Anyone heard of Ashermans Syndrome?
I lost my baby last February and had a dnc in March. After my dnc I had a really bad infection that could have killed me if i wouldn't have caught it in time. Since then my cycles have been messed up. They have been shorter and lighter and also very irregular. I finally went to my OB today and got some bad news. She is pretty sure i have Ashermans Syndrome. I have to schedule a sono where they are going to put dye in my uterus so they can see how bad the scaring is. After that i have to have surgery to cut out all the scare tissue and I will have to take estrogen for a few month because it will help in the healing process. After a few months I can start trying again. It is so heartbreaking to know that I have been trying for the last yr to get pregnant and there was no way it was going to happen. It bad enough that I lost my baby and know I cant have one until I have this all fixed. I am so thankful for the 3 girls I have but it still hurts so bad. Has anybody ever had this and got pregnant again?
I have no experiance with it sorry hun so here is a bump for you.
Everything was relatively painless and quick. Look up ashermans.org
I have already :). Did you go to a specialist or just you OB. How was the healing time. I am so glad everything is going okay for you. I hope you get your bfp soon.
Quoting LilysMommy813:
Yes I have heard of it. You are at an increased risk of ashermans with a blind d&c, but m/c can increase your risk in general. I had a saline infused sonogram because I had persistent bleeding after my second mc (1st d&c, 2nd induced vaginally) they found lots of scar tissue in one area and retained placental tissue 10 weeks after I delivered. I had a "hysteroscopic lysis of adhesions" they used a camera to guide them to the problem area and basically performed a d&c. I was then on estrace for 25 days and day 16 started provera for 10 days, stopped both and got a normal period 2 days later. I am currently cleared and TTC
Everything was relatively painless and quick. Look up ashermans.org
They say it is rare. I had only heard of it because i googled light af after dnc back in July. I brushed it off and figured surely it couldnt be what is wrong with me. As I was telling my OB what was going on she said I bet you have Asherman's. She was shocked I knew what she was talking about.
Quoting Angela4boys:I've never heard of it?



- mama91605
on Feb. 6, 2013 at 9:23 PM