Topic: Rough survey on how we are doing with recruiting LLMD's
kam
Honored Contributor (10K+ posts)
Member # 3410
posted
I know when I was first dx, there were only 3 LLMD's in CA.
Now, they have much more. How many more I am not sure.
I also know when I moved to AZ we only had one or two LLMD, but now have 3.
Just curious as to how we are doing in other states.
Posts: 15927 | From Became too sick to work or do household chores in 2001. | Registered: Dec 2002
| IP: Logged |
Dawnee
Unregistered
posted
Well I know there is finally one in Tennessee... better than none.
seekhelp
Frequent Contributor (5K+ posts)
Member # 15067
posted
It doesn't sound like a very exciting career with those low marks. It's like trying to sell a foreign car to a Big 3 Executive.
Posts: 7545 | From The 5th Dimension - The Twilight Zone | Registered: Mar 2008
| IP: Logged |
posted
Well, I know my LLMD is training new doctors in his office. He has them sit in on office visits and then start to do follow-ups with him checking in at the end.
I really think more of this needs to be done!
Posts: 27 | From my own little world | Registered: Oct 2008
| IP: Logged |
posted
Training them is easier than keeping them, except in CA where the lyme law is some protection. As soon as they get a whiff of controversy or some local/insurance pressure, they disappear. This is why the state boards keep going after lyme docs, so as to discourage others from helping us.
Posts: 8430 | From Not available | Registered: Oct 2000
| IP: Logged |
posted
In WA state, I've been to 2 personally, know of one ND, and another MD. My doctor has had a trainee with him once that I know of.
The documentary "Under our skin" was shown at Bastyr University, and it was well attended. There was no way of knowing how many medical people were there, but the Q&A went real well.
I said something optimistic about it, and my doctor responded it's going very slowly. We're in the same place as when the book "Cure Unknown" talks about what was known in the 70's.
Posts: 563 | From New Mexico, USA | Registered: May 2007
| IP: Logged |
blinkie
Frequent Contributor (1K+ posts)
Member # 14470
posted
Can someone please explain the "lyme law" that protects our California LLMD's?
What is the law and how does it protect them?
thanks!
Posts: 1104 | From N.California | Registered: Jan 2008
| IP: Logged |
kam
Honored Contributor (10K+ posts)
Member # 3410
posted
Good question.
SEveral things popping my my mind.
I recall watching a presentation in SAC re: the law. But, do not recall the web site now.
I also know that a NP my Lyme Doc suggested I see because she was closer to me stopped treating patients for lyme because one lady took her to court for prescribing long term abx.
I assume that was before the law was passed.
Hopefully, someone will come along and help us out.
It does sound like we need this type of law passed in other states.
It was not for just LLMD's but for all doctor's so they would have the right to treat as they see fit.
I noticed when I was looking for help with a dx, the ones that really were interested in my health were the ones that were not being paid by the insurance companies.
Posts: 15927 | From Became too sick to work or do household chores in 2001. | Registered: Dec 2002
| IP: Logged |
klutzo
Frequent Contributor (1K+ posts)
Member # 5701
posted
When I finally found out that my Fibromyalgia was really Lyme in 2003, there were 5 LLMD's in our county.
Now there are none, unless you count alternative practitioners who say they can cure it w/out ABX. We have 2 of those that I know of.
There are 2 LLMD's in the county just east of us, but only one is affordable to those who aren't filthy rich.
klutzo
Posts: 1269 | From Clearwater, Florida, USA | Registered: May 2004
| IP: Logged |
kam
Honored Contributor (10K+ posts)
Member # 3410
posted
Daisy, Glad to hear Washington State now has LLMD's.
When I first came down sick, people had to travel out of state for help.
Posts: 15927 | From Became too sick to work or do household chores in 2001. | Registered: Dec 2002
| IP: Logged |
posted
I have heard that ILADS membership has increased, also thanks to the recent SF conference.
Posts: 13171 | From San Francisco | Registered: May 2006
| IP: Logged |
The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:
The
Lyme Disease Network of New Jersey 907 Pebble Creek Court,
Pennington,
NJ08534USA http://www.lymenet.org/