There is little that can describe the devastating effect that my hair loss has caused me. My hair started thinning many years ago, but it wasn't until diagnosed with lupus and frequent flare ups of this disease that my hair loss has increased to the point that I no longer feel feminine. Since my disease becomes more active with sun exposure and exposure to fluorescent lights, I have to have my head covered at all times upon leaving my home. I have little experience with wigs and wig toppers. I want to learn more about wearing them and be able to encourage other women that there are solutions to make us feel beautiful again. I will definitely share my experience with any wig or wig topper. I am very excited at the prospect of empowering others through my own experiences.