LymeNet Flash: Does any one have experience with Dr T in Montana or Dr H in California?

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»	LymeNet Flash » Questions and Discussion » Seeking a Doctor » Does any one have experience with Dr T in Montana or Dr H in California?

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Topic: Does any one have experience with Dr T in Montana or Dr H in California?

mcg08002
LymeNet Contributor
Member # 24617

posted

I am going to see Dr T (LLND) in Montana and Dr H (LLMD) in California in May.

I just want to know people's experience's with these two doctor's. This would be so much help!

Just So I know what to expect.

Thanks!

--------------------
Stephanie, University Student.

Ehrlichia [POSITIVE]
IGG/IGM AB [H] 1.49
indexLyme AB interp. EIA [A] POSITIVE
IGG P93 AB [PRESENT]
IGG P41 AB [PRESENT]
IGM P41 AB [PRESENT]
IGM P23 AB [PRESENT]
Lyme IGM WB interp. [A] [PRESENT]

Posts: 145 | From Idaho | Registered: Feb 2010 | IP: Logged |

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

posted

-
You've posted about Dr. T before so I remember that she seems very knowledgeable.

Hopefully, others who have seen her will be by to post their basic experiences and PM you privately, precise details. In the meantime, to save speculation, it's helpful to post the website so everyone is aware that she is ILADS-educated (since most NDs - like most MDs - are not):

http://www.natfamilymed.com/

http://www.natfamilymed.com/aboutdr.html

In 2008 - completed a clinical rotation in New York City with Dr R., MD who specializes in treating Lyme disease and other tick-born infections.

This preceptorship was sponsored by the International Lyme and Associated Diseases Society (ILADS) via the Turn the Corner Foundation

=======================

http://www.LymeNet.org/SupportGroups/UnitedStates/Montana/Support.shtml

Montana Lyme Support Group

=======================

As for Dr. H - several here do see him. He has more years of experience than Dr. T. but both are ILADS-members.

You might also contact the leaders of the California support groups. I had several wonderful conversations with a couple people when I was considering this doctor (but, sadly, I could not manage to pull that together).

http://www.lymenet.org/SupportGroups/UnitedStates/California

California Lyme Support Groups

-----
www.lymedisease.org

CALDA - California Lyme Disease Association

===============

VERY important to read:

http://www.lymebook.com/steven-harris

Chapter 1 from the book "Insights Into Lyme Disease Treatment"
-

[ 03-29-2010, 09:44 PM: Message edited by: Keebler ]

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

Robin123
Moderator
Member # 9197

posted

Hi - pm'ing you.

Posts: 13116 | From San Francisco | Registered: May 2006 | IP: Logged |

Imaginit
LymeNet Contributor
Member # 20399

posted

Hi mcg--
I think I have written to you about Dr. T before--I have been seeing her for about a year. PM me if you want more information.

Posts: 123 | From Montana | Registered: May 2009 | IP: Logged |

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