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Any long term LDN users?

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Hi Alice

I almost have a full year of L.D.N use under my belt, well twenty days short of a year!

What a ride it has been like many others I have at the outset been surprised at how well my annoying symptoms behaved,or went away never to come back again. At least in my case,while on this real inexpensive drug the symptoms, some, not all by no means,left and have never returned.

Like Optic Neuritis GONE....

Neuralgic pain GONE

Bladder Incontinence GONE

In the last eleven months I have purposely not taken my nightly pill only three times but after a small return to pre LDN symptoms I promptly resumed my treatment and there was no permanent setback.

It has made me very mad. Because if I had been prescribed this a year earlier I probably would still be working, as it is I now am a burden on the SSDS(Social Security Disability System) and I can no longer work towards my retirement plans. I think a lot of us can relate to that.

I have now had small local anaesthetic type of procedures done with no detrimental effects ie sebaceous cist removal and a cap on my tooth, at no time did I stop taking my LDN before this, So I would infer that normal freezing Dentists use or that Dr.s inject are not affected by LDN use or we use to little to be of any concern.

I also believe we do not ever become accustomed to or accommodate this small dose so a break is unnecessary but it does reinforce the need to continue as we see the drawbacks to stopping this treatment almost immediately.

In my experience almost any pain killer that you can buy over the counter will not work against the effects of LDN. Booze is still gonna get you drunk and Marijuana will still get you high!

I still need a wheelchair to shop or do any activity that necessitates much walking or standing but then I also had a major car wreck years ago that destroyed the ligaments in both of them.

I am also still dizzy but then again I am a guy.Most people that know me say he's nuts anyway.

I have seen a few transient improvements that never amounted to a lot but then again I am SPMS and have had MS since before 1981. I have also seen people (friends actually) that are not taking this and I can say I am doing better than them by far!

Reg.

-------Original Message-------

From: low dose naltrexone

Date: 09/14/04 11:09:00

low dose naltrexone

Subject: [low dose naltrexone] Any long term LDN users?

Hi, I am considering taking LDN for ms but would like some feedback from any long term users - at least one year to see how its working. Can anyone help?Alice

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