I don’t feel good! Do you hear this often from your child / teen / adult with FASD and not sure how to respond? I provide some links on research and share what we do.
For anyone that had a great day today, I’m happy for you. For anyone that does not recognize the day, I honour that. For those that had a tough day, I send you much love. I had a tough day. A disappointing day that turned out differently than the plan. My daughter was going to … Continue reading Mowing Mother’s Day
Why not try leaning instead? How are you doing? We’ve passed the one year mark for living in a global pandemic and I don’t know about you, but I have been feeling very alone and struggling to keep my anxiety down and my motivation up. I haven’t written much here about life in the pandemic. … Continue reading Are you hitting the wall during COVID-19?
Reflections on a one caregiver's journey on shifting parenting perspectives and changing expectations in supporting an individuals with Fetal Alcohol Spectrum Disorder.
Sharing (with permission) a wonderful piece about parenting a neurodivergent child and Groundhog Day by Lisa MacColl (Motherwell Magazine). While there is no mention of FASD, these are definitely similar experiences to supporting an individual with Fetal Alcohol Spectrum Disorder which is why I asked to share. Groundhog Day, February 2nd, conjures any number of … Continue reading Parenting, Groundhog Day and FASD
An interesting discussion on looking for the small positives, turned into a connection with my daughter and discovery that today is National Bubble Wrap Day.
Some of the groups I'm in have posed questions about when is it too old to believe in Santa. While the maiden has on and off mentioned she still believes over the years since she has gotten older, this year she never mentioned anything until Christmas Eve. She wrote a note, poured a glass of … Continue reading A Day Late … but Santa Arrived
At first I wasn't sure how I was going to end this series. When I wrote the original post in 2016 all the wishes were together, and this one flowed with the rest. As a stand alone it wasn't going to have much to it. In the original post I wrote that she didn't ask … Continue reading 12 Wishes for My Daughter and FASD: 2020 Edition
If my daughter had a time machine, she may choose to go back in time and be born without FASD. But if she chose that I would never have become her mum. My wish is that she could go back in time, receive a diagnosis earlier and therefore receive supports and interventions to lessen the struggles we … Continue reading Wish #11 for My Daughter and FASD: A Time Machine
During the adoption process, no one provided me with any education or training on FASD. No plan was established should I require access to services. We have been though some really trying times. Many people used to ask me, given what we have been through, would I still adopt my daughter if I could do … Continue reading FASD Wish 10/12: Know she is loved