Guest guest Posted July 6, 2007 Report Share Posted July 6, 2007 hi,i'm emiliano from italy i'm affected by ms from 1985.mine ais a very rare and strange form that for 18 years has no givven big problems so that nobody considered it as ms. in 2000 i was in bayres(argentina)for my job and one day walking in the main central road of the town(florida is the name of this road)i had some problems to the left leg that become lazy and difficolt to move. when i was back in italy i went to several doctors,but none of them understod it was ms.after 4 mounths finally i found the right neurologic doctor that hearing my description of all the strange sinptoms (sensibility,diplopia,urologic difficolty etc etc)sent me to the hospital for the mg risonance test and the mielin damage went out. due to the fact that until today i can walk(even if with a visible disturb of movement)without helps my form was classified as benign ms. now day i can feel that a low progression of disability is running and i belive (in agrement with the doctor) my ms has become a sp form. i'm doing betaferon every two day but i have heard about ldn in ms therapy and about its good effect against ms simptoms and progression. i wish to know more about thi drug,becouse here in italy it is not more considered and the trial is not performed well. if someone could give me informations i will be very grate to him. best regard emiliano(excuse me for my bad english) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 6, 2007 Report Share Posted July 6, 2007 > > hi,i'm emiliano from italy > i'm affected by ms from 1985.mine ais a very rare and strange form that > for 18 years has no givven big problems so that nobody considered it as > ms. > in 2000 i was in bayres(argentina)for my job and one day walking in the > main central road of the town(florida is the name of this road)i had > some problems to the left leg that become lazy and difficolt to move. > when i was back in italy i went to several doctors,but none of them > understod it was ms.after 4 mounths finally i found the right > neurologic doctor that hearing my description of all the strange > sinptoms (sensibility,diplopia,urologic difficolty etc etc)sent me to > the hospital for the mg risonance test and the mielin damage went out. > due to the fact that until today i can walk(even if with a visible > disturb of movement)without helps my form was classified as benign ms. > now day i can feel that a low progression of disability is running and > i belive (in agrement with the doctor) my ms has become a sp form. > i'm doing betaferon every two day but i have heard about ldn in ms > therapy and about its good effect against ms simptoms and progression. > i wish to know more about thi drug,becouse here in italy it is not more > considered and the trial is not performed well. > if someone could give me informations i will be very grate to him. > best regard > emiliano(excuse me for my bad english) > Emiliano, Your english is fine. If you want to know more about Low Dose Naltrexone (LDN) a good place to start is by reading this website: http://www.low dose naltrexone.org/ If you have questions, post them here and there are many people who will try and help you. That's what we're all about. Art -- Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 7, 2007 Report Share Posted July 7, 2007 HI EMILIANO, I'M from the U.S.A. I was dx with MS IN OCT.2006 was taking BETASERONE from oct-april ,when I started the LDN 4.5 MG WHAT I HAVE FELT AND SEEN WAS IMPROVEMENT. I am very happy that I stopped taking the betaserone and started the LDN.You can get detailed information about the LDN by going on the ldn website I just put ldn on my searchengine and it comes up.Or you can contact CRYSTAL in this group and she will give you the web sites for LDN to look into.I hope your symptons improve as mine did.I know taking the BETASERONE made me feel and look worse.REGARDS ,BEST OF LUCK,DJ [low dose naltrexone] ldn and betaferon in ms hi,i'm emiliano from italyi'm affected by ms from 1985.mine ais a very rare and strange form that for 18 years has no givven big problems so that nobody considered it as ms.in 2000 i was in bayres(argentina) for my job and one day walking in the main central road of the town(florida is the name of this road)i had some problems to the left leg that become lazy and difficolt to move.when i was back in italy i went to several doctors,but none of them understod it was ms.after 4 mounths finally i found the right neurologic doctor that hearing my description of all the strange sinptoms (sensibility, diplopia, urologic difficolty etc etc)sent me to the hospital for the mg risonance test and the mielin damage went out.due to the fact that until today i can walk(even if with a visible disturb of movement)without helps my form was classified as benign ms.now day i can feel that a low progression of disability is running and i belive (in agrement with the doctor) my ms has become a sp form.i'm doing betaferon every two day but i have heard about ldn in ms therapy and about its good effect against ms simptoms and progression.i wish to know more about thi drug,becouse here in italy it is not more considered and the trial is not performed well.if someone could give me informations i will be very grate to him.best regardemiliano(excuse me for my bad english) Got a little couch potato? Check out fun summer activities for kids. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 7, 2007 Report Share Posted July 7, 2007 tanks a lot for your answ. regards ---------- Initial Header ----------- From : low dose naltrexone To : low dose naltrexone Cc : Date : Sat, 7 Jul 2007 05:32:13 -0700 (PDT) Subject : Re: [low dose naltrexone] ldn and betaferon in ms > HI EMILIANO, I'M from the U.S.A. I was dx with MS IN OCT.2006 was taking BETASERONE from oct-april ,when I started the LDN 4.5 MG WHAT I HAVE FELT AND SEEN WAS IMPROVEMENT. I am very happy that I stopped taking the betaserone and started the LDN.You can get detailed information about the LDN by going on the ldn website I just put ldn on my searchengine and it comes up.Or you can contact CRYSTAL in this group and she will give you the web sites for LDN to look into.I hope your symptons improve as mine did.I know taking the BETASERONE made me feel and look worse.REGARDS ,BEST OF LUCK,DJ > > > > [low dose naltrexone] ldn and betaferon in ms > > hi,i'm emiliano from italy > i'm affected by ms from 1985.mine ais a very rare and strange form that > for 18 years has no givven big problems so that nobody considered it as > ms. > in 2000 i was in bayres(argentina) for my job and one day walking in the > main central road of the town(florida is the name of this road)i had > some problems to the left leg that become lazy and difficolt to move. > when i was back in italy i went to several doctors,but none of them > understod it was ms.after 4 mounths finally i found the right > neurologic doctor that hearing my description of all the strange > sinptoms (sensibility, diplopia, urologic difficolty etc etc)sent me to > the hospital for the mg risonance test and the mielin damage went out. > due to the fact that until today i can walk(even if with a visible > disturb of movement)without helps my form was classified as benign ms. > now day i can feel that a low progression of disability is running and > i belive (in agrement with the doctor) my ms has become a sp form. > i'm doing betaferon every two day but i have heard about ldn in ms > therapy and about its good effect against ms simptoms and progression. > i wish to know more about thi drug,becouse here in italy it is not more > considered and the trial is not performed well. > if someone could give me informations i will be very grate to him. > best regard > emiliano(excuse me for my bad english) > > > > > > > ________________________________________________________________________________\ ____ > Need a vacation? Get great deals > to amazing places on Travel. > http://travel./ ------------------------------------------------------ Leggi GRATIS le tue mail con il telefonino i-mode™ di Wind http://i-mode.wind.it/ Quote Link to comment Share on other sites More sharing options...
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