Susan & List!
What a great article. This is all so confusing do you all realize how many
diseases have the same symptoms. I was told I have Lyme, CFIDS, Fibromyalgia
and M.S. all at the same time. Now the CF & FM I guess would go hand in hand
with a body that is run down by Lyme and the MS and Lyme are often confused as
we all know. But I was told I had all three. The CFIDS and FM my doc showed up
on lab tests along with a strong indication for Lyme on my Western Blot, I had
a band for late Lyme disease and I am sure that is what is was and hopefully
is no longer. But what scares me to death are the docs who label you M.S. and
buy you a wheel chair. Terrible!
Some time ago I read an article about our Ex President George Bush. He
got the Gulf War Syndrome as well as his wife and the family dog. The
Government who loves us all so much ignored this syndrome and told these men
it was in there heads, oh no here we go again. I hate to inform these doctors
but we know when we are sick. So it is contagious and the doctor who
discovered the Syndrome is here in Louisiana. Dr. Edward Hyman is his name I
know because I tried to see him but he was working strictly on Gulf War
Syndrome. He is treating his Gulf War patients with antibiotics as well. You
see it could be that the I.V. would have gotten rid of my Lyme but it takes
two or more years of continuous treatment for it to work if it is going to
work at all. I saw a video a woman finally got well after four or five years
of abx. First off insurance companies will not pay for these things, only for
about two months if that, and if you want to talk about hard on the body, this
is another factor that makes CS so important to mankind, accessibility and
potency.
For all we know we are getting the Mycoplasma Syndrome in epidemic levels.
I worked in the Medical Insurance industry for twelve years before they fired
me for having a body that would not move. I saw more cases of aches and pains,
Chronic Fatigue, Vision problems in young people. Eye pain and vision problems
such as I had. It seemed like everyone was aching all over, or everyone has
Arthritis or going blind for no reason and guess what the doctors would tell
them Multiple Sclerosis. What a wicked label that is once you are given that
you are given no hope and they are probably wrong on the diagnosis 70% of the
time or more. FRIGHTENING! How can this be, it does not seem to me when I was
younger that everyone was ill with these strange undiagnosable illnesses.
This is most fascinating and I don't see why CS would not be able to kill this
Mycroplasma dead in its tracks.
After all it must need oxygen to live or it would not need other cells and
tissues to be host ( sounds good) to survive. Sounds logical. Boy I sure wish
we had a doctor on this list. Well great article and I am going to look into
this further this would sure explain allot for allot of people. Do you realize
how many blank looks I got from doctors when I would tell them my symptoms.
They thought I was crazy but I was just Lyme.
Thanks Susan Great Article,
Candace
