The Faces of APS

Wednesday, April 12, 2006

APS & Thrombophilia Support Groups

At the APS Friends & Support site, you read messages from others under headings interesting to you. You can start new messages or add comments to the string of messages that already exist. It can be found by going to http://www.apsforum.com.

A forum run by Heidi & Tina founders of the APS Foundation of America, Inc., a non profit organization.

This forum is an information source and a friendly support group for people who have Antiphospholipid Antibody Syndrome or for anyone who's lives are touched by it. It is sometimes referred to as APS, APLS, or APLA and is known as Hughes Syndrome or "Sticky Blood" in the UK. APS is an autoimmune clotting disorder that causes recurrent clotting events including premature stroke, repeated miscarriages, phlebitis, venous thrombosis and pulmonary thromboembolism.

If this disease touches your life in some way, please feel free to join in our discussions! :) We're glad to have you visit!

Antiphospholipid Antibody Syndrome Support: http://groups.msn.com/AntiphospholipidSyndromeSupport

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