I have a wonderful, bright, and talented young boy who has ASD (Autism Spectrum Disorder). Initially, when he was diagnosed, I felt lost and unsure about what it meant for my child to be autistic. I went through various stages of grief, just like many of you out there.

As parents, we often envision a “normal” life based on societal expectations and what we believe to be predictable. However, I had to let go of those expectations and hit the reset button.

Let me tell you, while we celebrate the major milestones, it’s the small victories that touch our hearts the most. I’ve learned to appreciate the little things we often take for granted. For someone with a disability, even everyday tasks require hours of practice, occupational therapy, speech therapy, physical therapy, and feeding therapy.

In this space, I’ll not only share my struggles but also my wins. Despite feeling lost at times, I’ve managed to gather a wealth of knowledge that I want to pass on to all the parents who are going through similar challenges.

Let’s face it, none of us are perfect. Let’s accept that we’ll make mistakes along the way. What truly matters is how we learn from those mistakes, how we pick ourselves up, and keep moving forward. That’s what makes us resilient and shapes who we are.

By taking the time to read and seek information on how to support your loved one, you’re already winning. So keep going, and together, let’s navigate this journey of love and parenthood.

Please kindly note that the information I share is based solely on my personal experience as a mother. I am not a medical professional, therapist, or expert in the field. I have gathered my knowledge through my own struggles and endeavors to seek answers. It’s important to consult with qualified professionals for specific advice or concerns related to medical, therapeutic, or related matters.