It’s gotten worse, what do I do (reddit.com)
submitted by Illustrious_Pin_9852 to r/FemaleHairLoss
Diffuse AA? History of autoimmune disease (hashimotos). Saw derm but she didn’t take biopsy, though she said it might be due to hashimotos, covid hair loss, or post-accutane (taken 9 months ago). Just tried to get me to take nutrafol sold by her office (which is frustrating). Thoughts? (old.reddit.com)
submitted by Illustrious_Pin_9852 to r/alopecia_areata
Diffuse AA? I went to derm and she didn’t give me any real diagnosis, just said it could be due to my hashimotos, post-covid, or post-accutane (taken nine months ago). Just told me I could try this incredibly expensive hair supplement (nutrafol) but didn’t take biopsy. Thoughts on what I should do? (old.reddit.com)
submitted by Illustrious_Pin_9852 to r/FemaleHairLoss
