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My web site and making women aware of AS.

My blog is on my web site called

My Ashermans Syndrome Story. 

 

I am so happy to have found this web site.  Marni I had the same vision as you and started my web site to bring women together with their stories and to help eachother.  I also feel it is so important to make all women aware of AS.  I know for myself if I was told I could get AS from my D&C's I would not have done them.  With my first miscarriage I was scared of having a D&C so I chose not to and took meds to miscarry.  I would have done that again if I had known all the risks.

 

Thank you

Leanne

 

http://www.myashermanssyndromestory.webs.com

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Comment by Laura Rosendale on June 5, 2011 at 5:31pm

I am concerned because I had two  D&Cs.  Did you have the D&C s after your miscarriages?  Did you have periods? What is your next step? Sorry for all the ??s 

 

Comment by Leanne Hester on June 4, 2011 at 9:06pm

After 3 miscarriages, I had blood work and a sonohistogram (sorry for the spelling).  They thought it was a septum and while on the srugery table when the doctor went in he say it was not a septum but severe AS.

Do you think you have AS?

 

Leanne

Comment by Laura Rosendale on June 4, 2011 at 2:59pm

Hi Leanne,

 

How did you know you had AS? Thanks

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