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Hi everyone

I have read all the messages and learned a lot from them and I feel with

each and every one of you because its really frustrating that things happen

because of negligence especially if they could be avoided.

Unlike most of you I have developed Ashermans gradually over the years with

no apparent cause and this is why it took like 6 months to diagnose it

after a lot of blood works and hormones and clomid. My periods just stopped

coming. The DR assumed it is hormonal or that I am not ovulating.

After all the treatments with hormones we did HSG and it showed that my

Uterus is full of scar tissues. He did operative hysteroscopy and he put me

on premarin 5mg a day for six weeks with the last 10 days he added

progesterone. After two weeks I asked for u/s to check the lining and

another HSG to check the adhesion, he refused promising that everything is

all right. My period came and the flow was great for six days so my hopes

soared high. He put me on a rest cycle and after that he wanted to give me

clomid because I want to get pregnant as soon as possible( I'm 40.4 yrs and

have a 10 yrs old son).Well my next period was nothing to talk about just

some spotting for a day and a half.

Did another HSG and a comparison between the two showed no improvement.

At the appointment with him to discuss my situation he told me that he did

the best he could and that he was stuck for the adhesions are calcified and

that it is not his fault and that a laproscopy should have been done to

assist him because he felt that if he was more aggressive during the hyster

he would have perforated my uterus and then a he should do a

hyestroractomy(spelling??). I tried to do some research on calcified

adhesions but didn't find any.

I'm changing Drs. again and hoping because frankly I'm fed up with them

trying things on me.

Has anyone heard about calcified scar tissues? Are they correctable?

Any imput will help.

Sorry for such a long email but I feel so frustrated and obsessive about

ashermans that I'm stuck to my computer reading anything that is connected

to this horrible syndrome.

Thank you all

Leila

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