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BMJ 2007;335:1152-1154 (1 December), doi:10.1136/bmj.39374.504884.BE
Siri Lowe, patient
Pemphigus Vulgaris Network, London
siri.lowe@btopenworld.com
Twelve years ago, Siri Lowe developed pemphigus vulgaris, a potentially fatal autoimmune blistering disorder. As her story shows, it can have a devastating impact on patients' lives, as can the side effects of the necessary treatments
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I deteriorated quickly and in only five weeks moved from being strong and healthy to being unable to eat solid food, drinking through a straw, and being in agonising pain. I remember walking the London streets in a total daze thinking, "This can't be true, it's like the script of a bad television play." I had no idea how living with a chronic disease would change my life.
There's no cure for pemphigus. No smart drug to take it all away. It is nearly always controllable, but that control comes at a
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