Sharing A Child’s FASD Diagnosis with Them

How do you share difficult life changing news with a young child? That’s a question I’ve been thinking a lot about since we received T’s FASD diagnosis in January. The hubby and I shared the info with the school right away as it would better inform the way they supported T. We’ve held off onContinue reading “Sharing A Child’s FASD Diagnosis with Them”

Advocating For Your Child

I took a nervous breath as the hubby hit ‘Enter’ on the Zoom call for the School Services Team meeting. This meeting held this past week was when we learned the school’s plans for supports for T when he enters Grade 2 this September. Advocating for your child is a necessary part of being aContinue reading “Advocating For Your Child”

Playing Sidekick to My Incredible Hulk

Our T has found a kindred spirit in a superhero with anger issues and the irony is not lost on me. Last week’s loan from the school library was a non-fiction book featuring the green Marvel superhero and we enjoyed reading it over several nights. I love that reading comics or books inspired by comicsContinue reading “Playing Sidekick to My Incredible Hulk”

Hitting the Reset Button

During a work call, I got a call from T’s daycare teacher. She was not her usual calm self. She said an older student had ran off the bus during drop off and pushed T against a wall. She had to shield him from further harm. A few hours earlier, the hubby and I receivedContinue reading “Hitting the Reset Button”

Disconnecting to Move Forward With a Clearer Head

During our recent week away, I had one focus: unplugging and recharging. Special needs parenting often leaves caregivers feeling perpetually foggy headed. Thanks to amazing colleagues, I checked out of work. I told family to e-mail me about urgent issues, but I tuned out everything else. I slept very well – passed out before 11Continue reading “Disconnecting to Move Forward With a Clearer Head”

The Power of Inclusion

When all kids are included, accommodated and set up for success, everyone wins. Maintaining a positive relationship with T’s school is a priority for the hubby and I. We try to be open, transparent and collaborative with his teachers and principal. We shared his recent FASD diagnosis and we’re thankful his school has been soContinue reading “The Power of Inclusion”

Escape Room

“What am I escaping from?” asked the exasperated dad after the resort staff asked if he wanted to try their Escape Room game. The staff asked another dad, walking quickly with a kid in tow and he asked, “Do I get to escape from this?” He looked at me with T in one of hisContinue reading “Escape Room”

Waves

“I get back up and I do it again. I get back up and I do it again…” One of my wishes with our vacation is to overfill T’s bucket with happy memories – so he has them during grayer days. I loved watching T play at the beach, with its soft white powder andContinue reading “Waves”

Finding the Bright Spots

Perfection is the enemy of progress. I thought about this expression by French philosopher Voltaire after T broke his four-week streak of perfect spelling tests. T’s teacher recently introduced Words of the Week; six words given on Mondays that he practices for a test on Fridays. T crushed the first four weeks and we postedContinue reading “Finding the Bright Spots”

Into the Unknown

Step by step, the unknown becomes known… Our adoption was finalized five years ago between Valentine’s and Family Day and is now always celebrated between these days. On this Family Day, we went for a morning hike at Hilton Falls Conservation Area. It was a beautiful sunny day and 1 degree compared to yesterday’s -12.Continue reading “Into the Unknown”

Cool As A Cucumber

Making cucumber kimchi and sledding down icy hills helped us keep it chill this weekend. Six weeks into the new year and I’ve been working hard at my resolution: to be the calm in T’s storm. It’s a life lesson I wish I could’ve applied earlier in my parenting journey – especially now that T’sContinue reading “Cool As A Cucumber”

The Diagnosis

After 5.5 years, we’ve answered a longstanding question about our son’s life and then uncovered more questions. When T was 18 months old, he received a prognosis of at-risk Fetal Alcohol Spectrum Disorder (FASD). It’s been quite the journey since as the hubby, T and I experienced the highs and lows of life with aContinue reading “The Diagnosis”

Making Popcorn

One freeing lesson I’ve learned is that every child’s potential pops at their own time. You may have seen this meme – the photo of popcorn with a message that reads: “Popcorn is prepared in the same pot, in the same heat, in the same oil, and here the kernels do not pop at theContinue reading “Making Popcorn”

Resolutions

Through virtual schooling, T learned about setting goals for the New Year. The related assignment is the last thing we had to catch up on and complete this weekend before we return to in-person learning this coming week. I often write about how we struggle with T to sit still and concentrate long enough toContinue reading “Resolutions”

Brittle and Faith

“There is a crack in everything. That’s how the light gets in.” This is an excerpt from Leonard Cohen’s song “Anthem” that I saw posted on Instagram. After a year of best laid plans falling apart, we began 2022 by making something just to break it: peanut brittle, using this easy recipe from In Diane’sContinue reading “Brittle and Faith”

Making Marriage Work in Special Needs Parenting

This Monday, we celebrated an amazing human’s birthday: the hubby turned 41. He took this week off work and I joined him for downtime on Monday. It was the first time we had to just the two of us in forever. When we started the adoption journey, a former manager told me to avoid adoptingContinue reading “Making Marriage Work in Special Needs Parenting”