15/02/2026
Hello Everyone,
This post is for all our friends who haven’t seen this on Instagram..
It’s been a while since we shared an update, and yes we’ve missed you all😘
Shamel has been making progress. He is attending more physiotherapy 💪🏽 sessions and bravely trying new things for the very first time. ♥️
Life feels completely different when you’re a parent to a child who needs extra care every single day.
Some days are so heavy, and exhausting 😔 but through it all, we choose to see the good side of life when ever possible..
Just two years ago, we were unsure if he would even make it. 💔Today, he is thriving. To us, that isn’t just progress - its a miracle🌟
Spinal Muscular Atrophy stole a lot from us including of the future we dreamed of.. It showed us how uncertain life can be.
But it also taught us to see the value of things we once took for granted - breathing, eating without struggle, walking freely, and even a normal everyday routine.. 🌈
But despite it all…
We are profoundly grateful.. 🥲
*Grateful for what we have..* 🍃
*Grateful for the of love we’ve received and continue to receive..*💖
Grateful for every tiny milestone… it reminds us that hope is still alive.. 🌱
Thank you from the bottom of our 💕 for standing by our side, for holding us up in our hardest moments, and for continuing to walk this journey with us.
Without your love, it would have been much different..
♥️♥️♥️
Achintha, Dula, Shamel