Category Archives: Uncategorized

The R Word – AGAIN

New Entry from Jody’s Spectrum Scene Blog:

Catching up and sharing from the files of my ramblings. This particular set is from
April 26, 2016.

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

“There’s a bunch of RETARDS running times today!”

Kicked in the guy and barely catching my breath at the very memory of overhearing this comment at last night’s track meet in Bushnell. Last night. In 2016. Essentially in our own back yard.

Let me clarify, this was not an A-Town or BPC athlete. In fact, his wasn’t a jersey I was familiar with so I can’t say for sure where he was from. What caught me most was his parents never said a thing about his outburst other than to fan the flames of his disgust. Apparently his team’s times weren’t as good as what he thought they should have been and other teams beat his, so of course, he surmised, it was a bunch of “retards” running times.

Rude. Disrespectful. I could go on and on with the adjectives that ran through my mind as I struggled to remain calm. That family moved on to find the rest of their disgruntled team and I breathed a sigh of relief not to have to be around them any longer without leaving our vantage point for our son’s next race.

What broke my heart most was that I didn’t have the fortitude to speak up and share that what was being said was hurtful and actually inaccurate. I doubt it would have made difference, but at least I would have had the peace of knowing I’d done my part in spreading awareness and if not stopping, at least slowing down the hatred.

I just cannot wrap my mind around why so many people find it perfectly acceptable to use the “R” word when referring to someone that has upset them, angered them, or even simply disagreed with them.

I’m ashamed of myself for not speaking up. Despite rationalizing the situation with the reality that I couldn’t catch my breath, how could I speak, I know I should have. I can’t expect others to speak up when I don’t, but I can ask, please, stop and think before you speak. And if you have children, please ask them to do the same.

from thespectrumscene http://ift.tt/2lBGGer
via IFTTT

Labels Don’t Change the Important Stuff

New Entry from Jody’s Spectrum Scene Blog:

Catching up and sharing from the files of my ramblings. This particular set is from November 30, 2015.

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

Our oldest daughter asked me the other day, “What kind of autism does Ben have?”

It was a fair enough question as she knows other kids with specific diagnoses such as Asperger’s Syndrome and PDD-NOS, but these labels aren’t something we’ve necessarily talked all that much about when it comes to her brother.

This could be for a variety of reasons:
a) He’s a person, not a diagnosis.
b) There are so many variances even within the different types of autism that no two kids are alike.
c) Specific types aren’t always diagnosed as young as Ben was when we initially took him to Easter Seals.

But, if I’m honest with myself, it’s probably as much
d) we don’t know
as anything.

Initially, this was a little frustrating at best, but the more I’ve thought about it, I’ve begun to wonder if it really matters what kind of autism it is? Beyond knowing how to best help him learn to help himself, do the labels really matter? Yes, they can help us better understand him and how he deals with things, even help point us in the right direction in terms of research, therapy, and assistance, but they don’t change the important stuff.

The bottom line is that he is a person first. Sure, he has a few little quirks that set him apart from his peers, but in all honesty, don’t we all?

Ben’s official diagnosis was simply “autism” along with a side of expressive/receptive language disorder and a slight motor delay. All that really tells us is that yes, he does in fact have autism, communication is going to be a challenge area for him, and he may have a slightly different gate when walking and running than others.

I find myself returning to one of the most poignant pieces of wisdom a dear friend shared with me the day before our diagnostic clinic: Ben will be the same boy coming home from the clinic that he was going into Easter Seals. He will still be your son. You will still love him to the ends of the earth. No label can change that. Diagnosis can help you know which direction to turn, but it will not change anything about who he is or the fact that he is still your son and you are still his parents.

THANK YOU

We still laugh and cry. He still wins my heart over every single time he looks me in the eye. We still hug and kiss and love, all the same as before our D-day. Yes, labels can help us know where to head for understanding and assistance, but they don’t define him or us.

from thespectrumscene http://ift.tt/2lBHoIz
via IFTTT

Normal or Extraordinary?

New Entry from Jody’s Spectrum Scene Blog:

img_8844

Catching up and sharing from the files of my ramblings. This particular set is from October 26, 2015.

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

Normal is just a setting on a washing machine.

I’ve read it and heard it a million times over since our son’s autism diagnosis, but when I read that, I often think the truth is, all special needs parents really want is a chance at normalcy. Sometimes I wonder if that isn’t what all parents want: normalcy. I wonder this because I look around and I see people fighting battles of all kinds.

No one is immune to the pressures of this life. Some battle autism, some battle cancer. Others I know press on despite the challenges of dyslexia, ADD and ADHD. Some families live with epilepsy hanging over their heads, and others wonder when the next bout of chest pains will come for their athlete.

Some families wonder where the next job move will take them and how their kids will adjust to the move. Others wonder if they’ll even have a job next month or next week, and if not, how will they provide for their family?

Other families are looking at their growing children and wondering where they will attend college and how, as parents, they will pay the tuition; or if their students will join the military and if so, where will they serve?

We all have challenges of some sort. And I think we all hold on to the glimpses of normal we see in our family life. Perhaps it is those glimpses which get us through the next challenge and the next and the next…knowing that somewhere down in the depths of who we are as a family, there is some sense of normalcy and what that means for our family. Perhaps “normal” is different for each of us.

Perhaps it’s a dad and a son going out to do morning chores together, perhaps it’s that same dad and another son singing happily as they head to the truck to make a Sunday afternoon run to the grocery store. Perhaps it’s a mom and her oldest huddled around old photo albums looking for just the right baby picture to submit for senior honors, or the same mom and her youngest snuggled up as the littlest reads a story for the one who rocks her world.

It’s in these moments of what may seem all too normal to the outside observer, that I realize we are given moments of extraordinary to get us through until the next normal. I hope that I don’t spend all of my moments wishing for the normal, when I could be experiencing the extraordinary.

from thespectrumscene http://ift.tt/2mtgSyS
via IFTTT

Necessaries vs. Importants

New Entry from Jody’s Spectrum Scene Blog:

Catching up and sharing from the files of my ramblings. This particular set is from September 21, 2015.

NECESSARIES vs. IMPORTANTS

So many times in life we get busy with all the “have to’s” that we simply run out of time for the “want to’s”. If we’re not careful, our “necessaries” can begin to push away our “importants”. A friend mentioned “importants” to me one time many years ago and it took me a while to digest it all, but once I could work through what that meant in my heart and mind, I couldn’t ever forget it.
My work is necessary. My deadlines are necessary. There are certain things I have to do with my job every week for me to be able to keep up with things there. These are necessary. But my family – they are important. I won’t get fired as wife and mom if I don’t take the time to snuggle with my family tonight. We will all live to see another day if we don’t share laughter and one-on-one time with each of our kids at some point this week, but that doesn’t mean it doesn’t need to be done. I need that snuggle time, laughter and connection with each member of my family.
The varied ages and interests of our children necessitates variety and flexibility. For one child, it may mean sitting down to an intense game of Stratego, for another, a simple though no less intense round of Go Fish! Another child may only need session of roughhouse wrestling, while another just needs a good belly laugh from tickling and bear hugs. The other opens up during shared time in the kitchen. Each child is different. These are not difficult moments, but it takes time. If I’m not careful, I can get wrapped up in my list of necessaries and overlook the ticking of the clock until it’s nearly bedtime. It’s then that I realize what a treasure I’ve missed with my kids. And I promise myself again and again that it won’t happen again, but this is life and we are human. We make mistakes and thankfully, we do grace and forgiveness in our house. We do love and laughter. We do do-overs. We do life.
My challenge this week and every week is to remember to focus on my “importants” at least as much as my “necessaries”.

from thespectrumscene http://ift.tt/2kpYGEE
via IFTTT

A Country Baptism

New Entry from Jody’s Spectrum Scene Blog:

Catching up and sharing from the files of my ramblings. This particular set is from September 14, 2015.

A COUNTRY BAPTISM

Sunday is typically family day for us. We do all we can to keep that as a constant, but as our children grow and are more active in their schools and communities, it becomes more difficult. We’re also finding that as the children grow and mature, they develop close friendships and make plans to spend time with those they don’t see in school (ie: church friends) on the weekends. We’ve begun to joke in our home that we share custody of our oldest son with another family from our church as the two boys are often together over the weekends since they attend different schools.

This past weekend, we were able to enjoy a rural worship service with our church family (ie: all the kids together) at the side of a pond, complete with live music performed from a floating dock, and the testimonies of more than a dozen people who had answered the call to be baptized. This is always such a touching time as we listen to the stories of those who are about to be baptized, ranging in age from elementary up through long since any school days. It’s a time to reflect on our own stories and rejoice with those who are stepping out in faith.
As I sat with my family on the hillside, soaking up the warm September sun and the chill of a morning breeze, our spectrum son snuggled up to me, pointed to those in the lake and said, “Mommy, I like that.”
Truly, I think that he meant “I like to be in the water.” as he absolutely loves to go swimming, but at that moment, no words could have been more perfect. As most Ben comments do, it got me thinking, wondering if he really understood what was happening, why people were going into the lake fully dressed, just to be tipped under water and then brought back up. I wondered if he understood the statement they were making, the commitment to live like they never have before marking the transformation that had taken place in their hearts.
I can’t speak for my son and what his understanding that morning was, but I know that his maker loves him just as much, no, even more than I could ever imagine, and I’m so thankful that we live in a community which will continue to rally around him, teaching, doing, leading and loving him every step of his journey.

from thespectrumscene http://ift.tt/2kpKrzX
via IFTTT

Our Son, Your Boy

New Entry from Jody’s Spectrum Scene Blog:

Catching up and sharing from the files of my ramblings. This particular set is from September 3, 2015

I’ve mentioned before how amazing our community is about rallying around its youth. This is never so apparent as it is during the Avon Fat Steer Show. Young exhibitors work all summer long to ready their animals for show – washing; rinsing; leading; guiding; studying their feed and growth rate, making adjustments when necessary; raising their stock for eventual show and sale.

It is so refreshing to see our community take an interest in the young people who work so hard. Watching these kids in the show ring is nothing short of amazing. Truth be told, any one of those animals could very easily walk right out of the ring, kid in tow, leaving behind anyone who tried to stop them along the way. But for the most part, they do not. The endless hours spent in preparation are evident in the way that animal and owner work together. On the occasion that an animal acts up, or gets away from an exhibitor, they are never on their own. Everyone around the ring stands on the ready to assist.

Outside the show ring, friends and neighbors gather to catch up, not on markets and weather, but on life. This is where I see the epitome of community. Countless smiles and rumbles of laughter greeted me each and every time I visited the fairgrounds with our kids. Most often, I was flanked by both of our youngest, now aged 6 and 7.

Thanks to this amazing community, these kids don’t know a stranger at the fair. Even when all the sights and sounds and long hours at the fair have taken their toll on Ben, and there is simply too much stimulation for him to handle, not once did I get a disapproving glance. Those moments we took solace in our quiet spot, a chair with our cattle – those were the moments we retreated, the moments Ben needed to curl up and regroup in the safety of mom’s arms and lap.

While my son wrapped himself in a ball tighter than seems humanly possible and buried his face into arm as I gently squeezed the anxiety away, friends and neighbors greeted me with sympathetic eyes and a knowing smile – not an “I know what you’re going through” but an “I can see this is a time Ben needs you so I won’t speak, but just know that I’m here” kind of smile. I can’t explain the words which aren’t spoken other than to tell you these are the moments that refuel me. These are the times I am reminded that while Ben is our son, he is very much your boy and we are so completely in this together. And I cannot thank you enough.

from thespectrumscene http://ift.tt/2kpzTR9
via IFTTT

I’m Back … for now anyway

New Entry from Jody’s Spectrum Scene Blog:

Life has taken some unexpected turns over the last couple of years. HA! I have to laugh – isn’t that the understatement of the year? And I have to think it’s not just true for me and my family, it’s just life in general. Sometimes, things we enjoy and think we will never give up simply have to be put on the back burner because there are other things which need our attention. “Important” and “urgent” can come to define, even dictate what gets our attention, and sadly, this blog is often one of the first to go.

While I continue to write, those thoughts don’t always make it here. I want to say, “I’m sorry, ” but I really can’t do that in good conscience because it is a choice that I make based on where my family needs me most. Here, thespectrumscene, hasn’t been the answer to that of late and I’m okay with that because while I haven’t been “here,” I’ve been “there.” There is where my family has needed me. There has covered many miles, included countless bleacher seats cheering on our middle set, involved more sets of clues and puzzles than the mind can imagine while playing with our littles, and even some deep discussions while walking the path with our oldest. I wouldn’t trade these moments for life itself. This is who I am, who God made me to be, and I am thankful that while I am “there,” thespectrumscene remains “here” as my outlet for sharing my thoughts and our experiences not just as a spectrum mom, but as a mom; not just as a spectrum family, but rather as a family.

I can’t promise that entries will be regular forever, but I can promise that while I’m there, I’m thinking of here, and when the day allows, I’ll visit to share the joys and struggles, the ups and downs, and all that makes our family us. I hope that our experiences will encourage other spectrum families and remind everyone that regardless of the challenges, there are perfect moments in every day, even the ones we really have to search for them.

from thespectrumscene http://ift.tt/2kjKYIF
via IFTTT

Christmas Time is Here

New Entry from Jody’s Spectrum Scene Blog:

Christmas time is here
Happiness and cheer
Fun for all that children call
Their favorite time of the year
    Snowflakes in the air
    Carols everywhere
    Olden times and ancient rhymes
    Of love and dreams to share
Sleigh bells in the air
Beauty everywhere
Yuletide by the fireside
And joyful memories there
    Christmas time…it is one of my favorite times of year and this is one of my favorite Christmas songs because it hits so close to home. 
    It seems more than just me enjoys a walk down memory lane as in the last two weekends, I’ve been able to enjoy Christmas walks in different towns. This weekend, I was blessed to have my folks and one of my kids with me as we strolled down decorated cobblestone streets and stopped to enjoy two of our children caroling with a group from their school. We even fortuitously enjoyed a wonderful performance of A Christmas Carol in Thirty Minutes by a community theater group with which our kids were once performed.
    That evening, we were blessed with another wonderful evening with our church family, enjoying the labor of love our young people pour into musical performances. Eighty minutes of performances by children aged 6-18 poured over us as a praise offering to our creator.
    Such joy fills my heart to watch my children interact with those whom they’ve shared the stage and been reunited with after many months, to see children I don’t even know laugh and run and play while my children entertain their families with Christmas carols even my parents were raised singing, and to sit and listen while songs of praise are offered by sweet young voices, along with sibling banter and encouragement between sets.
    All of our children performed last night. Rob played his guitar for most of his siblings and a couple of friends. Tom and Jac sang Hark! The Herald Angels Sing. Ali serenaded the full church with a sweet rendition of I’m Dreaming of a White Christmas, and much to our surprise, even invited the congregation to join her in a sing-along, which after an endearing chuckle, everyone joined in, bringing the dearest smile on our baby’s face. And Ben, Ben shook his bell sticks with all his might while he sang Jingle Bells. As loud as he sings his heart out at home, the church platform seems to have a silencing effect on him. Perhaps it’s the lights, perhaps it’s all the people as the church was incredibly full, but for whatever reason, he started very, very softly.
    My “mommy heart” broke as I saw the disappointment on his face at hearing people talking while he tried to sing. I don’t think people were trying to talk over him. I really think it just happened as he was so soft, they didn’t realize he had begun, but as they realized he was there and trying, the most precious silence descended upon our crowd. As the room grew quiet, Ben’s confidence built and he began to sing out, finishing strong, replete with that signature Ben smile and twinkle in his eye.
    We are so incredibly fortunate to be here, in this place, at this time – a place we can truly call home, where our children can do their thing, in their way and in their timing, and be so completely loved by so many.

from thespectrumscene http://ift.tt/2hgduYT
via IFTTT

Being Someone’s Person

New Entry from Jody’s Spectrum Scene Blog:

img_2950
My cousin got married this weekend. Biologically, she’s my cousin but truly, she is my sister in every sense of the word. More than that, she is my person.
We are incredibly huge Grey’s Anatomy fans, my cousin and I. She took to calling me her person before I got to that episode on Netflix a few years ago. I could not for the life of me figure out why she began referring to me as “person” instead of Jo, Leggz, or even Mom as was our normal. Then I saw it: the episode.
It doesn’t matter if you aren’t familiar with the show, I’m betting you can relate to the concept of “your person.”
You and your person are always on the same team, even if it means you have to do something you really don’t want to do. Even if you’re incredibly busy, you’ll make the time to check in with each other – even if it means you sit with them while they work. They’ll dance with you when no one else will, and when the day is just too much, they’ll lay down with you. They’ll listen to you complain about your life, and they will have your back. They’ll listen to you at your craziest moments and tell you what you NEED to hear, even if it isn’t what you WANT to hear. You act like a married couple because when you are together, you are always together and you talk about growing old together. You understand each other’s logic, even if it makes zero sense because you have your own language and sometimes you don’t even need to say anything, you can just make a face and they can read you word for word. On your worst days, they’ll hold you. You know you can always share secrets because they will keep them; they are your safe spot. And, you never have to worry about losing them because they’ll always be “your person.”
This is the epitome of my relationship with my sister/cousin. Of course,our relationship has changed and grown with us over the years. I’ve seen her grow from a skin and bones preteen to a strong, beautiful woman who will open her arms to children offering them love, support and security in a crazy world, but use those same arms to fight off the crazies which threaten the very security she offers those she loves.
Events of the weekend got me to thinking how very blessed I am to not only have her as my person, but also to have my own bevy of people figuratively around me each and every day – figuratively only because many of them are miles away, but I know they are “there” for me at a moment’s notice. This group has seen me and my family through the mountains and valleys of life and I simply could not be more blessed by them – everything from marriage, birth and death of babies, raising our children through the teen years (God bless my people!), and not the least of which, Ben’s autism diagnosis and subsequent therapies. We simply could not have come through all that diagnosis entails without our people praying for us, encouraging us, and simply “being there.”
Thank you for being our family, for having our backs, understanding our (okay my) ramblings, even when it made zero sense. Thank you for being our people.

from thespectrumscene http://ift.tt/2cygJ8B
via IFTTT

We Are Never Alone

New Entry from Jody’s Spectrum Scene Blog:

Dear God,

Thank you for going to school, going to church, playing at home.  I love you.

Amen

*****

THANK YOU

This is the prayer of a little boy on 9/11/2016, a little boy we once were told may never be able to communicate effectively.

Fifteen years ago, I stood in disbelief as the events of 9/11 unfolded before us, pregnant with our twins and suddenly questioning everything I thought I knew about life and how we would live it. My hopes and dreams for the world our son and his unborn siblings would grow up in were being tested.

I shook my head, not able to comprehend the way our world had just changed and held my son tight as often and as long as he would let me.

Our leadership stepped up. President Bush reassured us, “I can hear you, the rest of the world can hear you, and the people who knocked these buildings down will hear all of us soon.”

America united and over time, peace in our hearts was restored.

Four years ago, I also stood in disbelief as doctors, therapists, and other professionals, told us our son may never be able to communicate with us, may never understand what we tell him or be able to express himself effectively, may never be able to build friendships or relationships of any sort. He may lash out at us. He may run away from us. He may never this or never that…my hopes and dreams for one of my sons were again being tested.

Once again, I shook my head, not able to comprehend the way our world was changing and once again, I held my son tight.

Diagnosis day is different for every family, and in fact, different for each person in that family as we all feel and process differently. For us, it was confirmation of something we already knew in our hearts. Yet, hearing the words still pack quite the punch.  For me, it was the beginning of a battle in a war we’d already begun.

A month later, another initiative in this battle to hold onto our son and help him move forward commenced with Easter Seals’ Intensive Therapeutic Autism Program (ITAP).

ITAP’s director and her staff quickly became trusted confidants as we began traveling to Peoria for Ben to participate in their three hour program twice a week. Ms. Wiebler assured us that she could hear us, she could hear Ben, and after only a few days into the program, she already knew that everyone would hear him very soon. We united and over time, peace in our hearts was restored.

Life may never be what we once expected, but the peace the prayers of this little boy on the anniversary of an event so breathtakingly terrible brings to my heart reassures me that I am heard; my faith in our creator reassures me that he is heard; and the moments we slow down, allowing ourselves to both hold and be held reassures me that we will never face any battle alone.

from thespectrumscene http://ift.tt/2crqIC2
via IFTTT