Jaksokuvaus
Welcome to this episode of Alopecia Life, and for sharing your time with me and our guest, Susan McLemore, today. A couple months ago, I was searching for something on Facebook, and I discovered Susan and a really cool thing she organized. I wanted to find out more, and we were both excited to talk about the community that supported her family after they were diagnosed with alopecia. I hear so often, after children are diagnosed, that parents want to do something, anything really...to support...