When my son was diagnosed with Alopecia Areata at 8 years old, our family entered a world we knew very little about.
It started with a small patch of hair loss. Over time, his alopecia progressed, eventually becoming Alopecia Universalis.
As his mom, I watched him navigate changes in his appearance, questions from others, difficult moments, and moments that showed me just how strong and brave he truly is.
Through our journey, I also began learning more about the alopecia community. I realized how important it is for children, adults, parents, siblings, and supporters to feel seen and supported.
That's where Alohugs, Inc. began.
Alohugs, Inc. was created from our personal experience, but its purpose reaches far beyond our family.
I wanted to create something that celebrates the beauty of a smooth scalp while also providing the emotional "hug" that can mean so much along the journey.
Whether you have alopecia yourself, love someone who does, or simply want to show your support, there is a place for you here.
Alopecia may be part of our story, but it doesn't define the whole story.
There is still joy.
There is still confidence.
There is still community.
And there are always hugs. šš
Welcome to Alohugs, Inc. ā Embracing the Journey, Hugging the Transformation.
ā A Mom, an Advocate & the Founder of Alohugs, Inc.