So I have more growth than I have had since I lost the last of my hair spring of 2012. Still patchy but more coverage than before. I also have eyebrows and eyelashes that are long enough to wear mascera.



In addition to Alopecia Universalis I have Rheumatoid Arthritis and Autoimmune thyroiditis. The RA was diagnosed 13 years ago. Dec 2016 my Rheumatologist and I finally called it quits on Remicaid. I had been on that for about 10 years when it started to fail. In Feb 2017 I started… Continue

So my hair has started to grow back ... kind of. I guess what I have now would be AA. It is very patchy. I feel kind of ungrateful saying this but I actually wish it would just go away. Way less than 50% of my head has hair so it looks terrible. I don't tolerate my wigs anymore so I always wear a scarf to work and usually a hat outside of the office. I am so tired of covering my head!

So - it has been a weird week.

First - I have been thinking very hard about the awesome things associated with AU such as the fact that I never, ever have a bad hair day. I have also realized when you are bald people seem to think you are prettier than before - are their expectations of beauty less than when you had hair? Like it is so shocking that a bald woman can be attractive? Not sure. They should look at this website and see all the breath taking pictures of bald women! Also…

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March 2012

I am now head shaved and getting permanent make-up. I have also noticed I now lack arm and leg hair - so there are a few perks to alopecia universalis i guess

I decided that if I was going to get brave and try to go wigless and scarfless then vacation in the Caribbean was a good place to try it out. I still wore my wig to dinner every night…

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