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Use your EpiPen! |
Nut-allergic Ruth Holroyd encourages fellow allergics to use their EpiPen. On two occasions she did not – and only just survived... |
Who would have thought that I, a 36-year-old intelligent young woman, would suffer two severe anaphylactic attacks in the last two years, both with my EpiPen in my bag, and still not take action and administer the medicine that could have reversed the reaction and hastened recovery… and potentially saved my life. I have been lucky. I have also been stupid and careless and should have known better. I wanted to share my experience in case it is similar to other allergy sufferers, and also in the hope that others can learn from my mistakes. My own allergy I grew up in a fairly poor family. I never really felt I was missing out but we never had chocolates in the house or snacks as kids do nowadays. We rarely went out for meals and life was much simpler. Home-cooked food and simple basic
ingredients. I know I didn’t like nuts but that was as far as it went. I always used to get a tingling on my lips and in my mouth within seconds of eating any nuts. Consequently I’ve always stopped eating the offending food and only had minor sickness. Until recently, when the pattern seemed to change. And again... I don’t know why I didn’t use my EpiPen on either of these occasions. Perhaps it was because I had no swelling or tingling in my mouth. I was not sick. The two major triggers I used to have were not symptoms in these two recent attacks. My advice to fellow anaphylaxis sufferers is to tell all your family and friends that you have an allergy. Show them your EpiPen and demonstrate how to use it. Really drum into them that if they suspect you are having a reaction that they should take charge and administer the drugs. It’s easy and fast and simple to do. First published in 2009 If you found this article interesting, you will find many more articles on anaphylaxis here, and reports of research into anaphylaxis here.
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