Positive Options for Antiphospholipid Syndrome (APS): Self-Help and Treatment

by Triona Holden, M.D. Graham Hughes (Foreword), M.D. Robert Roubey (Foreword)

This book contains information on an increasingly common autoimmune disorder. Also called "sticky blood" and Hughes Syndrome, APS makes one's blood clot too easily, creating high risk of stroke, thrombosis, and premature heart attack. It is also implicated in many other health problems including repeated miscarriages, neurological problems, eary dementia and migraines. It is often associated with lupus, and mimics the symptoms of other diseases, including MS.

Symptoms include; migraines and headaches, recurrent miscarriage, memory loss, slurred speech, blood clots, poor circulation, muscle pain and cramps, blurred vision, extreme fatigue, epilepsy, strokes, thrombosis and a form of angina. Because of lack of knowledge of APS in the medical establishment, sufferers are often misdiagnosed with MS or other more life-threatening conditions.

This book helps the reader identify the symptoms and provides important information on diagnosis and treatment of APS. It contains many moving stories, explaining how people eventually got a diagnosis, their symptoms, the impact of APS on their lives and whether or not treatment has worked.

Written in collaboration with Dr. Graham Hughes, the major researcher of APS in the UK, this book provides a clearly written informative look at an important but little-known disease.

144 pages, Paperback

First published March 1, 2003

Reviews

[Emmie Marigold · Rating 4 out of 5]

The info isn’t groundbreaking, but it’s really solid for people who are just getting diagnosed. I’ve been diagnosed for 4 years so I didn’t learn anything new, but appreciate the info being out there for others

[Lisa Leu · Rating 5 out of 5]

Very helpful for anyone suffering with APS.

[Susan Montgomery · Rating 4 out of 5]

Good introductory book on this syndrome.

[Debi Achey · Rating 5 out of 5]

excellent and not too difficult read that explains all my bizarre symptoms of APS. Will need to educate my doctors on why it is so important to keep my INR (blood thinners at higher range for symptom management.