Guest guest Posted August 19, 2010 Report Share Posted August 19, 2010 Here’s Zillah Damon’s story on “Life with MS” and her use of LDN in Wales Online http://www.walesonline.co.uk/news/health-news/2010/08/19/zillah-damon-on-life-with-ms-91466-27090695/ Like most, she too wishes she found out about LDN sooner! Don’t forget, if you haven’t signed/supported the EU petition, please do. There’s almost 2,200 signatures with some excellent comments, thanks to those who have already supported this. This really is our human right to be able to have access to LDN and make it available as front line treatment. There’s lots of Drs out there who DO want to prescribe LDN but until the Govt have said ‘”it’s OK”, they do risk having their licence suspended. So let’s help them as well http://www.ipetitions.com/petition/ldnnow/ Many thanks, Jayne Crocker Chairperson www.LDNNow.com Important! Please sign our LDN petition to the European Parliament by clicking here tel: +44 (0) 7877 492 669 Dr Steele MBE, talking about LDN LDNNow are a political/pressure group of individuals dedicated to getting Low Dose Naltrexone (LDN) accepted into modern medicine and trialled for the myriad of uses it shows benefit for. .. Quote Link to comment Share on other sites More sharing options...
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