The next time you see me, my hair will not be perfect. But, it will be my own.
Over the last few years, I have been dealing with Alopecia Areata. It started with thinning hair, but eventually the hair loss became significant and I couldn’t hide the bald patches any longer.
My hair loss was emotional: much more than I expected it to be. I faced insecurities, a loss of confidence, and shame. One day a few years ago – quite suddenly actually – I decided it was time for a wig. That too, was emotional: also much more so than I expected.
I shared my reality with some, but for the most part, I have tried to hide the truth. In time, I became more accepting. I adjusted. I started to share my story with a few more people. I have also met others with Alopecia: some children. Talking to others dealing with this condition has helped me to feel more normal and accept my reality.
Fortunately, over the last few months, my own hair has been growing back. What’s more, I have had no hair loss since. Now that the length has evened up, I have decided to lose the wig. I have also decided it’s worth sharing the truth and raising awareness.
I know my hair loss could begin again at any time. I know, too, that many others deal with hair loss much more significant than mine.
This blog is usually about education. Today it is about education of a different sort: September is Alopecia Awareness Month. If you want to learn more, please visit The Canadian Alopecia Areata Foundation. Today, I made a donation to this foundation; if you are interested and able, I invite you to donate to a cause close to your heart.