Abby’s eczema story

Meet Abby, a university student with a story to share. Her bravery in opening up about her struggles with eczema isn’t just about her journey—it’s about helping others feel less alone.

“Eczema has been a lifelong challenge, starting from my early childhood. Classmates teased me, asking, “What’s on your arm?” My response: “Eczema.” Their next question: “Is it contagious?” left me defending myself despite lacking the words to educate them.

Over time, I learned to advocate for myself and seek solutions. I realized that eczema is highly individual, and different treatments work for different people. However, hearing stories of people overcoming eczema added immense pressure and self-doubt, making me question what I was doing wrong.

Eczema lingers in my mind, impacting my choices for moments of enjoyment. Should I swim in my friend’s chlorinated pool and then suffer later or miss out on being with my friends? It often felt unjust and robbed me of simple joys. Eczema profoundly affected my mental health, particularly during my formative years when insensitivity compounded the struggle. No child should endure such experiences.

The summer of 2023 brought the most severe flare-up of my life. My entire arm peeled like a snake, and securing a dermatology appointment was impossible. My understanding of eczema expanded when I discovered Eczema Society of Canada (ESC) and explored its resources, revealing the complexities of eczema triggers and treatments.

I wish everyone had access to the relief they need. I’ve come to terms with living with eczema throughout my life, understanding that while it’s a part of me, it doesn’t define me.”

ESC sincerely thanks Abby for sharing her story. If you are struggling with eczema and need support, please contact us at info@eczemahelp.ca or visit us at eczemahelp.ca or on our social media channels.

September 2023