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Anonymous (reply to Anonymous)

I have been diagnosed with LS since 2002 (40) and using the .5 cream for years then was recommended to use the 1 in 2014 which for me drastically changed and accellorated the other complications that are part of LS. My entire labia minora has been absorbed and the upper flaps of the labia magora are starting to dissipate. I did not fully understand in my diagnosis that eventually the vigina would be absorbed by the body. It's not just the skin change it is a structural change. I think anyone that is diagnosed with this needs to seek out a support group and get as much help as they can give you. Because beyond the creams there doesn't seem to be much more help the medical practise has. As I understand it is a autoimmune condition, is a gene within the family , , not contagious, command patient history traumatic experience during childhood, quite often excessive skin production on other areas of body. You need to live as healthy and positive life you can to slow it down . All the best to everyone including males who also can develop this.

March 9, 2017 - 9:54am

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