LymeNet Flash: Anyone in Eugene, Oregon?

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»	LymeNet Flash » Questions and Discussion » Seeking a Doctor » Anyone in Eugene, Oregon?

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Topic: Anyone in Eugene, Oregon?

Grateful
Member
Member # 6893

posted

Can anyone recommend an LLMD in Eugene, Oregon? (Yes, I am asking about Northern Va., etc., area in my previous post -- my daughter is considering relocating or moving between the two areas.)

Many thanks for your answers.

Posts: 24 | From Alexandria, VA, USA | Registered: Feb 2005 | IP: Logged |

bettyg
Unregistered

posted

grateful,

talk to keebler; she's from oregon; she says NO LLMDS THERE!

wash. state has 30-35 !! so perhaps she would like to move there!

send me a pm if you are interested and then i'll send to you! [Smile]

IP: Logged |

Keebler
Honored Contributor (25K+ posts)
Member # 12673

posted

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True, no LLMDs here but we have one LL ND who is a member of ILADS (and possibly one or to other NDs who are LL).

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You might refer to your previous post on March 9:

http://flash.lymenet.org/scripts/ultimatebb.cgi/topic/2/8538?

--

I sent you a PM on March 10 with the Oregon Lyme Disease Network website and contact:

http://oregonlyme.org/index.htm

You might see if you have that PM still in your profile as I also sent the contact for the LL ND.

If you need that again, please PM me or contact the Oregon Lyme Disease Network above for other options.

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Posts: 48021 | From Tree House | Registered: Jul 2007 | IP: Logged |

Grateful
Member
Member # 6893

posted

Still have it, thank you. It's just that sometimes, in my experience elsewhere anyway, sometimes the mention of a specific town will prod someone's mind. Not here though, alas!

Posts: 24 | From Alexandria, VA, USA | Registered: Feb 2005 | IP: Logged |

Keebler
Honored Contributor (25K+ posts)
Member # 12673

posted

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Grateful, that's very true.

The Oregon Lyme Network is usually pretty much up on any new developments.

It's nearly written in stone that no MD is allowed to properly treat lyme in Oregon. We all hope that will change but the Oregon Medical Board is a might foe and any change will likely not be soon.

Still, the Oregon Lyme Disease Network is working on education. There are some doctors who quietly are coming to understand more. So, be sure to connect that that group.

---

I do have a call into a ND in Salem. His name came to me by someone new to all this and I left a msg. asking him to call me back about the scope of his knowledge and practice regarding lyme and TBD and to ask if he would want more lyme/TBD patients.

Until I talk to him I'm not comfortable giving out his name but will PM you when I hear back from him.

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[ 04-03-2009, 05:49 PM: Message edited by: Keebler ]

Posts: 48021 | From Tree House | Registered: Jul 2007 | IP: Logged |

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