I do. I'm sorry, it sux! How was it diagnosed for you? I had an MRI 2 years ago, and every doctor has clung to the diagnosis since. We're about to head towards IVF, and a doctor recently told me that our chances are lower than they ordinarily would be (like 20% for an IVF). Ugh.
__________________ TTC #1 since 8/06
PCOS, Adenomyosis, MFI
IVF #1 April 2009
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Do you know if you have cycstic adenomyosis? I was just diagnosed yersterday. This was found in my first U/S for my fist IUI cycle. She originally said it could be blood from a period, she said if it did not disappear at next U/S it was probably adenomyosis. In my U/S yesterday it was not gone, she diagnosed it as cycstic adenomyosis. My Dr says it does not affect pregnancy. The cycsts are in the muscle of your uterus, not the lining. I have been researching this all morning and am yet to find a website that says there is any link to infertility.
Anybody else been diagnosed with this and heard different?
My GYNO thinks I could have this. I saw her this morning. She isn't ruling out Endometriosis, but thinks the chances are minimal, considering she didn't see any signs of it in 2002 when I had a septum resection.
At this point, she wants me to take bcp 3 months at a time to help with spotting. She's also prescribed a supplement from the bcp to help with the pcos symptoms.
__________________
"We can't solve problems by using the same kind of thinking we used when we created them."
-Albert Einstein
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