Re: Need LLMD in Oregon for my cousin's child

[Guest guest]

Hi Natasha, 

Good luck finding the Virgin in this search  for a dr.   We live in

Oregon and also travel to RW City.  I've heard a Seattle dr speak and I felt

really good about him.  I know of a few good naturopaths in the Ptld area who

treat but not everyone's insurance covers naturopaths.  If theirs does, let me

know and I can give you the names.

Bend support group

info@...

Southern Oregon support group

sold@...

Good luck to your family.

Elaine

________________________________

From: Natasha Moiseyev <nmoiseyev@...>

Sent: Fri, August 13, 2010 9:15:54 PM

Subject: [ ] Need LLMD in Oregon for my cousin's child

 

Hello all --

I already have a rep for basically seeing the Virgin in grilled cheese

sandwiches, Lyme-wise, but my cousin came to vacation with us for a week and her

daughter has unmistakable Bartonella marks on her thighs and some cognitive

issues that she mentioned to me unprompted. Ack. It's becoming a club of

everyone we know! Their son has autism spectrum issues and if his sister is

infected odds are pretty good that he is too.

They live in Bend, OR.

They are freaked out about how to get help. I downloaded an Igenex form for

them and they have a pediatrician friend who will sign the request for them.

But then what? They could come down to Redwood City to see our LLMD, but that

is not the most realistic thing. Perhaps people know of a great LLMD in

Oregon? If they had to they could get to Seattle -- it's about 6 hours from

them.

Please tell me privately if you have any recs (or ones to stay away from).

Thanks much -- love this list.

Natasha

[Guest guest]

Recommend you contact the Oregon Lyme Disease Network. Their website is

oregonlyme.org.

My understanding is that it's extremely difficult to get properly treated in

Oregon. Many Oregon patients end up going either to California or Washington

state. I am aware of a naturopath who treats Lyme in Corvallis. Contact me

privately if you want that info.

>

> Hello all --

>

> I already have a rep for basically seeing the Virgin in grilled cheese

> sandwiches, Lyme-wise, but my cousin came to vacation with us for a week and

her

> daughter has unmistakable Bartonella marks on her thighs and some cognitive

> issues that she mentioned to me unprompted. Ack. It's becoming a club of

> everyone we know! Their son has autism spectrum issues and if his sister is

> infected odds are pretty good that he is too.

>

> They live in Bend, OR.

>

> They are freaked out about how to get help. I downloaded an Igenex form for

> them and they have a pediatrician friend who will sign the request for them.

> But then what? They could come down to Redwood City to see our LLMD, but that

> is not the most realistic thing. Perhaps people know of a great LLMD in

> Oregon? If they had to they could get to Seattle -- it's about 6 hours from

> them.

>

> Please tell me privately if you have any recs (or ones to stay away from).

>

> Thanks much -- love this list.

>

> Natasha

>

>