LS? Join the LS group here....

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HI Sue....

I just sent you a private email about joining my LS group hon.. I hope you do since there is SO much information specifically on LS there that will be quite beneficial for you.

For anyone else I may have missed (I usually tried to catch that if it was mentioned when joining) but if not the link is here:

http://health.groups.yahoo.com/group/LichenSclerosis/ You join the same way you did this one..Hope to see you there too. and yes hon believe me your feelings are quite normal. *smile* AND indeed things 'can' be turned around!!

HugsDee ~

RE: Estrace to Chelle/estadiol v estriol

I think it's just wonderful to have such a great support group out there. It's so great to know that we aren't alone. Is there anyone out here who has vulvar lichen sclerosis? I think I could really use a friend. I'm sitting here writing this and it's really hitting home for me. I've known about this since January and to tell you honestly I was in shock. I had a bad experience with the Clobetasol Propionate Cream and the ointment.

I'm on no treatment as of the second week of January. I've really tried hard to get this out of my mind. I guess I kind of just blotted everything out. I try hard to forget the fact that I have this disease and then reality sets in. It's here to stay and not just some kind of bad dream. All of this has left my emotions all over the place. I'm waiting for an appointment to see Dr. in Boston. There is no where to run and hide. I guess I need to face this headon. How the heck does one do this? I want to take a negative and turn it into a positive but how? I hope my feelings are normal...'