It’s nice to take a break…

It’s been a while since I’ve posted an update; just thought I would take some time off. Jake’s been doing great! We had a great summer with lots of swimming and a little bit of therapy. It was really nice and relaxing!

One of the best things that Jake has learned over the summer is how to dress himself with no help from me! Oh my, how I’ve waited for this day! Up until about 4 weeks ago I had to help him with his clothes. I was getting frustrated thinking, he’s 8 he should be able to do this now. But like everything else it takes time. One day after swimming I told him we needed to get changed and he said “I think I can do it by myself”. He ran upstairs and was up there about 20 minutes. The look on his face when he came out of his room was priceless…he yells “I DID IT!!!”. This was HUGE!! We’ve been working on this skill since he was 3; that’s 5 years! It is SO nice for him to be able to dress himself! Now I can send him upstairs and in about 5 minutes he’s dressed and ready for school!

Jake also learned to swim! He was very reluctant at first and I didn’t think he would do it this year. We took swim lessons at the beginning of summer and let’s just say it was trying for his swim instructor. She showed him the basics but he wouldn’t really even try with her. When we would go swimming Jake wouldn’t put his face in the water, he cried when I tried to help him swim and wouldn’t jump in the pool. About two weeks after his lessons he started working on his own and then overnight, he was swimming, going under water and jumping in the pool. 

Jake started 3rd grade two weeks ago and for the most part it’s been going well. He’s had to adjust to a lot of changes which has been the hardest part for him (and me). Going from the lazy days of summer to a stricter routine and then having two teachers instead of one as well as getting to know new kids in his class, is a lot for Jake. In my opinion, the hardest part of the new school year is more is expected from him. He’s older now and as many of us know or may remember third grade is difficult for most any child and having autism makes things a bit more difficult. But Jake’s learning the new rules, mostly the hard way. He has learned not to write that his teacher is mean, not to cheat on a test, not to yell no to his teacher and is learning how to work with a team. He’s adjusting as best he can but it’s a struggle. It’s been a struggle for me as well, I pray every day that he is a good listener and is following the rules. We are fortunate to have two outstanding teachers this year that are challenging him and working with him to find his strengths and help him with the areas of weakness. I really do believe it will be a great year for our boy!

Currently, Jake is interested  in logos for things like NBC and comparing them to their original logo and telling me how and when it originated and then showing me what the logo looks like today. I honestly never cared and never thought about different television logos or movie logos or toy logos but now I find it interesting. The best part is Jake is initiating conversations. He has found something he enjoys researching and wants to share it with me. And I love this!!

We’ve walked this autism journey for a little over 6 years now. The biggest and smallest tasks take a lot of time. Much of the time I want to rush it but it always backfires on me when I do this with him! As he gets older things change and I am constantly trying to figure what will work this time to help things click. I can go from feeling overwhelmed, frustrated and angry to feeling great pride all within a minute, at times. But it’s all worth it to see him succeed! And he’s doing just that. He’s growing and learning and talking with us more and more each day. 


Summer Fun



2nd grade wrap-up

It is hard to believe Jake has only a week left in the 2nd grade! In some ways it feels like this school year has been long but mostly it feels like it flew by.

Jake has an amazing teacher and advancing to 3rd grade is very bittersweet! The first day we met Mrs. Hansen, Jake was drawn to her and responded to her quickly. She wasn’t all gushy and sweet and over-the-top nice. That sounds a little strange, but Jake doesn’t need that or want that all the time especially meeting someone for the first time. She was extremely nice and kind but her tone let Jake know she was his teacher and he would follow her rules. He quickly fell in love with her; wanting to make her proud and to show her he could do anything she asked of him. Jake had some rough days but overall he has absolutely loved being in her classroom and told me just a couple of nights ago that he wanted Mrs. Hansen to be his teacher forever. That says something about a teacher when you’re child doesn’t want to leave their classroom.



One of the things I love the most about Jake’s teacher is she not only teaches the required subjects but also teaches respect for others, kindness and the inclusion of others. And in return, from what I’ve seen when I’ve been in the classroom, the kids show her as well as their classmate’s kindness, respect and are always including each other in different activities. As a mom of a child who is autistic this means so much! I know this is only 2nd grade but this is where and when our kids learn this stuff and hopefully take that with them as they go through life. Jake has always been welcomed and cheered on and made to feel important by his peers. Even when Jake is having a rough time I have heard encouragement from his friends trying to help him get back on track.



Jake loves being a part of his classroom and doing what the other kids are doing as well! Last week the 2nd graders had their spring musical where they had to dress up as a classic storybook character. We chose Tom Sawyer. At first, Jake wasn’t sure about this as he isn’t a fan of wearing anything except his normal clothes. But he wanted to do it! He asked me several times if he wore his costume would he would still be Jake? He wanted to make sure people wouldn’t forget he was Jake; this made me smile! He wore his costume with pride and I have to say he was such a cute Tom Sawyer!! He put aside his anxiety and for this kid, that is HUGE!!



The progress we’ve seen with Jake this year has been fantastic! He has learned to speak up for himself, he’s become much more independent and able to initiate small conversations with us at home. One of the best things I’ve personally seen is his ability to carry information that he has learned during the school day over to home. Most of the time what he learns at school, stays at school. And what he learns at home, stays at home. But I’m seeing that he is able to make the connection now and do the things he is able to do at school at home and vice versa. He will also remember things Mrs. Hansen wants him to tell me and many times he will make me repeat to him what he said so he knows I get it (something we do with him all the time). Jake is also learning to be proud of himself and his accomplishments. He may have always been proud but hearing him verbalize it is so cool! Recently we were talking and I asked him “Who is proud of you?” and he said “Mommy, Daddy, Sissy and Mrs. Hansen!” I asked him “Who else is proud of Jake?” He thought for a moment and said with a huge smile “I’m proud of Jake! I am proud of me!”



autism acceptance

April 2nd is National Autism Awareness day. It is neat to see that in the short time we have been on this journey how many people now know what autism is or at least some form of the definition. When Jake was first diagnosed, nearly 6 years ago, I had to try to explain what autism was to us. Being new, I had a hard time. I don’t have to explain it very often anymore which is awesome! Accepting someone with autism is great but being aware is even better, in my opinion. When you are aware then you are more likely to accept. Autism is a large part of our lives and knowing that because of days like today, Jake can be Jake and others get it 🙂

For the past week or so I’ve talked to Jake about autism and what it means to us; to him. It is hard to explain to a child who has difficulty processing information. I really want to make sure I use the best words so he understands, words that don’t scare him or make him self-conscience which could lead to insecurity. Anyway, it is not easy. Over time he will understand more and more, it is just a slow process that we will talk about for a long time until I feel he fully understands.

The color chosen for autism awareness day is blue. Everyone is supposed to “light it up blue” and wear blue to show their support. I think it’s great but having a child on the spectrum who doesn’t fully understand the “rules” wants to wear red because that is his favorite color. Jake will wear blue, in fact, he has a lot of blue in his closet but when I was showing him the shirt he was going to wear he said he had to wear red. I asked him why and without missing a beat he tells me “I like red and that is my color” he walks away; end of discussion.

I think it is so awesome that the school district we live in recognizes the special needs community and does their part to raise awareness not only for autism but for other disabilities as well! Tomorrow, Jake’s school will be wearing blue to show their support, raising awareness and acceptance to those who are autistic. I love it! If you see Jake tomorrow, he will be wearing his red shirt and probably smiling! There is a meme that says Autism; Always Unique Totally Interesting Sometimes Mysterious. That’s my boy and I love it!!





things are starting to click

This year has been different for us. I know it is the beginning of March but I feel as if we’ve been in 2017 a lot longer! We’ve seen a lot of changes in Jake. He recently turned 8 and we’ve had just as many birthdays, Valentine’s and Christmas’s. But this year it is as if he is experiencing them for the first time. We have our traditions and do the same thing each year because that is how Jake likes it; change is not good in the Dickan household. 

This past Christmas Jake loved the decorations. He was super excited to get our tree and looked in awe each time a new present appeared under the tree. When he would find one with his name on it, he would look at me with this quizzical look and ask “is this for me?” I would tell him it was because it had his name on it; he would stare in a little bit of confusion and then it would turn to excitement. I asked him if he remembered getting gifts before at Christmas and he said he did. I couldn’t help but wonder if he just went through the motions, not understanding. On Christmas morning he was excited to see what Santa brought and to open his gifts. With each gift he was thrilled, like most kids, but there was something different. It was as if this was his first Christmas. You know the ones where our kids finally “get it”. 

The same thing happened on his birthday. He saw his presents and kept asking if they were for him. Valentine’s day I had a card for him and he looked at it and again asking “Is this for Jake?” (he often talks in the third person), I asked him if it had his name on it and he said it did and then asked “why are you giving me a card?”.  I said “It’s for Valentine’s day and I love you!” He smiled and said “cool!”.  Everything seemed new to him. I asked if he remembered past birthday’s and Valentine’s days and gifts and he just smiled. I’ve tried to get more out of him to no avail. 

In a way, it is all so strange to me. How can we do the same thing for 8 years and then all of a sudden it is brand new? Autism. Although, we have been on this journey for 6 years we are all still learning. I just scratch my head, try to keep up and understand to my best ability. It is hard and frustrating most every day. But thankfully Jake is happy. I wouldn’t change who Jake is but I sure would love to get inside his sweet head and know what he is thinking, why he is thinking it and to see the gaps that keep him from being able to tell me these things. One day…






What I want to tell the person who called my son weird!!

I heard what you said when you thought no one was listening. You called my son a name; you said he was weird!  It wasn’t said in a joking way it was said with disgust. It hurts my heart for Jake and I pray he wasn’t nearby when you said what you said. He knows what weird means and has been called this before. He tells me from to time he is weird and I have worked hard trying to get this label out of his head.

Just so you know, we are all a little weird in our own ways. I don’t think there is one human on the planet that doesn’t have their own quirks or something that others think is different. I mean, God created each one of us as individuals and no two people are alike. We all have similarities and differences, that’s what makes us all unique; in my opinion. It’s a sad world when someone feels he or she needs to point this difference out in a child to make themselves feel better especially when this child has special needs!

I’m sure you said this because he makes you uncomfortable and you don’t know how to talk or relate to him. Try treating him with respect and he will open up to you! Please know that I do everything in my power to keep him calm and help him try to have conversations. Jake needs help talking to people, he is still learning social skills and needs someone who will respect his autism and to be patient.

Jake is autistic and if that makes him weird then I have some books I want to share with you or we can have a conversation or two; if that would help. Jake did not choose to be autistic nor did he ask to be called names by adults or anyone else. Jake is different. I love this about him! He is smart and is developing a sense of humor. It may not be what you might expect or understand but he is pretty funny. Jake is developmentally delayed which means he isn’t like other children you may know who are 7 years old. Jake’s autism is a processing disorder which means when you talk to him he may not fully understand and might need a minute or need you to repeat the question so he can process the information. It isn’t because he is weird; he is autistic!

Before you judge my child or any other child think about this; what entitles you to call anyone, especially a child, a name?

I also want you to stop and think about all the hard work and time that we have given Jake, as well as all the hard work Jake has completed to get where he is today. We have spent countless hours and not to mention thousands of dollars over the past 6 years to help him to be able to do what he does today. But I’m sure you don’t think about these things because you’re too annoyed that Jake doesn’t talk to you or seem interested in you. Jake is interested, and although you think he isn’t paying attention; he is! He watches every move you make and hears every word that comes out of your mouth. I will say this again, he just needs someone who will approach him, treat him with respect and to be patient!

Jake is awesome and yes, I’m his mom so I’m biased, but he works every minute of every day learning to accomplish new things. There are a lot of people who see the strides he’s made and see the possibilities that await him in the future. I’m just asking you to take a moment when you are with my son and give him a chance before the name calling begins. When given the opportunity he will change how you view autism and all kids with special needs.


Jake’s Mom ~ the one person you don’t want to mess with when it comes to my son who is autistic!

Jake doing what he loves best; iPad on his exercise ball 🙂

the first time…

The past few weeks we have seen a lot of growth in Jake. These weeks have been full of many “firsts”. These warm my heart and make those very long day’s worth ever second. For those with children on the spectrum, no matter where they fall, persistence pays off. The hours of tantrums, tears and emotional break downs, both the child and the parent, there is light. It might not be this huge TA-DA moment but they are there. Keep hoping and doing what you do. Even if your child is not on the spectrum but you find this parenting thing so hard; there is always that light and the hope for what will be in the future!

Here are a few things Jake has been up too lately:

  • Jake told me he loved me! I didn’t say it first. He called my name and said “I love you!” I honestly, had sort of given up expecting to ever hear him say these words to me without me saying them first.
  • Jake has been talking nonstop. Less than a year ago I wondered if we would ever have any type of real conversation. His conversational speech has improved just over the past couple of weeks. He is always telling me something he has read or seen or something he thinks is interesting. He wants to make sure I am listening and asks questions and we go back and forth. Ask him anything about Transformers and he will tell you! This is the majority of our conversations but hey, I’ll take it! I always wanted to know the history of Optimus Prime – ha!
  • Loud noises have always bothered my boy. He will cover his ears, fall to the floor, curl up in a ball and cry. Jake used to do this with all loud noises but lately if they are expected they don’t seem to bother him in the slightest. This past Friday we attended the school’s annual fundraising race. The music was really loud, the kids were even louder and Jake didn’t seem to mind how loud it was. I was watching him to see if he needed my help but he did not! He danced, cheered and shouted with his friends!
  • Jake ate a lollipop. He doesn’t eat and won’t try any type of candy. He had gotten one at school one day for being a good helper or something, got in the car opened it and started sucking on it! What?!?! He didn’t eat the whole thing but he tried something new!
  • Jake tried a popsicle. He hates cold things and has been offered popsicle’s many times but this past Friday he decided to try one. He might have licked it once but he held onto that thing like it was a prized possession!
  • Jake allowed his hand to be written on with a sharpie, something for school, and didn’t hate it.
  • Jake got a temporary tattoo at school. Now this one was a little harder for him, he really wanted it because it was part of the race day. After I put it on him he wanted it off. He hid his arm and wouldn’t let anyone see it. He picked at it, licked it and did everything he could to get it off. BUT he didn’t cry or freak out; huge moment here!
  • Jake will say hi and wave to people he knows and responds when someone says hi to him. This has been a long long work in progress and one of the biggest moments thus far in our journey. It is almost strange for me to hear a child say hi to Jake and he responds with hi. I really couldn’t believe it when this happened the other day! (Thanks Dr. Allison!!)

Jake wouldn’t be where he is without the many wonderful therapists (I’ll write more about them later) that have helped Jake. Right now he has this amazing teacher. She treats him with respect and pushes him just enough. Jake trusts her, he loves her, he respects her and because of this he feels secure to try many new things.  Jake had the best 1st grade teacher and I didn’t think he would be lucky enough to have another great teacher but we do; Jake is blessed!



So you can see, anything is possible! Keep encouraging, offering and keep moving each day. You just never know when your child will do something that you didn’t think he would ever do! Jake may never get his hands super messy finger painting, he may never run through a sprinkler, write without a struggle or try unfamiliar foods. But just because he refuses something today doesn’t mean he will always refuse. There is this hope that I have and with that hope I am certain he will do many more things that today he doesn’t!




keeping it real

Life with an autistic child is hard! Jake is 7 1/2 years old and although he is verbal and incredibly smart we still have many challenges. I write a lot about his progressions but many times I don’t elaborate on the hardships we face daily. I am a “the glass is half-full” type of person. There is always a positive side of things and my dad brought me up to always look for the “good” things that happen, focus on those and don’t dwell too much on the difficult. Therefore, I tend to write about Jake’s struggles but I don’t focus on those too much because I know in the end they will work out. All of that being said, I do see Jake’s challenges and look for them all the time because without seeing where he is having a hard time I won’t know what to work on with him.

So I wanted to invite you in to see some of our daily struggles with Jake.

Life with Jake is very rewarding but it is extremely hard and can be extremely frustrating. I get frustrated daily and sometimes I feel I stay frustrated the entire day. I stay tired. My mind doesn’t shut down unless Jake is asleep. Jake is in the second grade and these are some of the things that he has a hard time doing without help.

Jake cannot dress himself. He can put on his own underwear and shorts but it is hard for him and starting the day trying to get him to dress himself sets him up for a troublesome day. So most mornings I dress him from head to toe. Socks are incredibly difficult for him, I’ve tried every brand but his motor skills aren’t where they need to be just yet and he struggles. Jake is fully potty trained and stays dry each night. YES!! This is a HUGE deal. It only took 4 years to get where we are today. Jake cannot wipe himself though, we try and we work on this with him but let’s just say he can’t do it yet. Jake cannot bathe himself. I still have to give him a bath, wash his body and hair. He is learning how to wash his body but in order for him to get clean he needs my help. Jake hates the shower and won’t even try it! You might think, just keep trying it and eventually he will like it. I do try but each time I bring up the subject panic sets in for Jake. He has never liked the rain and the shower is very similar. The thought of water sprinkling on him gives him so much anxiety and the fear that comes across his face is nearly heartbreaking. I know he won’t always be like this but like everything else it is a work in progress. Jake cannot brush his teeth alone. He has difficulty holding the tooth-brush and moving it around in his mouth and he doesn’t fully know how to spit. I have to brush his teeth and try showing him how to spit. He can spit a little but has a hard time with this concept. Jake cannot blow his nose. We work on this too. He has a hard time drinking from an open cup. He can do it but usually spills which brings tears and having to change his clothes because having the smallest amount of wetness on his clothes brings anxiety. Jake has difficulty expressing his needs and often resorts to grunting or pointing. Jake is afraid of change or unexpected issues. Here’s an example, the other day the emergency alert came across the TV. You know the one with the loud noise saying this is just a test. Jake just sees the emergency and freaks out. He ran to me crying that there was an emergency and we wouldn’t be able to go to Target. It took me about 15 minutes to help him calm down and understand that it was just a test and there was no emergency. He chose to hide under his blankets to find his calm before he could move on and accept that things were really okay. Hiding under blankets brings him so much peace and allows him to regain control. Jake is deathly afraid of the dark. A few weeks ago our power went out in the middle of the night which left his room dark and his sound machine cut off. We woke up to blood curdling screams. Fortunately, he has a battery operated lantern and that helped him go back to sleep and the power was only off for a couple of hours.

I could go on but you can see some of the daily struggles Jake faces. I’m sure many of you have typical kids that do some of these same things and Jake’s three older siblings had their own struggles. My point is; it is just different! It isn’t the same. I could talk to Jake’s older brothers and sister, they would understand and within a minutes or a couple of days working on the problem they would get it and we would move on to the next issue at hand. With Jake it might take weeks, months or years. I have more to do, more to teach and a lot more words come out of my mouth each day and all of this makes me really really tired! I do insist that Jake does more for himself but when I am exhausted I have to think ‘can I handle the break down that might come from me making him put his own clothes on? Do I have the temperament at that moment to not get frustrated and work with him to brush his teeth?’ Triple or quadruple the amount of time it takes to teach something like holding a pencil to another child and that doesn’t compare to how long it took Jake to learn.

I am thankful there are some things I have never had to teach Jake. When he began reading around the age of 2 1/2; I was dumbfounded. Today he is reading above grade level and I didn’t have to teach him one bit of that. Math comes pretty easy to him as well; the word problems is where he gets stumped. He can memorize anything and won’t forget it! I haven’t had to work with him with any these things. Am I bragging? Heck NO!!! I am thankful that these few areas I could rest and thank God for helping me out!

This is autism. This is real! It isn’t, by far, the worst thing that I could have to go through. It is just hard. I am able to go to sleep each night, rest and gear up for another day and I am thankful for that. Jake is funny, he has one of the sweetest smiles, his facial expressions make me laugh constantly (they always have) and overall has a sweet disposition. Jake has determination and won’t quit until he figures something out. He loves Transformers, Thomas, PJ Masks and Mickey Mouse Club House. I love that he can go from the fighting of transformers to sing the hot dog dance with Mickey Mouse! I love that he is still a child. He does his own thing without thought to what others think. He speaks his mind whether with words or with his body language. He can be defiant one minute and the next doing exactly what was asked of him. It is a roller coaster!

This is our journey with Jake 🙂