Hi folks,
About the bill that will protect our LLMDs from losing
their medical licenses:
STATE SENATE:
As a result of our calls and letters, there are signs
that Senator Hannon is starting to pay some attention
to the OPMC Due Process bill - S5057/A7757.

This means that we have to INCREASE THE PRESSURE on
him now to bring the bill up for a vote in his Senate
Health Committee.

PLEASE, anyone who has not yet contacted Senator
Hannon. do so immediately.

If you have already contacted him in the past couple
of weeks, this is the time to get friends and family
to do the same.

If you don't think they will actually get around to
it, please ask them whether you can send a note in
their name. But be sure to get their permission
before you do that.

Senator Hannon is a sponsor of the bill, for which we
have to thank him. The problem is that he has
sponsored many bills, and we need to keep on him to
give our bill a priority so it can get out of his
committee ASAP. Otherwise, there will not be enough
time for it to get passed through the entire Senate.

Hannon contact information:

His district office:

516 739 1700

His Albany Office:
518 455 2200

E Mail:
[email protected]

Just thank him for sponsoring S5057 and ask that he
move it out of committee as soon as possible.

STATE ASSEMBLY:
The bill was voted out of the Assembly Health
Committee last week. We thought it would come up for
a vote in the Assembly this week, but it was not on
the calendar - which seems to be just an
administrative matter and doesn't mean there is any
problem.

Any of you who have had trouble getting treated, OR have lost a doctor to state persecution, OR have to travel long distances to see your LLMD OR have to wait too long between appointments with your LLMD , OR have complained that your LLMD is not accessible enough - you need to make sure this bill is passed .

This is true no matter which state or country you live in.

If you haven't noticed yet, we don't have enough of them.

That's because the persecution by the NYS disciplinary board, the OPMC, has got doctors across the country afraid to treat us.

It's great that we can count on each other for support and information. But it wouldn't be so great if that was all we had because we lost our doctors.

Please take the time to contact Senator Hannon and to get your friends and family to do the same.

We have more and more patients sharing fewer doctors.

ONE, count him..ONE Lyme pediatrition in the entire WORLD..
and he treats thousands, works 7 days a week, 12 hours a day..
and is well past retirement age with noone brave enough to follow him full out.

..and our leading LLMD's have to watch their backs every day, operating under these pressures.

No non-LL's will touch this because they know of the liscencing pressures..which generate from financial concerns of insurance companies.

This won't stop unless the medical review board procedures are reformed so they can't do this anymore..

and it won't stop uless WE..the patients do something.

make the calls and get everyone else to.

If not for any other reason do it for the thousands of kids that will be infected this Spring.

Mo

Probably all of us here are pretty sick, and it's hard to have time and energy to be altruistic when you feel like you can barely survive yourself.

So please understand that this action is for you and anyone else in your family who is sick!!!!.

If the OPMC is permitted to keep harassing doctors, we could wind up all losing our medical care no matter which state we live in.

Now is the time to reach out and touch someone.

The LLMD you save may be your own!

------------------
If you get the choice to sit it out or dance...

Or maybe I saw this and sent a letter and forgot!

But I always try to respond so I know if I have sent a letter or not...that is so sad!

Was wondering how you are doing?

Linda..

Let's get it together, can we?

HA!

Maybe if we put both our brains together, we could form 1/2 a brain? Ya think?

Thank you for sponsoring S5057, the OPMC Due Process bill. I hope that you will see that it comes up for a vote in your committee as soon as possible. I have had Lyme Disease for 7 years and have finally been properly diagnosed January of this year.

The Doctor I go to doesn't take insurance due to the fact that he treats aggressively for success in conquering this horrible dibilitating disease. Insurance companies don't "allow" Doctors to treat aggresively with out persecution or scrutiny.

My insurance company should not dictate my health. They are not doctors. Alot of the literature available from my insurance company on Lyme is outdated. On their audio directory they talk about the lyme vaccine "Lymrix" which has been off the market for many years. It is really pathetic and unsafe how much control the insurance industry has.
Thanks so much,

Heather xxxx
xxxxxxxxx Aberdeen, NJ 07747
732.000.0000