LymeNet Flash: Has anyone had experience with university clinics around NYC?

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 had experience with university clinics around NYC?

UBBFriend: Email this page to someone!

Author

Topic: Has anyone had experience with university clinics around NYC?

thejab
Junior Member
Member # 31985

posted

I've seen a few research related university clinics and am unsure as to tx being better or worse at these settings

Posts: 4 | From scranton, pa | Registered: May 2011 | IP: Logged |

Abxnomore
Frequent Contributor (5K+ posts)
Member # 18936

posted

In my experience the only place to get the right kind of help is by seeing a lyme literate doctor who is a member of ILADS and follows Dr. B's guidelines.

I don't know of any university clinics that can properly help with this illness and not in NYC either. The one at Columbia is for research. They don't actually treat patients there.

Posts: 5191 | From Lyme Zone | Registered: Jan 2009 | 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/