Guest guest Posted November 17, 2004 Report Share Posted November 17, 2004 That's a wonderful story I wish more people would see it. Reg -------Original Message------- From: low dose naltrexone Date: 11/17/04 16:19:28 low dose naltrexone Subject: [low dose naltrexone] Have to share I don't post very often but tonight is night 170 for me on LDN and I have nothing but great things to say about LDN! I had my first MS incident was in 2001. I had a bunch of tests that were inconclusive. The symptoms went away and I never thought of it again until April '03 when my hubby was in Iraq. My feet went numb/tingling as did other unmentionable parts of my body. It was enough for my neuro to get my beloved home. With steriods, I went back to normal except for my feet and fatigue. I did have another flare-up in May of this year just before I started LDN but again that was pretty mild with just my left hand and left side of my torso going numb. I overreacted and I got steriods cause we were going on vacation. Never again... I became pyscho mommy/wife.Up until two weeks I was on Copaxone. I had been on Avonex for a year before I started LDN but my neuro wouldn't give me LDN without me on something else so that's why I went to Copaxone. I just up and decided that I didn't need the Copa anymore and now I can say I'm CRAB free and happy about it. I am sleeping better, my fatigue is gone as much as it can be with three activity-involved children. Also, just today while driving I realized my feet are almost completely back to normal. My life is good!Thanks for letting me share and for all the great info and support this group gives. ____________________________________________________ IncrediMail - Email has finally evolved - Click Here Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 18, 2004 Report Share Posted November 18, 2004 That is great, . My 16 year old son has been using LDN for MS for almost 6 months, and he is doing equally well on it. He used Avonex and Rebif for a total of 21 months prior to LDN, so I know what you are saying. Just wanted to wish you well and say hello! Take care, and keep in touch! Kim --- In low dose naltrexone , " noemkat " <noemkat@y...> wrote: > > I don't post very often but tonight is night 170 for me on LDN and I > have nothing but great things to say about LDN! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 18, 2004 Report Share Posted November 18, 2004 WONDERFUL NEWS.....ALL OF YOU INSPRIE ME DeLores decrosby@... -----Original Message-----From: Reg Kreil [mailto:regkreil@...] Sent: Wednesday, November 17, 2004 6:33 PMlow dose naltrexone Subject: Re: [low dose naltrexone] Have to share That's a wonderful story I wish more people would see it. Reg -------Original Message------- From: low dose naltrexone Date: 11/17/04 16:19:28 low dose naltrexone Subject: [low dose naltrexone] Have to share I don't post very often but tonight is night 170 for me on LDN and I have nothing but great things to say about LDN! I had my first MS incident was in 2001. I had a bunch of tests that were inconclusive. The symptoms went away and I never thought of it again until April '03 when my hubby was in Iraq. My feet went numb/tingling as did other unmentionable parts of my body. It was enough for my neuro to get my beloved home. With steriods, I went back to normal except for my feet and fatigue. I did have another flare-up in May of this year just before I started LDN but again that was pretty mild with just my left hand and left side of my torso going numb. I overreacted and I got steriods cause we were going on vacation. Never again... I became pyscho mommy/wife.Up until two weeks I was on Copaxone. I had been on Avonex for a year before I started LDN but my neuro wouldn't give me LDN without me on something else so that's why I went to Copaxone. I just up and decided that I didn't need the Copa anymore and now I can say I'm CRAB free and happy about it. I am sleeping better, my fatigue is gone as much as it can be with three activity-involved children. Also, just today while driving I realized my feet are almost completely back to normal. My life is good!Thanks for letting me share and for all the great info and support this group gives. ____________________________________________________ IncrediMail - Email has finally evolved - Click Here Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 18, 2004 Report Share Posted November 18, 2004 Thanks for the information. I am thinking good thoughts for you and your family I pray only good things come your way sounds like you deserve them. God Bless you and yours Joanne -----Original Message-----From: noemkat [mailto:noemkat@...]Sent: Wednesday, November 17, 2004 6:18 PMlow dose naltrexone Subject: [low dose naltrexone] Have to shareI don't post very often but tonight is night 170 for me on LDN and I have nothing but great things to say about LDN! I had my first MS incident was in 2001. I had a bunch of tests that were inconclusive. The symptoms went away and I never thought of it again until April '03 when my hubby was in Iraq. My feet went numb/tingling as did other unmentionable parts of my body. It was enough for my neuro to get my beloved home. With steriods, I went back to normal except for my feet and fatigue. I did have another flare-up in May of this year just before I started LDN but again that was pretty mild with just my left hand and left side of my torso going numb. I overreacted and I got steriods cause we were going on vacation. Never again... I became pyscho mommy/wife.Up until two weeks I was on Copaxone. I had been on Avonex for a year before I started LDN but my neuro wouldn't give me LDN without me on something else so that's why I went to Copaxone. I just up and decided that I didn't need the Copa anymore and now I can say I'm CRAB free and happy about it. I am sleeping better, my fatigue is gone as much as it can be with three activity-involved children. Also, just today while driving I realized my feet are almost completely back to normal. My life is good!Thanks for letting me share and for all the great info and support this group gives. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 18, 2004 Report Share Posted November 18, 2004 > Thanks for the information. I am thinking good thoughts for you and > your family I pray only good things come your way sounds like you deserve > them. God Bless you and yours Joanne Thanks Joanne and everyone else for the warm wishes. I pray the best for everyone here as well. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 18, 2004 Report Share Posted November 18, 2004 congratulations Kristiin! So glad LDN is doing some awesome things for you. Kathy On 17-Nov-04, at 4:18 PM, noemkat wrote: > > I don't post very often but tonight is night 170 for me on LDN and I > have nothing but great things to say about LDN! > > I had my first MS incident was in 2001. I had a bunch of tests that > were inconclusive. The symptoms went away and I never thought of it > again until April '03 when my hubby was in Iraq. My feet went > numb/tingling as did other unmentionable parts of my body. It was > enough for my neuro to get my beloved home. With steriods, I went > back to normal except for my feet and fatigue. I did have another > flare-up in May of this year just before I started LDN but again that > was pretty mild with just my left hand and left side of my torso > going numb. I overreacted and I got steriods cause we were going on > vacation. Never again... I became pyscho mommy/wife. > > Up until two weeks I was on Copaxone. I had been on Avonex for a > year before I started LDN but my neuro wouldn't give me LDN without > me on something else so that's why I went to Copaxone. I just up and > decided that I didn't need the Copa anymore and now I can say I'm > CRAB free and happy about it. I am sleeping better, my fatigue is > gone as much as it can be with three activity-involved children. > Also, just today while driving I realized my feet are almost > completely back to normal. My life is good! > > Thanks for letting me share and for all the great info and support > this group gives. > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 18, 2004 Report Share Posted November 18, 2004 Hello , That's really good news! Such an incentive for all of us here. Thank you for sharing this. Wishing you and your family the best. Regards Joanne --- In low dose naltrexone , " noemkat " <noemkat@y...> wrote: > > I don't post very often but tonight is night 170 for me on LDN and I > have nothing but great things to say about LDN! > > I had my first MS incident was in 2001. I had a bunch of tests that > were inconclusive. The symptoms went away and I never thought of it > again until April '03 when my hubby was in Iraq. My feet went > numb/tingling as did other unmentionable parts of my body. It was > enough for my neuro to get my beloved home. With steriods, I went > back to normal except for my feet and fatigue. I did have another > flare-up in May of this year just before I started LDN but again that > was pretty mild with just my left hand and left side of my torso > going numb. I overreacted and I got steriods cause we were going on > vacation. Never again... I became pyscho mommy/wife. > > Up until two weeks I was on Copaxone. I had been on Avonex for a > year before I started LDN but my neuro wouldn't give me LDN without > me on something else so that's why I went to Copaxone. I just up and > decided that I didn't need the Copa anymore and now I can say I'm > CRAB free and happy about it. I am sleeping better, my fatigue is > gone as much as it can be with three activity-involved children. > Also, just today while driving I realized my feet are almost > completely back to normal. My life is good! > > Thanks for letting me share and for all the great info and support > this group gives. > > Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.