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» LymeNet Flash » Questions and Discussion » Medical Questions » The Best LLMDs - NY

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Author Topic: The Best LLMDs - NY
seekhelp
Frequent Contributor (5K+ posts)
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If you could recommend the very best LLMDs, would they be in NY? Which ones? How long are the waiting lists? Approximate cost? Do they require face-to-fsce follow-up visits monthly?

Kind of dreaming here, but I want to have some idea. I assume NY is the closest to MI for quality docs.

I have no idea if insurance would even pay an out-of-network benefit for a LLMD residing out-of-state. Any luck with that for those who tried to submit?

Posts: 7545 | From The 5th Dimension - The Twilight Zone | Registered: Mar 2008  |  IP: Logged | Report this post to a Moderator
djf2005
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i dont want to list all this info on here.

PM me and i can send you the requested info.

i see a dr in NY, his patients are former patients of the dr B and he is considered to be one of the best.

derek

--------------------
"Experience is not what happens to you; it is what you do with what happens to you."

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Posts: 2269 | From Lansdowne, Pa | Registered: Mar 2007  |  IP: Logged | Report this post to a Moderator
sixgoofykids
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Derek, I agree, but I don't think he's currently taking new patients (at least the last time I called he wasn't).

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sixgoofykids.blogspot.com

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JKMMC09
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There are three LLMDs in NY who I consider "Top" LLMDs, One in NYC, another in Westchester, and another further upstate.

I take my daughter to the LLMD in Westchester, he has been a true God-send for us. He has been treating 20-25 years and has a lot of experience...he's seen it all. Going through the "LymeLands" as we have, you come across all kinds of LLMDs, you will know when one suits you...it may not be the first you you see, or the second. We have gained a lot from all of the consults prior to finding our amazing LLMD.

Insurance will cover oral meds prescribed by these docs, maybe some IV, and reimburse a % of in-patient (not over the phone) appointments. As far as appt. frequency goes, it really depends how sick you are. My daughter needs to be seen every week, sometimes we can get away with every 2 weeks. You will need a local doctor to correspond with the LLMD and for bloodwork, etc.

Appts. vary in price. You can PM me for info, if you need it.

[ 10. December 2008, 12:01 PM: Message edited by: JKMMC09 ]

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seekhelp
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Tried PMing you Derek. I can't since your mailbox is full. Can you clear it? [Smile]
Posts: 7545 | From The 5th Dimension - The Twilight Zone | Registered: Mar 2008  |  IP: Logged | Report this post to a Moderator
onmyway
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Just sent you my thoughts!!!!

Onmyway

Posts: 131 | From Georgia | Registered: Oct 2008  |  IP: Logged | Report this post to a Moderator
HopefulinNY
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My doctor is in Westchester. He is excellent. I have spoken to several people in the waiting room who have gone to him for years and believe that he has made all of the difference for them. Some have seen other LLMD's prior to seeing mine. People come from all over the country to see him. He was one of the early Lyme warriors, and continues to be. I will PM his name and address.

Hope this helps!
HopefulinNY

--------------------
Lyme diag. 2005, confirmed with LLMD Dec. 2007, 2 years of Marshall Protocol, Bicillin,mal.Dr.Z herbs, EBV, HHV-6,Babs,Bart?(3 kids positive for Lyme)

Posts: 10 | From NY | Registered: May 2008  |  IP: Logged | Report this post to a Moderator
   

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