Home Forums General Discussion Any advice please..supplements, food, a new test, symptoms

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  • #464938
    mouse
    Participant

    Supplements
    My doctor has suggested these supplements. Vitamin adk, activated charcoal 4 a day, fish oil, curcumin, resvesteral, b complex, magnesium, trace minerals, liposomal glutathione. Will there be any side effects with the liposomal glutathione or the activated charcoal? Is this too many vitamins to take at once? Should I be rotating these? I am taking boron.

    Aperiomics Test
    I have recently discovered a test called Aperiomics. It’s a test for thousands of bacteria, fungus, parasites and virus. Rheumatoid diseases seem to be a mystery. Does it apply here? Would this test be something to pursue?

    Food
    My doctor tells me what you eat to makes a difference. Would I want to see an allergist or is this something that changes constantly? I did eat pork chops last night, something I never eat and I am having some extra pain today, some neuropathy and stiffness.

    Hot flashes, fatigue, jittery feeling
    I have been having hot flashes but my blood tests come back normal. Does anyone have any suggestions. Fatigue and jittery feeling? What can I do about this?

    Female, 59 years old. My issues began with a drug reaction.
    ANA 1:32 Homogeneous, Nuclear Speckled
    Rheumatologist/Osteopenia, osteoarthritis, UCTD,
    Gastroenterologist/little gastritis,11/20,
    Cardiologist/heart/bradycardia,7-20 had a little tachycardia
    Benign limp node removed 4 years ago
    My last panel of antibody blood tests taken in 8/20 were all negative accept ana.
    Taking Vitamin D and magnesium. My doctor has given me B12 to take and wants me to take hormones. Getting physical therapy soon.

    #464941
    Spiffy1
    Moderator

    I am a firm believer in iGG and perhaps IGE food testing. My boat did not begin to turn around until I added the food changes. Other people will say that it did not make a difference for them. But it can take up to five years to totally detox from inflammatory foods. So if people are still not symptom free, I think diet does have something to do with it pretty much every time whether we like to admit it or not. There is a percentage of people though that does so well on AP alone that no diet change was necessary, but most of us, I believe, are multifaceted when it comes to our healing. Many of your symptoms above could be food related. You can have bloodwork done through the standard labs or if you want to pay bigger bucks there are those companies like Cyrex that offer food testing. I had the Cyrex Array 10 but the most helpful thing to me early in was the simple IGG testing through Quest. It sounds to me like you have an excellent doctor willing to look at the body as a whole. If he or she is prescribing these things you may feel more comfortable working with your doctor sort of building one at a time. If you start all and have side effects it will be hard to know which one is causing it. Ask your doctor’s thoughts in stair stepping your supplements and maybe have him or her order them by greatest importance. As far as the test you found, ask your doctor if he or she feels like it could be useful information. We are all filled with viruses and bacteria. Some are beneficial and some are not. I have a tendency to be curious about things and might would like to see what it finds. But yet so often nothing is done with the information that is presented. But, hey, sometimes it is…so I would definitely ask about this. Let us know what you find out!

    Flare fall of 2014...muscle aches, joint pains, fatigue, hair loss, rashes, etc.
    RA Factor 71 in Jan 2015 down to 25 as of September 2017
    DR4/DQ8 HLA...biotoxin illness
    IGG food allergy to wheat, egg, and dairy...probably all grains
    Vit. C&D, probiotics, milk thistle, turmeric, fish oil, methyl b 12, methyl folate, digestive enzymes, Candisol, Ubiquinol, berberine, chlorella, Moducare, LDN, monolaurin, Triphala, Patriot Greens, Paractin
    MTHFR compound heterozygous
    Igenex IGM positive Lyme, minoMWF

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