New Entry from Jody’s Spectrum Scene Blog:
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New Entry from Jody’s Spectrum Scene Blog:
from thespectrumscene http://ift.tt/2cygJ8B
via IFTTT
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
*****
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.
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New Entry from Jody’s Spectrum Scene Blog:
Nearly three years ago, I wrote about how our spectrum son looked me square in the eye backstage at play practice, put his hands on my cheeks, and asked, “Mommy, can we please just go home?” http://ift.tt/2b5qltO
I wrote about how defeated I felt by autism that it was stealing the joy our boy had flourished in on stage as a soldier boy just a year previous. I wrote about how disappointed I was to be giving up, to let autism win, to walk away from something I knew our boy had so completely enjoyed before.
In rereading that piece tonight, I realize now that hindsight really is 20/20, or at least a little closer to anything we can see in the heat of the moment. Reliving the emotion of walking out of rehearsal knowing that was the end of Ben’s show season, I failed to recognized something even more monumental in the life of an autistic child than performing on stage – I failed to recognize that he was his own advocate. He didn’t need me to speak for him, interpret for him, or seek help for him. All he needed me to do was to LISTEN to him. He needed me to listen and honor his request, and once I did, I had my boy back. My smiling, happy, laughing, joy-filled boy had returned to me.
I relive the moments of despair from that season three years ago every time I go backstage at the Opera House our other kids have come to know as another home. Tonight was no exception as tonight was audition night for the younger set (read: Ben & Ali).
Ali is very much like our bigs, ready to jump on stage and perform at a moment’s notice in any way, shape or form her director requests. She is clearly one of the happiest kids around when her feet hit that black platform. Ben is more of a depends on the day kind of kid. He absolutely LOVES to watch his siblings perform and he typically wants to have his moment in the spotlight as well after all is said and done, but it really just depends on the day as to whether he actually wants to be “in” a show. Fortunately, I have come to realize this is perfectly acceptable, even applause-worthy considering his placement on the autism spectrum, particularly if he is in fact able to articulate his desires as to whether or not he will participate.
And so it was, time to head to our beloved Opera House for Oliver Twist auditions. Kids were given a script and encouraged to read part of a scene and then sing Twinkle Twinkle Little Star. Our director, Ms. M., gave me a script and suggested a few different parts for Ali to read. When I asked Ben if he’d like to read, too, he hopped right up and joined in. They took to the stage and read the scene with two older girls, smiled and giggled as they returned the books to Ms. M.
She then suggested they sing a song together. Ben took Ali by the hand, stepped forward and belted out the most flat rendition of Twinkle Twinkle Little Star you’ve ever heard. I have no idea what it was that made him decide he was going to sing off-key, but I had asked him to sing loud, and loud he did. It took all I had not to belly laugh as I watched his eyes dance. Ali, bless her heart, just sang along, best she could, hand in hand with her best friend, BenBen.
I have no expectation of lead roles for these two or even lines for Ben as I realize his struggles can be exemplified on stage and that can start a downward spiral for the other kids, but I am so thankful that he wanted to participate, albeit on his terms. (Yes, I can still hear him in my mind and I am still smiling.)
And just as important, I am ever so thankful for a place like the Ellisville Opera House where everyone knows your name, everyone gets a chance, and everyone is loved. I can’t think of a greater gift to give our young people. If you’d like to contribute to that atmosphere, mark your calendar for September 30 – October 2 to attend a performance of Oliver Twist I’m sure won’t soon be forgotten.
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New Entry from Jody’s Spectrum Scene Blog:
There’s an article making the rounds entitled, “My Child Has The Kind of Autism Nobody Talks About.” It’s not an easy read. In fact, it really pushes the emotions of this spectrum mom, not because it’s wrong, but because there are some aspects of it with which I can definitely relate.
Autism isn’t an easy road. There are many challenges, many struggles, many difficulties. But it is these trying times which make the milestones, the victories all the sweeter.
I tend to not write so much about the difficult times, but rather focus on the successes, the overcoming, the persevering. I do this because it is my intention that our spectrum boy will someday be able to read through all these entries and get a glimpse of his childhood through our eyes. I don’t want him to ever feel like he was a burden; like he was a challenge; like he was someone or something to be persevered through and overcome. Autism is a part of him. It cannot be separated out from him. It does not define him, but it is very much a part of him.
I could write volumes on the frustrations, the hours upon hours of therapy and work devoted to helping him, not to mention the gallons of tears cried in frustration; but these aren’t the stories on which I want dwell. Yes, these are an important part of our journey and help us to work through the times we get a message saying something along the lines of “just wanted to alert you to some issues this morning…”
Yes, there are issues and for some they are many, frequent, daily, perhaps even hourly, but I also don’t think it’s fair to stereotype all autistic kids into a group which is identified as being nonverbal kids with behavioral issues, Yes, that is the reality for some, but not all. Not Ben. While communication is something we will continue to work on for years to come, he is very verbal, so much in fact that we spend a fair amount of time asking him to quiet down a bit. It’s a wonderful problem to have indeed!
Bottom line, these kids are kids and every single one of them is loved for exactly who they are. And this, I have to believe, is exactly how it was intended to be.
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A quick scan through social media can lead you through any number of lists: to-do lists, don’t-do lists, top 10 lists of this that and the other.
I happened upon one this evening from TheAutismSite.com blog which touts the Top 9 Signs that Your Toddler May Have Autism.
1. Lack of Smiling
2. Rare Imitation of Social Cues
3. Delay in Babbling & Cooing
4. Unresponsiveness to Name
5. Poor Eye Contact
6. Infrequently Seeking Attention
7. Lack of Gesturing
8. Repetitive Behaviors
9. Delayed Motor Development
As I read through this list, I found myself shaking my head. You see, our spectrum son wouldn’t have fit into more than one of these categories his first two years of life. He was very much a “normal” kid, there were just some things that were different as compared to his older siblings, not wrong, but different. Because of my husband’s involvement in education as a career, he knew long before I did what we were looking at, but even I knew something was different. Because our son was meeting typical milestones, our doctor suggested a “wait and see” approach to answering the oddities that were quickly making our son “him”; again, nothing wrong, just different.
It finally took a long talk with a trusted cousin whose son had recently been diagnosed with Asperger’s Syndrome before I could wrap my mind around the possibility that what I considered as a “maybe” could very well be a “reality” and even at that point, I had to call our pediatrician to ask for a referral to Easter Seals so that we could begin the diagnostics process not because we wanted him to be autistic, but because we knew we had to find answers for our son.
It would be another 18 months before we would have the diagnosis and even begin to know who and what to ask in order to better help our son, but I shudder to think if we had given up based on a list such as this simply because, well, he didn’t fit the mold of that list. My point here is that as parents, we know our children, and quite often, we know when we need to move on in seeking help for our children. I think back and realize how easily we could have written off the oddities that just made Ben his own little person, but we knew there was more to it than a different personality. Because we followed our gut instincts, we were able to get him the help he needed so that he could enjoy things like an afternoon at the park or the beach and time spent with peers. These still are not easy things for him to tackle, but because of the efforts of countless people along the way, they are at least a possibility. And the smiles that come with the requests to go back to the beach are simply priceless.
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“Autism is hard – kicked in the gut hard.” This thought hit me Sunday as I’d been through dozens of sets of clues with our spectrum son in just a few short hours that seemed to stretch into days. Autism is hard.
It’s tears and fears; worry and frustration; heartbreakimg and heart-sinking. And that’s just for me, I can’t even begin to imagine the struggles he faces and works through every single day.
It’s also full of sighs and smiles; love and hugs and kisses and sometimes even snuggles, but never for very long; it’s belly laughter so big you need to catch your breath and dry your eyes; it’s pride in him, and joy bigger than life itself as he smiles and laughs and runs at us with all his might.
A few moments of quiet allowed for reflection and took me back to those many, many clues and all the emotions that came in those hours with our boy. Further reflection took me to his four siblings and I realized that autism isn’t so hard. It’s not our life, it’s only part of our story. Parenting – parenting is hard.
Seasoned parents warn young moms to “Enjoy these moments!” because they will be gone all too soon. “Carpe Diem!” “Seize the Day!” “Don’t wish these moments away!”
Confession time: I LOVE being wife to Chris and mom to Rob, Tom, Jac, Ben & Ali. LOVE LOVE LOVE LOVE LOVE it! There’s no question this is at least part of what God made me to do. I truly love it. But, I do not love every single moment. I do not love the frustration and the heartbreak, the tears and fears, the struggles and the growing pains, but I am thankful in all of them – thankful that I am able to live these days with these people.
Parenting is hard, but I sure wouldn’t trade it.
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It’s been a terribly long time since we’ve spent any time here at all updating what is going on. Unfortunately it mirrors out life pretty closely in that these days we are often busy and don’t get much done other than what NEEDS to be done. We have made some technology changes that hopefully will eliminate some of those challenges and make updates easier. Here is to trying to do better!
Sometimes, we are afforded the opportunity to just be & enjoy a few moments with our family & perhaps even share a part of our history with our kids – part of what makes us who we are. Not nearly often enough for our liking, but sometimes, it comes in the form of a trip “home” – “home” because it’s never quite the same, at least not for us. But it is still part of who we are and how we came to be that person.
Last weekend offered such a time, and we grabbed on with both hands and no matter how hard the kids tried, we wouldn’t let go…at least not for a while. And when all was said and done, they conceded, it was a good time. “It” being the hour plus we spent driving around the greater Pearl City area, where Chris grew up and still has treasured memories of his younger years. Since his parents moved to Iowa nearly 8 years ago, we don’t make it back very often, but his aunt and uncle were celebrating 50 years of marriage, so we made the trek. 50 years. That’s a lot to wrap my mind around. So much has happened in the 16 we’ve been married, I can’t hardly imagine 50. And they still live, laugh & love, just the way they “always” have, at least as long as I’ve known them. I especially love the way they laugh. Aunt Faline in her quiet snicker, with a smile from ear to ear, usually shaking her head at Uncle Gene, who still giggles like a little boy. I know this because he sounds an awful lot like our Tom. Funny, they bear a striking resemblance to one another as well.
We had plans to head to a cousin’s after the celebration for a wonderfully relaxing escape from reality. Truly, less than 24 hours, but such a restoration of the soul comes when there is belly laughter and the enjoyment of watching kids play and play and play and did I mention laugh? Oh those boys, they had us in stitches.
On the way to the cousins, though, we diverted from the path & headed out for an adventure touring Pearl City and all its wonders. Don’t laugh, there’s a lot of history wrapped up in that little area. Why, we saw some incredibly huge chicken farms, quite expansive dairy operations, and even happened upon the Blackhawk Monument, which for a history buff like our oldest, is pretty cool stuff. But the stop that got them all, even the littlest two, was that of Babb’s Grove Cemetary. You read that right: the cemetary.
I spent all the years of my youth with a cemetary bordering our farm, so it was a treat to run & play hide & seek with my brother among the headstones. We were always very respectful, as much as kids could be anyway. We always stayed close to the stones & never ran carelessly in “the open spaces”. It didn’t happen often, but it was a treat when we were allowed to go & look around. At that point in our lives, who knew people actually lived in the 1800s? Funny the things I remember. So, it never strikes me as odd that the kids would enjoy a walk through a cemetary, especially if they knew they had family there, but apparently, this is an oddity. Imagine, our family “odd” in any way…
So we happened upon Babb’s Grove while Chris was telling of how he spent many years hunting in the area when he all but stopped in the middle of the road. (It’s a one-lane country road, not a big deal.) I sensed he was putting two and two together, so to speak, and waited patiently. We turned into this small, unmarked cemetary as he said, “I think I have ancestors in here.”
He’s been doing some family tree research in his “free time” and remembered reading about Babb’s Grove cemetary. He just wanted to see if he could find any Baumgartners and assured us, “I won’t be long.” After about 10 minutes, I texted him, “Do you mind if the boys join you?” and the adventure took on new meaning. The boys had a mission; and they were successful! Tom found the Baumgartner line & Rob, whose eyesight is apparently much more keen than any of ours, found their great, great, great, great grandfather’s gravesite, one John Baumgartner. There were two others, whose connection we haven’t quite determined yet, but we will, in time. Perhaps that’s another adventure for another day.
Wow! I guess we are a little behind in getting a post on what’s going on in the Janssen household these days. We need to try and be a little more diligent. I’ll ATTEMPT to hit the highlights since our last post, and hopefully we can fill in the holes of what I miss.
I think the big news of the year is in the spring Ben did get an official diagnosis of Autism. He is on the spectrum although many of the professionals agree he is on the higher functioning end. That being said it is still amazing the small little victories we enjoy. Small things like Ben telling us he had a tummy ache last night and then confirming that by getting sick an hour later after we got home. I strongly believe that this whole experience will teach us to always notice and celebrate the little things. With this diagnosis, he has started therapy twice a week in Peoria at Easter Seals. This has been quite a change in our schedule as Peoria is over an hour away and he goes for 3 hours a day 2 days a week. It has been an adjustment, especially with summer ball schedules mixed in, but we do believe we are seeing good progress with the process.
Speaking of summer ball, the “big 3” have been busily enjoying summer ball this summer. All three teams started the season strong with multiple wins and it has been an exciting summer. Robert is finishing up his last summer of summer ball and has decided to go out with a bang. He has had the best season he has had in quite some time. He is fielding much better and is hitting the ball well. He has made some new friends in having guys from Abingdon and Bushnell on their team this summer and he has really enjoyed it. Thomas’s team has had a good summer as well. They’ve won some and lost some, but in his usual manner, Tom has continued to ALWAYS be upbeat and hustling! Jac had a different experience this summer in that she and a classmate were the only two on a team from Bushnell. There were more from her class involved in summer ball, but they combined girls from Avon and Bushnell and then split them on two teams. She found a strong love of catching, and of course Dad will try and foster that love. With a little coaching she has started to really come around as an up and coming catcher. Ben and Ali spent a lot of time at the ball fields this summer and have their favorite playgrounds, but also due to the extreme heat this summer have spent some evenings at home either with one of the big 3 or Mom or Dad.
Robert managed to have a few other experiences this summer in that he was involved in the Senior Rascals performance of Dear Edwina. He’s moved into the Senior group now. He tried telling us he had a very small part with only a few lines. He’s old enough that we would drop him off for practices and didn’t see the play until performance, and found out he was not completely honest. He didn’t have an overabundance of lines, but certainly had times when he stole the show with his lines but especially his non-verbal communication. Great performance. Rob spent a week with his Grandfather at Lincoln’s New Salem park near Springfield where he attended a day camp essentially training him to be an “interpreter” at the site teaching people about the site and the history. He really enjoyed it and the staff was very complimentary and was really advocating for him to return! This was also the summer of work for Robert in that he got his first taste of real employment. Rob decided he wanted to sign up for detasseling this summer and it’s meant some early mornings with hot working conditions, but he has enjoyed the paychecks.
Thomas and Jaclyn have also stepped up and been helping out bunches at home with the busy schedules. Thomas enjoyed a week of Bible camp last week at Faith Bible Camp, and this week both he and Jaclyn are spending their time at Lincoln’s New Salem park. We are so looking forward to the reports of their experiences this week. Ben continues to make progress and work on things both at Easter Seals and at home. In the fall he will be attending Pre-school at least part days to try and make that transition as well. Ali continues to keep us all smiling with her love and care for all of her siblings, but with a special bond with Ben. We can see already that she, Rob, Tom and Jac will all play a critical role in Ben’s future and they are all so caring and helpful in that regard.
Jody continues her work as Church Secretary and the challenges that it brings. Chris continues his work as Junior/Senior High Principal at Spoon River Valley and the challenges that the job and the schedule bring. We are all so thankful for the opportunities and blessings that God has provided. Jody has been struggling with a hip injury sustained from a fall on the ice last winter. Jody and Chris are both scheduled to run in the Macomb to Peoria run on July 21st to benefit St. Jude Children’s Research Hospital. Jody’s training has been disrupted by the injury and her running will probably be adjusted on Saturday, but so far the recovery is going well.
We have such busy schedules that we don’t often take the time to personally get in touch with our friends and family that mean so much to us, however, we are so blessed for each and every one of you. A short electronic note either here or on Facebook always means so much!
After several failed attempts at getting this posted on our blog, here it finally is!! I am sooooooooooooooo not the tech person in our family. Bet you couldn’t have guessed! Without further delay, the 2011 Janssen Family Review:
It seems we think the same thing each year, “How can it possibly be time for this already?” But alas, here we are, once again experiencing the truth of the matter that time does in fact fly when you’re having fun!
Adventures come in so many different forms, we just never know where we’re going to find our next one. Our greatest adventure of the year has been brought to us by that beautiful spirited bundle of energy & joy we all know as Ben; our Benton Alfred; our own little Alpha-Ben.
Our year began with concerns of little things that we always just thought made Ben, well, Ben. Things that were not necessarily wrong, but just different from what we had experienced with the older kids. Through many ups and downs and more conversations than we can count with professionals who have become almost as much family as any others, we still don’t have an official diagnosis, but we suspect he is on the Autism spectrum. This has lead us to speech therapy on a regular basis during the school year and while he still has bad days, there are so many more good days to balance it all out and for that, we are thankful beyond measure. As Rob pointed out one night last summer, “We all have bad days sometimes.” He’s so right.
Speaking of Rob, he’s another one of our great adventures! We often joke he is our experimental model because who really knows what they’re doing the first time around anyway? Oh how many times I’ve felt that way as we find ourselves split between the toddlers years with Ali and the teen years with Rob. Perhaps these are the years which caused cavemen to coin the term “man-cub”; not yet a man, but far beyond the years of the cub. All joking aside, Rob is one of the most genuine people I know and we are so blessed to be his family. He is a phenomenal big brother (especially to the youngest two) and quite the history buff. Highlights of his year include getting contacts; working for Mrs. Peterson & our wonderful neighbor, Jim; and all the fun that comes with JH youth group at Checkrow. He’s also quite the marketing mastermind when I let him loose to come up with different ideas for my growing photography business, PhotosbyJo, landing me three junior high dances, high school homecoming & prom yet to come, not to mention a few family shoots which have come out of those. This has been such a fun time for both of us, especially for me as I watch him grow and develop an interest in something that has been a passion for me for so many years. I am so thankful for the opportunity to do something I love with people I love and create precious keepsakes for those who come to me. There will come a time these captured moments are all we have to hold in our hands of those we hold so dear in our hearts. I don’t take this responsibility lightly & absolutely love seeing these precious moments unfold in the pictures I’m blessed to create.
While I’ve been snapping the shutter for decades, the business side of this adventure got its start in the summer of 2010 when I was trying to figure out a way to help Chris raise funds for the St. Jude run and I have been blessed that it has grown from there. You can see some of my work on my facebook profile: PhotosbyJo.
St. Jude is such a wonderful organization that a portion of my bottom line goes to support their amazing efforts. So touched by all the emotion of last year’s run, Chris & I made a decision that we’d run for St. Jude together in 2011. And that day, we decided we’d run together until we couldn’t run any more. There is just no way to describe the emotional overload of doing something like this. I had never run a day in my life before hitting the pavement to train for last summer. Oh, I liked to think that I tried in college, but those were never successful attempts, unless of course, you count run a block, walk 5 success. However, I’ve found that something happens when it becomes personal; when there’s a person you know & love, no matter how long it’s been since you spent time with them; when you realize nothing will stop you from running to help find a cure for that person, and every person like her, and heaven forbid, your own children should they ever be effected by this horrible monstrosity called cancer or other inconveniences such as autism. I say this because Autism Speaks allows us to raise funds for autism research as we participate in different runs as well.
Ironically, when you do something like this, you find yourself reflecting. A lot. I found myself wondering how it was even possible that I ran 7 miles in one day when a few short months before, running even a minute was a stretch. Chris was the ultimate cheerleader telling me he had no doubt I could do this & not to worry, I wouldn’t even feel it on run day. He was so right. It was just an emotional high outdone only by our wedding day and the birthdays of each of our children. I also found myself thinking I just couldn’t stop. There are too many things in life that provide stress, I wanted – no I NEEDED to keep running, not only for my health & to help St. Jude & Autism Speaks, but also for my own sanity. That road has taken a beating from my feet and relieved my frustrations more times than I can count. I choose to love my life, no matter what the adventure of the hour may be, and running helps me to keep that focus.
Fortunately, my running buddy (also a St. Jude first-timer in 2011) found herself thinking the same thing about not stopping and we have continued to hit the pavement together throughout the fall. We enjoyed the first annual Ghouls & Goblins run in October & we’re gearing up for Get Lit! through the Festival of Lights in East Peoria on New Year’s Eve WITH OUR HUSBANDS. So very excited about this!
And now, my cousin has decided to join us for the 2012 St. Jude Run, too! It’s quickly become a family event. Even our kids got involved this year by helping to organize a Kids Helping Kids event one day last summer which brought in more than $500 for St. Jude! Rob played his trumpet uptown in front of Main Street Cafe, then took donations at the pump at Caseys. Tom & Jac corralled their Girl Scout & Cub Scout groups to help with a car wash & bake sale. What a fabulous day for our little town to come together!!! Thank you to so many of you we saw that day!
In the midst of our Ben-venture early in the year, we realized Ali wasn’t talking. At all. Not even trying. With a speech therapist at our disposal thanks to Ben, we quickly acted on her advice and Ali began therapy with another specialist and we now spend one-two mornings a week on speech for Ben & Ali and one morning in a preK group for Ben – by Wednesday noon, mom is therapied out. It is so worth it, though, as there are often days I remind myself not to stifle her banter, we wanted her to talk. We have reached the pinnacle of why I wanted to name her Aliyah Lillian – the joy in hearing her little two-year-old voice say, “My name is Ayeeya Yiyyian Janssen.” Okay, the truth of the matter is, she is named after my brother and Chris’ grandmother, but I still LOVE to hear her say those words, especially when she giggles with me after she’s done…another grand adventure, that little Ali-bean is!
In addition to Scouts, Tom & Jac both still enjoy AWANA kids club at church and joining Rob on stage at the Ellisville Opera House with the Spoon River Rascals. Tom was the mayor of munchkin land, Jac was a munchkin, and Rob headlined as The Cowardly Lion in their production of The Wizard of Oz this fall. What a joy it is to watch our kids literally come alive on stage. It’s almost sad to realize this is the end of an era for the Janssen trio as Rob will be advancing to the Senior Rascals this summer while Tom & Jac stay in the younger group. It’s enough to choke a mom up.
All three kicked off the Christmas season with a production of Chris-Myth Busters at church. Rob opened the show with Christmastime is Here Again, while Tom & Jac were leads in the show which highlighted truths of God’s Word, despite not knowing many of the specific facts of that first Christmas so long ago. I found it humbling to lead the charge of this group of Checkrowite kids who only practiced together twice before the performance. It was a definite leap of faith, but God is faithful and nothing is impossible through Him. Those kids rocked it!! We may not know all the facts of the night of that babe’s birth so many years ago, but the truth is God sent him for us. Great job, kiddos!
That pretty much wraps up the year in a nutshell for the Janssen family. Sure we still have the daily grind of work & running kids here & there. Chris is still the JH/HS principal at Spoon River Valley Schools in London Mills; still the chairman of Avon Businessman’s Association (read Avon Fat Steer Show); and still loving the thrill of being a volunteer fireman. I’m still working part-time at Checkrow; teaching Caterpillar Club (preK) there for Ben & his friends once a week; still Cubmaster for the local Cub Scouts; still Troop Leader for Jaclyn’s Girl Scouts group; and still juggling the adventures of keeping a family of seven on task…and loving every moment of it!
Alpha-Ben
Yogi & BooBoo all snuggled up
BULLSEYE! Tom at Cub Scout Camp 8.2.11
Jac as a fashion model for Halloween
so blessed – most handsome date AGAIN! 🙂
Merry Christmas, everyone!