Showing posts with label Causes. Show all posts
Showing posts with label Causes. Show all posts

Wednesday, June 3, 2020

IWSG ~ Unity

“Unity to be real must stand the severest strain without breaking.” – Mahatma Gandhi
LINK
*Insecure Writer Support Group aka IWSG is a safe haven where writers share their fears and insecurities, hopes and dreams through a monthly post. Want to join in? Click on the image to find out more or to find other participating members.



I'd planned on giving some humorous answer in response to this month's optional question about a deep, dark writer secret I have, but my heart is too heavy to be funny, right now. I'm not going to go on and point out all the current wrongs in the world or preach on how we should handle them. I just want to offer you a silent nod of encouragement and comfort. 

Thinking of you all . . .

Thursday, April 23, 2020

It's O-Kay To #ReachOutToConnect

***I was inspired by Cheryl Rainfield, one of the sweetest and kindest authors I know, to share my thoughts and feelings about how the Covid-19 pandemic is affecting so many. Find Cheryl's post HERE.
***

Fear. Isolation. Loneliness.
Anxiety. Apprehension. Lack of motivation.
Sadness. Confusion. Depression.

You may have felt some or all of these emotions during your lifetime. You may be feeling then now since #socialdistancting and #selfconfinement began. Since your daily routine stopped abruptly, leaving you reeling with unknowns and what-ifs.

It feels like yesterday. 
And then like forever-ago.

That's normal. Understandable. It's O-kay.

YOU ARE NOT ALONE. 


It's hard. I totally get it. There is plenty to fear, plenty to feel isolated over, and plenty to box each one of us into the confinement of any of those emotions. But we can battle our way through this.

TOGETHER.
  • Give yourself permission to feel. Yes, feel whatever it is you're feeling. #NoShameInCoping
  • Take comfort in knowing there are many out there feeling as you do. Revisit old photos, journals, or newspaper clippings. Remember the good, and know more good will come your way. #ShieldYourMentalHealth
  • Reach out to others through email, a phone call, or even set up an online virtual meeting. #ReachOutToConnect 
Loneliness and the feeling of isolation (or even of claustrophobia) can hit anyone, even someone in a busy household. I'm married, a mother to four, owner of three cats and a GSD puppy, and a business owner with my husband - plus I write. We're still coming in virtual contact with customers and with each other, yet at times I feel alone. 

Solution:
A few of my good friends and I have been setting up a virtual call at least once a week since the pandemic began. I can't tell you how therapeutic these cyber chat sessions have been. We even share a drink together. Our kids, husbands, and even our dogs and cats steal the screen to make their own virtual appearance during our meetings.

SELF CARE
For most of us, life is one big ball of hurry up. We are running here and there, whether during work hours, family time, or adult time. So much so that we find it hard to slow down, let alone come to an almost complete standstill like during our current world pandemic. Here are some suggested activities to help with self care during this time. 
  • read a book
  • jot down your thoughts in a journal
  • take a walk with the dog
  • make yourself a special sweet treat
  • clean or rearrange rooms in your house
  • do a craft you've always wanted to do
  • knitting or sewing
  • learn calligraphy
  • exercise
  • play an instrument
  • virtually taking up yoga
  • watch an old movie you used to love
  • flip through old photographs
  • do a treasure hunt in your basement or attic
  • light candles
  • drink plenty of water
  • pray
Helpful Self-Care sites.
  1. OCD
  2. Stress
  3. Mayo Clinic
  4. Stay-At_Home
  5. Ways To Stay Healthy
*Some information previously share in my newsletter.*
  1. I also have a Young Adult Health (Mental & Physical) Page on my website with helpful links to mental health & illness, eating disorders, drug addition, healthy teen project, and more. Please feel free to utilize that page. FOUND HERE.

I'm hoping you connect with some of this and that you find it helpful. If you do, please share it with others you think could benefit from it. Want to share this information or have some helpful thoughts or links to share? Please use hashtags #NoShameInCoping, #ShieldYourMentalHealth, & #ReachOutToConnect.

My hope is that you believe you are not alone. We are much stronger when we stand together. 

Wishing you health, happiness, and peace . . . 


Sunday, September 1, 2019

IWSG ~ Book Lovers Unite for World Suicide Prevention Day & a Bookish Giveaway!

I'm foregoing this Insecure Writer's Support Group monthly question to share a cause that is dear to me and has, in the past, caused me some insecurity. I'd love it if you'd comment, sharing from your experiences or opinions, but I completely understand if you don't. A huge 'thank you' goes out to this month's co-hosts: Gwen Gardner, Doreen McGettigan, Tyrean Martinson, Chemist Ken, and Cathrina Constantiner! For more participants, go HERE.


The first annual Book Lover's Unite for World Suicide Prevention Day Tour will kick off on Sunday, September 1st and will culminate in a twelve-hour Facebook Live Event on World Suicide Prevention Day, September 10th.

The purpose of this event is to spread mental health awareness among the book community, eradicate the stigmas associated with mental health, share our individual journeys in an accepting community, discuss books that effectively represent mental health issues, and raise money for the International Association for Suicide Prevention.


Mental illness is often misunderstood. Some believe it's feeling sad, while others think there's just something wrong with that person. And the biggest misconception is that the person suffering with mental illness can just think happy thoughts or maybe try smiling to make it all okay. We have a lot to learn about true clinical mental illness, but smiling more is definitely not a cure.

Without further blah-blah from me, here's the exciting author line-up for the Book Lovers Unite for World Suicide Prevention Day Tour:

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                         LINK                                             LINK                                        YOU ARE HERE!
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My Spotlight On September 4th

I talk about mental illness and depression from personal experience, one I RARELY expose. 

When I was around twelve years old, my mother was diagnosed as a severe or manic depressant. (Today, I believe it would be classified as bi-polar. Please correct me if I'm wrong.) For the remainder of my school-aged years, my father spent most of his time refereeing for her, while I shielded my younger brother of four years from any of the backlash. Yelling, throwing things, crying, complaining, grabbing my arms, being dissonant, and over-dosing on sleep. That's what I remember her doing all those years.

Growing up was tough. She threatened suicide sometimes, which made coming home from school kind of scary. I never knew what I might find. My mother wasn't a bad person. Frankly, she had a huge heart, always wanting to help others or be involved. But so often, her emotions (or so we thought) prevented her from doing so. She was sick, but nobody back then looked at it that way. She was moody or ornery or high maintenance. Other than taking her to therapist after therapist - that always failed - she never got any other help, partly her own doing. Everything was everyone else's fault. I even agreed to go to therapy with her in my later teen years to help her, and all she ended up doing was telling the therapist how wrong I was about everything. I don't think that's what she meant. It's just her view of reality was so eschewed that she didn't know any other way to act or communicate. 

Her behavior, attitudes, and roller coaster emotions were so confusing to grow up with, which made being the oldest extra rough. My dad tried everything, but nothing could ever make her happy, make her well. And that unhappiness needed an outlet. I've never, EVER said this out loud (Well, other than to my husband), but most of that unhappiness landed on me - the oldest child, a girl who was expected to grow up so fast. I feel like this is me crapping on my mom, but people have to realize that a family member with a mental illness is a family with mental illness. It affects every single member.

It wasn't until my mid-thirties that I realized how emotionally damaged I really was, the reason I had a hard time to show love, the reason I was terrified to accept love. I know this must sound seriously messed up to some of you, but I've never put my feelings about all of this into words. I've tried. I've just never been strong enough. I think I am now.

I've had a young adult story about a patient of mental illness and the affects it has on a child growing up within that perfect storm stewing within me for over fifteen years. I know I must write it. I think I'm finally ready. I want children/families with members suffering from mental illness to know that they can advocate for their loved one . . . but they also should advocate for themselves. 

Something I wish someone would have told me when I was younger.

Thank you for listening. <3 

Please scroll to the bottom of this post to enter for your chance to WIN the special giveaway I'm offering up.
Facebook LIVE Event!

Join us for a twelve-hour Facebook LIVE event on September 10th - World Suicide Prevention Day!



Want to lend some support?



Enter my giveaway . . .

What you'll get:
  • a Book Lovers Unite for Suicide Prevention day T-shirt
  • a Meditation Sidekick Journal from Habit Nest
  • some book swag from my books
 I'll be keeping this giveaway open until the Live Facebook Event on September 10th, so the more you spread the word the more chances you'll have to win!



a Rafflecopter giveaway

This is a safe zone. If you'd like to share an experience or feelings about mental illness and/or suicide, you are more than welcomed to do so. Thank you for stopping by to visit the Alleyway!

Thursday, May 14, 2015

Childhood Apraxia of Speech

There are a multiple of valiant causes in today's world. I'm sure we've all been touched by at least one cause in some way. A family member or friend's struggle with a disease. Or maybe an acquaintance through social media drowning in medical debt. They are all worthy. 

Today, as I've done before, I'm sharing with you one cause that is near and dear to my mommy heart. 

Childhood Apraxia of Speech is a motor speech disorder, where the brain has difficulty sending messages to the parts of the body that are responsible for verbal communication. The child is fully aware of what he or she wants to say, but physically can't. As you can imagine, this poses loads of frustration for the child. 

I could go on and give you specifics about signs, false signs, and processes to proper diagnosis and treatments, but I won't. Instead, I'll share with you a piece I wrote for Apraxia - KIDS/CASANA a few years back. For those who've read this piece before, feel free to skim to the end. It's be great if you'd tweet a message to help raise awareness! To the new and/or young parents out there, I hope you find comfort in my family's experience. Finding someone who understands your plight can make all the difference in your world.

As the mother of three young children, I figured I’d seen it all from ADHD, tonsillitis, surgeries, colds, and runny noses. I was wrong.

CJ was born on a crisp November day in 2003, two weeks earlier than expected, and with a true knot in his umbilical cord. He should not have survived.

Feeling tremendously blessed, we took CJ home and, for the next six months, went about the busy life of raising four children. The latter half of his first year was spent with picture books in his hands and puzzle pieces scattered on the floor. He was fanatical about pictures. So much so, that by twelve-months old he had mastered 60-piece puzzles with no aid at all, pointing out objects in the pictures. He figured out how to communicate his wants and needs. I used to joke, calling it our private language. He excelled in every area of growth, except for the normal sounds babies make.

His first birthday came and went, but did not take with it his inability to make sounds other than the grunts and groans we’d grown accustom to. With no improvement in articulating formidable sounds over the next months, I spoke to our pediatrician about my concerns. She set up an appointment for CJ, who was 22 months old at the time, to be evaluated by a speech therapist. Her trust in me as a parent would never be forgotten.

CJ was officially diagnosed with Apraxia of Speech.

As a family, we dedicated ourselves to learning sign language and used amazing DVDs to do so. Once CJ was given his “Picture” book, he could hand us little images of his wants and needs. It was then that I finally understood what he had been telling me all along.Hearing CJ’s diagnosis being described as a neurological disorder could have crippled me. Instead, I collected research and questioned his two therapists on ways I could help him at home in addition to his therapy regiment. I searched magazines, the internet, and any other source to find pictures of everything under the sun. 

Shrinking the images and laminating them into a deck of cards made it easy to take to any ice rink or field my older kids were playing at. We would use car rides as therapy by flipping pictures to CJ and encouraging him to form the sounds. My older children helped, too. Slowly we saw improvement.CJ had lots to say. He only needed help finding his voice.

My greatest joy was the first time I heard him say, “Mama.”

The next three years were spent in therapy, where CJ and his therapists developed a fond relationship, one that would unexpectedly follow him into elementary school. There, he entered special services for speech therapy. His original therapist took a job at the school and could keep an eye on CJ, one of her star little guys. We were so blessed.

But soon, it was evident that CJ had met and even surpassed the official state benchmarks to receive services any longer. It was then that an image of a chubby 22-month-old sitting at a lone table in his therapy room and swooning over the mini M&Ms, which had become his expected reward during speech, wafted across my mind. I knew how hard he had worked. I had educated myself enough about Apraxia to know that it could continue to affect him as his vocabulary and the demands on his system increased, especially around third and sixth grades. I could not let his hard work go to waste.

Through my advocacy, CJ was allowed to remain in speech therapy for the remainder of kindergarten, first grade, and the beginning of second grade. He is still in the second grade and was recently discharged from the program; however, I asked for a written agreement, stating that CJ will be allowed back into the program, with ease, if his speech skills backslide when entering third grade. Given that his original therapist is at the school, I am confident she, as his advocate, will insure CJ’s continued care.

The most important message I have through CJ’s story is parental advocacy. There is nothing wrong with standing up for your child’s well-being, as long as it is delivered in a positive manner. Parents can be their child’s voice, until he or she finds their own.

Every child deserves a voice.

For more information, feel free to visit ASHA or CASANA. Please copy and paste a tweet for us! Raising awareness can help in ways you'll never know, but that doesn't lessen the value. Thanks in advance. 

Childhood Apraxia of Speech Awareness Day!!! Help give kids a voice!   

What is Childhood Apraxia of Speech?    

Every child deserves a voice. Childhood Apraxia of Speech Awareness Day!!!   
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Thursday, February 12, 2015

Eating Disorders & Young Literature

Writers have power. We hold the ability to point out wrongs in the world and work out ways to make them right through our stories. Using good or positive efforts of a character can also bring real life to the forefront. Our interpretation of reality can influence opinions. We can motivate. But all scenarios we consider to include in our fiction come with responsibility. 

I have a soft spot for kidlit, as you already know. That's what I do. That's what I write. The offbeat, quirky, or aloof character with a special talent aka paranormal, naturalistic, or magical is what attracts my heart the most. 

This past summer I began searching the deepest parts of my passion for writing, why I love the creepy and strange over the contemporary or normal - whatever normal really means. I discovered that any characteristic with the spice of supernatural feels safer to me, like tapping into the emotional reality of a contemporary situation would be any different. #Snort ... But for some odd reason, my brain and heart saw it that way. 

T-Shirt Purchase Link Only 4 A Few More Days
That revelation moved me to a place inside myself that, I know now, had been waiting to be released for a long time. Though creating characters with otherworldly issues will always be a love of mine, I decided to take the life's journey of a character I'd had in my heart forever and give her her due. I spent the next three months mapping out a contemporary young adult story, fully outlining each and every chapter, and completing a full-length synopsis.

This story is real life. It's very dear and close to my heart. It's fiction, but some of its scenes have been inspired by my life as a teenager. And that's what leads me to my true purpose today: raising awareness for eating disorders. 

February is Eating Disorder Awareness Month. It's a plague of mind, body, and soul that can touch anyone at any age, but most prevalent among tweens, teens, and college students, who are still trying to discover who they are, who they are supposed to become, and where they fit into their world. For us writers that's middle grade, young adult, and new adult fiction. 

Last year, I provided links to sites where you can find out more about the truth behind eating disorders, how people use them to cope with life-out-of-control. You can find those HERE. But this year, I'll leave you with the blurb I created for that YA contemporary story I mentioned above that I'm currently writing.
Seventeen-year-old Carly Foster learned early in life to keep her emotions hidden. Weighed down by the instability of her mother’s severe depression, she exists behind a wall of ginger smiles and loyal school work, the ability to feel dulled and numb. Her only reprieve is dance, where the safety of rhythm and movement free her to feel.
Liam Blake moves into town in a raging storm of aloofness, yet stalked by the popular crowd like a celebrity. His ‘rich boy’ status is in total contrast with his disheveled leather jacket and grimy baseball cap. Carly finds him rude, always staring at her but never saying a word. Though strange, his attention awakens a longing in her heart, which frightens her. So when an offer to study dance through a prestigious program, she clenches on to her Liam distraction and chance to escape her family pain. But then her mother is diagnosed with a physically debilitating disease, forcing Carly to abandon her dreams. 
Crushed beneath the gravity of it all, Carly spirals, plummeting off a ledge of self-destructive anorexia and drug use that sets the stage for a dangerous night she may never recover from. And, for reasons Carlie is still unaware of, Liam is the only one able to catch her … if she’ll let him.
My hope is in sharing even a glimpse of my experience with eating disorders through fiction, I'll inspire at least one young person to discover that they are stronger than their problems.
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Wednesday, January 21, 2015

The United States Navy Lost My Father’s Military Records.

If you have care and respect for our US Veterans, then please read this!

My dad served our country through the United States Navy from 1963 – 1967, beginning in the Naval Reserves while still in school from November 1962 to June 1963. He was deployed to Vietnam twice and was stationed out of Tan Son Nhat Air Base, Saigon, Vietnam. He served his country humbly because 'that's just what we do.' Though his official service ended with his final honorable discharge in November of 1968, exiting the Navy with the ranking of AX2, Anti-Submarine Warfare Tech, he has silently continued in dedication to make this country a better place.

He has been an amazing husband and father, raising me and my brother while married to our mom for 46 years now. From his steadfast faith in God to caring for his ailing parents, his goodness has touched many. Like millions who've come before him and many who will come after, service like his is the backbone of our country. It consistently honors our founding fathers’ pledge to build a land of opportunity, bravery, equality, and justice, through selfless deed after deed. A US citizen, who’s lived his life from day to day in the shadows of politics and economics that so often shroud the true beauty of this great land. These people are our foundation. They are many.

As a child, I recall my father’s playfulness with my brother and me, yet his stern guidance to teach us right from wrong. This skill continued and was felt by many of our friends who knew him as their baseball or ice hockey coach. I'm sure some of you reading this recognize these same silent qualities in people you've known all your life - parent, friend, teacher, or neighbor. Someone who doesn't seek the limelight, but whose only goal is to live a good life and leave this country with a bit of light to flourish after they’re gone. 

Just over 26 years ago, our family was dealt a tough blow. My mother was diagnosed with multiple sclerosis to add to her existing battle with depression. As you can imagine, her MS diagnosis only compounded her highs and lows. She also has heart disease and other ailments that require a boatload of medications and hands-on care. Her bodily functions have slowly and painstakingly deteriorated over the years. It has been hard to watch her body constantly fail her to the point she’s been unable to hold her grandchildren. Her fight is one of heroism, but also degrading blows – blows which my father has always taken with her. He is her shield. But even the toughest shield ages and can’t keep up the same productivity. Many reading this can surely relate.

Always her faithful caregiver, my father has put her before himself in all and everything, just as he did all those years ago with our country. The Vietnam War could have taken his life. Thankfully, it did not. Instead, it spared him to return home and be a productive citizen. He has spent his life doing so until recently receiving his own diagnosis - cancer. The shield is developing cracks all his.

My brother and I now face the heartbreaking reality of setting up in-home care for our mom, while my father has surgery for the cancer and for his recovery. We both have four children and will do everything to care for her, but we can’t do it alone. I’m in awe that he’s been doing this alone all these years.

He is a proud man, so asking for help has been hard for him. But it got us thinking about his military service and if Veteran Affairs could be of any assistance. His initial reaction to the idea was that he’d given to his country without the expectation of anything in return and that there are thousands of vets coming home now in need of more care than he needs. (Yeah, my heart pounded a little harder after hearing him say that, too.) Finally, he agreed to let me take him to the VA to see if they could lessen his load of taking care of himself so he could still be available to care for our mom. But to our horror, we discovered the military records he was given upon his honorable discharge were incomplete. They lack the TDY orders proving his was ‘Boots on the Ground’ in Vietnam. Without that proof, the VA can’t offer him any help.

The Navy lost my father’s military service records. Seriously?

We petitioned the Military Achieves in Missouri in November, but have received no response. The only positive help we've been given is from Senator Susan Collins’ office in Maine, where my parents reside. However, a phone call from her office this morning shared with us some bad news. They have found nothing to prove his service as of yet. Again – Seriously? My father will not only be worried about his limited ability to care for my mother during his surgery and recovery, but he’ll also be worried about the expense and care he will need. His surgery is in less than two weeks.

This is a man who our country should be grateful to have as its citizen. And there are millions like him.

After receiving the news from the senator’s office, my father text me this: Makes me feel like I imaged serving, or it was a dream. I’m very disappointed. I can guarantee you his memories aren't his imagination, the atrocities he witnessed or the friends he lost. It’s all real. He could have died in Vietnam, not once but twice. If he had, would he now be a ghost? A never-had-been because the Navy can’t find his records, proof that he served?

This is heartbreaking. Obviously he is crushed, but not for the VA’s refusal to offer him the benefits he earned by serving in the armed services. He is devastated because it seems like he didn’t exit, as though his sacrifice didn't matter to anyone. I, for one, NEVER want a service person to feel this sort of abandonment. What about you? 
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Monday, October 20, 2014

Teenage Depression ~ Sometimes You Just Can't Smile & Where's Lenny Lee?

***I have two posts for today, so if you're here to celebrate a fantastic teen's birthday feel free to skip to the latter part of this post. If you're Lenny, QUICK! Scroll to the bottom.

List of Participants
I'm please to be part of this ingenious blogfest hosted by Stephen Tremp, Michael Di Gesu, Diane Wolfe, and Alex Cavanaugh. 

It's meant to bring awareness of disease prevention and early detection regarding medical conditions that may be averted or treated if caught in the early stages. Our desire is to motivate people to go in for early screening, and if a condition is caught early and treated, then our world just became a little better place to live. 

Here's my contribution.


Most everyone knows or has heard the name Robin Williams. He's been in countless films and comedy shows, igniting smiles and lightening hearts in millions over his professional career. He started making me laugh when I was in elementary school, while watching him during his stint as Mork for Ork on the television show Mork & Mindy. His sudden passing stunned many. But the hand he had in his own death was the real shocker. Bewilderment and sadness that a man with the capacity to give such joy to others yet somehow could not feel it himself spread rapidly. It also placed a spotlight on the mental disorder of Depression, how well some people can wear a fake outer skin, and how it affects loved ones of the sufferer.  

All of us can have a sense of being depressed ~ sadness, gloom, dejection. We all have crappy days. Our bodies are chemically engineered with sparks of electricity firing at all angles throughout every day. We are emotional beings, which plays a part in our genetic make up. Events and circumstances can flair our emotions and affect our chemistry. It happens to all of us. But it eventually wears off, after we've had time to reflect or maybe spend time with a friend. Clinical Depression is an entirely different animal. Sufferers can not just make themselves happy or change their outlook. It can be an emotional up and down daily battle. Tell her to just smile, as I've been told, will not work for them. 
 
By collective definition, Clinical Depression: a depression so severe as to be considered abnormal, either because of no obvious environmental causes, or because there action to unfortunate life circumstances is more intense or prolonged than would generally be expected. 
NOTE: I by no means am a physician or councilor, or an expert on depression. However, I've had personal experience dealing with the disorder, suffering from Post-Partem after my third baby (take that Tom Cruise) and taking care of a clinically diagnosed family member for years.
Saying that, my focus here is on our youth, particularly teenagers. I write for children and love seeing the world through their eyes. But their world is not always rose petals and lollipops. Many kids have real life issue to handle. My current young adult project ~ a teenage girl who cares for a severely depressed parent, what she has to sacrifice, what that does to her, and how she deals with it all ~ has lent me lots of research into depression and teenage depression. 

The teenage years are by far the most volatile emotionally. Everything is a tragedy, a calamity. In their minds, no one understand what they're going through. We all remember feeling like that at some teenage point.

These years are the inner battle of adolescent Meism slowly losing ground to the revelation that the world does not revolve around them. Of course, there are loads of variables attached here. Everyone is an individual, different situations, circumstances, environments, etc... Each handles those uniquely. 

Feeling down or 'bad' is real to any of us, but especially during the middle grade and high school years of self discovery. Where do I belong? Who am I? Who do I want to become? In today's world, there's a lot of stress on these kids to answer those questions.  

Yes, there is a difference between feeling down and feeling as though one has been sucked into a black hole. But do not take any sense of depression lightly. You and I do not know the true workings of another's inner mind and heart. Pay attention. A life could be at stake.

Here are a few of the more common warning signs that might give you pause to a teenager suffering from a form of depression:
  • Sleeping excessively
  • Sudden disinterest in food or compulsive overeating leading to weight loss or gain
  • Memory loss
  • Unusual irritability
  • Irrational and/or rebellious behavior - skipping classes, driving recklessly, forgetting regular obligations like babysitting or work 
  • A sense of hopelessness
  • Outwardly feeling sorry for self
  • School work suffering; drop of letter grades
  • Apathetic attitude toward what was normally important to them: grades, athletics, music, etc...
  • Begin dabbling in alcohol and/or drugs
  • Isolate self
  • Disinterest in friends
  • Talk of death/dying
  • Headaches, fatigue, other aches and pains.
  • Overdoing actions or obnoxious in public
  • A heredity edge - (a symptom you might not be aware of: family history of depression)
Here are sites, organizations, articles, and books with more information on teenage depression, how to help, and how to manage it. 

Beyond the Blues by Lisa M. Schab
Anxiety Workbook for Teens by Lisa M. Schab
Mindfulness for Teen Anxiety by Christopher Willard

Thank you for reading, and please take this post to heart. Depression can happen to anyone, even those least likely to fall victim. Don't be afraid to ask questions, be attentive. You're not nosy. You care. <3


original image credit
I first met Lenny Lee through the blogosphere, while reading a post written by the fabulous Candace G. Her admiration for this young eleven-year-old kid struck a cord inside my heart. I then followed Lenny's trail to my amazing writer pal Sharon Mayhew and discovered Lenny's courageous journey and battle with cancer. 
Most of you will remember Lenny for his blog Lenny's World and from his imfamous sunshine logo. 
Dear Lenny,

You are one of my heroes. Your resilience amazes me. The way you see the world through hope-filled eyes and recognize the glass as half-full comforts me. There really is a better tomorrow. Thank you for being a light in my life and in the lives of your blogging buddies. 
We HEART U!
Happy 15th Birthday!!!
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Wednesday, June 4, 2014

Today's Health Care System ~ JOKE

Normally, I chat about children's literature in one form or another. On occasion, I toss in a post about my trials through mommydom and wifyhood. There's even been a few that fetch to tickle your funny bone or inspire you.

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Once in a while I'll throw you a curve ball. 

Ready?

Welcome to a new meme created by me, for me, and about me. Honest, it's not as self-absorbed as it sounds. I have in issue, a gripe, I'd like to share with you. 

Normally, I keep inspirations here on a positive note. But this is a subject that has been gnawing at my sides for a while now and I'm wondering if some of you have similar thoughts and feelings on the subject.

Health care.

According to Dictionary.com, the term health care means: 
"The field concerned with the maintenance or restoration of the health of the body or mind."
Ever have an issue with your health insurance company? Of course you have. We all have. Like any oiled machine--note I refrained from using the word 'well'--parts wear and systems need updating. Understandable, right? 

Sure.

I mean absolutely no insult to anyone utilizing state or federal programs. We take care of our own, and I'm 100% good with that. What frustrates me is this: No matter how loyal you are to your insurance company, your doctors, or your hospitals, everyone is out for themselves. Period.

Approximately five years into our marriage, my husband was diagnosed with Sleep Apnea (AP-ne-ah). According to the Mayo Clinic, sleep apnea is a potentially serious sleep disorder in which breathing repeatedly stops and starts. You may have sleep apnea if you snore loudly and you feel tired even after a full night's sleep. There are two main types of sleep apnea - Obstructive sleep apnea (the more common form that occurs when throat muscles relax) and Central sleep apnea ( which occurs when your brain doesn't send proper signals to the muscles that control breathing).

Of course, there is a lot more to it, such as pauses in breathing ranging from a few seconds to as long as a minute. This obviously puts stress and strain on vital organs and affects the patient's waking hours as well. For the purpose of this article, I'll stop there. But you can check with sites such as National Heart, Lung, and Blood Institute or American Sleep Apnea Association for more information. 

My husband went under two separate sleep studies, which lead to a prescribed BiPAP machine (Bilevel Positive Airway Pressure). A CPAP machine (Continuous Positive Airway Pressure machine) can also be used in treatment. Let me reiterate the machine was prescribed by a doctor - a physician who specialized in sleep apnea. My hubby used the machine for a while. Then, like the stubborn man he can be, he tired of it. 

Fast-forward to about six months ago. His sleeping patterns and snoring had gotten so bad, neither of us had slept in months. He finally returned to the doctor for sleep apnea treatment. It had been so long since his last sleep study, he needed to undergo another one. Okay, whatever. Let's get this done so his body stops aging more quickly because of his lack of breathing/oxygen while sleeping. And, or more selfishly on my part, so we can sleep and function.

HOWEVER ... when his doctor submitted the necessary test to our insurance company they deny her request for his testing. Why you ask? 

Because, in their opinion - His condition is not life-threatening enough and unless he shows other signs such as a stroke they are denying her request. The insurance company wants him to have a freaking STROKE before they'll let him have the test, which he's had twice in the past - both of which came back positive and his condition has only worsened over the years??? 

What is wrong with our health care system? We have been good citizens. We work hard. Raise our children well. Help others. Pay our bills - including the overpriced insurance company premiums. And this is what we get in return. Bah...

So I barked, which encouraged my husband to bark at his doctor and the insurance company. 
And guess what? 
He had the test.
And guess what?

Ding, ding, ding...it's sleep apnea, again. Go figure.

Obama's health care blah, blah, blah ... is suppose to bridge this gap for those of us Americans considered The Middle Class. (key in booming music)

Enough said. 
This is me. Frazzled. 
Utterly distressed.
Angry.
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I would very much appreciate you chiming in, here. Tell me what you think. Share your healthcare experiences (or nightmares). This inquiring writer wants to know.
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