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Posts Tagged ‘Autism’

Some days Skylar really struggles with going to church.  Yesterday, as I sat in worship, I got to thinking about why it is often difficult to take an individual with special needs to church.

It is difficult to explain the fears that many parents of special needs children have in taking their children into a worship service.  I hear from many families that they gave up going to church a long time ago!

Why is that?  Well, let me share with you my own thoughts on this matter.  Let me start off by saying that I am not speaking for all families that have a child with special needs, just MY family!  So here we go!

1)  PEOPLE STARE

This is a biggie!  I can’t even begin to tell you about the stares that we get.  You would think that it would be better in church, but nope..it isn’t!  This seriously saddens me!  I understand people’s curiosity, but for the love of all that’s holy, quit staring!  This wasn’t as much of an issue with us when Skylar was younger, but as she has grown into her teenage body, it has become more of an issue.  When you have a younger child in service who is a bit restless people don’t even think twice about it, but when you have a child who is taller than her mom and the age of a young high schooler, people are staring when she is hugging me tightly, holding my hand, rubbing her face against mine for that deep pressure input, or moving “a bit more than she should” during worship.  You know what?  If you can’t move during worship, when can you move?  One thing I won’t ever do is tell Skylar that she can’t dance during worship or tell her that she is singing too loud!  That is how she worships and I will never try to change that!  

2)  PEOPLE ARE JUDGEMENTAL

We do make Skylar stand and join us during the worship segment of church.  Some days she adamantly says “I am NOT singing with you today!” but we still ask her to stand and read the words on the screen.  

When it comes time for the message, we allow Skylar to use her i-pad (with the volume completely silenced). Some of you might think that is wrong and that is ok, but until you’ve walked a mile (or a quarter of a mile for that matter) in my shoes, then please keep your judgements and opinions to yourself!  This keeps Skylar happy and entertained so that Chris and I can listen to the sermon and be encouraged by God’s word!   My guess is that most people see Skylar on her i-pad, think that she is some teen that is bored, make a snap judgement about our parenting abilities, and then give us dirty looks, roll their eyes, or make comments loud enough for us to hear them.  Guess what?  When this happens, most people would be so hurt and angry that they wouldn’t darken the doorstep of your church ever again!  But oh no…not me!  I have been known to turn around and say “Just so you know, my child has autism!” which in turn usually leads to a horrified expression and something along the lines of “I’m so sorry!  I had no idea!”.  My point is not to shame people, even though that is often what they are trying to do to me, instead it is to educate people.  I hope that you will think twice before making snap judgements.  Church should be a safe place for people, instead many people feel more judged at church than any other place they go.  

 

3)  MOST CHURCHES DON’T HAVE PROGRAMS FOR INDIVIDUALS WITH SPECIAL NEEDS

When we meet other families with children who have autism and they find out we go to church, one of the first questions they ask is “Does your church have a special needs program?”  None of the churches that we have attended here in Prescott have had such a program.  This is something that we, as a church, need to step up and do something about.  This would be such an amazing ministry and blessing to families in our community!

Several months ago we were talking to some friends of ours that are church planters, who are very aware of Skylar’s needs.  The pastor said “Julie, as a church body, we are failing your family!”  I appreciated his candor.  He then went on to ask a question that I had never been asked in over 10 years of having a child with special needs.  ”What can we do as a church to serve families and individuals with special needs?”  Here are my responses:

-Churches need a buddy system!  We need individuals who will step up and hang out 1 on 1 with our kiddos during service.  Most of the time, most churches only have childcare/Sunday School for children through 5th grade.  Even though Skylar is in 8th grade, she wants to be with children that age.  Why not let her attend those classes?  If she had a buddy, whether it be an adult or an older member of the youth group, she could enjoy their lesson and be happy in that classroom.  The buddy doesn’t have to be the same individual!  Imagine if 4 people stepped up and said “I’ll take one week a month and hang out with Skylar!”  That would be awesome and I can guarantee you that not only would they be a blessing to us, but Skylar would be a blessing to them.  What a great thing to be teaching our youth!

-Churches need to come alongside families that have individuals with special needs and get to know them!  Many of us have learned more about patience, love, forgiveness, mercy, and grace than we could have ever imagined by parenting a child with special needs.  I, for one, know that my faith has grown by leaps and bounds this past 11 years.

So there you have it!  These are the reasons that we often find it tough to take Skylar to church. I pray that you will be open to getting to know individuals with special needs at your church!  I am confident that they will bless you far beyond anything you ever imagined.  Their joy is contagious!

This past Sunday was just like most Sundays!   Skylar woke up in one of “those” moods.  She immediately started saying she didn’t want to go to church. Unfortunately, it set my mood for the morning and I was just dreading going into service.  As I stood during the first worship song, Skylar LOUDLY whispered “I’m NOT singing with you today mom!”  I tried to clear my mind of the stress and sadness and I immediately prayed that the Lord would comfort me.  I also asked Him to bless sweet Skylar through the music.  I remember questioning whether or not I was doing the right thing by continually forcing her to come to church and wondering if she gets anything out of it.  The third song we sang was a mix of an older worship song and the chorus to Hallelujah (Skylar calls it the Shrek song as it was sung in the first Shrek movie).  As I closed my eyes to focus on the chorus, I suddenly heard Skylar’s sweet soprano voice carry over most of the voices around us.  My heart was overwhelmed with joy at the sound of her praising God!  As a tear rolled down my cheek, I thanked God for such an immediate answer to prayer, for comforting me, and for Skylar, who is such an amazing blessing to our family!  I truly believe that the Lord gave me a glimpse of what hearing the angels singing will be like!  

Whatever you do today, make it great!

JuJu

 

 

 

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Hello friends!  So excited to share the adventures of our Elf on the Shelf, Gracie with you today.  I need to give a shout out to my grandmother and Aunt Carol who shared the Elf on the Shelf craze with our family last Christmas.  I admit that I was originally against adding in this tradition, but I am really glad that we decided to do it!  The girls LOVED Gracie, but I’m pretty sure that Chris and I had even more fun with Gracie’s antics.

For those of you who are new to my blog, both of our girls are on the autism spectrum.  They are very literal and we usually know exactly what they are thinking, as it just spills out!  Hailey cracked me up with her almost daily comments about what Gracie had done.  I’ll add her thoughts below the pictures.

WHAT A “CUTIE”

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This was our first morning with Gracie and the girls thought she was pretty funny. Hailey jumped in on the fun and continued to take parts of the orange away during the day.

GOING FOR A SWIM

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“Good thing she didn’t eat all the Cheerios, Skylar would have been mad!”-Hailey

ENJOYING THE VIEW FROM ABOVE

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“That’s hilarious!  She must not be afraid of heights like you are mom!”-Hailey

HIDE AND SEEK

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TAKING A BUBBLE BATH

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We went down to Phoenix for an overnight trip and the girls didn’t want to take Gracie with us.  They wanted to see what she would do while we were out of town. This presented a challenge for Chris and me.  Gracie got all settled into her bubble bath right after the kids got in the car.  When we returned home the next day, the marshmallows were pretty stiff from sitting out for about 24 hours.  Hailey said, “Well that can’t be comfortable!  Why would she want to bathe in hard marshmallows?”

TAKING OVER

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“I can not believe that Gracie knocked the angel off the tree!  That should definitely put her on the naughty list!”-Hailey

SUCH A JOKER

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CELEBRATING SKYLAR’S BIRTHDAY

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“I can’t believe Gracie didn’t eat all of her cake!  It was SO good!  Can I have the rest?”-Hailey

JUST A SIP

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“Well that’s a waste of a perfectly good straw!”-Hailey

A LITTLE LIGHT READING

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This is a really blurry picture, but Hailey’s comments were some of my favorite.  She said, “Oh my word!  Why is she reading Twilight?  Who told her those books were good?”

MISSING SANTA

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REPLACING OUR STOCKINGS WITH UNDERWEAR

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“Wow!  I hope those are clean!!!”-Hailey

SUGAR HIGH

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GREEN MILK

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“EWWW!  How’d she do that?  That is really weird!”-Hailey

VANDALIZING

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“What a waste of toilet paper!  You’d better save that, I’m sure we’re going to need it!”-Hailey

Thanks for reading about our adventures with Gracie!  The girls were excited that she left a note saying goodbye and that she would be back next year.

Blessings for a great New Year for all of you!

Make it great!

JuJu

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Dear Ann Coulter,

I’ve long thought that even though we, as Americans, are politically divided, that underneath it all, we are all still human beings.  Human beings that want what is best for this country. Human beings that care for others. Well, that thought ended last night!  I can’t even begin to put into words my utter disappointment when you took to Twitter and called the president a “retard”.  Really?

When you use that word,  you hurt thousands of individuals with disabilities.  One of those individuals is my sweet daughter.  We were told over 10 years ago that she had “mental retardation”.  These past 10 years she has taught us more than we could ever teach her.  She has taught us patience, joy, encouragement, forgiveness, hope, acceptance, and unconditional love.

Ann, our daughter is NOT a joke!  She is more than you could ever aspire to be! Open your eyes and your heart.  And for the love of all that’s holy, please think BEFORE  you open your mouth or pull out your smart phone.  Think of our sweet girl and know that you hurt her, and all those like her, with your insensitive and hateful words!

Ann, meet Skylar!  You could learn a LOT from her!

Signed,

JuJu ( A mother who will stop at nothing to protect her children!)

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Last week I shared a post about what I’ve learned since starting to homeschool with a virtual academy.  If you missed that post you can read it HERE.   We are now in our 7th week with homeschooling and we are definitely into a better groove.  We still have days that are tougher than others, but overall we are doing well!  When I get overwhelmed or discouraged, I like to focus on the positives of our situation.  It makes me feel so thankful for where we have been and how far we have come. So,  today I want to share with you my favorite things about homeschooling so far.

1)  SEEING THAT “LIGHT BULB” MOMENT

-There is nothing better than witnessing the moment when your child “gets it”!  I have been so blessed to be able to witness many light bulb moments since starting school 7 weeks ago.  I have found that most of these moments for my girls happen during math.  It truly excites me to know that I’m a part of my child’s learning!

2)  SEEING THE EXCITEMENT ON THE GIRLS’ FACES WHEN THEY DO WELL

-In the program that we are using, the girls typically have a short assessment at the end of each lesson.  It is usually anywhere between 6 -10 questions and tests whether the girls have captured the information from their lesson.  Immediately upon completing the assessment, a screen pops up with their score.  I absolutely love the reactions that we see when they get 100%.

Skylar squeals with excitement and screams “I got 100!”.

Hailey usually says “I totally ROCKED that lesson!” or “Oh yea, I am SO smart!”.  I love hearing those words!

3)  SEEING THE GIRLS APPLY WHAT WE HAVE LEARNED TO OUR EVERYDAY LIVES

-Pretty early on we did a science lesson on the scientific process.  You know….observations, forming a hypothesis, testing, dependent and independent variables, conclusions, etc.  Well, a few days following our lesson Hailey opened the refrigerator and said “If I don’t put these tacos in the fridge, then they will go bad!  How’s that for a hypothesis mom?”  I loved it!  Since then, she has formed MANY hypotheses!

-We also did a lesson in history/geography on longitudes and latitudes.  Chris and I have been watching reruns of the show Alias.  In one of the episodes they were using a GPS device and the longitude and latitude coordinates popped up on the screen.  Hailey was walking by and quickly said “Hey!  Did you see that?  They just showed the longitude and latitude of where they are.  Now they will be able to be rescued!  That’s cool!”

I truly love these moments!  They may seem little to some, but they are HUGE to us!  I also love that I have been able to share these moments with other parents that have children with special needs and that they rejoice with us.  One thing having 2 girls on the autism spectrum has taught me is:

EACH AND EVERY VICTORY IS WORTH CELEBRATING!

4)  NO MORE “MORNING RUSH”

-This was my least favorite thing about getting the girls up and ready to go to school each day.  Both of our girls move at their own paces and trying to get them to move faster would only lead to frustration, tears, and bad attitudes.  By the time I got the girls dropped off at school I felt like I needed to come back home and take a nap. Chris even mentioned this week how much he doesn’t miss the morning chaos.  He said that the absolute chaos often sent him to work in a bad mood and it would take half his morning to really relax and be settled.

5)  FLEXIBILITY

-We are pretty routined, but it is nice to know that we can pick up and go when needed.  My sister moved this past week and we went down to Phoenix on Monday and Tuesday and helped her unpack.  The girls worked solely on Math and Language. Hailey also worked on Spanish.  I knew that this would most likely stack the end of our week heavier, but it allowed us to help my sister and her family.  We also got to see my niece swim in her high school swim meet.

-We don’t have to follow a strict schedule each day.  As long as we complete all our lessons for the week (5 Math, 5 Literature, 5 History, 5 Spanish, 3 Science, and 3 Art) we are good.  If we choose to do all 5 Math lessons on Monday, that is fine! This week we did only Math and Language on Monday and Tuesday because those are the subjects that the girls can work on a bit better on their own.  That allowed me to help my sister a bit more.

So these are my 5 favorite things about homeschooling so far.  I look forward to adding more things to this list as time goes on.

Do you homeschool?  I’d love to hear your favorite things about homeschooling! Please share them with me in the comments.

Hope you all have a great weekend!

Make it great!

JuJu

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I am so excited to share with all of you that Skylar finally got an adaptive bike! Let me share how Skylar came to be riding this fancy set of wheels!

Many of you might recall that I shared here on my blog several months back about how we were trying to raise funds for an adaptive bicycle for Skylar.  The bike we were originally looking at was priced at about $1,600.  Shortly after writing that post I received an e-mail from a couple, Henry and Yvonne, who were in a Bible study with my parents when they lived in Virginia years ago.  Both Henry and Yvonne are avid bikers and they wanted to come alongside us and help us pick out the perfect bike for Skylar.  We kept in touch over the next several months via e-mail.

Over the course of those few months my mom did a jewelry fundraiser and we sold autism bracelets to help raise the funds for the bike.  We also had multiple people who donated money to her bike fund as well.  We had raised a significant amount of money and were encouraged until the beginning of May, when Skylar’s physical therapist actually priced out the specific bike Skylar needed and it was over $2,200. That definitely took the wind out of our sails!  After seeing the cost of that, I told Chris that we needed to specifically pray that God would provide exactly what we needed!

A couple of weeks later while I was in Tucson, I received another e-mail from Henry and Yvonne.  Henry told me about a gentleman, Bill, that he had read about on one of the biking message boards he regularly reads.  You see, Bill has a passion for biking and a heart for individuals with special needs.  Bill had already built bikes for individuals with Autism, Down Sydrome, and Cerebral Palsy.  The best part was that Bill lived in the Phoenix area which put us in pretty close proximity to him.

Henry asked if I would be interested in connecting with Bill to see if he could build a bike for Skylar.  Of course I said “YES!!!” and within hours I had already heard from Bill and set up a meeting for the following week.  I actually sent a copy of what the physical therapist had stated she needed and information about Skylar’s cognitive delays, low muscle tone, and issues she has with her feet.  I was overjoyed and so encouraged when he wrote back and said that he would be able to build a bike for her and for a fraction of the price!

It took about 3 weeks for the bike to be built and we were so excited when we got word that it was ready for pick-up!  The pictures below are of Skylar and Bill, who is also known as “Yoda”, and the first time she got to ride her bike out in front of his house.

I can not begin to describe to you the range of emotions that I felt as I watched her peddle her new bike around the cul de sac.  Her huge smile made my heart burst!  I loved hearing her words as she rode her bike.

Look guys! I’m riding a bicycle!

I totally love my new bike!

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Thank you Mr. Yoda for building me this bike!  It is perfect!

We left the next morning for Albuquerque and were thrilled to take the bike with us so that my parents could watch her ride.  I asked my sweet friend Sara, who was my co-worker in the health office when I was the school nurse, if she would come up and snap some pictures of Skylar and her new wheels!  Sara just started her own photography business, Two Brunos Photography, and I have been an admirer of her photography skills for years!  If you live in the Albuquerque/Rio Rancho/Santa Fe area and want to have pictures taken, check her out!  You won’t be sorry!

I’m so excited to share some of my favorite photos that Sara took with you.

And this is my most favorite!  She was on her way back to the car and singing her heart out!  It truly was just the most perfect moment!

I am thankful for so many things!

I am thankful for Henry and Yvonne who put us in touch with Bill!

I am thankful for Bill Irvine who made our dream of getting Skylar an adaptive bike a reality!  Thank you just doesn’t seem like enough!

I am thankful for my friend Amy, from Ohio, who spread the word about our efforts! Her family and friends were so generous in their donations!

I am thankful for so many of you who bought autism bracelets and other jewelry to help us raise the funds for the bike!  And for those of you who sent money with a simple note “I want to help Skylar!”

I am so thankful for my mom and dad who continue to pour their love and energy into this sweet girl who has brought us so much joy!

I am so thankful for Sara, who gave her time and talents to capture these pictures of Skylar and her new wheels!  You can like her page on Facebook here!

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I am so thankful for all of you who continue to pray for Skylar and Hailey and the long journey that we have ahead of us!  We couldn’t get through without all of you and those prayers!

If you would like to get in touch with Bill “Yoda” Irvine regarding having a bicycle built and for pricing information, please shoot me an email and I can send you his information.  You can do so by either clicking the link in the upper right-hand corner of my blog or sending me a message to iamjujublog (at) yahoo (dot) com.

As always, I’m happy to answer and questions you might have.  You can either leave them in the comment section or send me an email.

I hope you have a wonderful week!

Make it great!

JuJu

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I know, I know!  It’s been a long time since I’ve posted a No Filter Friday!  For those of you who are new to my blog, this is the time that I love to share things that the girls have said or done that have left us red-faced, laughing, and sometimes speechless.  I have mainly shared stories of Skylar and her lack of filter here on my blog, although Hailey also lacks a filter, just to a lesser degree. In many ways it is refreshing how brutally honest the girls are, but it can be embarrassing. This is by far my favorite thing about having 2 girls on the autism spectrum.  The “lack of filter” is hilarious!  If you are new to my blog or missed previous posts, you can click here for a complete list of No Filter Friday stories.

Yesterday, we took Hailey to her gymnastics class at the Y.  We sit in this little room off to the side so that I can see Hailey and so that Skylar can see the TV.  Picture a room the size of my kitchen with about 8 adults and 15 kids in it.  That will give you an idea about how packed in there we were.

Skylar sat with a bunch of little kids most of the time watching Toy Story 2.  Not long before gymnastics was over she got up and walked over to the area in front of me that houses multiple recumbent bikes.  What a great idea to have excercise equipment so that we can workout while our kids do!  Now just to actually get on the bike instead of sit behind it, but I digress!

Skylar looked at the bike and said to me “Mom, I’m going to do a bit of excercise!”.  I responded with “That’s great honey!  Way to go!”

After a few minutes of pedaling she let out a large sigh and exclaimed very loudly:

OH MY! MY BISCUITS ARE BURNING!

I just burst out laughing and said “Your biscuits are burning? What are your biscuits?”

Skylar gave me the look that only she can give.  The look that blatantly screams You don’t have a clue!  She then said:  Mom, you know what I’m talking about!  My bum, my bottom, my behind, my butt!  You know….MY BISCUITS!

Thank you Skylar for the lesson on all the things we can call our bum!

Gotta love this girl!

I hope you all have a wonderful weekend!

Make it great!

JuJu

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These are our dear friends the Hopkins!  Buddy was tragically killed last Thursday, June 21st by a hit and run driver who hit him from behind while he was jogging.  We can not even begin to put into words our grief over the loss of this amazing husband, father, son, and friend.

I met Heather in 2008 when she walked into my health office at the elementary school where I worked.  Their family had just moved to our town for Buddy’s job and Heather was struggling.  We talked for quite some time and during that conversation I learned that her son, Garrison had autism.  I told her about Skylar and I could tell that she was instantly relieved to know that she had met someone who was walking a similar path as she was.  As I sat there chatting with her, I was overwhelmed with the need to get up and hug her.  I got up from my desk, told her I needed to hug her, and the rest, as they say “was history!”

We spent countless hours with the Hopkins family.  Buddy kept us laughing with his hilarious comments and that one-of-a-kind smirk.  We were sad to see the family move away from New Mexico but kept in contact all these years.  We enjoyed all of their return visits and I was so blessed to be able to go to Texas and spend time with their family a couple of summers ago. Heather is truly one of my very best friends!

Buddy loved his family more than anything on this earth!  His love for Heather and the kids shined through in his daily life.  He coached his girls’ softball teams and he was constantly taking Garrison camping with the Boy Scouts.  He also had a passion for Special Olympics and was at every event to cheer Garrison on!  Buddy was constantly serving others!  What a legacy he left behind!

Two days before Buddy was killed, Heather and I had spoken and we made plans to meet up in Flagstaff next week as their family would be travelling on vacation.  We were so excited to see each other as quite a bit of time had passed since we had last seen them face-to-face.  Instead, we will now be going to Flagstaff to attend Buddy’s funeral and support Heather and the kids in any way possible!  It is truly unreal!

I can not even begin to imagine the tough days that Heather and the kids have ahead of them.  While I know that they will have a difficult journey emotionally, it is my heart’s desire that they will not have to struggle financially as well. No, money will not take away the pain of this tremendous loss, but I’m hoping that the outpouring of love and support shows Heather and her family how much people care! This is where all of you come into play!

I am asking all of you who are willing and able to donate in one of the following ways to help out Heather and her sweet family!

1)  A fund has been set up at the American Airlines Credit Union in Texas.  You can donate at any one of their branches under “The Buddy Hopkins fund”!

2)  You can also donate via paypal. This is an easy way for all of my international readers to donate!  You can send any donation to: Hdhopkins@hotmail.com

3)  You can mail a check made out to Heather Hopkins to me and I will forward them on to her.  The address to mail them to is:

Julie Coryell

2200 Lone Oak Way

Prescott, AZ 86305

I challenge everyone to donate $20 (or more if you can) to this precious family!  And I am asking that all of you share this post with as many people as you can.  Please help me come alongside this sweet family and help ease the financial burden they face.  Those of us who have children with autism, or any special need for that matter, know the financial difficulties that come with that.

I’m so thankful for each and every one of you!  So many of you have supported our family!  Heather has been one of my biggest supporters since entering the blogging world and I want to do anything I can to help her now!

Make each day count!

JuJu

*Please share this post via Facebook, Twitter, email, or any way you can to help spread the word about how we can help Heather during this difficult time!*

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Happy Friday!  It has been quite awhile since I have posted a No Filter Friday story. Life has been hectic, as I’m sure it has been for all of you.  Thank you for all of the sweet e-mails, messages, & text messages that have said something like “We’ve missed the No Filter Friday posts!  We need our dose of total honesty!”

For those of you who are new to my blog, this is the time that I love to share things that the girls have said or done that have left us red-faced, laughing, and sometimes speechless.  I have mainly shared stories of Skylar and her lack of filter here on my blog, although Hailey also lacks a filter, just to a lesser degree. In many ways it is refreshing how brutally honest the girls are, but it can be embarrassing. This is by far my favorite thing about having 2 girls on the autism spectrum.  The “lack of filter” is hilarious!  If you are new to my blog or missed previous posts, you can click here for a complete list of No Filter Friday stories.

Today’s story is not embarassing, but actually shows Skylar’s inability to lie.  Or maybe I should say her inability to lie well!  Many times when we ask her if she is responsible for a mess or the “mysterious” disappearance of the cookies from the pantry, we don’t even have to wait for an answer….her face gives her away immediately!

A couple of weeks ago I was sitting at the dining room table when Chris and I had the following exchange:

Chris:  Julie, do you know which one of the girls used my toothbrush?

Me:  No. What makes you think one of them used your toothbrush?

Chris:  I put it in my drawer after I used it and it is now on the counter.

Me:  Well, I doubt it was Hailey because she is such a germaphobe.  Skylar should be coming upstairs in a few minutes, just ask her.

A few minutes pass and Skylar makes her way into the bathroom where Chris and I are getting ready.  Chris picks up his toothbrush and says “Skylar, did you use my toothbrush?”

Without a moment’s hesitation Skylar responds with:

That is YOUR toothbrush??

Chris:  Well, that answers that question!

Me:  Why did you use dad’s toothbrush buddy?  Your toothbrush is right here.

Skylar:  It is such a pretty toothbrush so I decided to use it.

Chris:  Well, it’s your toothbrush now!

Skylar:  Oh good!  I like that toothbrush!

Me:  Chris, maybe if you didn’t have such a girly toothbrush this wouldn’t have been an issue!

Chris:  Whatever!  That’s what I get for living in a house full of girls!

I hope all of you have a wonderful weekend!

Make it great!

JuJu

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Ten years ago today was by far one of the worst days of my life!  I had awoken early as I was singing at church with my friend Louanne.  I went in to check on Skylar and found her unresponsive.  I immediately picked her up and brought her into the living room.  Within minutes she started seizing, 911 was called, and we were swept away by ambulance to the hospital.

Chris, Jenny, and I sat in a darkened emergency room waiting to see the pediatric neurologist.  She had already had a CT and an MRI.  As we waited to hear whether a brain tumor or a structural abnormality were the cause of the seizure, I prayed that the Lord would equip me for whatever road we would walk.

Outside of our room at the nurse’s station, there was music playing, streamers, and chips, salsa & queso for Cinco de Mayo (we lived in Tucson).  I remember saying “I will never, ever think of Cinco de Mayo without remembering this day!”

So last year on Facebook I mentioned that each May 5th we celebrate a sweet girl who has overcome so many different obstacles.  We thank God for each and every day that He has allowed us to have her.  My sister-in-law, Diane quickly replied “Happy Cinco de Skylar!”  I loved that so much!

So today I wish you a Happy Cinco de Skylar!  Please join us in celebrating an awesome kiddo who has brought so much joy to our lives!

Make it great!
JuJu

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A few weeks ago I was down in Phoenix for Skylar’s physical therapy evaluation. Afterwards, we met up with my sister at her favorite local hangout, Luci’s.  Before we headed out for the 2 hour drive home I ran to use the restroom. The beautiful apple artwork above was hanging on the wall.  As soon as I saw it, I immediately had so many thoughts start running through my head.  I ran back to the table & grabbed my phone so that I could snap a picture. Oh yes I did!

Many of you might ask “What is so special about these apples?”

Well, I immediately saw my girls in these apples!

-They are both different in many ways from many of the people we come in contact with, but they are absolutely beautiful souls!

-Unfortunately, many people see individuals on the spectrum (or any individual with special needs) as “less than” other human beings.  They feel a sense of pity.  When I look at the picture above I think how the red apple is different from the rest, but it is still an apple!  My girls are still beautiful, unique human beings!  They aren’t “less than” anyone!

-Different isn’t bad! Different is different! Sometimes it is hard, but many times it is beautiful!

As I drove home I thanked the Lord for the beautiful reminder of how differently beautiful my sweet girls are!  It was just what I needed!

Thanks for letting me share!

JuJu

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