Two weeks later, I began to experience flu like conditions, with a fluctuating fever as high as 104 farenheit, but the worst part was if I went into the direct sunlight, my heart beat rate doubled in frequency.
I have never been one to run to doctors for anything and tried various home remedies for about a week and finally went into an emergency room at the hospital. There I was diagnosed with a fever of 'unknown origin' and released with a prescription of antibiotics for 10 days. I took one pill that night and woke up feeling completely healed the next day.
From that point forward however, I suffered from short term memory loss, and loss of short term memory(2 different things). Also insomnia, severe chronic fatigue, depression, head aches, back aches, knee and elbow joint pain, and would wake up every morning about 3AM completely exhausted and couldn't go back sleep.
After about 7 years into this ordeal, and after several doctors prescribing sleep aids and anti-depressants, one of which was the foremost physician for the treatment of contagious diseases in Louisiana, and none would give me antibiotics, I decided to treat this obvious case of Lyme's disease myself.
I had been communicating with the Lyme's Disease Foundation at the University of New York in Stoney Brook, and they had sent me a clinical update for physicians regarding the diagnosis and treatment of 'late' Lyme's disease. To make a long story short, after studying the information I got from the Lyme's Disease Foundation, and suffering for 8 years without any kind of effective diagnosis or treatment, I administered 500 mgs of tetracycline hydrocloride for 4 months and I was cured, with no relapses, and it never came back.
I am convinced that what I went through would have killed most people, and I would not be alive today if I had not taken my health and treatment into my own hands and cured myself. Sorry to say, but the depression was more a result of the doctors not taking me serious when I walked in and advised them that I had late Lyme's Disease. The doctors seemed to resent my walking in and 'telling them what was wrong with me. I was more mentally disturbed by the doctors refusing to prescribe antibiotics, than the bacteria that was living in my brain and spinal fluid.
So, I hope if you are suffering from what has been diagnosed as MS, Alzheimer's or an auto-immune disease that you will consider researching Lyme's disease as a possibility.
Here is something I just discovered is the possibility that it can be sexually transmitted:
https://www.lymedisease.org/lyme-sexual-transmission-2/
One physician has even proposed that although there is no statistics presently, he predicts that Lyme's disease may be a bigger epidemic than Aids.
Here is a great resource for more info:
https://www.lymedisease.org/lyme-times-lyme-disease-journal/
Lyme disease is much more common than previously thought, with over 400,000 new cases diagnosed each year in the United States.
That makes Lyme disease in this country about twice as common as annual new cases of breast cancer and four times more common than annual new cases of HIV/AIDS, hepatitis C virus (HCV) infection and syphilis combined.https://www.lymedisease.org/lyme-disease-genital-lesion/
1 comment:
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