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I was wondering how I could access the information

sent in to the group prior to my joining. I know there

is a way to retrieve this information and I would

appreciate help. I am especially interested in the

info on Estrace and Premarin. I tried Estrace and had

a horrible reaction. I wanted to die it burned so

badly! It turns out that Estrace contains Soy, to

which I am very allergic. My doctor gave me a

prescription for Premarin and it doesn't seem to

bother me. Has anyone else had this experience? Also,

can anyone recommend a doctor in the Northern NJ area?

I was seeing a doctor at the University of Penn., but

he recently died in a car accident. I then started

seeing the doctors at the Vulvular Pain Center in NYC

(including Dr. Glazer) but I haven't been too happy

with my treatment, with the exception of a NP. It is

costing me a fortune (800.00 for the first visit and

450.00 for the follow ups. Most of this is not covered

by my insurance.) I just don't know where else to

turn. Does anyone have any ideas? I have had v for

over nine years and seen so many doctors. I can't tell

you how much of a comfort it is for me to have this

group. Over the years I have been told by so many

doctors that it was all in my head and been through so

many treatments that made me worse. Although I spend

most of my time lurking in the background, I really

benefit from all of you. Thank you!!

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