Forum Replies Created

  • IngridG

    Member
    October 28, 2020 at 11:22 am in reply to: Do you have theories about why you have Parkinsons?

    Amelie, it could be a combination of the toners, but mostly about the very strong EMFs (electro-magnetic fields) of the copy machines. Try to go close to a copy machine with a tri-meter to see how potent they are. Also cell phones, computers, WiFis, etc. keep away from all of them.

  • IngridG

    Member
    September 15, 2020 at 4:32 pm in reply to: When did you first suspect that you had Parkinsons?

    I have probably had it for years without knowing it. I only became concerned about a year ago, after I fell 3 times in 3 months, without tripping over anything, but falling backwards and injuring my spine. This spring I fell again and the problem is that I cannot get up easily. I always blamed my stiffness, fatigue, insomnia, internal tremors, etc. on Epstein-Barr , mercury and other culprits. Knowing what mercury poisoning does to the brain and the way that viruses invade one’s nervous system, I suspected PD.

  • IngridG

    Member
    September 10, 2020 at 6:00 pm in reply to: Do you have theories about why you have Parkinsons?

    My theory is that is was caused by an overload of mercury, viruses and life-long Hypoglycemia. In my 20s I was injected several times with mercurial diuretics to loose weight, which I did not loose. The side effect of these injections were 30 cavities that were filled with amalgams, 50/50 mercury.

    Then, I was exposed to the Epstein-Barr virus, Shingles, Rickettsia (Human Ehrlichiosis),resulting in CFIDS/ME, MCS, etc.

    Glucose matabolism is very important for any brain and Neurotransmitters, so severe Hypoglycemia since age 9 has contributed also, I believe.

    I have just been diagnosed with Oxalate Cristal disease, which can have profound problems in the body, though I, and many others, don’t have kidney stones, but the Oxalate accumulates in the joints, muscles, organs and probably in the brain also. The best information is on Sally K. Norton’s website, though she does not write about Parkinson’s, she has devoted her life to make this known. Many people, like myself, have increased their vitamin C consumption because of Covid19 and noticed increased pain in their feet, joints etc. that is how I found out. I ate a “very healthy” diet for many years with lots of greens, nuts, chocolate, Kiwis, celery juice, etc, all of these foods are very high in Oxalates. I wonder has anyone done research on oxalate effect on Parkinson’s ??? It certainly affects the stiffness in my muscles, pain and balance. I do not take any medications, as they never agreed with me, but plenty of alternatives.

    I believe that is most important to eat a diet free of chemicals, GMO, gluten and sugar. Please let me know what you think about my theory, blessings, Ingrid