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!
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