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Re: Resent ILADS meeting

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Perhaps I am too new to this to understand. However, if we don't

have licensed doctors, we can't get patient care....

I agree that new research and patient care are very important. I

also know that I am one of the lucky ones who have found a LLMD

(Rheumatologist) who is willing to treat me with long term IV

antibiotics. But she is being cautious. I know there are a lot of

people that are looking for doctors in this area and are having to go

out of state. If we can get the politics resolved, there may be many

more doctors to be willing to provide such medical treatment. (And

not be afraid of loosing their liscense.)

It is sad that this is the case. But it seems to me that this is

critical to providing aid - especially for the many who have no

doctor to turn to right now.

~Beverly

Reston, VA

> My Lyme doc, who is member of ILADS, > The International Lyme and

Associated

> > Diseases Society, told me rather distressing news. The last

meeting was

> > devoted to the political side of Lyme. Not one minute was spent

on patient

> > care or new research. They are spending all their time trying to

keep

> > their careers. Its such a shame. Did you know that 24 doctors in

New

> > Jersey alone, have had their practices viewed by governing

bodies? This

> > was over several years period. I guess many doctors decide to

fight

> > silently.

>

> On top of this, my doctor is worried about prescribing my

oxycontin. Will

> this ever end? ~

>

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