Guest guest Posted June 27, 2005 Report Share Posted June 27, 2005 I believe it's called the MS hug. I just started having a belted ribs feeling a couple of months ago, and have been on ldn for 15 months. I prefer hugs from my husband! LOL Arlene Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 27, 2005 Report Share Posted June 27, 2005 In a message dated 6/27/2005 12:50:10 PM Eastern Daylight Time, workerchris24@... writes: Been there and done that!! How does the LDN work for you? Chris Doesn't work as well as some have reported. In fact I was tempted to stop it several times, but the fact that it is supposed to stop progression kept me taking it. I never had the vivid dreams, but I did toss and turn a lot in the beginning. After about 8 months, I started to get SOME bladder control. But, I would try it and stick with it for at least the 6-9 months as suggested by Dr Bihari. Like I said earlier, I've been taking it for 15 months and plan to continue. Good luck to you. Arlene Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 27, 2005 Report Share Posted June 27, 2005 hopefully the LDN will help! thanks! Lynn Re: [low dose naltrexone] ? symptom ? Lynn/Marcie I believe it's called the MS hug. I just started having a belted ribs feeling a couple of months ago, and have been on ldn for 15 months. I prefer hugs from my husband! LOL Arlene Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 27, 2005 Report Share Posted June 27, 2005 Been there and done that!! How does the LDN work for you?arlizotte@... wrote: I believe it's called the MS hug. I just started having a belted ribs feeling a couple of months ago, and have been on ldn for 15 months. I prefer hugs from my husband! LOL Arlene Sports Rekindle the Rivalries. Sign up for Fantasy Football Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 27, 2005 Report Share Posted June 27, 2005 I seem to get the idea that the effect of the drugs usefullness is directly related to the level of progression u are in when u start to take it. I am still walking and on some days can prolly do a half mile. I'm not that bad yet. Has the drug seemed to slow up the progression and how impaired were u when u started the treatment? Besides the bladder has there been any other positives? Thanks-Chrisarlizotte@... wrote: In a message dated 6/27/2005 12:50:10 PM Eastern Daylight Time, workerchris24@... writes: Been there and done that!! How does the LDN work for you? Chris Doesn't work as well as some have reported. In fact I was tempted to stop it several times, but the fact that it is supposed to stop progression kept me taking it. I never had the vivid dreams, but I did toss and turn a lot in the beginning. After about 8 months, I started to get SOME bladder control. But, I would try it and stick with it for at least the 6-9 months as suggested by Dr Bihari. Like I said earlier, I've been taking it for 15 months and plan to continue. Good luck to you. Arlene Stay connected, organized, and protected. Take the tour Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 27, 2005 Report Share Posted June 27, 2005 In a message dated 6/27/2005 4:10:16 PM Eastern Daylight Time, workerchris24@... writes: I seem to get the idea that the effect of the drugs usefullness is directly related to the level of progression u are in when u start to take it. I am still walking and on some days can prolly do a half mile. I'm not that bad yet. Has the drug seemed to slow up the progression and how impaired were u when u started the treatment? Besides the bladder has there been any other positives? Thanks-Chris Chris It seems like that to me too. I think it did slow progression in some ways. I was using a cane most of the time when I started, but I probably could have used a walker at times. I use one now all the time in the house. I didn't see much in the way of symptom relief, but I know a lot of other people on this forum have. Perhaps someone else can chime in. Arlene Quote Link to comment Share on other sites More sharing options...
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