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Low Dose Naltrexone


kimis

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kimis Collaborator

I remember reading on this forum that someone was taking this. I looked it up and I want to try this drug. I can't remember who was talking about it though. Anyone have any experience with it? It sounds wonderful!


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heathen Apprentice

This drug is used to treat narcotics overdose. I'm not sure why it would be used for Celiac symptoms.

kimis Collaborator

yeah Full Dose Naltrexone (50mg) is used as an opioid blocker, but Low Dose Naltrexone (1.5 - 4.5 mg)is used for people with autoimmune diseases.

Looking for answers Contributor

The Whitaker Wellness Center in Newport Beach uses it to reverse or halt damage from autoimmune diseases. I know of several people who greatly benefited from it. I got a prescription but then never took it because my husband and I want to get pregnant and i don't want to be on any medication as a precaution. Also, Dr. Mercola has a lot of information about it on his site and recommends it. It's very interesting stuff and seems very worth looking into.

Lori2 Contributor

My brother-in-law used it for his Rheumatoid Arthritis. It worked for him.

txplowgirl Enthusiast

It is prescribed for Fibromyalgia patients also. I have been trying to stay off the precriptions trying to keep my fibro and Rhumatoid arthritis under control with my gluten free diet. But I think next time I go in i'm gonna ask for it for my Chronic fatigue, I understand that it helps with that too.

I finally had to break down and get a prescription for sleeping pills, my Melatonin and 5-HTP stopped working.

kimis Collaborator

I asked my gastroenterologist about it and he didn't know what I was talking about. I see my rheumatologist on Tuesday and I'm gonna ask him to put me on it. I tried a few of his drugs and they didn't help so I think it's my turn to call the shots.


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Looking for answers Contributor

You may only find that doctors who specialize in intgrative medicine are the only ones who will even know about this. The reason why is that it is not branded by any pharmaceutical companies per se. I had to get my from a compounding pharmacy.

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    • AlwaysLearning
      Get tested for vitamin deficiencies.  Though neuropathy can be a symptom of celiac, it can also be caused by deficiencies due to poor digestion caused by celiac and could be easier to treat.
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      EXACTLY! I was asked yesterday on my LAST video call with Standford and I stated exactly yes absolutely this is why I need the name! One, get proper care, two, not get worse.Im falling apart, stressed out, in pain and just opened email from Stanford stating I was rude ect.I want that video reviewed by higher ups and see if that women still has a job or not.Im saying this because I've been medically screwed and asking for help because bills don't pay itself. This could be malpratice siit but im not good at finding lawyers
    • AlwaysLearning
      We feel your pain. It took me 20+ years of regularly going to doctors desperate for answers only to be told there was nothing wrong with me … when I was 20 pounds underweight, suffering from severe nutritional deficiencies, and in a great deal of pain. I had to figure it out for myself. If you're in the U.S., not having an official diagnosis does mean you can't claim a tax deduction for the extra expense of gluten-free foods. But it can also be a good thing. Pre-existing conditions might be a reason why a health insurance company might reject your application or charge you more money. No official diagnosis means you don't have a pre-existing condition. I really hope you don't live in the U.S. and don't have these challenges. Do you need an official diagnosis for a specific reason? Else, I wouldn't worry about it. As long as you're diligent in remaining gluten free, your body should be healing as much as possible so there isn't much else you could do anyway. And there are plenty of us out here who never got that official diagnosis because we couldn't eat enough gluten to get tested. Now that the IL-2 test is available, I suppose I could take it, but I don't feel the need. Someone else not believing me really isn't my problem as long as I can stay in control of my own food.
    • AlwaysLearning
      If you're just starting out in being gluten free, I would expect it to take months before you learned enough about hidden sources of gluten before you stopped making major mistakes. Ice cream? Not safe unless they say it is gluten free. Spaghetti sauce? Not safe unless is says gluten-free. Natural ingredients? Who knows what's in there. You pretty much need to cook with whole ingredients yourself to avoid it completely. Most gluten-free products should be safe, but while you're in the hypersensitive phase right after going gluten free, you may notice that when something like a microwave meal seems to not be gluten-free … then you find out that it is produced in a shared facility where it can become contaminated. My reactions were much-more severe after going gluten free. The analogy that I use is that you had a whole army of soldiers waiting for some gluten to attack, and now that you took away their target, when the stragglers from the gluten army accidentally wander onto the battlefield, you still have your entire army going out and attacking them. Expect it to take two years before all of the training facilities that were producing your soldiers have fallen into disrepair and are no longer producing soldiers. But that is two years after you stop accidentally glutening yourself. Every time you do eat gluten, another training facility can be built and more soldiers will be waiting to attack. Good luck figuring things out.   
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