LymeNet Flash: Seeking LLMD's in southern California

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»	LymeNet Flash » Questions and Discussion » Seeking a Doctor » Seeking LLMD's in southern California

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Topic: Seeking LLMD's in southern California

kimwg
LymeNet Contributor
Member # 19094

posted

Hi All,

I am one of those "recovered" lymies who never comes back to tell you that you CAN get better... my bad. But that doesn't mean I don't care. I've recently been corresponding with a friend of a friend who has a lot of neuro lyme symptoms and ambiguous titer/western blot (only 1 band positive, probably for 41 but I'm not sure).

Anyway, he lives in Nicaragua (btw, this is where I am pretty damn sure I got lyme) but is currently in SoCal, looking into diagnoses after an MRI showed demyelinization on his spine. I'm putting him in touch with my Seattle LLMD, but does anyone have any good contacts in SoCal? He's supposed to head back south April 6th, so time is of the essence. Please PM me with any leads!

Thanks
Kim

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Wildlife biologist working in tropics since 1997; tick bites in Nicaragua in March 2007, started getting sick May 2007; diagnosed with Lyme based on serological testing in Jan 2009; treatment starting Feb 2009. Wish me luck!

Posts: 116 | From Seattle | Registered: Feb 2009 | IP: Logged |

Robin123
Moderator
Member # 9197

posted

Pm sent -

Posts: 13171 | From San Francisco | Registered: May 2006 | IP: Logged |

Siciliano
Frequent Contributor (1K+ posts)
Member # 15920

posted

Hi,

Kim, how wonderful that you are better!! I am so happy for you! [kiss]

I have sent you some information. That is very nice of you to want to help someone else. [Smile]

--------------------
I'm sorry but I am no longer accepting any private messages due to my own battle with lyme.

Posts: 3897 | From New Hampshire | Registered: Jun 2008 | IP: Logged |

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