Holidays provide time for rest and reflection. Family Day is a special holiday, because it comes after Valentines and the anniversary of finalizing T’s adoption in court. When T was a toddler, we loved reading Todd Parr’s Family Book, which spoke about families in all forms – nuclear, single parent or multi-generational households, same sexContinue reading “Chosen Family”
Tag Archives: FASD
Stand Under My Umbrella
Six years ago today, also a Wednesday, T, the hubby and I became a forever family. In many ways, it feels like a lifetime ago when our adoption was finalized in court – and in other ways, I think with awe, “Has it been only six years?!” So many moments have happened since – joyousContinue reading “Stand Under My Umbrella”
Sweet Dreams
Time flies. It’s hard to believe but our little guy turned lucky number 8 last weekend. T had been counting down excitedly for weeks. But his birthday week got off to a rough start. Last Monday, T woke up around midnight and threw up. A lot. Then woke up every hour after to throw upContinue reading “Sweet Dreams”
Family Traditions
Time spent and memories made with our loved ones are what really count in the end. When my sister learned her chemotherapy was not working, it was sad watching her come to terms with her time left. She said the saddest thing was not getting to spend more time with family and friends. Shortly afterContinue reading “Family Traditions”
All That Matters
Our family’s recent and first experience with COVID reminded me what’s truly important in life. Yes, the dreaded COVID finally hit our family and I was a single parent for nearly two weeks. Shortly after my sister’s funeral during the holidays, our family was longing for respite. No more bad news, please. A few daysContinue reading “All That Matters”
The Wedding
We took our 7-year-old to his first wedding this past weekend. Well, at least the first wedding he’ll remember. He attended his first and only wedding in 2016, a friend’s destination wedding, when he was 1. As with all social events, we had some initial apprehension of how T will be. But we believe it’sContinue reading “The Wedding”
Sharing Our Son’s FASD Diagnosis with Him
There are crucial conversations in life that stick out vividly long after they’ve happened. Coming out when I was 14; telling my parents I was moving out; our wedding vows; the adoption worker telling us we were matched with T. Over the Christmas break, I had two more: one that was planned and another thatContinue reading “Sharing Our Son’s FASD Diagnosis with Him”
Marshmallow Halo
Processing and understanding death is hard for kids. Sometimes, stuffed animals can help. T’s Auntie’s – my sister’s – death a few days after Christmas was sudden and despite the unexpectedness, T is doing ok. I continue to check in with him every day to see how he’s doing. Kids often don’t tell you howContinue reading “Marshmallow Halo”
In the Arms of an Angel
Our family faced a sudden loss – for T, his first experience with losing someone – over the holidays. My sister passed away last Thursday, a few days after being admitted to the hospital on Christmas Day, after a short and brave battle with cancer. My family and I are still processing and making senseContinue reading “In the Arms of an Angel”
Believe in Your Goodness
Faith is not believing things will always work out but that you will be ok regardless of how they do. It was an up and down week at school. So the start of the holidays was so welcomed. T made a lovely note for Santa last night. When he woke up this Christmas morning, heContinue reading “Believe in Your Goodness”
I Believe In You
How you see yourself makes a huge difference in how you experience the world. The hubby and I had our first parent-teacher interview last Friday with T’s Grade 2 teacher. The conversation focused on T’s challenges: focusing and completing his work; avoidance behaviour like taking long bathroom breaks, and social interaction. I felt deflated, becauseContinue reading “I Believe In You”
Second Chances
What parents won’t often admit: When they ground their kids, they are punishing themselves too. After T’s unfortunate incident with taking the lollipop from the store, we grounded him last weekend; no electronics and he would not have his Halloween decor, bought on the same trip to the store, until next year. It may seemContinue reading “Second Chances”
The Boogeyman
This is a very hard post to write, but I’ve learned that fears die down when you face them. I’ve been enjoying the ramp up to Halloween – recently catching a matinee of “Halloween Ends.” Yesterday night, a real horror scenario played out: T took a lollipop from a store without paying for it. ThisContinue reading “The Boogeyman”
On a Night Like This
When the unicorn of a night out without T presents itself, I grab it by the horn and go for a ride. Going into parenthood 6 years ago, I knew weekend night outs by myself would be rare. When we do go out, it’s usually with friends; company that we enjoy. Parenting a child withContinue reading “On a Night Like This”
Secret Sauce
Asian cooking and special needs parenting have one thing in common: assembling your ingredients. Hear me out. I have not gone off the deep fried end; not yet, anyway. As parents of a child with FASD, the hubby and I have learned so much. We’ve been blessed with help to create a toolkit of ingredientsContinue reading “Secret Sauce”
The Traveller
What’s the meaning of a name and does it express one’s desire in life? For social studies this week, T completed an assignment that asked to research his name. It turns out one of the meanings is “traveller.” To see the world was one thing the hubby and I prioritized during life before T. TravelingContinue reading “The Traveller”
Cross Country Race
Our little guy competed in his first cross country school meetup today. For a kid who is endlessly active, gym is a class T struggled with the last few years. For his mid-year report card last year, his gym teacher gave him an “I,” as he didn’t participate enough for her to give a properContinue reading “Cross Country Race”
Walking Towards Hope
Inspiration exists in all forms and they are so important when traveling down unpaved road. Thanks to our FASD service provider, the hubby and I recently joined a cohort of parents and caregivers for a weekly support group. It’s an 8-week pilot initiative hosted by Surrey Place, an amazing organization that has supported T sinceContinue reading “Walking Towards Hope”
Rain
God bless the innocent unfiltered honesty of children. During a drive to a family lunch today, there was torrential downpour. The visibility was bad and the conditions got quite dangerous at one point. Suddenly, T says matter of factly, “Good thing I don’t live with my mother. She’s homeless. I would be soaking wet!” T’sContinue reading “Rain”
Guiding Light
Earlier this month, Pa would’ve turned 100. I thought about him when T had his first swim lesson. T’s always loved the water. The outdoor pools saved our pandemic summers and T loves swimming in lakes during our outdoor adventures. He’s very comfortable in the water and it was time he learned proper swim technique.Continue reading “Guiding Light”
My Life With T 