Melissa Johnston Miles

Mom, author, nurse, teacher . . . reading the world around me

Dragon Con 2016

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I was fortunate enough to attend my first Dragon Con last weekend in Atlanta with my family. This was the 30th anniversary of the pop culture, fantasy, and sci-fi convention, and I was joined by more than 77,000 others on this adventure. According the the post- convention press release, “Fans came from around the world and all 50 states, with this year’s convention attracting people from as far away as Japan, New Zealand, and Fiji.” In other words, I was in good company.

What I knew about Dragon Con is that people engaged in cosplay–dressing up as their favorite characters from movies, comics, television programs, video games, and just about anything that reflects their interests. I knew this because I’ve assisted my young adult kids in making these costumes and/or purchasing items to make them look authentic. I vaguely knew that they held panels for people interested in writing because my daughter, who volunteered this year in media relations at the con, had told me about them last year.

What I didn’t know about Dragon Con could fill Lake Michigan. Here’s just a few facts that I found impressive.

  1. The con has it own awards/recognition program called Dragon Awards. These recognize the creators of science fiction and fantasy in books, comic books, games and filmed entertainment.
  2. The con raises money for charity. According to the press release, $98,000 was raised this year for its 2016 official charity, the Atlanta Center for Self Sufficiency, which helps put homeless individuals on a pathway to achieving a healthy independence.
  3. The con attracts famous actors, writers, producers, etc. There was some serious talent in that place. There are far too many to name, but a few of the individuals that I’ve watched in television during my lifetime were in attendance such as Alex Kingston, William Shatner, Gillian Anderson, and Jason Isaacs and Adam Baldwin. There was a pool of talent at the con that would appeal to people of all ages and interests.
  4. The sheer size of the con! I mentioned the numbers above, but nothing would prepare you for how many individuals (costumed or not) were crowded into a huge area of Atlanta. Event organizers added more than 215,000 square feet to the venues, including the AmericasMart Building 2. The con consumed meeting space in the Sheraton, Marriott Marquis, Westin, Hyatt and the AmericasMart buildings.
  5. The con is quite civic minded. In addition to the fundraising efforts, there was a blood drive held in which over 6,000 units of blood and blood products were donated to an Atlanta blood bank. Also, disability services were visible everywhere and provided assistance to individuals with special mobility/seating needs.
  6. The diversity of the people attracted by Dragon Con was one of my biggest surprises. There were people there who were less than half my age as well as people (almost!) twice my age. There were people there of every race, gender and socioeconomic level. Some costumes were Captain America shirts from Walmart and some looked professionally made to the cost of thousands. The attendees for the most part were gracious with posing for pictures, and seemingly unflustered by the long (and I mean long!) lines, wait times and sheer crowds you had to part to just move anywhere. I loved seeing families there with their kids, all in costume having a great time. 14317415_1242873745744756_2617542351912526429_n
  7. I’m saving the best for last. 🙂 I was stunned at the writing community that was in attendance. There were some terrific panels at the con on the writing craft as well as specific elements of publishing. Brandon Sanderson, who is probably best known for finishing Robert Jordan’s epic fantasy series, The Wheel of Time, was on a panel that I attended. I ran into him outside of one of the hotels and he was warm and gracious in answering a question and then chatting for several minutes. The authors who attended seemed very willing to interact and share insights with attendees. I was impressed with the breadth of options of panels to attend that focused on writing.

    My takeaway from Dragon Con 2016 is that there is truly something for everyone there. If you’ve ever read or watched anything related to science fiction or fantasy, if you’ve ever watched superhero movies or read comics, if you enjoy art or especially if you like people watching–this is the place to be during Labor Day weekend in Atlanta. 14195279_1059995960781223_8651517751153972000_o

     

    Have you been to Dragon Con or think you might be interested? If so, I’d love to hear your comments! For more information on Dragon Con 2017, please visit the website www.dragoncon.org for more information. You can also follow them on Facebook and Twitter.

 

Photo Credits: Sarah Maney

 

Picture Books that Get The Big Picture

As an author, a mom to a special needs son and a pediatric nurse, I am always on the lookout for books portray a realistic representation of the American demographic. We are not all “the same” and that is one of our country’s greatest strengths. One underrepresented group of kids that I’m particularly sensitive to are kids with ‘disabilities’ that make them look or act different from other kids. Here are some picture books for very young children that can begin to introduce characters with special needs in a positive light.

  1. Keeping Up With Roo by Sharlee GlennRoo cover

    I will admit that this book hits close to home. My older sister Mary Beth was always so excited to be an aunt. But each of her nieces and nephews, as they grew older, came to realize that she was different than other adults. This is what happens to the main character Gracie in this story when she starts school. When Gracie brings her friend Sarah home from school, she feels embarrassed about Roo’s behavior. Like all children who have a family member who is “different”, Gracie has to comes to to terms with her aunt’s differences and realize what is really important in life.

     

  2.  Susan Laughs by Jean Willis

    I love the fact that this picture book focuses on all of the things the main character images (1)Susan does that are exactly like every other kid in the world. It isn’t until the very last page of the book that the reader will discover that Susan is in a wheelchair. I took care of a beautiful, smart and sassy little girl who uses a wheelchair and I see her on every page. I highly recommend this book to parents of preschoolers. When you reach the end of the book, the illustration of Susan in her wheelchair provides the perfect teachable moment to discuss all of the similarities Susan has with your own child.

 

3. My Brother Sammy Is Special by Becky Edwards
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I love the way this book explores the complex sibling relationship that occurs when one of the sibling’s has special needs. Generally that sibling is parented differently, with a different set of rules and expectations. The author allows Sammy’s brother to express his resentment and frustration, but ultimately focuses on his love and concern for his brother. This book would be the perfect gift for any child with a special needs sibling.

4. Just Because by Rebecca Elliott

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What I love most about this book is that the younger brother Toby is too young to understand exactly why his big sister Clemmie can’t do the things that other kids can–but he doesn’t need to. In his innocent and accepting heart, he just loves her like she is. The author depicts the positive things these siblings can do together, even if it isn’t what most siblings can do. The writing is beautiful and the illustrations are enchanting. Children with siblings like Clemmie are going to be faced with many challenges as time goes on, but this book’s purpose isn’t to tackle the hard stuff. It’s to focus on the love and affection that is at the heart of the sibling relationship. And it does it beautifully.

5. A Friend Like Simon by Kate Gaynor51OijiofOVL._SX402_BO1,204,203,200_

This book doesn’t focus on the sibling relationship, but on the struggles kids on the autism spectrum have making friends at school. I love this book. I see so much of my own son in the character of Simon. This story is told from the perspective of a kid who is trying to be Simon’s friend at school. But it isn’t always easy. It takes more time and effort to get to know kids who are on the spectrum, but this book shows that it can often be well worth the effort. As a mom of a “Simon” myself, I appreciate the kids who make the effort.

6. The Invisible Boy by Trudy Ludwig

51j3FlqSA9LFor any parent of a quiet child that’s felt left out of the “popular group” at school, this book is a true find. The illustrations by Patrice Barton add to the impact of the words because Brian (the invisible boy) starts out gray and becomes more colorful as he begins to see himself as fitting in with someone–anyone. This book truly shows that it only takes ONE kind child to reach out to an “invisible kid” and make them feel a part of a class. Parents, I urge you to teach your children to be this one child. There are “Brians” out there in every classroom. I’ve taught elementary school, and I’ve witnessed the change one child can make.

 

This list is certainly not inclusive of all the excellent books out there. However, these 5 titles resonated with me in a special way. If you have other books to recommend, please comment and let me know about them. I’d love to hear from you!

**Please note that I am not the copyright holder for any of these books, and am using the cover images to aid in readers locating the books at their local stores or libraries. 

 

The Rest of the Story

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A few weeks ago, our pastor asked me to share a story or memory about my sister during her memorial service. I managed to pull myself together enough to share a story that took place at my grandfather’s funeral many years earlier. I’ve had people ask me about it, and share with me how much they enjoyed the story. So, in the words of Paul Harvey (who happened to be one of my grandfather’s favorites) here is “the rest of the story”.

September 12, 1981 was the day my childhood abruptly ended. It began as an almost idyllic Autumn Saturday. My mom had taken us to Stone Mountain Park for the Yellow Daisy Festival, and we had spent the morning browsing through rows of handmade crafts and funnel cakes.

When we got back to the house, my mom dropped us off the swim while she went grocery shopping. I was thirteen years old that day, but by the time the sun went down I felt about sixty. The sibling dynamic in my family had always been skewed because my older sister had been born two months early, leaving her with disabilities. I functioned as the oldest sibling, even though it was never acknowledged formally. On this fateful day, my sister Mary Beth had decided to stay inside while my younger brother and I swam. After about thirty minutes of enjoying our typical pool antics—cannon balls from the side, diving for rings, contests for holding one’s breath underwater, etc.—my sister appeared at the back door looking as if she’d seen a ghost.

“Some lady just called,” she announced in an unrecognizable tone, “and said that she’d ‘heard in passing’ that Grandpa died.” She looked as if she’d seen a ghost.

I swam to the side of the pool. “Grandpa Callaway?”

She swallowed hard, still pale and shell-shocked. “No. She said it was Grandpa Walter.” But this simply couldn’t be possible. My grandpa was a doctor who still saw patients every day. He was full of life. I’d spend the weekend before with them in the mountains and he’d been perfectly fine.

I was out of the pool and to the door within seconds. I didn’t even bother to completely dry off before rushing to the phone hanging on the wall of the kitchen. I punched in the numbers to my grandparent’s rambling old farmhouse in the mountains from memory. As the phone rang, I tried to think of a reason for calling. I surely couldn’t explain to Grandpa the real reason for my call.  But he didn’t answer the phone that day and neither did my grandmother. At that moment, I just knew. The woman on the phone had been right. With my mom gone, I had to become the adult and hold things together until she got home and could find out what had happened. Once you take on the role of adult, there’s no going back to the innocence of childhood. I discovered this on that day.

The funeral was held at the church my grandparents had attended for years-a white frame building constructed in the early 1900s. It was traditional in every sense of the word. The day of the funeral, the place was packed. People stood along the sides and the back of the sanctuary, and people even stretched out the doors into the churchyard. After all, Doc Walter had treated most everyone in the valley at one time or another, having been the only doctor around for miles. People came out in droves to pay their last respects to the Doc.

My sister, Mary Beth, taped her favorite television programs years before anyone had ever thought to make VCRs. Armed with a Kmart cassette tape recorder, my sister would record an hour long program—the first half on side one of the cassette tape, and the rest of the show on side two. Of course, this meant you couldn’t talk, cough, or clear your throat during the entire program without suffering her withering stare and flapping hands to silence you. But come hell or high water, those shows were going to be taped. Mary Beth also traveled everywhere with her trusty tape recorder. So it was no surprise to anyone who knew her that she had it clutched in her arms when we walked into the church for the funeral.

Mary Beth had decided that we needed to record the funeral-partly because my grandmother was too distraught to attend. This task was delegated to my father—a man who has the biggest heart and the best of intentions, but doesn’t handle stress all that well. He scurried around through the packed room and placed the Kmart recorder on the top of the organ. He asked the organist, who was rather elderly, if she would please be kind enough to push the “record” button and the “play” button down when the service began. She nodded her agreement as she pounded out the hymns that the family had requested be played.

Everything seemed to be going according to plan until the organist reached up and hit the “play” button only—just as the family had been seated. Mary Beth had placed the cassette in the recorder on the “B” side, which contained the second half of a Little House on the Prairie episode that she’d previously recorded. She must have really wanted to have a recording of Grandpa’s funeral pretty badly if she was willing to tape over that show—it was her absolute favorite.

When the blood curdling screaming started , no one else in the church knew what was happening. They simply looked around the church, bewildered by the terrified sounding young girl’s voice screaming, “Pa, help me! Help me Pa, I’m blind. I can’t see!”

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Photo credit NBC

But we knew! We knew the minute we heard the voice of Melissa Sue Anderson, who portrayed Mary Ingalls on the popular show—the organist had hit only play rather than both record and play simultaneously.

Try to imagine a quiet, simple, mountain funeral suddenly and most unexpectedly, filled with the loud screams of a panicked young woman. You could see people mouthing the word, “Pa”—attempting in vain to discover who this “Pa” person was. Surprised and startled looks spurred my mother to jab Dad in the ribs, and he promptly pushed and shoved his way as gently as possible through the people obstructing his path to the organ.

As unobtrusively as possible, he pushed the “off” button on the tape recorder and weaved his way back to the front row of the church—only to find his oldest daughter hyperventilating and flapping her hands wildly, and his wife fixing him with her penetrating gaze.

“You turned it off,” my mother informed Dad. “Now it isn’t recording the funeral at all.”

The look on his face was a mixture of bewilderment, incredulity and hostility. I could literally see the gears of his mind churning in circles as he realized that Mom expected him to find a way back through the throng of mourners to turn the recorder back on—the correct way this time, in order to spare any further outbursts from Mary Ingalls. But he got up and did just that. And now you know the rest of the story.

Leaving a Kid (and part of your heart) at College

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So, it’s that time of year again. My Facebook feed is filled with posts and pictures of my dear friends leaving their kids at college. So much goes into that big day as any parent knows. I’ve been there and done that twice and it wasn’t easy either time. And endless loop of thoughts played through my head each time. Did I teach her/him enough? Does she/he know what to do in an emergency? What if she/he gets homesick but doesn’t call home?

My son has Asperger’s and we had to leave him at Georgia Tech in Atlanta. It was huge, busy, loud, and so terribly far from me. His mom. No one else knew him like me. But who was I to deny him his shot at this dream to go to Georgia Tech? Has it been easy? Heck no! That first year almost killed us both. But tomorrow he begins his junior year and he is still a Yellow Jacket through and through.

Flashback to 1986. What do you know? My mom felt the same way. She shared with me this journal entry that she wrote the day I started college. She gave me permission to include it in my blog.

I left her today.

So brave. So full of determination. 

She’s waited so long for this day.

It has been so long coming and there has been so much pain along the way.

But now.

She stands perched on the brink of her future.

Eager, and just a little bit afraid.

She’s a college student at last.

I have to admit I got a bit choked up when I read my mom’s words written about me. She knew me much better than I gave her credit for.

Here’s to fresh starts and new beginnings. To every college student and college parent out there tonight, just know that you’re not alone. You’re in good company. Go out there and knock ’em dead kids!

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photo credit for gif image. Odyssey Online

 

Saying Goodbye to My Sister

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My sister was older than me, so there’s never been a time in my life when she hasn’t been there. Until this past week. I’ve had plenty of time to reflect on her life and I want to take a minute to share some insights about what it’s like to live with a disability that makes you feel marginalized and even invisible.

Mary Beth was born in 1964 two months ahead of schedule. There were no neonatal intensive care units back then, so they just tried to keep her warm. She survived, but it was obvious by the time she started school that she had residual effects of her premature birth. Over the years I have watched her be cheated, robbed, beaten and worse. Thankfully most people in the world aren’t completely horrible and wouldn’t dream of doing things like that to a person with a disability. But there are plenty of decent people out there who just “didn’t see her.” And those are the people who can truly make a difference in the life of someone like Mary Beth.

On this day of her memorial service, I want to ask you for a favor. When you come across a person like my sister, take an extra moment to talk to her. Ask her about her hobbies. Ask her what TV shows she watches or books she reads. Ask her what kind of music she likes to listen to. And when she answers, just listen. Lately I’ve been replaying my last encounters with my sister and grading myself on how much effort I put into including her in conversations. And I don’t always score very highly. I’ve been wondering what it would feel like to sit there and listen to people talk about their careers, travel, kids, and other adventures when you don’t have those things. I’m so thankful for those people who invested their time and energy into her life.

On thing we can likely all agree on is that the world needs more kindness these days. This is one easy way to start spreading it around to those who need it the most.

Mary Beth, you were loved by so many people. You will be missed!

Pitch Wars Bio

For my regular blog subscribers, this post is for the Pitch Wars community.  But you might decide it’s worth the read anyway…. 😉

Hi Pitch Wars people, I’m Melissa and I would need about 20 lifetimes to experience everything that I want to! My bucket list could stretch from New York to California. Luckily my husband, kids and extended family just roll with it. My family is pretty cool and we were lucky enough to spend three years living in Europe where we traveled during basically every spare minute we had.

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I’ve had a hard time deciding on a career because I want to do so many different things, but I’ve narrowed it down to 3. My undergrad degree is in Nursing and I’ve been a pediatric nurse for about 25 years, but I also love to teach so I went ahead and got a Masters in Education and taught fourth grade for a few years. Finally, I write books– which is incredibly fun and has brought some fabulous people into my life. However, when it comes to how to find an agent and enter into the traditional publishing world, I feel about like this:

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My mom didn’t name me Grace for an excellent reason. I’m a complete klutz, and growing up in the south, I heard, “Bless your heart!” quite a bit. I’m pretty sure I have nine lives though because I’ve almost died about that many times–for real. I sledded under a barbed-wire fence, jumped from a thirty foot cliff into a small pool of water and missed all the rocks, was drug by the ankle under a horse running to the barn, spared by seconds from an inferno caused by a Sterno can flung into my Girl Scout tent at camp….I think you get the idea! It was probably Karma for teaching my kid brother how to fake unconsciousness to scare our teenage babysitters. My mom never could figure out why no one wanted to come back.

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The book I’m entering into Pitch Wars is my first MG book. I wrote it during NaNoWriMo this past November and have been revising/editing and getting feedback from CPs on it ever since. The title of the novel is SPARE PARTS, which comes from a cruel nickname that my MC is labeled with by a bully. Here’s a little snippet.

During her older sister’s ‎Quinceañera, eleven year old Esperanza (Espy) overhears a conversation that makes her wonder if her parents are keeping secrets from her. When her sister is diagnosed with an aggressive leukemia, Espy finally learns the truth: this is not the first time her sister Valerie has been sick. In fact, she had been conceived to save her sister’s life. Espy is filled with doubts, but knows she must be courageous and resourceful to help her family survive their latest crisis. She faces down judgmental critics of her parents’ decision, school and Internet bullies, her fears of medical procedures involving huge needles and plunges herself into doing whatever it takes to save Valerie’s life a second time. If she fails, she might lose her sister forever. 

My years of Pediatric ICU nursing combined with my years of teaching elementary school give me a unique background to write Espy’s story. If a mentor picks me, he or she should know that I have thick skin (think crocodile thick!) and am not afraid of criticism. In every job I seek out mentors, and writing is no different. I welcome the expertise! I’m a member of SCBWI and recently attended a writer’s intensive on writing middle grade literature. I entered a YA Contemporary manuscript last year during Pitch Wars and did get one request for a full. It was a great experience and I’m excited to get back into it this year with a shiny new manuscript.

There’s no point in telling you what I like to read, because I read basically everything. 🙂 If anyone took the time to read this entire post..THANK YOU!! 🙂 I’ll include you in my will. You might want to read some other cool bios too! Click HERE to do that.

Follow me on Twitter: @MelissaJMiles

 

 

Please don’t think discrimination doesn’t exist just because you don’t see it

In many ways, getting older is about as appealing as extensive dental work without Novocaine. However, there is one aspect of approaching fifty that I’m grateful for, and that is the increased realization that my view of the world is largely limited to my own experiences. I see the world through my personal lenses, and the world reacts to me by what it sees: forty-something, middle class, educated, white, etc. How do I change the narrow way in which I view the world? It’s actually pretty simple, and yet so many people refuse to do it. Just listen to the people who face discrimination every single day and allow yourself a glimpse into their lives. Why is this so hard for people? Because when we aren’t the object of discrimination, it’s easy not to see it as a problem. The knee-jerk reaction is to either get defensive, or else just deny the existence of the issue entirely.

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Old Navy (Photo from Twitter)

This morning, The Today Show had a segment on a Tweet from Old Navy that featured a beautiful family. Apparently there are some outraged Twitter users who are refusing to go into Old Navy stores again because they chose to feature this couple. I was honestly surprised that this image would cause any kind of uproar. But it illustrates the point that I made above. My husband and I are from the same racial background. I’m sure if we weren’t, or if one of our young adult children decided to marry someone of a different race, we would all be acutely aware of the fact that people living among us in 2016 still react this strongly to the issue on interracial marriage. Even though it still saddens me (because I just can’t understand how this family is hurting anyone in any way), at least seeing this blurb on TV educates me to what interracial families deal with.

Our son has Asperger’s, which causes him to feel set apart from society in many ways. Imagine him at the age of twelve (as if middle school isn’t hard enough) being told by his church pastor that he couldn’t participate in the confirmation class being offered because she thought, “he wasn’t ready.” There was another middle school aged child in the class, but he wasn’t allowed. We pleaded with the church pastor on two separate occasions to allow him to be a part of the class, explaining how excluded he felt. But this woman, with all of her lofty ideals about inclusion, didn’t see any problem. To her it was evidently completely acceptable to exclude him. As a parent, this was heartbreaking and we no longer attend this church. But until the world makes an effort to understand what it is like not to process sensory information normally, to be unable to determine a person’s meaning from a facial expression or their body language, this type of discrimination will keep going on.

Also within the past week, I read a blog by a mom whose son is in a wheelchair. It was heartbreaking to think of her little boy stuck in his chair watching the other kids run and play. Even though I’m a pediatric nurse and I’ve taken care of children in wheelchairs, I had never put myself in the position of one of these precious children or their parents. I found a blog with images of a playground in Australia that has the great swing featured in the image below. My favorite part was a sign mounted at the entrance that said, “Access for All.” Whether we have a child in our lives with this need or not, we should all be aware of the problem and support these types of play areas. One amazing little girl I’ve taken care of in the past was excluded from almost every preschool in the area because her “disability” made her a liability. Until she is old enough to enter the public school system, her parents are at the mercy of private programs and how far they will stretch themselves to give her a place to participate in a school environment.

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Sir James Mitchell Park in Perth, Australia

I’ll apologize in advance if this blog sounded preachy. It isn’t meant to be. But, I’d love to see everyone make a conscious effort to view life through the lens of others who are different than us. We’ve all heard that expression about walking a mile in someone else’s moccasins. It’s taken from a poem by Mary T. Lathrap. I’ll end this post with her words in the opening lines.

Pray, don’t find fault with the man that limps,
Or stumbles along the road.
Unless you have worn the moccasins he wears,
Or stumbled beneath the same load.

The Litmus Test

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I think anyone who has a disabled sibling understands the concept of the litmus test. It generally begins in elementary school when our classmates discover that our sibling is “different” than most kids. Which classmates pass the litmus test and become friends that we are willing to risk inviting over? The ones who don’t make fun of our sibling. We instinctively select friends who show acceptance to our sibling.

This continues well into adolescence when we are teenagers and enter the dating scene. We see someone we think is cute, everything seems to be going along great, and then BOOM…it happens. He or she makes a joke or a rude comment about our sibling, or even someone with similar issues. All the wind instantly leaves our sails as we realize that we can never bring this person around our family. Honestly, we are better off without them, but sometimes it is hard to realize that as a hormone riddled teen with a crush.

When it is time to pick a spouse, it becomes even more tricky. Not only does that potential life partner have to be kind to our sibling, he/she must be willing to buy into the fact that one day there will be some additional responsibilities placed upon us as a couple to care for this sibling once our parents are no longer able to do it. This takes a special kind of person. Someone who loves us enough to sincerely understand the concept of “for better or for worse” and really means it.

I recently thought about couples that I’ve known over the years where one of the pair has a disabled sibling. The siblings have conditions ranging from Down Syndrome, Autism, severe cerebral palsy, and other developmental and/or physical delays. Each of these people have married truly loving and supportive spouses that have the patience and kindness to support them in the difficult road that often has to be followed. We come with a good deal of emotional baggage when we’ve been raised in a home where our sibling’s needs often took precedence over our own.

I’m grateful to have found my husband who passed the litmus test with flying colors and continues to do so every day. Thankfully there are people out there who do. But for those of us who’ve grown up with a special needs sibling, we’ve unfortunately seen plenty of people through the years who fail the litmus test miserably.

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Photo by Contributed Photo /Times Free Press

Anywhere Doors?

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Writing Prompt:

Pick Your Gadget-Your local electronics store has just started selling time machines, anywhere doors, and invisibility helmets. You can only afford one. Which of these do you buy, and why?

This prompt immediately reminded me of the last Harry Potter novel when Harry, Ron and Hermione are discussing the Deathly Hallows, and each one picks the hallow that they perceive to be “the obvious” choice only to realize that they’d each chosen a different one. And they had good reasons for the choice based on their own lifetime experiences, as well as their strengths and weaknesses.

I imagine the same will hold true for this writing prompt. Each one of us who respond will be bringing our own unique background and experiences into our choice regarding which gadget we would choose. For me, it took only a moment to weigh each option and decide on the one that I would choose. It would definitely be the “anywhere doors” over the other two choices. My choice has to do as much with why I’d love to have a set of these doors as it does with why I wouldn’t want to own the invisibility helmet or the time machine.

I’m sure that I’ve said, “I’d love to be a fly on the wall” as much as anyone else. It is so tempting to want to observe situations that we can’t due to being a solid hunk of visible flesh. 🙂 However, as much as I’d love to be able to disappear at times, it does have major privacy and ethical issues. Just as I don’t particularly want the NSA listening to my phone calls, I don’t want anyone, friend or foe, to have the ability to spy on me without my knowledge. It’s just creepy. So I have to rule out the helmet and hope that anyone who knows me does the same!

Next, the time machine. This one was tougher, because who hasn’t wanted to time travel? To this day I love a good time travel story. But inevitably, toying around with the complexities of time travel is going to lead to trouble. Your current self will see your past self and think it’s insane. Or you will tinker with one small thing that will have tremendous ramifications for every future generation to come. It makes great novel fodder, but I think I’ll stick to my current time no matter how screwed up the world seems at the moment!

So, that leaves us with those doors. Now that is the gadget that truly tempts me, and seems to have the lowest probability to land me in serious hot water. Let’s say that in order for these doors to work, someone on “the other end” also has to have a set. I have family and friends all over the world. Many of my dear friends that we met while living in Germany are now scattered to the four corners of the world–literally. Also, my cousins live everywhere from New Hampshire to Washington State and many states scattered in between. What keeps us from visiting each other? The $2,000 in airline tickets we’d have to purchase for the family to visit! To be honest, our family would have extended our tour and stayed in Germany longer if maintaining family relationships back in the states had been as easy as walking through some doors. For me, this is the best choice of the three gadgets.

This was a great prompt, but seriously…can someone get onto the invention of these doors ASAP? I’ve posted a prototype of them in the picture I chose to go with this post. I’ll be in line for your first working set!

Pick Your Gadget

Pre-K Fun

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For those readers who do not know, I am a registered nurse as well as a certified k-12 educator. My current job is attending school with my patient who requires nursing care during the school day. I arrive at his house about 15-20 minutes before the bus picks us up for school in the mornings. I stay with him during the day, and the ride the bus home with him in the afternoon. However I want his day to be as normal as possible, so instead of hovering over him, I also participate in the classroom activities.

Since the teacher and para-professional in the room have plenty of other duties, I use the nap time and sometimes center time to get creative. I’ve missed making bulletin boards and doors from my days of teaching elementary school so this is a win-win for both myself and the teachers. The latest effort was a joint one between myself and the para to create a “Pete the Cat” bulletin board to showcase the shoes collected in support of the “Walk for a Cure” to raise money for Type One Diabetes research.

I can’t wait until we can do something new with the door for Christmas!
Happy Thanksgiving everyone!

Note: I’ve updated some new pics throughout the year. I can’t believe the school year ends in two weeks!

Update (as of December 2016) I still attend school three days a week with my same wonderful little guy. He’s now in Kindergarten, but I wanted to take a chance to update this school year’s fun creations.

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