Guest guest Posted April 19, 2003 Report Share Posted April 19, 2003 get on it right away and stop suppressing your immune system with drugs... they may stop the symptom (attacks by the IS) but in the long run wreak havoc with your body's natural balance. When you cut yourself your body knows how to heal that, LDN and the resulting endorphins/OGF suppresses the virus, rebalances the immune system, and gives your body a chance to heal. What have you got to lose trying this? $25/month? time? we've all wasted too much of all that already. Get on this drug immediately and see if it helps you as it has helped many others. You will know if it's working within 2 months, maybe sooner.... Good luck, I go on it next week -- my first experience with any drugs for MS. On Sat, 19 Apr 2003, Terry Humphrey Colquhoun wrote: > My girlfriend is 38 yrs old and is living in a nursing home. She is > being fed way to many drugs and what I consider a very poor diet. > Her symptoms are everything MS can throw at her, and the drugs are > just treating side affects of the other drugs. Some of these drugs > are actually counter-indicated for MS. Does anyone have any > suggestions or comments on the use of LDN and what kind of > expectations should we have? > > I also have Relapsing / Remitting MS for 25 years now and am preparing > to go on LDN myself. > > Any comments would be greatly appreciated. > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 19, 2003 Report Share Posted April 19, 2003 Hello, I agree completely;start the LDN right away!!!! I'd also advise the 4.5 doseage, as it will give you maximal endorphin production. Although I have a question. It was said "as it has helped so many others..... you'll know if it's working within 2 months.....". According to Dr. Bihari, of the 3000 plus people on it, is hasn't *not* helped anyone, or *not* worked* on anyone. Is there someone who gainsays this? I'd be truly interested to know. Thanks in advance, Rabbit ----- Original Message ----- From: G. Harding Terry Humphrey Colquhoun Cc: low dose naltrexone Sent: Saturday, April 19, 2003 10:22 AM Subject: Re: [low dose naltrexone] Severe MS get on it right away and stop suppressing your immune system with drugs...they may stop the symptom (attacks by the IS) but in the long run wreakhavoc with your body's natural balance. When you cut yourself your bodyknows how to heal that, LDN and the resulting endorphins/OGF suppressesthe virus, rebalances the immunesystem, and gives your body a chance to heal. What have you got to losetrying this? $25/month? time? we've all wasted too much of all thatalready. Get on this drug immediately and see if it helps you as it hashelped many others. You will know if it's working within 2 months, maybesooner.... Good luck, I go on it next week -- my first experience with anydrugs for MS.On Sat, 19 Apr 2003, Terry Humphrey Colquhoun wrote:> My girlfriend is 38 yrs old and is living in a nursing home. She is> being fed way to many drugs and what I consider a very poor diet.> Her symptoms are everything MS can throw at her, and the drugs are> just treating side affects of the other drugs. Some of these drugs> are actually counter-indicated for MS. Does anyone have any> suggestions or comments on the use of LDN and what kind of> expectations should we have?>> I also have Relapsing / Remitting MS for 25 years now and am preparing> to go on LDN myself.>> Any comments would be greatly appreciated.>>>> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 19, 2003 Report Share Posted April 19, 2003 yeah I agree, I guess the Missouri aspect of my personality is coming out: show me. I just remember hearing from a couple folks who said they had been on it for a while and weren't sure if it was working. I'll know immediately as my balance/walking is on a slide I can feel. I'll know immdiately if it halts that slide. I am very optimistic! It was the researcher at Penn State who I've been talking to who said the OGF that is part of the endorphin " bath " works even in vitro -- outside the body w/o help from the immune system. You might say he is totally confident in this treatment for autoimmune diseases like MS, HIV infections, and some cancers. Right now they are having success with pancreatic cancer patients, which you may know takes people very rapidly (i.e. they die). He and his team have had great success with LDN and these patients giving them hope where there was none before. I remain confident it will help me as well. On Sat, 19 Apr 2003, Rabbit wrote: > Hello, > I agree completely;start the LDN right away!!!! I'd also advise the 4.5 doseage, as it will give you maximal endorphin production. > Although I have a question. It was said " as it has helped so many others..... you'll know if it's working within 2 months..... " . According to Dr. Bihari, of the 3000 plus people on it, is hasn't *not* helped anyone, or *not* worked* on anyone. Is there someone who gainsays this? I'd be truly interested to know. > Thanks in advance, > Rabbit > ----- Original Message ----- > From: G. Harding > Terry Humphrey Colquhoun > Cc: low dose naltrexone > Sent: Saturday, April 19, 2003 10:22 AM > Subject: Re: [low dose naltrexone] Severe MS > > > get on it right away and stop suppressing your immune system with drugs... > they may stop the symptom (attacks by the IS) but in the long run wreak > havoc with your body's natural balance. When you cut yourself your body > knows how to heal that, LDN and the resulting endorphins/OGF suppresses > the virus, rebalances the immune > system, and gives your body a chance to heal. What have you got to lose > trying this? $25/month? time? we've all wasted too much of all that > already. Get on this drug immediately and see if it helps you as it has > helped many others. You will know if it's working within 2 months, maybe > sooner.... Good luck, I go on it next week -- my first experience with any > drugs for MS. > > On Sat, 19 Apr 2003, Terry Humphrey Colquhoun wrote: > > > My girlfriend is 38 yrs old and is living in a nursing home. She is > > being fed way to many drugs and what I consider a very poor diet. > > Her symptoms are everything MS can throw at her, and the drugs are > > just treating side affects of the other drugs. Some of these drugs > > are actually counter-indicated for MS. Does anyone have any > > suggestions or comments on the use of LDN and what kind of > > expectations should we have? > > > > I also have Relapsing / Remitting MS for 25 years now and am preparing > > to go on LDN myself. > > > > Any comments would be greatly appreciated. > > > > > > > > Quote Link to comment Share on other sites More sharing options...
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