Guest guest Posted July 6, 2010 Report Share Posted July 6, 2010 i was pn ldn for a long time and it helped but they wont give it to me anymore.................. LDN IS GREAT I DID WELL I HAVE MS FOR 30 YEARS AND CANT TAKE STERIODS AS I HAVE HAD BROKEN BONES, AFTER I FELL AND BROKE MY BACK THEY QUIT GIVING IT TO ME I RESEARCHED IT MYSELF AND IT HELPED I AM OUT OF THE CHAIR NOW ONA A WALKER AND WANT IT BACK ________________________________ To: googleldn ; ldnforcancer ; low_dose_naltrexone ; mscured ; Spotlight_ldn Sent: Tue, July 6, 2010 6:41:10 AM Subject: Fw: Galloway TV Show - The Real Deal - LDN - UK Â [LDN_RaisingAwarenessUK] Galloway TV Show - The Real Deal - LDN - UK [1 Attachment] Last year when Galloway was an MP, we contacted him with a view to him help raising awareness of LDN in the political arena. He put a BBC freelance reporter in touch with us and has contacted us again as he'd like to do a show on LDN this Friday 9th July. Is there anybody who would like to appear on his TV show this Friday who lives in/around the London area or willing to travel to London to be interviewed in the studio between 1 - 2pm? If you know of anyone, can you please contact me at jaynelcrocker@...? This is a great opportunity to get LDN 'out there'. Many thanks and apologies for the short notice. Jayne Crocker Chairperson LDNNow logo the one to use www.LDNNow.com <http://www.ipetitions.com/petition/ldnnow/> 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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