Have you had recurrent miscarriages and discovered you have Hughes Syndrome or Antiphospholid Antibody Syndrome? Or do you have Hughes Syndrome and are either pregnant or would like to be. This is a group for discussing your fears and worries, asking questions and supporting each other.

This can also be a safe place to talk about women's issues related to APLS as well.

The members of this list are not necessarily medically qualified and talk from their own experiences. Any advice or suggestions given on this list should not be construed as medical advice. Readers are urged to check specific treatments with their physician.

This list is a friendly, loving, supportive place and is not to be used for promoting any products, services or causes. Any information on this list is not to be forwarded or used for other purposes outside this list.

By joining this list you agree to abide by our guidelines and conditions (available on request and on subscription), so we can keep this a safe and supportive place for all members.