiple Sclerosis an Enigma. To receive 35% off the regular price, go to this link:
and enter this discount code at the checkout:VXXURQMH
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Sunday, April 1, 2012

HAWMC: Prompt 1. Time Capsule

WEGO, a health activist site, is sponsoring a month long challenge for leaders of health care. A quote from their blog reads:" If online health communities are an unruly high school, then Health Activists are its dedicated teachers – and WEGO Health is the teacher’s lounge. We help leaders to come together, to learn from each other, and to go back to their classrooms better at their craft."

Their first prompt of the month (no, this is not an April Fool's Day prompt) is to imagine what you might put into a health time capsule to be opened one hundred years from today. To read the full prompt, go to their website. Here is my response to this prompt: 
*******************************************************************************



"What do you think it is?"
"I don't know yet ... I can't get it open, it's covered in tape. It must have been up here in the rafters of this old barn for decades."
"Maybe it's a deed ... or a certificate of stock ... maybe it's something really valuable! Hurry up, open it!"
"Let me get one of those old tools we saw below, the one with the plastic handle and the flat end on the rod..."


The two brothers jumped down the short distance from the attic of their great-grandfather's barn. The tool they found was encrusted in rust and of no use to them, so they took they small packet into the house, where they placed it on the chopping block table. Reaching for a pair of zip scissors, they sliced off a sixteenth of an inch from one edge, and reached inside. The page inside was neatly creased and fell into two sections when unfolded.


"It's a letter, dated 2012, and signed by our great great great grandmother! Remember the story of the package of pages tied in ribbons that our great grandmother found about fifty years ago, the one that told all about life at the turn of the millennium? She gave it to the historical society when she found it. Dad told me that his grandmother wanted people to know what life was like for women born in the twentieth century. The pages were all about school-teaching, and learning to use primitive technology by typing on a keyboard ..."


"Read it! Why did she leave this note out in the barn? Why wasn't it with the rest of the pages? Is it really from her? Is it really a hundred years old? How old was she when she wrote it?"


"Give me a minute ... this one is hand-written, in the old style, with the loopy letters, and the ink is fading. Here's what I think it says:"

For whoever finds this note, please excuse the handwriting. My eyesight is worsening and the tremors in my hands are increasing, but I wanted to write this with liquid ink, so that it wouldn't fade away as print might. 

They tell me I have multiple sclerosis. I don't really believe them, for no one in my family, for generations past, has ever been labeled such. My father, his brother, and his mother all had Parkinson's Disease, and they showed the same symptoms that I have. But the doctors who diagnosed me disregard that history, for doctors in the past hadn't the modern technology of magnetic resonance imaging that we have. The clunking, banging, noisy scans reveal innumerable lesions on my brain, and on my spine. And the lumbar puncture, the long needle poked into my spinal cord, revealed bands in my spinal fluid, and that too is said to be an indicator of MS.

My first neurologist insisted on ruling everything else out, and said that I didn't have  PD because my arms did not jerk when he rotated my elbow. He prescribed what was thought to be important: a disease modifying drug that I would have to inject with a syringe every night, rotating among seven different areas of my body that had adequate layers of fat beneath the skin. Just the thought of that annoyed me, but he said that it would possibly delay the progression of multiple sclerosis' nerve degeneration by about a third. Small promise, I thought. But I went along with his prescription.

For almost five years I and my husband patiently, carefully, scheduled and rotated the injections, which always burned for twenty minutes afterward. But when I began to read about differences of opinion regarding the cause of this so-far incurable disease, and read that some disagreed that it was an immune disorder, seeing it rather as a metabolic disorder, I knew that my choice at diagnosis to change my eating style was a good decision, and was probably enough. No meat, no dairy products other than yogurt, nothing fried ... I'd lost a good deal of weight that first year, and hadn't had a relapse since diagnosis.

Oh, I'd had symptoms, but they were never called relapses. In my late fifties, a cataract could be causing the blurred vision. Weakness and vertigo in the hot humid summer was attributed to the weather, as it could be easily remedied by moving into a cooler space. Depression, anxiety and fear, loss of the ability to learn new things by reading, and forgetting my students' names were all attributed to life stresses. I had to leave my beloved classroom, and retire a few years earlier than planned. 

When that happened to me, I made my decision to discontinue the injections, and soon felt more like myself. My energy increased, my ability to read and write improved, and without the stress of the classroom and with antidepressant medication, I began to take an interest in life again. It was too late to save my teaching career, and my ability to remember new things was never going to return to what it had been when I could learn one hundred new student names and profiles every year, but I could begin a new career.

And that is why I'm writing today. I want to tell my children's children, and their grandchildren's grandchildren, to listen to their inner selves. I want to show them that taking care of their metabolism is important. I want them to know that eating a menu of vegetables, beans, seeds, and berries is a healthy choice. I want them to recognize that when a medication with slim promises doesn't help and causes more issues than existed before it is okay to tell a doctor 'No thank you.'

I suppose in a few more decades, or half a century ahead, or in the next century itself, all of this will seem primitive and ridiculous. When we look back at how illness was treated a century ago, in 1912, when people with Parkinson's Disease or assumed Multiple Sclerosis were told simply to go home and rest, limiting their strength by inactivity, we shake our heads and say they ought to have known better. 

Perhaps my descendents will look upon today's medical advancements as short-sighted. Maybe the nutritional aspects of disease symptoms will be looked at first in the next century. We look back today at the twentieth century's widespread use of pesticides and herbicides and shake our heads, realizing the damage they have caused to ourselves and to our gene pools. 

At any rate, whoever is reading this: you have the opportunity and responsibility to live a healthier lifestyle. We began to make  forward steps at the beginning of this twenty-first century. We recognized the faults of the earlier generations, and did our best to avoid the known carcinogens in our environments and in our lifestyle choices. 

Know that I love you, and want the best for you. It is up to you to seek it out.
Terry Crawford Palardy

PS: I asked my husband to tuck this note into the rafters of the barn because, as anyone alive today knows, the barns are often kept in better shape than the houses, for it is the barns that allow a space to earn a living. 


"Wow. It really is her note. She could be standing right here, talking to us."
"What are we going to do with this? Give it to the historical society? They can add it to the database and store it away with her other writings."
" I guess so. I don't know, it seems like something we ought to share with someone ... but who?"

The boys left the packet on the table,  planning to show it to their dad, later.
 ******************************************************************************

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Thursday, March 29, 2012

More Reviews for Multiple Sclerosis, an Enigma


I'm happy to post  more positive reviews of Multiple Sclerosis, an Enigma.  MSStation.org will be promoting the book during the month of April, and more reviews may follow.

Carmen Ambrosio, author of Life Continues, has written: 

"Bookended by the challenging generational demands of growing children and seriously ill elderly parents, dedicated educator Terry Crawford Palardy put everyone else's needs before her own for years--even as she experienced perplexing neurological symptoms.

Fluid dialogue and vivid descriptions reveal the author's protracted, diagnostic odyssey. Readers share alongside Terry the physical and emotional toll of getting to and through physician consultations, diagnostic procedures, tests, and treatments. The escalating frustration, confusion, and fear she feels when she interacts with certain medical, pharmaceutical, and insurance company staffers may be familiar to others who have a chronic illness or their caregivers.

Finally, Terry connects with doctors she trusts. A once elusive MS diagnosis becomes definitive. Throughout her ordeal, Terry resolves to preserve her dignity. She is bolstered both by her religious faith and by her husband's consistently calm, reassuring presence. His devotion to her is the embodiment of unconditional love. Despite losses and lingering unanswered questions, Terry remains true to her conviction to decide treatment options for herself.

When I finished the last chapter, I applauded Terry's determination to deal with multiple sclerosis on her own terms. It was a rousing ovation I hoped somehow she could hear."


And Faye Manos Quinn, another person experiencing multiple sclerosis, has written:

"Amazing! As I read along, I felt I was walking right beside her. In the story you could see that she was sticking to her recollections of symptoms throughout her life starting at an early age. And as I stated to her, I wonder also, were her family members misdiagnosed and had MS as well. We will never know. I felt comfortable walking beside Terry through her journey as I felt she had my heart in hand. I admired her for many years, but now is "special" to me! Quite brave to share such intimate details along this struggle we all experience in the Dragon of MS.

I recommend to all with MS and friends/family of someone suffering from MS!

Beautiful Read!"


Lauren DuBois, in France, posted this review of the book on Amazon.com:


"Terry's memoir is a story of courage and hope. It's so well-written that I feel I know the author personally. She writes of her life which was interrupted with the diagnosis of multiple sclerosis - a debilitating disease.
It's important for anyone who is newly-diagnosed or for family members, caregivers, friends to read this novel and get a good understanding of how MS can shake up a person's life.
Kudos to Terry for writing and sharing her innermost thoughts on her disability."


A winner of the book's Giveaway at Goodreads, Shane, sent this review:


"I entered this contest for my aunt. It took her a while to read it because of her condition but she finally emailed me to tell me what she thought. She wanted me to thank the author for allowing me to win this and that although she is in really bad shape, she said it gives her hope. I believe that she is going to be trying some of the steps that Terry took and will run some by her doctor as well. And she said she is going to start a journal to occupy her mind. Tv is getting old she said. All those channels and nothing to watch. LOL Her words Not mine. Sorry it took so long Terry. And thanks for the book. It put a smile on my aunts face and gave her some hope."
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