VVS

[Guest guest]

Evening ladies, how is everybody feeling? I don't know where to start

because I am frustrated and feel hopeless. How does a Dr. go about

giving a person a diagnosis of VVS, are there tests, a biopsy, or is

it a process of elimination? My first OBGYN Dr. told me he

believes I have this chronic condition but he couldn't say for sure.

Last week, I saw my second OBGYN Dr. and he didn't do an

examination, which I thought was strange. He referred me to a

neurology chiropractor (Dr.Rottacker) which is a fairly new type of

practice. Has anyone heard of it or tried it and had any success? I

had a consultation with him this past Saturday and he told me the

prudential nerve has a lot to do with the pain. I'm going to Stanford

hospital on Dec.13th to see Dr.Brodzinsky who is an OBGYN doc who

specializes in VVS. In the meantime though I don't know what to do

about my " contact pain. " During March through August, I used monistat,

antifungals, diflucan pills numerous times along with a one time usage

of Candida. I believe my skin is very dried out, thin and has no

elasticity to it. What can I do to repair it or heal it? I heard

something about Emu oil mixed with another ingredient. Any help would

be appreciated!