Jsack's Mom's Blog

Welcome to my blog where I share my special needs parenting journey with my heart, truth, and love, one story at a time. ❤️

Green

I’m happy to link up with Stream of Consciousness Saturday hosted by Linda G. Hill. Green is a symbolic colour in my family. We’re 1/3 Irish on my Mom’s side so you can imagine how important St. Patrick’s day was when I was growing up. We would say our prayers, honour St. Patrick and have my ancestors recipe of delicious Irish Mulligan stew.

There was one thing that confused me though could a certain colour of green denote danger? I was told if we were to wear Paddy green that it was bad luck. When you grow up with Irish ancestry a lot of superstitions are a part of life so I just didn’t question it.

I didn’t know what shade of green was paddy anyways so I chose not to wear until I was an adult. Then one day my Mom came to visit me and I was taking her shopping. I came out dressed in a new t-shirt I had bought recently and heard her exclaim “oh no you’re wearing paddy green!”

I went back to my bedroom and changed immediately. I know that may make some laugh as I was grown woman. But when my Mom starting making the sign of the cross and praying the Our Father I took this outburst seriously.

After we got to the food court I asked my Mom what was the superstition connected to that particular colour of green. She had told me my Great Grandparents immigration to Canada, tales of the Irish banshee that had a body of a dog and a face like a scary villain out of Grim’s stories. But really paddy green what was the fear of that?

She had explained that when someone in our family had worn the colour that a relative would die. At first I scoffed then I looked deep into her eyes and was ashamed because there was a belief and fear there.

Who was I to question the validity of a belief she held all throughout her life? After this insightful conversation we went back home and I made her a cup of tea and her favourite treat scones, like my Gram used to make. I cherish those memories and keep our Irish traditions alive with my own children.

My favourite thing about St. Patrick’s day is that there’s no expectations on this day. No need to get dressed up and go out to anyone’s for dinner, or get out of your pyjamas for that matter. The only thing you need to do is be happy, drink green beer, and sing Danny Boy.

In my family I make the green pancakes and potato patties like I would have as a child. And for one day out of the year I speak with an Irish accent. I’m putting those years of theatre training to good use. Also it makes my kids happy, and I love to hear their giggles when I break into song and kick up my heels in an Irish jig. I think the world could use a lot more happy traditions so I wish you a Happy St. Patrick’s day and may the luck of the Irish be with you.

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It takes a village

I recently took a physical for life insurance purposes. My nurse was kind and polite and when I was asked why do I take an anti-depressant when your otherwise healthy? I simply replied “I’m a special needs parent who’s always advocating, teaching, learning, researching, and loving my family I have to cope somehow.”

The look of surprise that crossed his face was something that I’ve seen before. I’ve had people ask me how do you do it, deal with autism, ADHD, ODD, SPD, and a genetic neurological disorder that affects everything from motor skills, to recessive language delay, to selective eating issues due to textures, smells, and shapes of food.

I have no other answer other than I don’t think about it I just do it. All of it needs to be done always. I need to advocate for my children so that they can have access to resources, funding, and therapy inside the school system and outside within the community. I need to keep up with the latest research on my son’s genetic disorder so I know how to help him specifically and what other co-morbidities I need to be aware of. I also need to teach him about number and letter recognition so he can begin to print what he knows. I have to deal with regression as it’s the part of his brain that’s affected by his micro-duplication.

I need to check, double check and help my son re-learn when he’s lost his ability to process what he’s learning in school. He’s come a long way with his progress from screaming if I tried to help him hold a crayon in preschool to printing his name confidently in elementary school. Now his world’s growing bigger as he attempts to make sense of all those letters on the page and learn to read. I remember what joy I felt when my Mom introduced the magical world of books to me.

I long to see that light in my son’s eyes that I know appeared in mine. Yet I see him stumble on three and four letter words and in frustration throw the book across the room. At the moment we’re working on his reading comprehension so that he can create the story from what he sees illustrated on the page. As for the phonics and word recognition I’m using a multi-sensory approach as well as his special education resources teacher does in the classroom.

1. First I print the word then I get him to to tell me the letters and we sound it out and say it together.

2. Next I have him build it with his alphabet letters on the line below.

3. After he prints the word with his pencil.

4. Then we go over the word and use it in a sentence and repeat with the remaining words.

Sometimes he only has enough patience for three words but to me it’s quality over quantity. I learned the Write, build, print method from an amazing website called Understood. I love this website as I now have a resource that’s there to help us both on our learning journey.

When I see the furrow in my son’s brow as he concentrates to maintain his alligator grip on his pencil I marvel at his independence. He sings a little song as he does so. Alligator grip then my pencil doesn’t slip. Then when he’s completed his task his beautiful smile makes his whole face light up. I’m excited to incorporate building Lego into his learning as we work on math next.

I have five months to prepare him to catch up with his peers and continue onto the next grade. He has an excellent team at school who’ve been there to help with his frustrations, transitions with the use of visuals and successes. My son teaches me just as much as I’m teaching him this why I choose medication for myself and seeking the guidance of a therapist.

No parent is an island and it takes a village to raise a child. When it’s a child with special needs it takes strength, courage, and a bigger, non-judgemental village. I need to be able to cope with this roller coaster of a life we lead. I need to stay on task and ten steps ahead of a sensory overloaded meltdown. Most importantly I need to take care of myself and repair what I feel is broken. My mental health and the well being of my children depend on it.

Welcome to Voices of Special Needs Blog Hop — a monthly gathering of posts from special needs bloggers hosted by The Sensory Spectrum and The Jenny Evolution. Click on the links below to read stories from other bloggers about having a special needs kiddo — from Sensory Processing Disorder to ADHD, from Autism to Dyslexia! Want to join in on next month’s Voices of Special Needs Hop? Click here!

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The Tear

What is it about the passage of time? I’ve heard that time heals all wounds, time passes on and time is short. It’s that tear in the fabric of time that intrigues me the most. Where you can be another version of yourself-someone who is stronger and makes better decisions and takes a different path in life.

Like the actress Gweneth Paltrow played in the movie Sliding doors her character was on the subway platform deciding if she should or shouldn’t get on the train. The director portrayed what would happen with her life if she stepped on the subway and who she was and who she interacted with.

It really fascinated me with the twists and turns within the plot of the movie. It showed me that you do have to be careful what you wish for. As I’m watching this the character in my favourite TV show #Thisisus is replaying the memory track of what his life was like before when he was a high school football star and adored by everyone. Kevin had colleges scouting him, a girlfriend who loved him and a close relationship with his family. Then it all came to a crashing end when he was tackled in the big game and suffered a broken leg.

He still had the beautiful girlfriend (who he would later go on to marry and divorce), a strong bond with his fraternal twin sister Kate, an emerging relationship with his adopted brother Randall, and his parents Jack and Rebecca that were there to love and support him to this jagged tear to his football dreams. Yet Kevin can’t see past any of that as he sinks into a depression that goes on to shadow his life in his current phase.

What would’ve his life been like if he avoided that devastating hit that changed his path forever? Would he have gone on to football stardom and become the proud recipient of the Heisman trophy, married the girlfriend and lived happily ever after? Even though he’s a television character Kevin and his life story is enthralling to me that he went onto to what appeared to be a good life making a successful living as an actor while recovering from the death of his Father, the rock in his life.

How would his life be any different if he would’ve just thrown the football, avoided the tackle and never have to lose his Dad at such a young age? It’s the conundrum I’m sure most of us have encountered at some point on our path what if I would’ve taken that subway train, stayed with the ex or gotten that scholarship to college. It’s the tearing of the dream that we have for ourselves that can hurt the most where we feel the regrets of time we’ve lost and where the what if’s eat us up inside.

Is the grass always greener over on the other side of the fence? Not necessarily, should we all just be living the life of our dreams with no regrets or resentments? I’ve always intended to raise my sons to follow their dreams, reach for the stars and be kind and giving human beings. It’s the life that we live that shows us who are true character really is. Excepting the hand we’re dealt and taking the leap of faith and being who we’re really meant to be that matters the most.

I saw myself becoming a famous actress and singer entertaining the world with my talent. Unfortunately I didn’t have the courage to pursue those idealistic dreams and leave my parents and go off to the big city. I didn’t believe in myself as much as I should’ve and that tears at my heart still today. But who am I to say that my dreams shall just wither and die? I can still realize them just in a different way, by performing in theatre and pursuing my passion for storytelling.

It’s the gift of words that sets my heart aflutter now as I’m passing on that love of reading and writing to my sons. It fills my eyes with happy tears as I sit and listen to my youngest champion son reading about Pete the Cat and his buttons as he acts and sings out every page. When I thought his brain might not be able to make sense of the letters with his autism and mental processing speed. Then as my heart swells with pride when my oldest rock star son starts reading me an essay that he’s writing for school and telling me he wants to be a writer like me when he’s older.

I wish for them not to struggle with their identities or what direction they should go career wise like I’ve done. To be able to avoid the “hits” that happen in life the fair weather friends, bullies on the playground, and young love breakups. If I could I’d protect them from it all but then they wouldn’t be truly living and discovering the world for what it is. Their time shouldn’t be spent wondering what if but really experiencing all that life has to offer them from school, friendships, love, and beyond!

It’s in these moments that I know I found the right path and even though my mind can wonder about the what if’s of the world it’s the life that I’m living being the best me I can be that matters. Not the one who made her way to Hollywood to become the actress of her dreams who may have caved in to all the pressure that a lot of celebrities fall under and resorted to drugs and alcohol as a way to cope.

I would rather be my authentic self who loves who I see when I look in the mirror, that prays with my children every evening for a better world for them to grow up in, and loves my husband with everything in me. That’s the bond of family that dreams, pride, fantasies, or ego can never tear away.

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Hotel living 101-special needs parenting

A month ago I embarked on a journey to pack up my truck and my kids and headed out on a new adventure. My husband has been working away for 3 months and after solo parenting, recovery from a broken arm, and listing our house for sale I was done! I counted the days till my kids were out of school and got out of dodge.

Once we arrived tired, sweaty, and dis regulated late at night that's when the real fun began. It was a long trip and after listening to my kids nit picking each other for 7 hours. I arrived disheveled and I needed a time out. I love my children but I was "needed out" and wanted to forget my name was Mom. But who would answer if I don't? My husband was off limits as he was attempting to sleep with working the next day. I went into action mode and set up the pullout couch for the kids. I jumped into my pyjamas and crawled into bed. My youngest son was stimming and in need of sensory input and regulation so we needed to fill that asap!

I walked around the hotel and read books and gave him deep pressure hugs that only his Mama can give. Inside I was praying for him to go to sleep as he jumped out of my lap and rolled around on the floor. I felt the need to explain to the front desk hotel staff that my son has autism and not able to follow the quiet time rule after 10 pm rule. He gave me a nod of understanding and I carried on with my regulation methods.

Finally by midnight my son was sleepy so I put him to bed. Meanwhile my brain was on hyper drive as the events of the day piled up and reduced me to tears. I lay there on the cold bathroom until my crying subsided then fell into bed into a deep sleep.

I woke up in the morning feeling like I had ran a marathon then someone had run me over and left me for dead. I needed to eat, shower, brush my teeth, and unpack. Breakfast was complimentary and a Godsend. My youngest son was fascinated with the pancake machine as he pushed the button an they fell onto his plate. Thank God for these little gifts as this held attention long enough for us to get through breakfast and back to our room.

5 ways to survive hotel living special needs style

*Beforehand research your list of hotel options and book one with pool, gym, and spa facilities. Luckily my husband's company took care of that for us in advance.*

  • Swim daily and spend as much time there as you can in order to wear your children out. That includes numerous trips to the water slide and to the hot tub. Water can have a regulating affect on children with sensory disorders if there's no Sensory Defensiveness present and they're comfortable being immersed in a pool.
  • Invest some time in the gym. I go there weekly with my kids to work out. Even at the ages 10 and 6 there's machines they can use like the treadmill, elliptical, spin bike, and free weights. It's a wonderful way to feel healthy and deal with stress.
  • Provide sensory friendly cut up fruit and vegetables for snacks. The crunchy foods provide the sensory seeking benefit as well as toning the jaw muscles. With my sons hypotonia condition in his jaw this is a huge benefit to his sensory diet.
  • Cut back on junk food for snack time. My kids tend to be sponges for everything they absorb like sugar and food dyes. Trust me you don't want a sensory overloaded mind and body meltdown within close quarters in a hotel room!
  • In one word Netflix plus additional DVD's, colouring books, crayons, felts, wipe board books, and washable markers on those inside days when you're too tired to move.

Maintain your children's sensory diet even while on vacation. Move as much as possible explore your local parks, playgrounds, and the city itself. On days when the weather's miserable have board games, puzzles, crosswords, and structured time on electronics. I stress this one as you don't need to struggle with the affects of a dopamine crash after a limit is not followed. We also signed up for the Kids Bowl Free summer program and that's fun for the whole family.

My kids became very creative through the pleas of I'm bored and built themselves and indoor bowling alley that kept them entertained for a few hours. They also did some crafts, painting, and worked on maintaining fine motor strength playing with thinking putty and play dough. Our favourite thing to do is play make believe as they pretended they were superheroes and the world was being covered in lava. I watched my kids jump from bed to bed and marvelled at their imaginations.

After a month of hotel living I'm confident I made the right choice to reunite as a family. I wanted my kids to have a fun summer instead of being stressed about keeping a clean house for showings while attempting to sell. Now I spend my spare time reading, writing, organizing housing information and counting off the days till our new homes possession date then the fun starts again with packing and unpacking. Whatever comes our way we'll get through it as being together as a family is the best place to be.

Come to the Voices of Special Needs Blog Hop. A monthly gathering of posts hosted by the http://www.thesensoryspectrum.com/and http://www.thejennyevolution.com/category/voices-of-special-needs/

Click on the links below to read stories from other bloggers about having a special needs kiddo. From Sensory Processing Disorder to ADHD, from Autism to Dyslexia! Want to join in on next months Voices for Special Needs Blog Hop. Click http://www.thesensoryspectrum.com/sensory-blogger

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Acting and other lies I tell myself

When I was a little girl I always wanted to be an actress. I remember late night movie watching with my Mom. We loved the classics of Audrey Hepburn, Lauren Bacall, and Marilyn Monroe. I felt happy and safe in that world of film. When I grew older and had opportunities to participate in school plays and Christmas concerts I jumped at the chance. 

 I memorized songs, dialogue, and full scripts for plays. Theatre had always been my first love and I joined a wonderful group and they quickly became my theatre family. I felt so loved and accepted there with my beloved Hope Pact. I sang with such confidence and determination. Then immersed myself into my character enjoying an Irish accent, and learning my lines, songs, while researching the history of my chosen role. 

Life has always been easier when I’m on my stage. I throw myself into the script and I don’t think of any outside influences. Now I still act but I’m in the background singing with a chorus or taking a secondary role. Where did the confidence go, why don’t I sing with grace and passion like I did before? 

Now I feel like I’m really acting avoiding the hurt I feel when someone has wronged me. I don’t lash out I don’t kick ass or take names like my personality would have me do before. I feel but I’m tending to hide the affects of those emotions more. I’ve always been a person who wore their heart on their sleeve. Which is still true but I act like I’m Teflon and things bounce right off of me. 

They don’t though, it’s just this one act play that has become my life of hiding those true thoughts and feelings. Does anyone care about all the tears I cry flooding my fragile ego until it sinks in an ocean of denial? This is my plight one I choose to accept and be proactive to change. Or continue on with acting and wearing those rose coloured glasses that impede my true vision.  The time to be real is now and stop acting like I’m wearing a titanium suit of armour. I will persevere I always do, find my voice again, sing with courage and conviction, and leave the actress on the stage where she belongs. 

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Ten Things of Thankful-Some kind of wonderful

It’s time to join up with the merry band of thankful crew. I’ve been on a little hiatus due to back to school craziness. It’s been a wild month of keeping track of all school responsibilities and I need to dive waist deep into some thankfulness. This is where my heart is and always will be whether in participating in the TTOT linkup or just reading all the wonderful talent that reside there. 

I’m thankful for having a more organized week and making each appointment and having my sitters lined up for the last week. My kids enjoy spending time with these special caregivers and I’m grateful for some me time and a date night with my handsome husband. 

I’m thankful for celebrating 11 years of marriage. There are times when life beats me down and I feel overwhelmed. I look towards my husband and he’s always there cheering me on and believing in my inner strength that I know I possess but need a reminder of when I’m feeling clouded by doubt. 


I’m thankful for the wonderful friendships I have in my life. I’m never without a kind word, strong shoulder, or zany sense of humour from my tribe. The real life friends make me feel so loved and appreciated. My online friendships have grown and have taught me to believe in myself and the power of my words. Words that can make a difference and be the change I wish to see in the world. 

I’m thankful for a successful week of charting and tracking my daily life habits. I’ve had 3 successful weeks of tracking my behaviours of food, mood, anxiety, sleep, and OCD I’m a journal. I’ve begun to see patterns of my behaviour that I can now work on changing and revitalize my self care regimen. 

I’m thankful for my behavioural therapist that I’ve been seeing for the last month. Cognitive behavioural therapy is the game changer in my life and I’m looking forward to more successes that I will accomplish with her support and expertise. 


I’m thankful for my sons doing well in school. It’s only been a month but they’ve both felt positive about being in their classrooms. Soon I will find out what funding is available for my youngest with autism and a teacher conference for my oldest to see how he’s doing in school. I’m proud of them both and the resilience and inner strength they’ve shown me. 


I’m thankful for a wonderful day spent at the women’s show. I met a lot of different vendors and listened to an amazing guest speaker. I sat in the sunshine and painted a wine glass and met some very interesting kind people. It was a rewarding day of being social followed by a 3 hour successful theatre practice. The most memorable part of my day was signing the poster asking the question in one word describing myself. I chose to say I’m inspirational and the loving energy that poured out of me from that moment onward was incredible. 

Speaking of theatre I’m thankful that I was cast in the lead role of the pantomime play! I was going to be brave and try out for a bigger role than in the previous years and I did. I’m memorizing a lot of dialogue, dances, and really enjoying my character. Performing is where my heart is when I’m on stage I feel like I’m invincible. 

I’m thankful for autumn days and walking along the river with leaves crunching under my feet. The pictures I take at this time of year thrill me as Mother Nature decorates these beautiful tapestrys of colour and wonder. 

I’m thankful for all things pumpkin now that it’s October. Halloween is a big deal in our household so let the dessert making and decorating commence. Stay tuned for guess what Halloween costume I’ll be wearing coming soon. 

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The Haircut

I see the long shaggy hair covering his eyes and he’s bent over trying to put his Batman in his Bat mobile. He’s getting so frustrated because he can’t see what he’s doing and this task is taking too long to figure out. I gently offer to help him and he runs away in anger and slams his door. He’s only four and already acting like a teenager. I pick up his toys, walk to his room and gather him in my arms. 

  
I wrap his blanket around him holding him tight in my Mama bear hug. Deep pressure soothes him and I rock until he stops crying. I brush the hair back from his eyes and I say the dreaded words “oh honey it’s time for a haircut.”

 Soon his body tenses and he’s ready for fight or flight. I rock him and tighten my hold till his fear ridden body is limp in my arms. 
The next day I tell my husband our son needs a haircut. He shakes his head and says “well I don’t want to do it.” Neither of us do it’s a two hour ordeal and the emotions overflow and we’re all stressed. We take turns holding our sweet boy who will turn into a howling banshee any moment. It’s my turn to perform the task of completing a decent haircut. 

I assemble my tools scizzors, buzzer, guards, comb, spray bottle, and a cloth. He will not wear a cape so we strip off his shirt and wrap a towel around him. I place his blanket in a clear plastic bag to protect it but so he’s still able to see it. Next I grab the iPad, thermos of water, and a bag of lollipops. 

I call my husband to help wrangle our son and it’s easier to catch a greased pig at a BBQ! He holds him tightly and I begin wetting down his hair. I’m being very careful to not spray his face at the same time singing his favourite song while his Dad finds him his favourite superheroes on YouTube. I begin to comb his hair and I cautiously snip his bangs. This is not an easy task as I venture close to his eyes. 

I comb his hair out a few more times and move to the sides. I gently approach his ears and I’m holding my breath while I cut around this delicate area. Next I move to the back of his head making sure to work quickly now as he starts to wiggle. I move over to other side and you can hear a pin drop as I cut around the other ear. The hair starts falling and covering his face and blanket in the plastic bag. 

I quickly blow it away and brush off his lap. He starts in with a low growl and I back off completely gently soothing him with my singing.  I carry on only to reach an impasse as he doesn’t want to sit any longer. I bribe him with a lollipop and ask his Daddy to hold him in his blanket bear hug. Instantly he’s soothed and I continue cutting. I’m not a hairstylist I have no professional experience whatsoever. Other than cutting his big brothers hair in the classic “page boy” style.

 I comb out his hair and continue cutting until he gets excited with the video and jerks his head and shoulders around. I narrowly miss stabbing him in the back of the neck! I tag team out with my husband and we trade spots. He plugs in the buzzers and I brush the hair away from our sons face and body. I prepare him for the buzzing sound and hold on to him tight because I know this is going to be a bumpy ride. 

His Dad works quickly and efficiently as I tighten my grip and sing louder overtop of the sound of the buzzers. He’s on my lap wiggling out of my arms and it’s like holding a bag of snakes! We’re almost in tears and we quickly wash his hands and face that are covered in hair. I pick up the hand mirror so he can survey our work and he starts to cry he wants all his hair back. A full sensory meltdown ensues while he can’t process what happened and why I can’t put the hair back. This is the invisible cloak that he wears as he tries to process all eight of his senses. 

I can only imagine what this has felt like for him. As much as we prepare him for haircut time it’s still unbearable. We let him run free and then I change him into his pyjamas while I make him a snack and give him something to drink. He sits at the table singing away between bites and I look at his happy face in awe. Just moments ago I imagined that the clippers felt like hot razors attacking his scalp as his body, brain, and central nervous system were in overload. He finishes up his snack, I wash his hands and face and hug him so tight while telling him how proud I am of him. 

He cuddles up with his Dad and watches a cartoon before storytime. I clean up the mess in the kitchen, sweeping, making lunches, and pour myself a stiff drink. I go downstairs and sit and sip while glancing up at my son and his Dad nestled together in the recliner. My husband says “thank you for being a brave boy for Mommy and Daddy.” 
His eyes well up with tears and he holds his Daddy’s face in his little hands and says “you hurt me Daddy.” I watch my husband’s face crumple and we look at each other and silently agree that this will be the last haircut he ever gets at home. This is our life with Sensory Processing Disorder. 

Welcome to the Sensory Blog Hop — a monthly gathering of posts from sensory bloggers hosted by The Sensory Spectrum and The Jenny Evolution. Click on the links below to read stories from other bloggers about what it’s like to have Sensory Processing Disorder and to raise a sensory kiddo!

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Ten Things of Thankful-Feeling prayful

There are times in life when some things just don’t make any sense. Death for one isn’t something I can fathom. Whether a loved one is young or old, natural causes or sudden tragedies it tears at my empathic heart. My husband and I recently lost a friend this week. The sadness overtakes me as this special soul leaves behind a beautiful, caring wife and three amazing kids. I think about the last conversation we had, the laughter, the reminiscing, the hugs of let’s keep in touch. Just when I start to ride a grief wave another loss happens, and I’m threatened to be pulled under by the melancholy cloud of darkness. I don’t think I’m supposed to understand death I’ve lost too many people to count in the last ten years. I’m beginning to believe that I’m just supposed to survive the affects of death and keep learning and appreciating the life lessons I’m taught. I will now begin to attempt to find some thankfuls as part of Lizzi’s TTOT linkup and glean a silver lining in a dark cloud. 

I’m thankful that even though it’s been a difficult week my husband has been able to talk about his feelings. He attended his childhood friends funeral while I attended an appointment. He told me it was good to see old friends and there’s comfort in knowing how many turned out for the sad day and how loved our friend was. 

I’m thankful that I kept my head and my heart busy with baking, walks in the sunshine, and movie time cuddles. My oldest (Captain) went with his Dad and spent time with family. The youngest (Mad dog) stayed home with me and enjoyed having me all to himself. 

I’m thankful that my Mad dog is making great progress with his behavioural aid sessions. His fine motor skills are improving so next we will continue working on having him sit for longer periods at circle time. It’s a large part of preschool and kindergarten and I want to prepare him for when he attends his new school. I’m so proud of his accomplishments in the last six months. ❤️

I’m thankful that I had silly, sweet, text conversations with my Captain while he was traveling with his Dad. We chatted from everything about wrestling (he’s a John Cena and Shane McMahon fan), Donald Trump versus the world, and how he wants to surprise his brother with the best beef jerky on the planet. I sure love my son and his creative mind! ❤️

I’m thankful for healthy meals, daily exercise, and relaxing in my hot tub with my family. When I have these things in my life everything just flows better and I feel so happy and loved. My fitness journey is ongoing and I strive to grow stronger in mind and body everyday. 

I’m thankful for catching up on housework, the dreaded laundry monster, and enjoying some beautiful summer weather. My moods are really tied to how much vitamin D I’m getting so the sunshine’s my elixir in life. 

I’m thankful for earth day this week. My Mad dog and I went for a walk by the river with his behavioural aid. We skipped stones jumped from rock to rock and took in the beauty and appreciation of our home. I’m grateful for the fresh clean water, the plants and trees providing me with oxygen and the flowers blooming and letting me enjoy their fragrance and aromatherapy. 

I’m thankful for reading, writing, and accomplishing my work tasks. I still have a few things to catch up on but I’m crossing things off my list and that’s a win/win in my world. Organization has never been my strong suit but as I see my piles of clutter becoming less I feel more in control of the direction I’m taking. It’s the old adage “cluttered space equals a cluttered mind.”

I’m thankful that I was able to apply that mindfulness to eliminating my digital and online clutter as well. Now that I’ve deleted data, cleaned up email accounts, and uploaded pictures onto my computer my phone/office is running at the speed of light! It’s amazing what a good feeling of satisfaction that can generate. 

I’m thankful for late night cuddles when my son can’t sleep. Late night talks and tuck ins when they miss me when it’s time to go to sleep. I’m getting to a point now where they don’t need me as much, especially my Captain. It’s so rewarding to see them growing and discovering the world and still wanting me by their side to chat about life and it’s mysteries. 

I’m thankful we had a successful follow up appointment with my youngest son’s sleep specialist. Since his diagnosis of autism in February and asthma in March we’re solving more health mysteries. The asthma medication has improved his breathing and shrunk his tonsils so much she doesn’t think he needs surgery! Now I will push for the MRI and see what’s going on inside his brain in regards to where the sleep apnea is originating from. Central sleep apnea is a a very serious condition-whereas the brain isn’t communicating with the heart and lungs about getting sufficient oxygen intake. Knowing my son is safe, breathing and sleeping properly is an answer to my prayers. Thank you to all you sweet souls who have expressed concern, said prayers, and empathized with us on this long, sleep deprived journey. This is the best outcome and update I could ever hope and pray for! I’m so thankful to God for these blessings. 💖

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Ten Things of Thankful-feeling the love

I’ve been thinking lately about the things that make me hapy. I always count my family, friends, and my ability to see the light in a grey cloud. I lived costal for nearly three years and one thing it taught me was to appreciate the sunny days when they happened. This was supposed to be part of the TTOT linkup but a faulty phone app froze and I missed the deadline. I’m going to post it anyways because life’s too short to not be thankful for my blessings! 

I’m thankful for a enjoyable spring break with my kids. It rained a couple of days but the last four have been perfect. We went for walks by the river, played in the backyard, made crafts, relaxing in the hot tub, and today was a perfect day for a water gun fight. And also seeing a sunset like this tonight. 

 
I’m thankful for learning how to paper mâché with my son’s behavioural aid. Even my oldest got into the fun as well. I’m excited to reveal our project for you next week. 

I’m thankful for getting caught up on laundry and housework over the week. You can’t tell I did much now so I’ll be back to the grind tomorrow. 

I’m thankful that my kids had a great experience at their dentist. The staff was friendly, professional and polite. Watching soccer on the flat screen was a big hit with both my boys and led to some interesting conversations. The office having IPads in the kids room was also a big hit with my kids. I was so impressed with how the staff addressed my concerns regarding my youngest son’s autism and comfort level. I’m so happy we found an office that’s close to all our other professional services. 

  
I’m thankful for relaxing, watching movies, learning Minecraft techniques, and baking with my son’s who are full of energy. We had a great time and I got a break this weekend from being there entertainment director. 

I’m thankful for sunny days, visiting with the neighbours, and digging in the dirt. It’s so exciting to see that spring has finally sprung    Now I’m anxious to get out and garden as soon as the morning frost disappears. Mother Nature has a sense of humour to be desired. 

 I’m thankful for coming to the blog to tell you what makes me happy and gives me a thankful heart. 

I’m thankful for you my dear readers and making it to 600 of you lovely followers. I’m grateful you like to pop by and read what I’m musing about. 

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I’m thankful for finding a local special needs community. A few faces I recognized from moving here and I look forward to making new friends for myself and my family. Special needs parenting can be lonely and isolating so to find others like our family is a blessing indeed. 

I’m thankful for having wonderful friends who invite me out to have fun, chat, and remind me that I’m not alone in life. Even my friends who are farther away who check in with a text, message, and a phone call just to see how I am. 

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Monday Musings A-Z challenge-Compassion


I was raised to have a compassionate heart. My Mom was a big believer in showing compassion instead of anger. She didn’t have an evil bone in her body and she believed that people judged others by what they saw in themselves. I still carry this belief and honour her memory by teaching my children the same. Some have called me naive because of this truth I hold to dearly. That’s one’s opinion but not my truth.
It will still baffle me as an adult when some members of society don’t show compassion. I see it in daily life when someone driving cuts off another car. I see it in a long lineup when someone throws their money at a cashier. I observe it in a restaurant when dining out with my family when my son becomes disruptive at the table.

The reason is he has autism, and he doesn’t sit still for long. Ten patrons can turn into twenty and he becomes visually overstimulated to his environment. He also “stims” when his body is seeking sensory input to regulate his central nervous system. He does this by jumping, rocking or dancing on the spot. I see the looks, overhear the whispers and take him outside to shake his wiggles out. I don’t attempt to try to shush him out of embarrassment because it can escalate matters quickly when he feels he’s not being understood.

This is why we eat at one restaurant in our town. The food’s amazing and we’ve become wonderful friends with the owners during our time here. They know my family and they know of my son’s autism. If things are loud and crowded in their establishment my husband will go in and order us take out. If we make a plan to phone ahead we put in our order so that it arrives when we walk in the door. I’ve been at this game changing strategy  for awhile now as he had a diagnosis of Sensory Processing Disorder first at the age of 3.

I had to prepare him for the world as it can be too loud, bright, and busy. I don’t feel that anyone owes my son any special favours all I would ask for is compassion. I recently shared on a Autism page of my son’s diagnosis. It was World Autism Awareness day and I felt brave sharing something so personal to our family. I made the mistake of not wearing my armour in sharing my son’s story. I had briefly discussed the judgements that we’ve received and even a personal attack on my parenting him through a sensory meltdown.

What I forgot in that moment of courage was that anything put out there on the Internet can be judged. That came to pass and I was stunned by the commenters lack of compassion. I thought to myself I don’t know this person’s story and yet she believes that she knows mine in one paragraph. I stayed in my #Mommitment mind, I may be judged on my words but I know my spirit. I didn’t reply and I was blessed that the admins of the page deleted the comment and left my story up.

It was liked and shared a few times and I felt relief that I wouldn’t be having to face that hurt again. It was such a strange feeling to be put on the spot like that from another parent. I will admit there’s a lot I still need to learn and not everyone wants to Light it up blue for autism awareness. Not all organizations are everyone’s cup of tea but I learn something from each of these groups and I gain support, understanding, compassion and that virtual hug of not feeling so alone. I just learned today from a amazing blogger friend  that autism by definiton means “to be alone.” This brought tears to my eyes and made me realize I never want that to happen to my sweet son.

My son has autism, but I don’t believe it defines him as a person. His precious giggle when playing hide and seek with his brother. His beautiful smile when he tells me he loves me with a sound, words, or a kiss. These things define him and when the world has gotten to loud and crowded for him and he reacts to his environment by melting down; he’s not being a brat, this is not a temper tantrum, all I ask is for a little compassion and understanding. It helps the eye of the society storm feel a little less scary to navigate.

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