LymeNet Flash: Looking for LLMD not far from Montreal, Canada

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 LLMD not far from Montreal, Canada

UBBFriend: Email this page to someone!

Author

Topic: Looking for LLMD not far from Montreal, Canada

alex2k
Junior Member
Member # 26823

posted

Hi,

I think I might have Lyme disease. I live in Montreal, QC and would like to see an LLMD. I have no problem driving to the US (closest cities: Plattsbugh, NY & Burlington, VT).

Thanks a lot!

Posts: 2 | From Montreal, QC | Registered: Jul 2010 | IP: Logged |

alex2k
Junior Member
Member # 26823

posted

...and I'd really like to have an appointment as soon as possible no matter how far I have to drive or pay (I'm sure I can get an appointment a lot faster in the US than here in Canada). I have been having lyme-disease-like symptoms for 4 years now with no diagnosis other than an over reactive immune system. A few days ago I found what I'm sure was a dead tick by my bed; that's made me think of infected ticks.

So, I'd really like to get tested for lyme!

Thanks a lot once again!

Posts: 2 | From Montreal, QC | Registered: Jul 2010 | IP: Logged |

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

posted

Hi,

Alex and WELCOME to our lyme site. We're glad you came to us for help.

I have sent you a private message (pm), click on the flashing envelope.

Also, check out our great "Medical Questions" forum where you can ask all the questions you might have and our wonderful, knowledgeable members will answer them. Just read some of the threads and you'll see just how informative they are!
[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/