Guest guest Posted February 1, 2006 Report Share Posted February 1, 2006 Many people go through feeling old symptoms come up. It is as if your body is working through it while it heals. Some people even feel the symptoms quickly going backwards, as if you go in reverse from what order your symptoms had come in the first place. I hope that is all that you are going through. Keep us posted on how you are feeling. Hopefully it will work its way through quickly. If not, look into reducing the dosage or changing the filler. My husband had new areas of numbness and tingling until he went down to 3.0 from 4.5mg Kindest of regards Aletha [low dose naltrexone] Relapse after starting > Hi Guys, > > I have MS and just started taking 3.0 LDN 11 days ago. After the > fifth day, I went into a full blown exasurbation, and I am still there > 6 days later. I was just wondering if anyone else has experienced > this, and how long did it last for you? I am hopeful, and hanging in > there until this one passes! Prayers for everyone out there going > through the same thing!!! > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 1, 2006 Report Share Posted February 1, 2006 > > Hi Guys, > > I have MS and just started taking 3.0 LDN 11 days ago. After the > fifth day, I went into a full blown exasurbation, and I am still there > 6 days later. I was just wondering if anyone else has experienced > this, and how long did it last for you? I am hopeful, and hanging in > there until this one passes! Prayers for everyone out there going > through the same thing!!! > ============= For those of you in the first 3 months of LDN therapy Dr. Bob Lawrence from the UK who has MS & uses LDN himself explains why the temporary increase in MS symptoms upon starting LDN. The increased symptoms are not lasting for 3 months generally but usually take place during the 1st 3 months. When starting this LDN(Low Dose Naltrexone) therapy in the treatment of MS, there may also be some initial transient, though temporary, increase in MS symptoms. Experience in using this method has demonstrated most commonly, such as disturbed sleep, occasionally with vivid, bizarre and disturbing dreams, tiredness, fatigue, spasm and pain. These increased symptoms would not normally be expected to last more than seven to ten days. Rarely, other transient symptoms have included more severe pain and spasm, headache, diarrhea or vomiting. These additional symptoms would appear to be associated with the previous frequent use of strong analgesics, which effectively create an addiction and dependency, thus increasing the body's sensitivity to pain. This temporary increase in symptoms may also perhaps be explained when we consider the manner in which this drug is expected to work. Initially, MS occurs due to a reduction in the activity of the controlling influence of the suppressor T-cells within the immune system. During an acute relapse, the overall number of T-cells is reduced, the normal balance of helper T-cells and suppressor T-cells is disrupted and the damaging helper (CD-4) T-cells tend to predominate. This is the situation most pronounced during an acute relapse but occurs similarly, but to a lesser extent, in chronic progressive MS. Under the influence of LDN there will be an expected increase in the overall numbers of T-cells but, because the CD-4, helper T-cells tend to predominate at this time, an increase in their numbers will expectedly tend to increase MS symptoms. It is only when the numbers of suppressor T-cells effectively " catch up " that the normal balance is restored and symptoms once again diminish and improve. In addition, because LDN stimulates the immune system and many of the drugs routinely used by the NHS in the treatment of MS further suppress the immune system, LDN cannot be used in company with steroids, beta interferon, methotrexate, azathioprine or mitozantrone or any other immune suppressant drug. If there is any doubt, please submit a full list of the drugs you are presently taking so that their compatibility may be assessed. In addition, because LDN will also block the analgesic effects of any opiate drugs (includes codeine, dihydrocodeine, morphine, pethidine or diamorphine) presently being taken, the use of LDN will initially greatly increase the level of pain experienced. It is therefore advisable that any opiate-like drugs be discontinued at least two weeks before this treatment is initiated. When starting the treatment it is essential that any untoward or adverse side-effects are reported immediately so that the treatment process can be further assessed and, if necessary, modified. Dr. M R Lawrence posted by Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 1, 2006 Report Share Posted February 1, 2006 --- In low dose naltrexone , " lmauro143 " <lmauro143@y...> wrote: > > Hi Guys, > > I have MS and just started taking 3.0 LDN 11 days ago. After the > fifth day, I went into a full blown exasurbation, and I am still there > 6 days later. I was just wondering if anyone else has experienced > this, and how long did it last for you? I am hopeful, and hanging in > there until this one passes! Prayers for everyone out there going > through the same thing!!! > Hi, I am only on 1.75 and am having my old symptoms return off and on. I think I am around day 7. After taking it at night my eyes shift back and forth can't sleep well and felt like I ws going to throw up last night. Mabey lower your dose so your body isn't " shell shocked " and work your way up to 3 after a few weeks. I'm not sure as i am having trouble too. good luck. I hate those relapses!!! Quote Link to comment Share on other sites More sharing options...
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