Wednesday, November 10, 2010

Welcome: An Introduction to Mullerian Anomalies

This is a blog dedicated to informing people about Mullerian Anomalies - what they are, how they are diagnosed, treatments, and the personal stories of the women who have them. The information you read here has been compiled by a group of courageous women who have a wide variety of Mullerian Anomalies. They are not doctors, but are experienced and pro-active patients of a medical system that rarely seems to have a grasp of this very special condition.

If you have recently been diagnosed with a Mullerian Anomaly, please consider joining the MA Support Group on Yahoo forums. The women who write the boards there are the same women who have contributed here. Their knowledge and expertise can be a great help to you as you navigate through your diagnosis and treatment.

Good Luck on your journey!

9 comments:

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Maria said...

Hello, girls!

At the age of 12, I was diagnosed with HWW syndrome: uterus didelphys + renal agenesis (one kindey missing)+ hemivagina. Back then my hemivagina was treated.

Now I am 29 and consider to start trying for a baby in 1-2 years. So I will soon have the operation to remove the septum. I am very scared, since I am not in my country (moved to Norway, bcs of my Norwegian fiance), and I am also worried about the time after the operation. I am extremely sensitive to pain.

Anyone that has done it and can share some experience?

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Unknown said...

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