Scroll
To Top
0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

*Important

The information contained in the Organizational Database (ODB) is provided for informational purposes only. There is no implied endorsement by NORD. NORD does not promote or endorse participation in any specific organization. The information is subject to change without notice. Every effort is made to ensure that the details for each entry are as current as possible.


Asherman’s Syndrome Online Community


Email Address

ashermansbook@yahoo.com

Description

The Asherman's Syndrome Online Community (ASOC) is an international community of women from all over the world who have been diagnosed with Asherman's syndrome. The purpose of this community is for members to give support to each other by sharing information. Asherman's syndrome is an acquired uterine disease characterized by the formation of scar tissue (adhesions) in the uterus. Most patients with Asherman's have scanty or absent menstruation (amenorrhea) but some have normal menstruation. Some patients do not menstruate but feel pain each month at the time that menstruation would normally occur. Symptoms can also include recurrent miscarriage or in some cases infertility. Founded in 1999, the online community serves women in countries throughout the world.

Please Note

The National Organization for Rare Disorders (NORD) web site, its databases, and the contents thereof are copyrighted by NORD. No part of the NORD web site, databases, or the contents may be copied in any way, including but not limited to the following: electronically downloading, storing in a retrieval system, or redistributing for any commercial purposes without the express written permission of NORD. Permission is hereby granted to print one hard copy of the information on an individual disease for your personal use, provided that such content is in no way modified, and the credit for the source (NORD) and NORD’s copyright notice are included on the printed copy. Any other electronic reproduction or other printed versions is strictly prohibited.

NORD's Rare Disease Information Database is copyrighted and may not be published without the written consent of NORD.