Re: testosterone for vulvar atrophy?
Hmmmm-vulvar dystrophy eh? I am still caught in the warp of Moscow, but will be home in Canada July 1st, and have an appointment booked with a vulvo-vaginal specialist Yea!The possibility of V.dystrophy seems to make a LOT of sense to me, although the common signs-white lesions, etc.are not apparant to the naked eye. For the past year I have been chasing the burning away with a tiny drop of cortizone (usually once or twice a week) but strangely, had a TWELVE WEEK period this winter where all felt very normal,and did not need to use the cortizone.Even had a return of sexual desire!!! Then Boom!! the old burning started again. It drives me crazy,because I have been compelled to "self-diagnose" and have explored possibilities such as oxalates/stress/allergies/irritant dermatitis(because a)my mother had horrendous exzema on her hands for years and b)I've always been super sensitive vaginally-have never been able to use bubblebath,bathsalts,etc).
The French gyn.I saw here in Russia was the worst experience of my life-he asked my age and put up his hand to say "Stop talking" and proceeded to tell me that he knew exactly what my problem was. He said "You have vaginal atrophy and there is no treatment for this condition". He said that the only treatment is testosterone and that he wasn't permitted to prescribe it in Russia. He then examined me,with some sort of probe (I think ultrasound)smiled and pronounced: "A beautiful atrophy! Go home my dear and be thankful you don't have cancer..you are not going to die". It was only that I lacked the courage, because on that day, after 2 years of constant burning,and that terrible,terrible man,I very much wanted to end the pain.
I AM improved. The estrogen in the compounded base DOES help,if I am vigilant,and use every night.But my gut reaction is that there is a problem that has yet to be diagnosed, and I DEEPLY appreciate your heads-up on V.Dystrophy...I had never heard of it, and from all my research, vaginal atrophy takes time to develop after years without estrogen. This symptom came out of nowhere..and became very intense, at which time, I began estrogen replacement with vagifem, and when this didn't improve symptoms long-term, I added Premarin in the vestibule...and after 3 years of this,one can't really say things are "normal" because I have to use the estrogen creme every night to obtain a semi-comfortable state. Sorry to be such a long-boring-story,but know each of you reading this, understand. Thank you.