Re: Re: LDN and MS exacerbation IT'S LOW DOSE!!!

[Guest guest]

Kathy, The key to LDN is LOW DOSE!! Taking 25 mg defeats the whole purpose of LDN. You are just suppose to tease the endorpins out to the blood stream. 25mg defeats the whole purpose of LDN. If I am wrong, someone please tell me. I am RRMS, 4.5MG nightly. I disolve 50mg tabs in 50ml of distilled water and use a baby dropper to take 4.5ml which is 4.5mg nightly. Who told you to take 25mg???? EdKathy Penrose <kathypnrs@...> wrote: Hi Hillerie, I took 25mg of the LDN. I get mine in 50mg pills and make liquid LDN. I take half a pill when I know I am having an exaserbation. When I first started LDN, I hadn't found this group yet. I just knew it sounded like the right way to go. I was prescribed the 50mg of Naltrexone. I didn't

know where to find a compounding pharmacy, which Windsor only has 1. I tried cutting the pill up but it just made a mess. So I took the half that I had made a mess with. The next morning my three month exaserbation was stopped. My pain was gone and I got up and went to the washroom without my cane! That night I took half a pill again and the next morning I felt great! I took it that way for 2 weeks by then I found a compounding pharmacy. It was a good thing because my head was buzzing day and night. My doctor when he heard this said maybe it was the neurons refiring. That was in Dec.,2003 and I still walk around the house without my cane. I only use my cane outside to help my balance on uneven ground. LDN is still correcting things that were wrong that I didn't know had anything to do with MS. I am SPMS stopped! Back in 2003 I was going out to buy a wheelchair and I never had to buy one thanks to LDN.Hillerie <hillieb2000@...> wrote: I was just wondering, what were you taking at 25 mg? Was it LDN?I was diagnosed with MS in 1991 and began taking LDN after tryingalmosst all of the ABC drugs with no halt in progression and Idiscovered LDN. I began taking LDN in June and was making steadyprogress when (around the holidays)I developed a urinary tractinfection which landed me in the hospital the middle of January withan exacerbation that I am still experiencing. I received three daysof solumedrol and stopped taking the LDN.After a week and a half in the hospital, I came home and started theLDN after the second day home.I don't feel a whole lot better and am scared to death and am tryingto remain faith ful that I will remitt from this exacerbation.Any advice?Thanks,Hillerie B. Maddox Hope all is well, Kathy Find your next car at Canada Autos

[Guest guest]

Yes Ed you are right, but for some reason for some people that are going through a terrable exasperation it can make it go away. I would not do it unless it was unbarable and not for long.

Aletha

Re: [low dose naltrexone] Re: LDN and MS exacerbation IT'S LOW DOSE!!!

Kathy,

The key to LDN is LOW DOSE!! Taking 25 mg defeats the whole purpose of LDN. You are just suppose to tease the endorpins out to the blood stream. 25mg defeats the whole purpose of LDN. If I am wrong, someone please tell me. I am RRMS, 4.5MG nightly. I disolve 50mg tabs in 50ml of distilled water and use a baby dropper to take 4.5ml which is 4.5mg nightly. Who told you to take 25mg????

EdKathy Penrose <kathypnrs@...> wrote:

Hi Hillerie,

I took 25mg of the LDN. I get mine in 50mg pills and make liquid LDN. I take half a pill when I know I am having an exaserbation.

When I first started LDN, I hadn't found this group yet. I just knew it sounded like the right way to go. I was prescribed the 50mg of Naltrexone. I didn't know where to find a compounding pharmacy, which Windsor only has 1. I tried cutting the pill up but it just made a mess. So I took the half that I had made a mess with. The next morning my three month exaserbation was stopped. My pain was gone and I got up and went to the washroom without my cane! That night I took half a pill again and the next morning I felt great! I took it that way for 2 weeks by then I found a compounding pharmacy. It was a good thing because my head was buzzing day and night. My doctor when he heard this said maybe it was the neurons refiring. That was in Dec.,2003 and I still walk around the house without my cane. I only use my cane outside to help my balance on uneven ground. LDN is still correcting things that were wrong that I didn't know had anything to do with MS. I am SPMS stopped! Back in 2003 I was going out to buy a wheelchair and I never had to buy one thanks to LDN.Hillerie <hillieb2000@...> wrote:

I was just wondering, what were you taking at 25 mg? Was it LDN?I was diagnosed with MS in 1991 and began taking LDN after tryingalmosst all of the ABC drugs with no halt in progression and Idiscovered LDN. I began taking LDN in June and was making steadyprogress when (around the holidays)I developed a urinary tractinfection which landed me in the hospital the middle of January withan exacerbation that I am still experiencing. I received three daysof solumedrol and stopped taking the LDN.After a week and a half in the hospital, I came home and started theLDN after the second day home.I don't feel a whole lot better and am scared to death and am tryingto remain faith ful that I will remitt from this exacerbation.Any advice?Thanks,Hillerie B. Maddox

Hope all is well,

Kathy

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