When my eldest two children where young, I had a spray bottle of water. I put in a couple drops of food coloring and told the kids it was "magic monster spray". I would get rid of the monsters under the bed, in then closet or just the ones they heard.
It always worked.
Except with Keargan. He insisted the magic didn't work. That he could still hear the voices, and see here monsters. Most of his nights were spent in my room.
Apparently Magic Monster Spray doesn't help with the voices that rage inside his head due to his schizophrenia.
Paths From Pooks Soul
A blog following Keargan, aka "Pookie", as navigates a world with early onset pediatric schizophrenia.
Monday, September 23, 2019
Sunday, January 4, 2015
Dear Suicidal Teens (And How Dear You Are, Indeed)
Dear Suicidal Aspie Teen (Or Autistic Teen, Or Teen With PDD-NOS, Or ADHD Teen, Or OCD Teen, Or Bipolar Teen, or Depressed Teen, or Gay Teen, or Trans Teen, or Bullied Teen, or Abused Teen, or Whoever You May Be):
I can’t promise that you’ll wake up one morning and your world will be filled with endless sunshine (or moonlight, if that’s more your style) and happiness and prosperity and that you’ll never have another self-loathing or suicidal thought ever again. I can’t promise that you’ll ever be the most well-liked person in your school or workplace or that you’ll never be bullied or loathed or put-down ever again. I can’t promise that your world will be any less overwhelming, any less dizzying, or any less difficult to live in than it is now. I can’t promise that you’ll become the next Nobel Prize winner, the next Pulitzer-winning author, the next Grammy-winning musical artist, the next Oscar-winning actor or actress, the next gold-medal Olympian, or what-have-you. I wish all of these things for you, of course, but I’m no psychic; I haven’t a clue what your future holds.
But having dealt with suicidal urges since the age of twelve, I do know this: staying alive is worth it.
Now, some of you may be thinking, “Yeah, well, staying alive may be worth it for you, but you don’t know me, and you don’t know the hell I live in.” And, indeed, I do not. I don’t know if you having a loving family or supportive friends; I don’t know if you have family or friends at all. I don’t know what it’s like to have your exact sensory issues, your exact deficits, your exact anxieties and fears, your exact tics and stims, your exact pain, your exact loneliness, or your exact regrets. I don’t know if you’ll ever graduate high school or college, and I don’t know if you’ll ever get a job (fun fact: I turn 20 years old in a month, I’m a straight-A student who supposedly has “decent social skills,” and I have never been employed a day in my life. It’s not just you, I promise). I know what it’s like to have my PDD-NOS, to have my weakness and inadequacies and painful memories and regrets, but I don’t know what it’s like to have yourstruggles, and I’m not going to pretend that I do.
But I know what you do have: you have yourself, and that “you” deserves a chance—a chance to try, a chance to experience, and a chance to find beauty in this world. See, there’ll be moments that you’ll be glad that you stuck around to experience. I can’t promise that the moments will be particularly abundant, but I can promise you that they’re there. There’ll be a song that you never heard before that sends chills from the tip of your head to the core of your being. There’ll be a time when you help a stranger, perhaps even an act so small, so inconsequential to you that you have no idea it was an act of kindness at all, and that stranger will tell you that you made their day, and your heart will beat a little lighter for a little while. There’ll be that hobby that you get into, a hobby that you may or may not ever be “good” at, that will fill you with awe and, well, fun! There’ll be a way that the sunset scatters across the clouds, a way that the leaves tumble from the trees or that the wind sweeps across a field of tall grass, a way that the rain will dance along the rooftops, that will take your breath away, even if for only a second. There’ll be a contest that you enter that you swear that there’s no way you will win or place in…but you do, because you’re more incredible than the self-loathing thoughts in your head will ever let you believe. There’ll be battles that you win, discoveries that you make, and joys that you have that bring you happiness just when you thought that happiness could no longer exist.
And maybe it’s presumptuous of me to assume that the little moments of happiness are worth dealing with whatever pain you are dealing with. But consider this: maybe you’re somebody else’s small miracle, somebody else’s stranger, smile, random occurrence that makes their day or even their life, and maybe your dark thoughts are being conniving little jerks that aren’t letting you see this.
Sometimes, you mean a lot more to a person than you’ll ever be able to believe.
Throughout most of my adolescence, I swore that my father merely tolerated me because he had to and that his life would be indefinitely better without me in it. It wasn’t his choice for his wife to give birth to his child when he was 48 years old, when his other children were already grown up and getting on with their own lives and when retirement was just over the horizon. It wasn’t his choice for that child to be “developmentally delayed” and for that child to need speech therapy and special education. It wasn’t his choice for my mother, through no fault of her own, to be forcefully removed from our family picture when I was six. It wasn’t his choice to have a daughter who threw deafening tantrums in the middle of crowded supermarkets and for strangers to judge his parenting skills. It wasn’t his choice to have a teenager that bit and scratched herself, that would almost get them both killed with her inability to distinguish “No!” from “Go!” from the driver’s seat of her small car, that made him stay up late at night sobbing with worry. It wasn’t his choice to have a kid like me. I thought that there was no possible way that he could have trulyloved me—all I ever seemed to do was drain and irritate him, and he didn’t deserve the trouble I put him through.
And I told him this in a therapy session one day; I told him how sorry I was for ruining his life and how I wish that I could be a better daughter, one that didn’t make things so worrysome for him. He was absolutely flabbergasted; he swore that I was the best thing that ever happened to him. Many days, I highly doubt that this is at all true, but the way his eyes almost glistened with tears (note: this is a man who passes large kidney stones and attends family members’ funerals without even hinting at a tear) that day tells me that I must mean something to the guy. He said that I keep him young, that his later years would have been so much less colorful without me in it. Now, I’m sure that I age him much more than I refresh him, but maybe the goofy poetry that I write inside of hand-made cards serves as a Fountain of Youth running behind those wrinkled eyes. Also, I’m his personal tech support; I’m the one that taught him how to use an iPhone and how to set up a Facebook account. That has to count for something, right?
See, we humans aren’t too good at telling our fellow humans how much they mean to us. It may well be that where you look in the mirror and see a burden, an aggravation, a chronic screw-up, others see a joy, a blessing, a person worth having around and a person that makes their lives better simply by you being in it. When you see yourself as unlikable, you may wonder how anyone else could possibly like you, either—I, personally, tend to expect that everyone sees me as bothersome or annoying and am often very taken aback when someone admits any sort of fondness towards me. But you are likeable, and chances are that there’s at least somebody out there who has a fondness towards you and who would be sad if they could no longer experience your presence.
And I know that you can know and believe all of this and that it still won’t take the thoughts and feelings away. I still feel absolutely worthless and useless many days, and I still don’t particularly like myself as a person sometimes. Knowing all of this about the beauty of living and about how loved I really am doesn’t do much to keep the images of a knife cutting through my throat or my body dangling from a tree by a rope from popping up from time to time. It’s an on-going battle, one that you may have to fight every single day or even every single hours. It’s not at all a fair battle, it’s not at all an easy battle, and it surely isn’t a fun battle, but it’s a battle worth fighting, and it’s a battle that you’re more equipped to fight that you may ever feel that you are. And the good news is that there are so many people fighting this battle alongside you and that would be more than happy to help you recharge your ammo. There’s the National and Regional suicidal hotlines for your area (United States: 1-800-784-2433 ; U.K: 08457 90 90 90 ; here’s a pretty comprehensive list: http://www.reddit.com/r/SuicideWatch/wiki/hotlines), as well as several online chatrooms, such as https://www.imalive.org/. There’s the members of this Aspie Life group. There’s me, if that’s anything. There are so many people who want you to win this battle, who want you to live, who want you to experience happiness and success and all that life has to offer. There are reasons to keep fighting. I promise.
I can’t promise that you’ll wake up one morning and your world will be filled with endless sunshine (or moonlight, if that’s more your style) and happiness and prosperity and that you’ll never have another self-loathing or suicidal thought ever again. I can’t promise that you’ll ever be the most well-liked person in your school or workplace or that you’ll never be bullied or loathed or put-down ever again. I can’t promise that your world will be any less overwhelming, any less dizzying, or any less difficult to live in than it is now. I can’t promise that you’ll become the next Nobel Prize winner, the next Pulitzer-winning author, the next Grammy-winning musical artist, the next Oscar-winning actor or actress, the next gold-medal Olympian, or what-have-you. I wish all of these things for you, of course, but I’m no psychic; I haven’t a clue what your future holds.
But having dealt with suicidal urges since the age of twelve, I do know this: staying alive is worth it.
Now, some of you may be thinking, “Yeah, well, staying alive may be worth it for you, but you don’t know me, and you don’t know the hell I live in.” And, indeed, I do not. I don’t know if you having a loving family or supportive friends; I don’t know if you have family or friends at all. I don’t know what it’s like to have your exact sensory issues, your exact deficits, your exact anxieties and fears, your exact tics and stims, your exact pain, your exact loneliness, or your exact regrets. I don’t know if you’ll ever graduate high school or college, and I don’t know if you’ll ever get a job (fun fact: I turn 20 years old in a month, I’m a straight-A student who supposedly has “decent social skills,” and I have never been employed a day in my life. It’s not just you, I promise). I know what it’s like to have my PDD-NOS, to have my weakness and inadequacies and painful memories and regrets, but I don’t know what it’s like to have yourstruggles, and I’m not going to pretend that I do.
But I know what you do have: you have yourself, and that “you” deserves a chance—a chance to try, a chance to experience, and a chance to find beauty in this world. See, there’ll be moments that you’ll be glad that you stuck around to experience. I can’t promise that the moments will be particularly abundant, but I can promise you that they’re there. There’ll be a song that you never heard before that sends chills from the tip of your head to the core of your being. There’ll be a time when you help a stranger, perhaps even an act so small, so inconsequential to you that you have no idea it was an act of kindness at all, and that stranger will tell you that you made their day, and your heart will beat a little lighter for a little while. There’ll be that hobby that you get into, a hobby that you may or may not ever be “good” at, that will fill you with awe and, well, fun! There’ll be a way that the sunset scatters across the clouds, a way that the leaves tumble from the trees or that the wind sweeps across a field of tall grass, a way that the rain will dance along the rooftops, that will take your breath away, even if for only a second. There’ll be a contest that you enter that you swear that there’s no way you will win or place in…but you do, because you’re more incredible than the self-loathing thoughts in your head will ever let you believe. There’ll be battles that you win, discoveries that you make, and joys that you have that bring you happiness just when you thought that happiness could no longer exist.
And maybe it’s presumptuous of me to assume that the little moments of happiness are worth dealing with whatever pain you are dealing with. But consider this: maybe you’re somebody else’s small miracle, somebody else’s stranger, smile, random occurrence that makes their day or even their life, and maybe your dark thoughts are being conniving little jerks that aren’t letting you see this.
Sometimes, you mean a lot more to a person than you’ll ever be able to believe.
Throughout most of my adolescence, I swore that my father merely tolerated me because he had to and that his life would be indefinitely better without me in it. It wasn’t his choice for his wife to give birth to his child when he was 48 years old, when his other children were already grown up and getting on with their own lives and when retirement was just over the horizon. It wasn’t his choice for that child to be “developmentally delayed” and for that child to need speech therapy and special education. It wasn’t his choice for my mother, through no fault of her own, to be forcefully removed from our family picture when I was six. It wasn’t his choice to have a daughter who threw deafening tantrums in the middle of crowded supermarkets and for strangers to judge his parenting skills. It wasn’t his choice to have a teenager that bit and scratched herself, that would almost get them both killed with her inability to distinguish “No!” from “Go!” from the driver’s seat of her small car, that made him stay up late at night sobbing with worry. It wasn’t his choice to have a kid like me. I thought that there was no possible way that he could have trulyloved me—all I ever seemed to do was drain and irritate him, and he didn’t deserve the trouble I put him through.
And I told him this in a therapy session one day; I told him how sorry I was for ruining his life and how I wish that I could be a better daughter, one that didn’t make things so worrysome for him. He was absolutely flabbergasted; he swore that I was the best thing that ever happened to him. Many days, I highly doubt that this is at all true, but the way his eyes almost glistened with tears (note: this is a man who passes large kidney stones and attends family members’ funerals without even hinting at a tear) that day tells me that I must mean something to the guy. He said that I keep him young, that his later years would have been so much less colorful without me in it. Now, I’m sure that I age him much more than I refresh him, but maybe the goofy poetry that I write inside of hand-made cards serves as a Fountain of Youth running behind those wrinkled eyes. Also, I’m his personal tech support; I’m the one that taught him how to use an iPhone and how to set up a Facebook account. That has to count for something, right?
See, we humans aren’t too good at telling our fellow humans how much they mean to us. It may well be that where you look in the mirror and see a burden, an aggravation, a chronic screw-up, others see a joy, a blessing, a person worth having around and a person that makes their lives better simply by you being in it. When you see yourself as unlikable, you may wonder how anyone else could possibly like you, either—I, personally, tend to expect that everyone sees me as bothersome or annoying and am often very taken aback when someone admits any sort of fondness towards me. But you are likeable, and chances are that there’s at least somebody out there who has a fondness towards you and who would be sad if they could no longer experience your presence.
And I know that you can know and believe all of this and that it still won’t take the thoughts and feelings away. I still feel absolutely worthless and useless many days, and I still don’t particularly like myself as a person sometimes. Knowing all of this about the beauty of living and about how loved I really am doesn’t do much to keep the images of a knife cutting through my throat or my body dangling from a tree by a rope from popping up from time to time. It’s an on-going battle, one that you may have to fight every single day or even every single hours. It’s not at all a fair battle, it’s not at all an easy battle, and it surely isn’t a fun battle, but it’s a battle worth fighting, and it’s a battle that you’re more equipped to fight that you may ever feel that you are. And the good news is that there are so many people fighting this battle alongside you and that would be more than happy to help you recharge your ammo. There’s the National and Regional suicidal hotlines for your area (United States: 1-800-784-2433 ; U.K: 08457 90 90 90 ; here’s a pretty comprehensive list: http://www.reddit.com/r/SuicideWatch/wiki/hotlines), as well as several online chatrooms, such as https://www.imalive.org/. There’s the members of this Aspie Life group. There’s me, if that’s anything. There are so many people who want you to win this battle, who want you to live, who want you to experience happiness and success and all that life has to offer. There are reasons to keep fighting. I promise.
Because I know that I can’t promise that you’ll ever win a Nobel, a Pulitzer, a Grammy, an Oscar, or an Olympic gold medal, that you’ll ever have an abundance of friends or your dream career or a lover or even a degree, but, you know, you just might, and the only way to find out is to stick around and see.
Submitted January 4th, 2015
Author: Paula Gomez
Click blue link for: Email Contact
Tags
abused,
adhd,
asperger suicide,
asperger syndrome,
aspergers,
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ocd,
pdd-nos,
suicide,
teen suicide,
trans
Tuesday, February 26, 2013
Asperger Syndrome Suicide
You wake on a typical weekend morning.
Your children are sleeping as you prepare breakfast. At 8:30am you
head upstairs to check in on your 14 year old son. A child with a
huge heart and beautiful smile, your heart breaks for him often. He
has Asperger Syndrome and struggles with the feelings that come from
not being accepted by your peers. He is very intelligent, which only
seems to fuel the problem. Even adults look at him, and due to his
intelligence, expect more from him then he is capable of. How do you
explain to a child that only things logically, that the reason people
shun him, or get frustrated with him, is simply because he is
different? There is no logic in that, yet it is the simple truth,
unfair that it may be.
These thoughts bombard you as you
slowly walk up the stairs, wondering what today might be and how you
will be able to help your son. You open the door as you call softly
to him to wake up. With a start you realize that he isn't in bed. You
step back into the hallway, figuring he was in the bathroom, or maybe
downstairs somewhere. You call for him several times, with no answer.
You aren't really worried. It's not
uncommon for your son to get up and go walking. It helps to soothe
him, comfort him. You hope he grabbed something for breakfast before
he left. He's struggled so much lately, he doesn't understand why
people treat him the way they do. He doesn't understand why the world
is so different then what he can understand or relate to. As you head
back into the kitchen, you pray again the prayer you've said so many
times, “Please God, help me find a way to help my son”.
Your laptop is sitting on the table.
You slide it over to you and post a quick comment on Facebook, asking
anyone that may know where your son is to get in touch with you as
soon as possible.
The hours tick away and you still
haven't heard anything. Your son doesn't typically stay gone for this
long, and you are starting to worry. You've had this nagging feeling
that something isn't quite right ever since you discovered that he
wasn't in bed this morning. You've been shoving it aside, but now
your starting to wonder if you should pay more attention to it.
An associate from work calls you. It's
doubtful she's heard that you posted on Facebook asking for info on
your son's whereabouts, and you don't really want to get into it on
the phone with her. You answer the phone, and in a style true to her,
she starts babbling about traffic being backed up on the interstate.
She is talking over excitedly and very fast. To fast for your ever
growing stressed emotions to keep up with. You vaguely hear her tell
you how traffic was stopped because of a body found on the side of
the road, and how it'd been there for hours before anyone bothered to
call 911. You finally tell her that it's been a very bad morning for
you, and that you have to get off the phone.
No sooner have you hung up your phone
then panic seizes you. Didn't your friend from work just say that the
body found had red hair? Surely she'd have said it was a teenager or
a child if it was your son. But, she said it had been there for
hours....hours! Oh no, she also said it was near where you live! That
can't be your son. Oh please Dear God, don't let that be your son.
You quickly snatch the phone back up
and call the local police department. You explain that your son, your
son that has red hair, is missing. Your transferred to an officer,
who asks you a ton of questions and then quietly tells you that two
officers are already in route to your home to get a statement.
There is a knock at the door. You
didn't hear the car pull up over the phone conversation. You quickly
run to the door and yank it open. As your mind registers that it is
two police officers, you stand on your tip toes to look over their
shoulder, praying that your son is standing behind them.
The tallest of the two officers look at
you with pity and an emotion that can only be sadness as he asks you
to step inside and find a seat. This can't be happening! Something is
wrong! Where is your son? That body on the side of the interstate can
not be your son!
You listen to the officers' words, as
if you are detached and standing a few feet away from yourself. It
seems that your son is the “body” that your friend told you
about. The police haven't pieced it all together yet, but it appears
that your son jumped from the bridge that goes across the interstate
at around 3:30am. He was hit by a tractor trailer. Through the next
several hours, until sometime in the afternoon, traffic went on as
usual. People noticed what appeared to be a “large animal in a pile
of clothes” but didn't have time to report it. Others thought it
was a body, but again were to busy to pick up their cell phones and
call 911, much less turn around to check. It wasn't until afternoon
that someone stopped and called 911 to let them know that a body was
on the side of the interstate, where it had lain since
3:30am.....alone and hit by several vehicles. The clothing matches up
to your son's clothing. There isn't any reason to do an
identification, the police will use medical means to finalize that it
really is your son. The police are certain it is suicide.
The next day, our best friend stops by
to let you know that the story was in the newspaper again. This time
the article states that the body that held up traffic for hours was a
14 year old that committed suicide. At the very bottom of the
article, almost as an afterthought, it reads, “the teen was taking
regular medication for Asperger's Syndrome and autism”. You look at
her incredulously. Your son committed suicide due to the challenges,
and lack of treatment, he faced having Asperger Syndrome, and it was
only mentioned at the very bottom of the article as an afterthought?
A Sargent said that your son was taking medication for Asperger
Syndrome when there are no medications available to treat it, as if
it's something that requires a magic cure? Why wasn't it mentioned
that your son being treated like an outcast and different, not just
from his peers but from adults, impacted him daily? Why didn't the
article talk about how tons of parents around the country are finding
themselves without the resources or tools necessary to help their
children? Why didn't the article list the few available resources for
this area? Why didn't it reach out to other families going through
something similar, other families that every day fear their teen with
Asperger Syndrome might also commit suicide?
* * * * * * * * * * * * * * * * * * * *
* * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * *
I wish I could say that I just made up
this story. However, I am saddened beyond words to say that I didn't.
This happened here over the last few days. As a mother frantically
searched for her beloved 14 year old son, motorist to busy to call
911 were driving by his battered and tattered body.
A newspaper quoted Sgt. G.A. Barger of
the North Carolina State Patrol as stating that the child was taking
medication for his “Asperger Syndrome and Autism”. To date, there
are no medications available to treat Asperger Syndrome. There is no
cure for Autism, and many parents advocate that a cure isn't needed,
merely the perception of “typical” people to change.
People have already started to judge. A
mother states that she has a child with Asperger's and she doesn't
understand why the article mentions it at all as her son is “bright
and a joy to be around”. She wonders what Asperger Syndrome has to
do with his suicide, or any other news article that has mentioned it
recently. Another mentions medications and how they only “make
things worse”. Another poster states that anyone with Asperger
Syndrome wouldn't want that for the rest of their lives. Yet another
newspaper article states that the child “suffered with
Asperger Syndrome”.
There are so many things I want to say.
I want to scream that children with Asperger Syndrome wouldn't suffer
if it weren't for the judgements, criticizing, and mistreatment from
“typical” people. I want to scream that there is not a medication
for Asperger Syndrome. I want to scream that Dan Akroyd, Bill Gates,
Daryl Hannah, Satoshi Tajiri, James Durbin, Paula Hamilton, Peter
Howson, Clay Marzo, Les Murray and others all have Asperger Syndrome.
There are so many more, Al Gore, James Taylor, Bob Dylan, Robin
Williams, Andy Kaufman, Hans Asperger, isaac Asimove and more. Do
they seem to “suffer”, need “medication”, or need a cure? I
want to scream that popular belief feel that Abraham Lincoln, Bobby
Fischer, Benjamin Franklin, Marilyn Monroe, Henry Ford, Isaac Newton,
Jane Austen, Vincent Van Gogh, and Virginia Woolf all had Asperger
Syndrome. How can all these people be broken and need a “cure”?
How can all these people not want to live simply because of their
diagnosis?
I want to scream at the world that I am
the mother of the sweetest, kindest, most caring teenage son. I want
to scream how his intelligence level is through the roof, but how he
lacks an understanding of social concepts. I want to scream out how
he tries to engage his peers in conversation, but the “typical”
teens shun him simply because he is different and different isn't
“cool”. I want to scream at the world that different is not bad
or wrong.
Yet, instead I will stand here and
speak for the family that is to grief stricken to speak for
themselves. I will stand and say that my son has Asperger Syndrome
and that his life has been difficult. I will stand and speak out and
let others know that my son's life, and the life of other teens with
Asperger Syndrome, is difficult because others refuse to accept
different as being acceptable. I will stand and tell others that you
can not say you are scared of someone with Asperger Syndrome because
of what one child with Asperger Syndrome did months ago, but instead
you should stand up and help find a way for these children to have
available the resources they need to help them succeed.
I am the mother of a child with
Asperger Syndrome.
I am proud to be the mother of a child
with Asperger Syndrome.
I support ALL parents of children with
special needs.
I won't ever quit speaking up for my
children's needs.
Always remember, if you've met one
child with Autism, then you've met ONE child with Autism. No two
children on the Autistic spectrum are alike, no two children with
Asperger Syndrome are alike. One thing they all share though,
resources are not available to help them reach their full potential.
Nor do they experience the acceptance in society that they should.
Please, don't be one of the passive
people that sit by and judge and criticize. Stand up today and speak
out.
For resources regarding Autism Spectrum
Disorder, you can follow the links below:
Autism Speaks Social Network for on-line chats with other parents in similar situations. Some use it to pose a specific question and get feedback, while others utilize it as a support group.
Autism Speaks Tool Kits http://www.autismspeaks.org/family-services/tool-kits
Autism Speaks Family Services web link - http://www.autismspeaks.org/family-services
Other Resources:
http://www.yourlittleprofessor.com/friendship.html
http://www.yourlittleprofessor.com/teen.html
http://teenautism.com/category/puberty/
http://www.aspires-relationships.com/. It seems to have a wide variety of resources that may be helpful.
There is an excellent online support group called GRASP – The Global & Regional Asperger’s Syndrome Partnership. http://grasp.org/page/grasp-support-groups.
You can contact me at any time for questions, support, or information at pathsfrommysoul@gmail.com
Monday, March 5, 2012
Light it up Blue for Autism
"In celebration of World Autism Awareness Day on April 2, Autism Speaks will again seek to turn the world blue. Our third annual Light It Up Blue initiative is fully underway with over 350 buildings already committed to turning blue.
Among the landmarks that will be turning blue on April 2, 2012 are Rockefeller Center, Top of the Rock Observation Deck and Madison Square Garden in New York City, Hôtel de Ville in Paris, France, the famous Tokyo Tower in Japan and Canada’s CN Tower, the Sydney Opera House in Australia and Michigan’s Mackinac Bridge.
Visit our website to learn how to participate and check back in early March to LightItUpBlue.org to register your events and see a full list of participating buildings.
Last year we had over 2000 buildings and landmarks turn blue. With your help, in 2012 we will more than double that number!!" (taken from http://blog.autismspeaks.org/2012/02/22/liub-2012-kickoff/)
Lowes has blue bulbs available. Please stop by to get your blue bulbs and light up your own home to raise awareness for Autism. Thank you.
Tags
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april 2nd,
aspergers,
autism,
autism spectrum,
blue,
light it up blue
Tuesday, January 31, 2012
15 Years Later
It's odd the things you remember in life.
I was in the passenger seat of an old, green Ford pickup truck. We were in the drive-thru at Burger King and I was insisting there was no way that I could eat anything, not even a bite. Yet, it was argued that I was pregnant and I needed to keep my strength and my sugar up. A song came on the radio and as I listened to the lyrics I began to cry. Tonight, writing this, I remember what food I was given at Burger King. It was a bacon, egg, and cheese croissant. I remember what I was wearing....a black shirt with a gray striped dress over it. Yet, I can't remember that song.
We went to meet our group of friends before heading to the funeral home. I knew I wanted that song to be played at the funeral. Pam agreed, and it was played. Yet now, almost 15 years later, the name of the song won't come to mind.
Exactly 15 years ago today, a beautiful blonde haired, blue eyed, six year old boy was murdered. Six years old....the same age my son will turn in three weeks. My son, who has blonde hair and blue eyes. My son who climbs, jumps, flips, and does stunts proudly and with no fear.....just like Jordy did 15 years ago. My son who asked today if he could watch Power Rangers on Netflix. Power Rangers....a show he's never seen, but that was Jordan's favorite.
Jordan's picture sits on the cabinet in my dining room. The picture frame has a motherly angel down the side of it. An angel.......the first time I saw Jordan the sun was shining on his blond curls, and I thought to myself that he looked like an angel. Those words would come back to me when I heard of his death.
I should've known. There aren't many things that can make multiple grown men cry. Yet, all they told us was to go to the pay phone and call Dan. So, we did. I remember thinking it was someone in their family.....their aged father perhaps. But I remember when I heard the person beside me say, “No, it can't be. Are you sure?” Then they looked at me, and suddenly I knew....it wasn't his family member. This was someone I loved. Yet, when he said the name in that horrible sentence, I didn't want to believe. Yet, somehow I felt it......inside.....where the core of all you are exists.
I was sitting in the passenger seat of a car, a small gray Honda. I doubled over in physical pain. I felt it.....the pain....it was driving through me. I raised my head and looked out the windshield. It was dark out, late. Most people were sleeping. Yet, I noticed lights coming on. Inside lights, then porch lights. I looked around for the source of what was waking everyone. I could hear it.....it was this primal scream that sent chills down my spine. It scared me. Even after I was taken back to the house and calmed down, I still didn't realize the screams I heard were my own. That would come to me later.
Each year, right after my birthday, I start to think about Jordan. I think of him often through the year, but towards the end of November I remember. Jordan's birthday is towards the end of November. The holidays. I think of him all through Christmas. He used to lie on the living room floor with me to watch the patterns the lights made on the ceiling. Then, into January....this month. Today.....15 years.
The news reporters all called it, “the worst case of child abuse in North Carolina history”. None of us would argue that point. We saw, we knew, we had tried to save him.
She is behind bars. Two consecutive life sentences and up for parole 25 years after her conviction date. She still claims to be not guilty. Facing the feelings I felt towards her was almost the end of me. God showed me that hating someone, seeking revenge.....that only destroys the hater and not the hated. I almost lost myself learning that lesson.
There are lots of lessons to be learned. There are some lessons that should never have to be learned. Jordan's death taught us all lots of lessons that we didn't need to know. It taught us a level of grief that to date has yet to exist anywhere else in my life. I'm sure those that love Jordy would agree.
I know that no matter how I write the words that come next, that they won't be able to convey the emotion behind my pleas. I know that words can't show you the tears that I shed as I type this. I know that words can't make you feel that pain that is still there.....in the core of my very being. I know that words won't allow you to hear the longing in my voice when I beg you to please do this one thing for me....for Jordan.
If you suspect child abuse, please please please seek assistance. Do not just pick up the phone, call your local Child Protective Service office, make a report, hang up and walk away. FOLLOW UP!! Call back, make sure it was investigated, make sure that the workers know you aren't going to forget. Let your presence be made known. Is the child in school? Report it also to the school. Is the child in daycare? Report it there. Do you happen to know who the child's pediatrician is? Report it there. Is the child school age but not in school? Report it to the truancy officer. Call the police. Call and report it to everyone you can. Each person you report it to will have to document the report and possibly investigate the allegations themselves. By reporting it to multiple people, you just gave that child that many protectors! Keep a ledger documenting what you saw....dates, times, who was with the child, what the abuse/injury was and never let that original out of your site. Include the dates, times and names of the people you reported the abuse to. Make copies to give to those who need it, but hold on to that original so that you hold those dates and times. So that if something else happens to that child, there are people that can be called who are able to move quickly to help the child. So that if the child is not protected by those in charge of protecting children, then there is a record of who to hold accountable.
Between 2006-2010, the average child mortality rate due to homicide was 52. That's 52 children dying each year as a result of child abuse. Homicide. Murder.
You can make a difference. You can save a life. You can do it for any reason you want, or you can do it for Jordan. It doesn't matter to me at all what your reason is, just please.....if you suspect child abuse, do something about it.
Wednesday, January 25, 2012
Update
I apologize for being so slack and not keeping this blog updated more. We went through a spell where Keeg, Pook's older brother was battling his health condition again that kept me busy. Then we had a family crisis and after that, I ended up in the hospital for a week and am only just getting back to my self!
We've had quite a few things happen in the last several months. First, I'll start with the chiropractor visit. We discovered that the top vertebrea in Pook's neck is slanted at a sharp degree upwards. This could, in fact, be blocking signals from flowing from his brain to the rest of his body like they should! This is big news for us.
You see, Pook's head has always been super super sensitive to touch/pain. However, from the neck down, he feels no pain at all. He's cracked his elbow when ice skating, and never once said it hurt! He sliced through the tendon in his pinkie finger, and never complained of pain! His neurologist has long said that he felt there was something blocking the signals that are supposed to flow freely between his body and brain.
So, can chiropractic help? We're hopeful that it can. So far, we have noticed changes in Pook, but have no way of knowing what is due to chiropractic and what isn't!
Now, let's talk about phonics. Pook still doesn't comprehend that each letter makes a distinct sound, or that putting those sounds together forms words. However, he is recognizing sight words on his own. He knows and can spell many words now, some of which are off, on, out, and exit. He picks the words on his own and once he says he knows it, he's retaining the information!! As you may recall, Pook typically gains new information but then looses it. Hopefully that's not going to happen anymore!
Also, Pook's memory has always been above and beyond, but now he can articulate the things he remembers even better. He has told us about events that happened when he was as young as 6 months old! He remembers details so vividly that there is no mistake that these are his memories and not something he just overheard. It's pretty spectacular (isn't God amazing!).
Pook also is starting to understand different emotions and the part they play in his actions. This is a huge leap for him and it's making things so much easier! He's started to express guilt when he does something wrong, and genuinely feels remorse for his actions that hurt others. There is still a significant delay in the amount of time between the actual action and his emotions catching up to it, but we're getting there and that is a start.
At this moment, it really seems that his Auditory Processing Delay is causing most of his frustrations. He acts on impulse, and then will cry for long periods of time upset about his action. He tells me, "I not want to do that, my body made me" or say that his "brain made me". My heart breaks for him when this happens. He's starting to realize that his actions have a bearing on others, and to feel that he can't control these actions is very upsetting to him.
He's only just now started addressing the issues he has resulting from the recent division in our family. He doesn't speak about his emotions, except to say that he misses Daddy. The rest of the emotions he discusses he puts on the other person. For example, if he was mad at me, he'd say "Mommy has a mad face". It can get confusing at times, but we're figuring it out!
Overall, Pook is making progress each and every day and I am thrilled! He's come a long way. One of his medial specialist told me recently that he'd have never come this far if I hadn't started his therapies so young. I encourage each parent to challenge any specialist or insurance company that wants you to wait until your child is older for therapy. Early intervention makes such a big difference. Fight for your child, cause at the end of the day, you're the only one that will.
We've had quite a few things happen in the last several months. First, I'll start with the chiropractor visit. We discovered that the top vertebrea in Pook's neck is slanted at a sharp degree upwards. This could, in fact, be blocking signals from flowing from his brain to the rest of his body like they should! This is big news for us.
You see, Pook's head has always been super super sensitive to touch/pain. However, from the neck down, he feels no pain at all. He's cracked his elbow when ice skating, and never once said it hurt! He sliced through the tendon in his pinkie finger, and never complained of pain! His neurologist has long said that he felt there was something blocking the signals that are supposed to flow freely between his body and brain.
So, can chiropractic help? We're hopeful that it can. So far, we have noticed changes in Pook, but have no way of knowing what is due to chiropractic and what isn't!
Now, let's talk about phonics. Pook still doesn't comprehend that each letter makes a distinct sound, or that putting those sounds together forms words. However, he is recognizing sight words on his own. He knows and can spell many words now, some of which are off, on, out, and exit. He picks the words on his own and once he says he knows it, he's retaining the information!! As you may recall, Pook typically gains new information but then looses it. Hopefully that's not going to happen anymore!
Also, Pook's memory has always been above and beyond, but now he can articulate the things he remembers even better. He has told us about events that happened when he was as young as 6 months old! He remembers details so vividly that there is no mistake that these are his memories and not something he just overheard. It's pretty spectacular (isn't God amazing!).
Pook also is starting to understand different emotions and the part they play in his actions. This is a huge leap for him and it's making things so much easier! He's started to express guilt when he does something wrong, and genuinely feels remorse for his actions that hurt others. There is still a significant delay in the amount of time between the actual action and his emotions catching up to it, but we're getting there and that is a start.
At this moment, it really seems that his Auditory Processing Delay is causing most of his frustrations. He acts on impulse, and then will cry for long periods of time upset about his action. He tells me, "I not want to do that, my body made me" or say that his "brain made me". My heart breaks for him when this happens. He's starting to realize that his actions have a bearing on others, and to feel that he can't control these actions is very upsetting to him.
He's only just now started addressing the issues he has resulting from the recent division in our family. He doesn't speak about his emotions, except to say that he misses Daddy. The rest of the emotions he discusses he puts on the other person. For example, if he was mad at me, he'd say "Mommy has a mad face". It can get confusing at times, but we're figuring it out!
Overall, Pook is making progress each and every day and I am thrilled! He's come a long way. One of his medial specialist told me recently that he'd have never come this far if I hadn't started his therapies so young. I encourage each parent to challenge any specialist or insurance company that wants you to wait until your child is older for therapy. Early intervention makes such a big difference. Fight for your child, cause at the end of the day, you're the only one that will.
Friday, November 11, 2011
RIP Dixie
RIP Dixie
I don't know where to start. I guess
first I need to tell you how we met Dixie.
Our family purchased a home in a very
rural area in March of this year. It's perfect....the location is all
we've ever dreamed of. We live in the midst of a forest, with a lake
nearby. Neighbors are practically non-existent and we never hear
sounds of traffic. Our lullabies are crickets, frogs and wonderful,
peaceful, calming sounds of night.
About a week after we started moving
in, my friend James and I were traveling with my three children to go
pack up some more belongings at our former home. As we came near a
stop sign, we saw something run across the road. We weren't quite
sure what it was, but thought it might be a dog. Living in a rural
area means that it's not uncommon to see animals get dumped. We
stopped at the stop sign, opened the driver's door, and whistled. Up
came running Dixie. She was wagging her tail so much the whole back
half of her was swinging from side to side. Without hesitation she
climbed into the drivers door, under his legs, across the center
console and stretched herself across my 3 children's laps.
I'd always told my daughter, Keara,
that when we bought a home, we'd get a dog. She'd waited 11 years.
When we bought our home, she told Pookie (our 5 year old son with
Autism) about our deal. He had prayed each night for a week for God
to give us a dog. When Dixie stretched out across his and his
siblings laps, he smiled as big as he could and with wide eyed wonder
told me, “Mommy! God gave me a dog!” Whose to argue with a
child's faith?
A few weeks after Dixie came into our
lives, it was warm enough for the children to go swimming. You know
the time of year....when the air outside is warm, the sun is bringing
a warmth to your skin that you longed for all winter, and though no
adult would ever get into the still chilled water, the kids all think
it feels great! As us adults sat on the shore with Dixie, our
children frolicked and played in the lake. Our 11 year old daughter,
got caught in a current. Though she could paddle and keep herself in
the same spot, she couldn't get up to shore. As I was getting ready
to get in to bring her to shore, Dixie jumped in the water. To our
shock and surprise, Dixie swam out to Keara, placed her collar under
Keara's hand, and pulled her to shore. Everyone was shocked and
thrilled.
Dixie seemed to also have been trained
as a therapy dog. Though we have no knowledge of her background, she
always stayed beside Pookie when he was out of doors. She would run
beside him on his bike, and even get in front of him if she felt he
went to far. He would lie down, resting his head on her and she was
content. When he would start to have a meltdown, she would come and
push against him.....calming him tremendously. She was in tune with
him on a level I'd never seen between child and pet.
As time progressed, so did Pookie. His
neurologist wasn't surprised. He'd told me the best thing I could do
for him, and his older brother that has Asperger's, was to get them a
good dog. He said he'd seen children advance and make progress with a
dog that otherwise wouldn't have been accomplished.
A few months after God brought us
Dixie, our daughter was attacked by a much larger dog. Dixie was a
cocker spaniel mix. The other dog was a German Shepard/Lab mix.
Dixie, despite being a fourth of this other dogs size, defended Keara
with a vengeance. I have no doubts that she saved my daughter's life.
At one point, Dixie stuck her entire snout into the other dogs mouth!
Dixie became loved by all the children
that came to visit. Being that I have children on the autistic
spectrum and with health issues, I am often visited by other families
that have children with special needs. Dixie always connected with
them. She offered them a sense of security and calm in a world these
children often don't understand. Somehow, Dixie made everything OK.
When my 14 year old with Aspergers,
Keeg, decided to walk to my parent's house, it was almost dark. I
hadn't realized he had left, but merely thought he was taking a quite
time in “his spot” in the woods near our house. When my daughter
and I began to look for him, it was getting close to dark. He didn't
answer, he wasn't in “his spot”, and we began to worry he was
lost. We walked the drive, calling for him, but to no avail. I
noticed that Dixie wasn't in the house, or outside. I knew that if
Dixie wasn't coming to us when we started to call her, then one of
two things was happening. Either Keeg was hurt and Dixie wouldn't
leave his side, or they were out of ear shot. This realization
prompted me to run back to the house so I could call 911. By now it
was dark, and it was cold out. Keeg was only wearing shorts and flip
flops. He has health issues and is unusually weak. I was panicked. As
I started to call 911, a call came through from my parent's. I heard
Keeg's voice say, “Hey Mom!” He hadn't realized the gravity of
what he'd done. He said that when he started to leave our property
and Dixie followed, he tried to run her home, but she wouldn't leave
him. He said she stayed with him the entire time. At one point he
said he saw some dogs and was scared, but Dixie barked a few times
and that was that. He had gotten scared on the way, and cold, but
Dixie kept him centered and moving forward. He said without her, he'd
have probably hid in the woods on the side of the road. But, Dixie
was there with him and so he knew it would be OK.
After that incident, Dixie got it into
her head that she could leave our yard and try to get to my parents
where she'd walked with Keeg that night. Although she occasionally
wandered to our neighbors home (often invited by the renters that
stayed there), she never went the opposite direction unless leashed.
Yet, for some reason she figured that if she'd gotten to go that
night, she was going to continue. Finally, we quit letting her go out
with the boys unless she was leashed. She spent her time in the house
and at times would drive me insane. She was used to running and
jumping with Pookie, and since she didn't have that outlet outside,
decided to do it inside. Pook of course missed the same play, and
actively participated indoors.
A week ago tomorrow, my husband was
involved in a terrible accident. He suffered a skull fracture and an
epidural hematoma, pooling blood and air pockets that put pressure on
his brain. He was air lifted to a hospital to be seen by a
neurosurgeon. We are blessed to have a large network of prayer
warriors, all who spread the word quickly and got many people praying
for him. He was blessed, and quite surprisingly to all, came home
after only 1 night in ICU, and 1 night on a general floor. He is in
pain, and has memory loss. He also doesn't remember much of what
happens in a day. He has to stay supervised for the most part, as
often he doesn't remember his injuries.
While we were in the hospital, Dixie
was left alone. Although she was fed, watered, and taken out.....she
had not been alone since God brought her to us. I remember my horror
when we got home from the hospital. There was not a square inch of
floor uncovered. Toys from the kids rooms were scattered throughout
the house, mixed with the garbage that had sat in the can unattended
during our hospital stay. I couldn't believe one stressed out dog
could have created such destruction.
I felt bad for having left her cooped
up and unattended. I let her out and stayed with her to make sure she
didn't run off. She stayed right around the house. Apparently her
extended stay inside, only being taken out long enough to use the
bathroom and only seeing someone for 10 minutes a day had fixed her
issue of running off. She stayed close to the house, only venturing
to the end of our personal driveway, then coming back. She was so
happy to see us.
The next day, I had to run into town
to grab some groceries. I couldn't find anyone to stay with my
husband, but had to get him something to eat. I timed my trip so that
he'd be sleeping and rushed to get things done. I came back in aprx
30 minutes. As I rushed to come in and check on him, Dixie jumped
from the van. I checked on my husband, and went out. Dixie stood at
the end of our personal driveway barking. I knew she was barking at
the trespassing hunters. I'd seen their truck on my way in. Despite
continually asking hunters to leave our property and the property
adjoining ours, and explaining that we have to children with Autism,
they still continue to return. Dixie stood at the end of the drive
barking as I carried in groceries. Suddenly, she quit barking and
started wagging her tail. She got excited and her whole back end
started to move back and forth. I couldn't help but smile. Dixie
would get so excited when she was going to get affection that she'd
shake her back end so much she could barely run. She took off down
the drive. I assumed that someone we knew was coming down the drive.
I was wrong. When I got the last of
the groceries in, I went to get Dixie in. No one had come up the
drive and I couldn't figure out what she had taken off the drive so
happy about. She wouldn't answer my call, and I didn't see nor hear
any sign of her.
I found her later. It was dark and I
was driving out the drive. I just happened to get a glimpse of her
green collar as I drove by. My heart sank. I backed up and cut on my
high beams. There was Dixie, laying on the side of the drive in the
grass. My heart sank as I realized she wasn't moving. “She's been
hit by a car” I thought. Then I thought, “She's just hurt. The
vet can save her!” I jumped out and ran towards her.....and then I
saw it. An arrow.....extending out of her. She was dead. My husband
said he was so scared and worried for me. He said it was as if I
crumpled, but was still standing on my feet. He said he'd never heard
anyone scream like that. My heart was shattering....all I could see
was our beloved pet, our family, lying there with that arrow
protruding.
I drove back home and called my best
friend. Halfway up the drive I stopped as my sobs and screams were
wracking me so much that I couldn't drive. I made it home and called
my best friend who advised me to report it to the police. I called
911 and was told a deputy was coming out. I drove down to sit beside
Dixie, worried that the coyotes or other animals would disturb her.
My husband insisted on coming with me, telling me he could never rest
knowing I was sitting there alone. I finally convinced him to go home
and lie down. I drove down the drive to turn around. There were
headlights coming towards me, but as soon as I spotted theirs, they
must've seen me. They turned around rapid fast and took off down the
drive. Instinct made me go after them and I was shocked to see a
small pickup truck, very similar to the one that was there when I'd
gotten home from the grocery store. I wrote down the tag number and
returned to give it to 911, hoping that the deputy coming out would
see them as he passed. When the officer arrived, I told him about the
truck. He had passed them on the way, but had not gotten the message
from dispatch. After getting all the needed information, he told me
that unless they confessed, he couldn't do anything. If they
confessed, the only thing he could do was give me the information so
that I could go to the magistrate for “destruction of personal
property”. I was dumbfounded. These hunters repeatedly trespass
posted private land, lured my dog from our property and shot it, and
nothing could be done. I was told that nothing could be done because
their was a leash law, and my dog wasn't on a leash when he was
killed. My heart sank. She'd been killed within 15 minutes of jumping
from my van. I saw her run down the drive happily to greet her
murderers, and never had a clue what was happening. I even remember
hearing the truck drive up and leave as I was calling out to her, but
never considered that any hunter would ever harm an innocent dog.
Especially not hunters that had already been told that there were two
children with autism living in the home. Did they have no heart?
After the officer left, I made a call
to my best friend. With my husband having a brain injury, he isn't
allowed to lift anything. There was no way I could bury Dixie as I'm
not strong enough to dig through the hard clay rock. She couldn't be
buried until the next afternoon, when a friend of mine would get off
work and come do so. I had to get Dixie to the house and protected
from the wild animals of night. I drove down to where Dixie lay. I
could have walked there in less then 3 minutes, but it was very cold
and I needed the warmth of the van. I took my camera and using the
flash surveyed the area. I could see where the hunters had stood next
to Dixie in the tall grass, even as she stood in the grass beside the
drive that was mowed that very morning. The hunters and Dixie were on
the neighboring property to ours.......property that is private and
posted as no hunting allowed. Using my headlights and the flash of my
camera, I walked a bit further down and saw a well worn path the
hunters had been using to get from their truck to the adjoining
property. I came back and took pictures of Dixie. I wanted to make
sure that somehow her death would not be in vain, and maybe the
photos would help that.
I sat with Dixie until my friend could
arrive. As we lifted Dixie to place her on a piece of wood, I almost
choked. When we lifted her up, we could see the other end of the
arrow. We could see the angle, and how far the arrow protruded from
her. Although I had never doubted that it was intentional, due to her
having been shot beside our drive, it had never occurred to me
exactly how cold hearted these hunters had been. They had stood
directly over her when they shot her. They shot her through the heart
and the evidence of this was pooling around her. Dixie would have
been looking up at them with her adoring eyes, tail wagging so much
that her behind swung from side to side. How could they have looked
at that adoring face and brutally murdered her that way?
We laid her Dixie in the van and
brought her home for the last time. My husband had been building a
storage building next to our home. We put her in there and wedged a
large piece of wood over the door. I laid awake for hours in bed that
night. I just kept seeing those so called hunters standing over her,
with her excited to be getting attention, and the arrow piercing her.
Although I was glad it had been a shot straight through her heart, my
own heart felt just as pierced. I cried throughout the night,
muffling my sobs so as not to disturb my husband who was still in
immense pain from his injuries.
I woke the next morning going over the
needed chores to be done. Then the image of her laying beside our
drive pierced through my mind. I got up quietly, pulled on my shoes
and sweatshirt, and headed out with my camera. I walked this time.
Though still cold, I needed that extra minute to prepare myself. I
had noticed the night before that the end of the arrow with the
quills had been broken off. I had remembered hearing in the past that
hunters mark that end of their arrow with their initials or an
identifying mark. They do this so that they know who made “the
kill”. I searched the area where I'd found Dixie and as I walked
back towards where their truck was parked, I found the broken piece
of the arrow that had the quills. Dixie's blood was still on it. I
found two pieces, laying next to each other. Yet, the very end,
beyond the quills, was missing. The part where the initials would
have been.
I then thought back to their returning
that night. I figured it had to be the same truck, despite it having
been dark and my vision being limited. Why else would they have
turned around so rapidly and taken off like a race car driver down a
curvy gravel road when they saw me? I wondered for a moment why, as
I'd done the night before. I felt that they must've been coming back
to take Dixie's body. I still haven't thought of any other reason
they would have had to return.
I came back home and headed straight
to the shower. I thought back over the last week. Finding out my
eldest son has to have a lung biopsy done, my husband's accident and
injuries, and now Dixie. I felt.....fragile. My husband woke as I
came through our bedroom. I got into the shower and as the water
poured over me, I lost it. The tears wouldn't stop and I was grieving
for so many things. I was grieving for Dixie's life. I was grieving
having to explain it all to my children. I was grieving for their
heartache. I was grieving for all the children that loved Dixie and
would have to be told. At some point, though I didn't notice, my
husband opened the shower door, turned off the water, wrapped me in a
towel and held me. I was thinking of all the ways I might have saved
her. If I hadn't taken her with me, if she'd been on a leash in the
van before I opened the door, if I hadn't carried in groceries first,
if I'd gotten someone else to dog sit while I was caring for my
husband. I must've spoke these out loud because I remember my husband
telling me over and over again that it wasn't my fault.
That afternoon, my two best best
friends came over to help me bury Dixie. James had been there the
first time we saw Dixie, and now he was helping lay her to rest. It
was a very emotional time for us and anyone watching the three of us
would have surely wondered as to our sanity. It took a long time to
shovel through the clay rock. When it came time to get Dixie ready
and to lower her, my dear friends sent me on an errand so that I
wouldn't have to see. By the time I got back, the grave was already
half way filled in.
Yesterday evening my children came
home. Due to their father's injuries, they had not come home yet. I
spent the evening consoling Pookie. After he fell asleep, exhausted
from his cries, our older two children came to me. They cried for
hours before falling into restless sleep.
Dixie was a blessing to our family. I
will never be able to understand how anyone could take the life of an
innocent. I've never been able to understand how someone could get so
angry at another that they would intentionally hurt their children.
Maybe these so called hunters thought that by killing my children's
therapy dog, that I would leave them alone and let them hunt here.
Maybe they figured I'd settle for keeping my kids inside at all times
for fear of them hunting next to my home. I guess I'll never know
what they were thinking. Part of me hopes that they will always see
her beautiful eyes and her wagging tail begging for love as they took
her life. Yet, what I really want is for pets and children to be
forever safe from these people. I want to make sure that somehow,
these people are never allowed near my home again. I want to know
that my children can jump on their trampoline, ride their bikes, and
check the mailbox without being worried that they'll be mistaken for
game. My children always wear hunter orange vest when venturing into
the forest, even the forest on our own property. Should they have to
wear it just to jump on the trampoline or to check their own mailbox?
I pray that somehow, some way, our
home is restored to the dream home that we envisioned it to be. I
pray that the children with special needs, and even those without,
can come here again and not worry about whether or not they may be
within feet of a hunters bow or gun. I pray that once again this home
and these woods can become that which God intended it to be.........
paradise.
RIP Dixie, You will always remain in our hearts. We love you!
Tags
asperger's,
aspergers,
autism,
Dixie,
hunters,
murdered,
therapy dog
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