Guest guest Posted July 24, 2003 Report Share Posted July 24, 2003 Hi! I don't often post to the list, but I do read the summaries I get sent from the list. I am involved with CF through my work and not because I have CF or have a child with CF and I have endless admiration for all of you coping the way you do. I just wanted to let you know that the organisation I work for (Cochrane Collaboration) has just published the latest version of The Cochrane Library containing reviews of medical interventions for a wide range of conditions - including CF. The abstracts of these reviews are available online free of charge via http://www.cochraneconsumer.com/index.asp?SHOW=Search Hope this information may be of some help to you, Nikki Nikki Jahnke Cochrane Cystic Fibrosis & Genetic Disorders Group Alder Hey Children's Hospital Eaton Road Liverpool L12 2AP http://www.liv.ac.uk/cfgd Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 24, 2003 Report Share Posted July 24, 2003 In a message dated 7/24/2003 10:50:08 AM Eastern Daylight Time, nikkij@... writes: > http://www.cochraneconsumer.com/index.asp?SHOW=Search It looks like a great site. Thanks. I have a friend who's daughter died from Cochrane Syndrome a few years ago. Rosemary in NY with 3 children (13, 10.6 and 6.6) with CF. I have a dog named TOBI and have coined the phrase " BREATHE DAMMIT " Quote Link to comment Share on other sites More sharing options...
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