chemo headscarves
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Every month, thousands with hair woes visit my site. The more the merrier! But it takes AGES to write posts and reply to emails. Don’t get me wrong, I love it! But running a website isn’t free. So I’m trying something new: I’m asking for your support. If Lady Alopecia has helped you, please consider buying me a (virtual) coffee or even become a patron of the site. Thanks!
I’m Emma. I’ve had alopecia for 24 years and I’m here to inform/hopefully empower people like me! Read my full story here. But I’m not a doctor, so any advice here is based on my own research and experience. I’m also in a few affiliate programs – see my disclaimer page for more. Or contact me here. Also, why not join a thousand fellow alopecians and get my-semi regular hair about life with irregular hair?
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