Emerging Worlds website/ lyme disease/Misinformation

[Guest guest]

Although I am not holding

the poster responsible in any way,

I want to comment that I went

to this website and was very

troubled by it's information on

lyme disease which I have.

It has information on it that

many/most lyme patients

would dispute along with their

lyme doctors e.g. how to diagnose,

that majority of lyme diagnosis'

are erroneous, and that there

is a vaccine out for lyme.

The vaccine as far as I know

was out some years back

but was pulled off the market.

The information was culled partially

from the CDC which many of us with

chronic illnesses know is not an accurate

source of information for many chronic

illnesses and certainly NOT for lyme.

I posted the page on Lyme to a lyme list

and requested opinions on it to see

how other lyme patients feel about it.

I have to say that although this website

may be acting in good faith, I would not

trust it's information based on it's

lyme disease information that will

mislead people and not help those

suffering with lyme, especially those

that do not know they have it, and

need to be diagnosed...

Again, just my take on it and no

ill will intended, but I think it's important

to dispel myths where we find them,

especially when there is so much

suffering going on and misinformation

already out there...

Best,