Guest guest Posted April 1, 2010 Report Share Posted April 1, 2010 I’m afraid the MS Society won’t be getting a penny from me either. The time they spent in writing to our local papers complaining about the press coverage we were getting about LDN and how they weren’t contacted to give a more “balanced” view on this treatment with MS, together with ripping our petition to the UK Govt apart (four pages) to one of our MPs was laughable! And yet they CLAIM to support further research into LDN. At least the press gave us an opportunity to respond to their pettiness, which we did with great pleasure! So it’s not because they don’t support LDN, that is their prerogative, I just find that a so called ‘charity’ who has the time to do the above is not worthy of funding. Jayne Crocker Chairperson www.LDNNow.com Important! Please sign our LDN petition to the European Parliament by clicking here (please note no funding required, please ignore the second page) 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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