Guest guest Posted February 5, 2004 Report Share Posted February 5, 2004 I think that story is why I keep reading all the posts. Sure I have my doc. in my back pocket for now, but what happens when the day comes that he says the same to me? I need to be prepared for that eventuality if it shows up, but until then I say halleluha for fads.This "fad" has been a Godsend when previously there was nothing else on the horizon, I hope he really isn't backtracking for your sake, as can you imagine life without ldn? I can and it scares the h**l out of me! Reg. -------Original Message------- From: low dose naltrexone Date: 02/05/04 14:13:35 low dose naltrexone Subject: [low dose naltrexone] I`m so angry Guys, I just got information today (second hand) that my neuro thinks that LDN is a "fad" from America. Now this is the guy who sanctioned a prescription for me in November and is now back tracking like mad, why? I don`t know. I have been taking LDN for 10mths now and getting great benefits from it, I can walk better, my fatigue has gone, some of my symptoms have improved, so basically in general my life is a whole lot better than it was a year ago, oh! and I have gone from having deterioration every month to none in the past ten. I know there is nothing you guys can do other than listen to my rants, which, by the way, makes me feel better sharing this with you. I have written to him twice, I was very civil both times and he won`t even answer my questions. Grrrrrrrrrr People like him just make the fight to get LDN recognised a whole lot harder. No wonder I hate doctors. That`s it rant over, thanks for listening.Lorna ____________________________________________________ IncrediMail - Email has finally evolved - Click Here Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 6, 2004 Report Share Posted February 6, 2004 I guess fads don't cost $1000 per month!!! > [Original Message] > From: loma1956 <district@...> > <low dose naltrexone > > Date: 2/5/2004 2:13:19 PM > Subject: [low dose naltrexone] I`m so angry > > Guys, I just got information today (second hand) that my neuro > thinks that LDN is a " fad " from America. Now this is the guy who > sanctioned a prescription for me in November and is now back > tracking like mad, why? I don`t know. I have been taking LDN for > 10mths now and getting great benefits from it, I can walk better, my > fatigue has gone, some of my symptoms have improved, so basically in > general my life is a whole lot better than it was a year ago, oh! > and I have gone from having deterioration every month to none in the > past ten. I know there is nothing you guys can do other than listen > to my rants, which, by the way, makes me feel better sharing this > with you. I have written to him twice, I was very civil both times > and he won`t even answer my questions. Grrrrrrrrrr People like him > just make the fight to get LDN recognised a whole lot harder. No > wonder I hate doctors. That`s it rant over, thanks for listening. > > Lorna > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 6, 2004 Report Share Posted February 6, 2004 Lorna are you Canadian too? If you want to see what the head nuero at the London MS Clinic thinks of Interferons go to www.mswatch.ca and check out the dialog magazine with the nurse on it. On Page 2 it tells you the Interferons don't work after the first year and on page 4 it says copaxone doesn't work after the 2nd year. It looks like LDN works longer and better. I was on Betaseron and since I had started it I graduated to a cane, then walker. I was just about to get a wheelchair. No I don't need anything. I do still use my cane outside because I am not sure the LDN has finished working to repair my knees! ----- Original Message ----- From: loma1956 low dose naltrexone Sent: Thursday, February 05, 2004 4:10 PM Subject: [low dose naltrexone] I`m so angry Guys, I just got information today (second hand) that my neuro thinks that LDN is a "fad" from America. Now this is the guy who sanctioned a prescription for me in November and is now back tracking like mad, why? I don`t know. I have been taking LDN for 10mths now and getting great benefits from it, I can walk better, my fatigue has gone, some of my symptoms have improved, so basically in general my life is a whole lot better than it was a year ago, oh! and I have gone from having deterioration every month to none in the past ten. I know there is nothing you guys can do other than listen to my rants, which, by the way, makes me feel better sharing this with you. I have written to him twice, I was very civil both times and he won`t even answer my questions. Grrrrrrrrrr People like him just make the fight to get LDN recognised a whole lot harder. No wonder I hate doctors. That`s it rant over, thanks for listening.Lorna Quote Link to comment Share on other sites More sharing options...
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