Posted in Down syndrome, Recreation/Leisure and Special Needs

Snow Day & Groundhog Day

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Snow Day & Groundhog Day

We had the 5th biggest snowstorm on record for Chicago yesterday.  So, today is a snow day at home with Nick.  That equals no concentration in the writing department.  I’ll be back next week with a freshly pressed blog (unless we have another blizzard).  Meanwhile, I’m tackling dust bunnies on the high kitchen cabinets.  Nick is tapping away with his tennis balls and pointing outside saying, “Brrrrrrrrrrrrr”!

Speaking of tackling things, here’s a re-blog about getting and staying in shape.  The first part is geared for individuals with Down syndrome.  I also included my top fitness tips to motivate you too! @https://nickspecialneeds.wordpress.com/2013/01/14/blog-37-just-do-it/

That’s what is in my noggin this week.  Stay warm my friends, it looks like 6 more weeks of winter!

~Teresa

groundhog

 

Posted in Autism, Behavior/ ABA, Down syndrome

Blog #112~Regression of Behaviors

 

Blog #112 Regression of Behaviors

Christmas 2014 was anything but merry.  The swimsuits, flip flops, suntan lotion and pool toys sat in a pile on the chasse in my bedroom.  We never made it to the Florida Keys for our vacation.  A member of our extended family came down with pneumonia and then a snowball effect of more health problems that included a 12 day stay in the hospital.  Nick wasn’t sure what to make of things.  He is 20 years old and has Down syndrome and autism.  All he saw was his Dad or me taking off all day on hospital visits which were an hour away.  Nick picked up on the fact that something was very wrong.  He was sad and angry and missed being with the extended family.  We spent that two week break unsure of the outcome and shooting from the hip.  In 20 years of raising Nick, I have NEVER seen such a spike in regressive behaviors.

When daily routines are interrupted a child with autism can feel anxious and behaviors regress.  Strict routines, normalized school or work schedules without any unexpected occurrences enable a child with autism to progress best.  However, because the holidays are busy, stressful and filled with the hustle and bustle of foods, gifts, and family; a parent can expect to see behavioral changes.

Back to Nick and those behaviors that spiked, which included the following:

*Increased stimming with objects and louder vocal stimming

*Pushing microwave fan, phone intercom and now house alarm system much more

*Throwing objects and dumping things like a one man wrecking crew.

*Spitting and rubbing snot on flat screen TV, windows, on our clothing.

*Squirting liquid soap in his eyes, rubbing lotion all over himself

nick lotion

*Multiple, violent meltdowns

*Peeing his pants several times

And to top it off, I left a bottle of Febreeze out by accident………Oh nooooooo!

febreeze

FYI, Febreeze and a flat screen TV don’t mix well.  So, we had to purchase a new one……..

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By the way if you Google search “Febreeze on a flat screen TV” there are several entries of other kids doing this.  Nice to know we’re not alone. 🙂

I reported all of this in the school/home communication book.  The school staff wrote back that Nick was definitely not himself. He was trying to pull fire alarms, pinching his cheeks hard as well as a staff member.  To make matters worse, just as Nick was back in his school routine we had two snow days.  On top of that, the kids were off two more for the end of semester and MLK Day.  Oh, and there was a full moon over the holiday break.

autism and full moon

The house is quiet now, and I can focus on writing again. Yesterday, I did a little research on regression of behaviors and holiday breaks.  As I reflect on Christmas 2014, a couple of things stand out.  First of all, Nick’s behavior was magnified because his parents emotional fatigue and lack of emotional availability.  For over two weeks we were back and forth at the hospital.  Nick picked up on the stress.  Secondly, as a family we should have communicated in private about medical updates.  I think back on one particular day.  As I briefed Al on the hospital visit, Nick came over crying and wanted a hug. I had to remind myself that he understands much more of what we are talking about.  He also picks up on the negative vibes of conversations. Finally, one tip I read in my research was so obvious.  But when you are in the thick of things it can be overlooked.  That is, don’t let your kids be aimless.  It’s essential to find ways for them to occupy your child.  When kids are on a school break, they have less structure in their day. Bottom line, they’re going to get into more trouble and conflict because they have the opportunity to do so.

While there was no kayaking, bike rides, beach and pool time or key lime pie over Christmas we did make it through.  Things are slowly on the mend. The cousin’s presents and white elephant gifts are tucked away for now.  The Hormel Cure 81 Ham sits in the refrigerator awaiting a belated Christmas celebration at a later date. The gift of Christmas 2014 is being reminded of how precious life is and how quickly it can be taken away.  In addition, I have a new perspective of how important it is to respect Nick’s needs when there is a school holiday break. That’s what is in my noggin this week.

~Teresa

 

Posted in Uncategorized

MLK Day

MLK Day

Taking this week off to honor of Martin Luther King Jr. Day.  I’ll be back with a fresh blog next Monday.  Here is one of my favorite quotes of his:

~Teresa

MLk Quote

 

Posted in Autism, Down syndrome, Health Issues and Special Needs Child

Cold Season Survival

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Cold Season Survival

Since we are in the trenches of the cold and flu season I wanted to post some survival tips that I use with my son who has special needs. Nick has Down syndrome and autism.  So, tackling the cold and flu season very challenging.  Here is some great information on this subject that I wrote a few years back:

https://nickspecialneeds.wordpress.com/2013/01/07/blog-36-what-i…-runs-all-over/

Cheers to a healthy start to the new year and surviving the cold and flu season.  That’s what is in my noggin this week. 🙂

~Teresa

Posted in Autism, Down syndrome

Happy New Year!

Happy New Year!

Happy New Year 2015

Whew, it was a long two week Christmas break. Having a child with Down syndrome and autism presents many challenges over the holidays.  So yes, I did the happy dance this  morning when the bus pulled up.  More on this after I wrap my mind around it.

This week I wanted to share a blog I wrote last year around this time.  I hope that it will inspire you @https://nickspecialneeds.wordpress.com/2014/01/20/blog-81dreams-for-the-new-year/

Thank you for reading and sharing Nick’s world. And by the way, I did keep those bird feeders filled up. That’s what is in my noggin this week.

~Teresa

Posted in Autism, Down syndrome

Christmas Break

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Thank you for reading and sharing Nick’s world this year.  Have a Merry Christmas and we wish you a Happy New Year!   Enjoy your holiday with  family and friends. 

I am taking a two week break from the blog, but there’s plenty of good stuff in the archives to dig thru and enjoy in the meantime.  You can also check out the Facebook page for more photos, links and video clips of big guy. We look forward to sharing more fire alarm updates, stories, and information about Nick, Down syndrome and autism. 

Cheers,

~Teresa

Posted in Uncategorized

Re-Blog~ #78 Christmas Past

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Re-Blog~ #78 Christmas Past

With the busy holiday season upon us, I opted to re-blog “Christmas Past”.  Here is a little photo album of Christmas past with my boys @https://nickspecialneeds.wordpress.com/2013/12/16/blog-78christmas-cheer/

Wishing you all the best and take time to make memories with your family. They do grow up fast.  That’s what is in my noggin this week.

~Teresa

 

Posted in Autism, Down syndrome

Blog #111~ Constant Child

 

Blog #111~ Constant Child

Last Saturday morning, Nick watched the same DVD over and over.  It was a continuous loop of Thomas the Tank Engine’s, “A Big Day for Thomas”.

Thomas the Train

Twenty years later I didn’t see myself listening to the dialog, and able to recite every line.  At this rate, there will be no break between Nick watching Thomas and my grandchildren following suit.  I can see it now, Hank Jr. saying, Hey Uncle Nick want to watch Thomas the Tank Engine with me?”  I also didn’t imagine stumbling over plush toys that my son dropped from the second floor.

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I didn’t picture myself scrubbing red marker stains off his clothes at age twenty.

Note to school staff:  Markers + Nick = Skin, and Clothes…….

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This got me thinking, having Nick is like caring for a constant child.  Nick is twenty years old and he has Down syndrome and autism.  He can’t stay at home by himself and requires continuous supervision.  Don’t get me wrong, he has made strides doing much more independently (like unloading the dishwasher, putting away groceries, recycling, vacuuming, etc.).  And he does watch age-appropriate movies and listens to grown-up music on his iPod.

Nick tabor hills

But at the end of the day, I’m still wiping snot off the flat screen TV and microwave.  Out in public, he can never be more than arm’s length for fear he may take off running, or to pull a fire alarm.

30 Fire Alarm pulls since 3rd grade. Is there a bumper sticker for that?

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I’m not writing this to get sympathy.  I’m simply putting a lens on what the world looks like having a young adult with Down syndrome and autism.  It’s not the end of the world.  But it is a very different world, then I expected.  The stimming, banging, tapping, yelling, dumping, phone intercom and microwave button pushing is constant and mind-numbing at times.  And you never know what he’s going to drop off the top of the staircase.  All I can do is continue working with him to foster independence.  I’ll keep redirecting his inappropriate attention seeking behaviors and have him clean up his messes.

I’ll take Stuart Little and Dora the Explorer over shaving cream any day……

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I will remind myself that the laughter, silliness, sweet kisses and unconditional love of this constant child helps to offset the rest.

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That’s what is in my noggin this week.  Now back to operation red marker removal. 🙂

~Teresa

 

Posted in Autism, Down syndrome

Blog #110~Autism Holiday Survival Tips

Blog #110~Autism Holiday Survival Tips

The Christmas holidays can be a land mine for individuals who have autism.  The changes in schedules, crowds, noises and the lights can result in way too much external stimuli to process. My son, Nick is 20 years old and has Down syndrome and autism.  As I flip the calendar to December, I can feel my anxiety level begin to arise. We all handle holiday stress in different ways. The movie, Christmas Vacation conveys this so well.

“I don’t know what to say.  It’s Christmas and we’re all in misery”

Christmas vacation cig pic

Here are 10 tips for surviving the holidays with your child who has autism:

  1. Start early, get as much done ahead of time with holiday preparations.
  2. Don’t rush, allow enough time to get from point A to point B. Give more notice when it is time to transition. This will help to avoid meltdowns.
  3. Be flexible and relax your expectations over the holidays.
  4. Pare down where you can, whether it’s decorations, presents, or parties. It’s okay to say no or bow out early.
  5. When possible try to stick to routines. Sometimes it’s easier to hire a babysitter or respite worker to stay at home with your child while you go to holiday parties.
  6. Make social stories using visuals or written words (depending on your child’s level of comprehension). This will act as a script for your child to follow.  If they can see what’s expected, they will understand the plan and won’t be as anxious.

Task strip for a trip to the mall…..

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Task strip for airline travel……

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7. Provide pictures of family members and friends that you don’t see that often prior to visiting them. If your child doesn’t like to hug then try a special handshake, high five or Nick’s favorite….

Elbow Bump 🙂

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8. Give your child opportunities to help out. Allow them to make choices between two things. This gives them more control during the holidays, (when we all feel a bit out of control at times).

Nick helps out with the luggage, which gives him heavy sensory work….

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9. Find a quiet place for your child to unwind. Most of us know how to do this on our own (bubble bath, crack open a bottle of wine, exercise, etc.). But a child with autism can get overstimulated and not know how to decompress. They may need you to help them to settle down and relax.

10. Get rest when you can and take time to pause and reflect on the blessings of the season.

Christmas vacation reflection

I hope these survival tips will help your family and child with autism.  As you flip over the calendar to December today, take a deep breath.  Your child will be feeding off your cues, so……

Keep Calm Christmas

That’s what is in my noggin this week.

~Teresa 🙂

Christmas 2

Nick and his brother Hank in 1999

Posted in Autism, Down syndrome, Fun Side of Nick

Re-Blog~ 5 Reasons I am Thankful for Nick

thankful

This week, a re-blog of #75 that I wrote last November:  5 Reasons I Am Thankful For Nick (who is 20 years old and has Down syndrome and autism). Click right here @https://nickspecialneeds.wordpress.com/2013/11/25/blog-755-reaso…nkful-for-nick/

Thank you for reading and sharing Nick’s world.  Wishing you all a blessed Thanksgiving. 🙂

~Teresa