Guest guest Posted September 11, 2003 Report Share Posted September 11, 2003 Great post Carol, thx for sharing :0) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 11, 2003 Report Share Posted September 11, 2003 That is great Caral. I am so happy for you. I hope that i am doing as good as you when I hit the year anniversary next June. Keep up the good works. Marie ----- Original Message ----- From: " sunynbrite56 " <sunynbrite56@...> <low dose naltrexone > Sent: Thursday, September 11, 2003 1:14 PM Subject: [low dose naltrexone] One year on LDN > Hi all... I just wanted to share with you my One Year Anniversary of > being on LDN. I started taking it on Sept. 6th 2002 and have had > nothing but positive days since. Of course, I still have a few MSy > days here and there. But, my life is nothing like it was before I was > off all my other MS medications and on the LDN. And, I have to tell > you, the past year has been a year of complete turmoil for me in all > areas. That of which I surely thought I'd be thrown into relapse > after relapse. But, to my suprise, and total thankfulness, I've not > had a relapse since early 2002. Yes, I do contribute this to LDN. > If any of you remember my first post, I did tell you I tried all the > ABC's and was on a handfull of prescription drugs per day. Nothing > helped me for 4 yrs. I'm happier and healthier, and now have my life > back...too bad hubby didn't stick around for it! Imagine..he couldn't > handle my MS! Oh well, his loss. Now I'm not sure he could handle me! > I'm able to do some dancing again, that's something I haven't been > able to do in over 5 years. So, I'm enjoying my Life!! Good for me! > Even my Neuro is impressed. He hasn't seen me in 8 months, walked in > the office and couldn't believe his eyes! I've lost all that > medication wieight, I'm not using my cane, I even did the Twist, > right there in his office~ he was hysterical!! After seeing the > progress I've made, and seeing my last MRI, and NO CHANGES, he is now > looking a bit more seriously into the LDN. Hopefully, more Dr.s will > get wise to the LDN and the good it is doing for us all. > Thanx for letting me share. Hope you all are doing well. God Bless > you all. > Carol > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 12, 2003 Report Share Posted September 12, 2003 ALL I CAN SAY IS *WOW* CONCRATS CAROL...THATS WHAT WE LIKE TO HEAR. IT GIVES US ALL HOPE. LOVE, SALLY > Hi all... I just wanted to share with you my One Year Anniversary of > being on LDN. I started taking it on Sept. 6th 2002 and have had > nothing but positive days since. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 4, 2004 Report Share Posted June 4, 2004 Dear , It's nice to hear that LDN sometimes works slowly. I've been on it for four months. I noticed some benefits of it immediately but it hasn't helped me as much as I hoped it would. I see no reason to stop taking it because it is so inexpensive and it's such a small dosage of naltrexone. I haven't posted much lately because I'm fighting a bout of fatigue. I shouldn't say I'm fighting it because all I'm doing is sleeping. I found that I don't have MS in my dreams so sleeping is a lot more pleasant than being awake. It's getting harder and harder to make it through the day. Not only am I fighting the MonSter but I'm fighting the state too. They're making me pay $700 a month to the nursing home that my wife is in. She was diagnosed with MS 8 years before I was and has been in a nursing home for over 6 years. I'm fighting like hell to stay out of a nursing home myself. Mama never sqid that there'd be days like this. Best, Chris Hello fellow MSers! Just wanted to let you all know that I've been on LDN for exactly one year this Memorial Day weekend. This time last year I could barely walk without pain and stiffness. At one point I couldn't even wear shoes or socks Now there are days when I forget I even have MS. (I also take collodial silver, calcium aep and digestive enzymes). So for those of you just starting LDN please hang in there. It may take a while but I honestly believe in it. I am not 100% healed but am doing so much better. The only problem I have are stilll some numbness in my legs and feet that are still s-l-o-w-l-y subsiding. . I plan on getting new MRIs done this summer and will update you all. Please stay positive, LDN works very slowly but it does work. I am praying and thinking of all of you as I read all your messages. Your friend, Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 4, 2004 Report Share Posted June 4, 2004 Hi Congradulation on your victory. I just realized that yesterday(June 3rd) was my one year anniversary with LDN too. I am also doing good. My spasms are much better and have been able to cut my spasms medication in half. But I had an MRI and they saw no progression in my disease. That was the first time that they saw no progression. I am so happy about that. Please let us know how your MRI turns out. Good Luck Marie ----- Original Message ----- From: Doherty LDN chat ; MS watch chat ; Spotlight LDN Sent: Thursday, June 03, 2004 9:16 PM Subject: [low dose naltrexone] One year on LDN Hello fellow MSers!Just wanted to let you all know that I've been on LDN for exactly one year this Memorial Day weekend. This time last year I could barely walk without pain and stiffness. At one point I couldn't even wear shoes or socks Now there are days when I forget I even have MS. (I also take collodial silver, calcium aep and digestive enzymes). So for those of you just starting LDN please hang in there. It may take a while but I honestly believe in it. I am not 100% healed but am doing so much better. The only problem I have are stilll some numbness in my legs and feet that are still s-l-o-w-l-y subsiding. . I plan on getting new MRIs done this summer and will update you all. Please stay positive, LDN works very slowly but it does work. I am praying and thinking of all of you as I read all your messages. Your friend, Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 4, 2004 Report Share Posted June 4, 2004 You know 700.00 isn't bad at all Our system here in Alberta has my brothers CPP cheque (945.00)going straight into the home he is in.and its only an extended care version of the hospital. I think you are lucky at that price! Of course this does depend on the care that she is receiving, food etc. Reg. -------Original Message------- From: low dose naltrexone Date: 06/03/04 23:24:03 low dose naltrexone Subject: Re: [low dose naltrexone] One year on LDN Dear , It's nice to hear that LDN sometimes works slowly. I've been on it for four months. I noticed some benefits of it immediately but it hasn't helped me as much as I hoped it would. I see no reason to stop taking it because it is so inexpensive and it's such a small dosage of naltrexone. I haven't posted much lately because I'm fighting a bout of fatigue. I shouldn't say I'm fighting it because all I'm doing is sleeping. I found that I don't have MS in my dreams so sleeping is a lot more pleasant than being awake. It's getting harder and harder to make it through the day. Not only am I fighting the MonSter but I'm fighting the state too. They're making me pay $700 a month to the nursing home that my wife is in. She was diagnosed with MS 8 years before I was and has been in a nursing home for over 6 years. I'm fighting like hell to stay out of a nursing home myself. Mama never sqid that there'd be days like this. Best, Chris ____________________________________________________ IncrediMail - Email has finally evolved - Click Here Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 4, 2004 Report Share Posted June 4, 2004 CONGRATULATIONS for your improvements. And THANKS SO MUCH for posting. It is always so wonderful to hear from those of you with extended experience with LDN. Wonderful rays of sunshine for the rest of us! Thanks Again - Cinders P.S. - I will be praying that your MRI supports what you already know, and that yet another Neuro gets impressed with the LDN improvement. Quote Link to comment Share on other sites More sharing options...
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