Dating can be an adventure filled with excitement—but when alopecia enters the picture, it might feel like you're lugging around a suitcase of "what-ifs." What if my bald look isn't appealing? What if I face judgment before even saying hello? Sound familiar? Fear not; you're in good company! When I first ventured into online dating, I was intimidated. The digital realm can be harsh, laden with filters and snap judgments. Initially, my profile showcased a mix of looks—some wit

Alopecia is a complex condition that affects countless individuals around the globe, leading to varying degrees of hair loss, from patches to total scalp and body baldness. This condition often carries an emotional weight, impacting those who experience it and their loved ones. As caregivers or loved ones of someone affected by alopecia, understanding the complexities of this journey is vital. While your support is invaluable, it's also important to recognize and prioritize y

Ahhh, alopecia—my ride-or-die companion for over twenty years! We've seen it all together—from curious stares to those well-meaning (but oh-so-awkward) comments. Each encounter has been a reminder of how much hair loss myths shape how others see us and how we see ourselves. Embracing my baldness didn't happen with the snap of a finger — it took courage, soul-searching, and unlearning many beauty "rules" I never signed up for. But I'll never forget the  day. The day I strolled

Meet Grace, an inspiring 10-year-old from Toronto, Ontario, who is transforming her journey with alopecia into a powerful message of self-love, creativity, and kindness. Alopecia, an autoimmune condition that results in hair loss, could easily lead one to feel isolated—but not Grace. To her, it's a superpower. "Alopecia is an autoimmune disease," Grace explains. "Basically, your hair falls out because your body thinks your hair is bad. It doesn't stop you from doing anything;

Experiencing alopecia goes beyond simply losing hair; it can touch your mental well-being and, at times, may feel overwhelming or even isolating.   Like  many, you might have believed that your first dermatologist visit would be a quick fix—perhaps a pill, a magical topical solution, and then poof! Problem solved. But for most, the reality is quite different. For me, that first appointment was disappointingly short. I left with more questions than answers, feeling unheard and

In the heart of the public health community, a beacon of inspiration shines through Anthony Gilding's journey. A graduate student, clinical researcher, and dedicated advocate, Anthony's narrative is one of resilience, self-acceptance, and unwavering passion. Join us as we dive into his personal experiences, interests, and vital impact on the alopecia community. The Early Years: A Journey Begins It all started when Anthony was just seven years old. He remembers the first signs

On October 17, 2023, I woke up to a “normal” day filled with too many snooze-button smacks, a mad dash to the shower, and a barely made-it exit from my house. But something wasn’t normal about this day, and I knew it as soon as I closed the door behind me. No wig. For the first time in my 20-year relationship with wigs, I had decided to leave home without one, heading to work unapologetically and fully bald. To say wigs have been my safety blanket is an understatement. I've h

From wigs to wings, a 20-year love-hate affair to self-love and freedom.