Low Dose Naltrexone LDN

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wmonique2
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Post by wmonique2 »

Tex,

has anybody asked Polly what she thinks about this treatment?

Thanks,

Monique
Diagnosed 2011 with LC. Currently on Low Dose Naltrexone (LDN)
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tex
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Post by tex »

:shrug:

I don't recall that she has ever offered any opinion on it. She may not have an opinion on it.

Tex
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It is suspected that some of the hardest material known to science can be found in the skulls of GI specialists who insist that diet has nothing to do with the treatment of microscopic colitis.
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wmonique2
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Post by wmonique2 »

Tex,

Yeah, I checked all the links you provided and she didn't chime in on any of them...The reason I am asking is because today I had an interesting conversation about this with a friend who is a doc in psychology and a medical researcher. She cautioned that serotonin turns to melatonin at night and that can cause serious sleeplessness, which is what some complained about (I already take melatonin at night). And also she explained that it suppresses our overactive immune system, which is what we have then it boosts it again.

Just thought I'll share her POV. Anyway, I am having her read the plethora of info on it.


love,

Monique
Diagnosed 2011 with LC. Currently on Low Dose Naltrexone (LDN)
Eric
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Post by Eric »

I did lots of LDN research months ago when I first heard of the treatment. Sleep issues seem to mainly occur when starting the med but soon normalize. My understanding is that LDN is what you might call an immunomodulator. It will suppress an overactive immune system, but it will also boost an underactive one.
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wmonique2
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Post by wmonique2 »

Eric,

Thanks for chiming in...I am still on the fence about using it. A little scared, actually because of the insomnia thing. I am already an insomniac...

Monique
Diagnosed 2011 with LC. Currently on Low Dose Naltrexone (LDN)
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Post by Eric »

Understood; the effect seems to vary, but most of what I've read indicates the majority of people find it tolerable/worth it. However, I've seen two or three accounts of people stopping the med after a few days because it wasn't comfortable for them.
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Post by Zizzle »

I wonder how many MCers have ever tried Plaquenil/Hydroxychloroquine (probably for associated autoimmune diseases?)? It's also an "immunomodulator." In fact, docs don't really know how it works, but it helps to control many Lupus-like autoimmune diseases including mine. I'm tapering prednisone, now down to 10 mgs/day, and still no sign of MC. My skin rash is 98% under control too.

Plaquenil is an anti-malarial, and I'm reading it's often used for people with Lyme-induced autoimmune conditions too. One possible side effect is stomach discomfort or D, but I haven't experienced either.

Just wondering if others have found it helped the MC...
1987 Mononucleosis (EBV)
2004 Hypomyopathic Dermatomyositis
2009 Lymphocytic Colitis
2010 GF/DF/SF Diet
2014 Low Dose Naltrexone
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Post by Eric »

Thanks Zizzle, I don't think I've heard of that but I'm interested since lyme is part of the puzzle I'm piecing together.
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tex
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Post by tex »

Eric,

FYI, Polly and several other members attribute their MC to an extended regimen of antibiotic treatment for suspected Lyme disease (which was never actually diagnosed, in her case).

Tex
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It is suspected that some of the hardest material known to science can be found in the skulls of GI specialists who insist that diet has nothing to do with the treatment of microscopic colitis.
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Post by Eric »

Thanks Tex. Lyme diagnosis was after I knew about the MC - refused abx treatment for lyme since they have caused such trouble in the past.
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wmonique2
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Post by wmonique2 »

Tex,

The LDN website claims that it helps with IBS, ulcerative colitis and Crohn's. Does that mean that it can help us? I don't see much difference between them and Crohn's and us. (I take mesalamine which is usually given to Crohn's patients).


Thanks,

Love

Monique
Diagnosed 2011 with LC. Currently on Low Dose Naltrexone (LDN)
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Post by tex »

Hi Monique,

Yes, there are absolutely no medications labeled for treating MC, so every drug prescribed to treat it is an off-label use. Therefore, doctors simply prescribe the drugs that have been used for treating other IBDs.

LDN is not simply used to treat IBDs, of course — it's used to treat virtually any autoimmune disease, so the possibility certainly exists that it may be helpful for treating MC, at least in some cases.

You're more than welcome, and if you decide to try this, I hope that it's effective.

Love,
Tex
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It is suspected that some of the hardest material known to science can be found in the skulls of GI specialists who insist that diet has nothing to do with the treatment of microscopic colitis.
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wmonique2
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Post by wmonique2 »

Thanks Tex,

I am on the fence about it. The only reason I am not plunging is the insomnia part of it and also I am scared to death that it would aggravate my symptoms although I am not sure that is has a direct effect on that.

I am gonna wait until I am more stable. Or maybe not, since if I tried it now it would certainly tell me if it's gonna help or not.

I am confused. don't know what to do. :lol:

Love,

Monique
Diagnosed 2011 with LC. Currently on Low Dose Naltrexone (LDN)
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Post by tex »

Monique wrote:I am confused. don't know what to do. :lol:
Active MC makes clear thinking and decision-making about a hundred times more difficult. :sad:

Love,
Tex
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It is suspected that some of the hardest material known to science can be found in the skulls of GI specialists who insist that diet has nothing to do with the treatment of microscopic colitis.
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wmonique2
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Post by wmonique2 »

Tex,

Thank you for clarifying that. I am no thinking clear enough to figure that one out :lol:


love,

Monique
Diagnosed 2011 with LC. Currently on Low Dose Naltrexone (LDN)
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