LymeNet Flash: Looking for Great LLMD or Treatment Center in US

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 » Looking for Great LLMD or Treatment Center in US

UBBFriend: Email this page to someone!

Author

Topic: Looking for Great LLMD or Treatment Center in US

improver
LymeNet Contributor
Member # 8380

posted

I know that we usually are state specific. I am in NJ but am realizing that sometimes you need to travel to get the best care.

I am looking for a Dr or a treatment center that looks at the big picture, Lyme, co's, viruses, toxins, hormones, detoxing, and other possible factors in this illness complex. Please let me know if you have suggestions.
If I sound desperate, I am tired of not getting better.

Thank you all.

Posts: 413 | From nj | Registered: Nov 2005 | IP: Logged |

Robin123
Moderator
Member # 9197

posted

Pm'ing you -

Posts: 13155 | From San Francisco | Registered: May 2006 | IP: Logged |

improver
LymeNet Contributor
Member # 8380

posted

Thank you. Tried to pm you back but your mailbox is full.

Posts: 413 | From nj | Registered: Nov 2005 | IP: Logged |

Robin123
Moderator
Member # 9197

posted

Hi - thx - I cleared a few -

Posts: 13155 | From San Francisco | Registered: May 2006 | IP: Logged |

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

posted

Hi,

Improver, I certainly can identify with your frustration in not getting better. This is a very difficult illness and the lack of understanding and knowledge by our Drs. is not right.

We must continue to search for that "right" doctor that is going to make a change for us. We have to remain strong and positive during this journey.

Having others who share our same frustrations is a comfort and knowing that we have them to talk to helps tremendously.

Improver, please come here and talk with us anytime you want. We have become like family here, we share so much of ourselves with each other.

I have sent you a PM. Let us know what else we can do for you, anytime. [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 |

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/