LymeNet Flash: Has anyone ever been to these doctors?

LymeNet on Facebook

LymeNet on Twitter

Follow @LymeDiseaseNet

The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive

The Lyme Disease Network is a non-profit organization funded by individual donations.

»	LymeNet Flash » Questions and Discussion » Seeking a Doctor » Has anyone ever been to these doctors?

UBBFriend: Email this page to someone!

Author

Topic: Has anyone ever been to these doctors?

mkc66
Member
Member # 36599

posted

I am looking for a Lyme doctor as close to home as I can get. Was given Dr. H of NY's name which am considering but found a doctor a little closer. Has anyone ever heard of Drs. B of NY? They are at *****,NY with office hours in **** once a week. I would like to go to the best place for treating my lyme. Am eager to hear back from those who are knowledgable. Thank you.

**edited names and cities of LLMDs per LN rules***

[ 03-09-2012, 10:29 AM: Message edited by: Lymetoo ]

Posts: 11 | From utica, ny | Registered: Mar 2012 | IP: Logged |

TF
Frequent Contributor (5K+ posts)
Member # 14183

posted

If you want to go to the best place, that is Dr. H. Forget everyone else.

It is going to be a long wait, and he is not always taking new patients. If he won't take you now, just call again in about a month.

Make an appt to see one of the physician's assistants.

Posts: 9931 | From Maryland | Registered: Dec 2007 | IP: Logged |

t9im
Frequent Contributor (1K+ posts)
Member # 25489

posted

Hi TF - there is also Dr. C who was in Cure Unknown. He treated one of Pam's son's.

--------------------
Tim

Posts: 1111 | From Glastonbury, CT | Registered: Apr 2010 | IP: Logged |

lyme-o
LymeNet Contributor
Member # 35115

posted

If you are referring to Drs. B, the brothers, do your self a favor and don't go. Total nightmare going there. You have to be your own advocate. PM me for more info.

Posts: 305 | From United States | Registered: Nov 2011 | IP: Logged |

Printer-friendly view of this topic

The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:

The Lyme Disease Network of New Jersey
907 Pebble Creek Court, Pennington, NJ 08534 USA
http://www.lymenet.org/