LymeNet Flash: Anyone see Dr. P in CT

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 » Medical Questions » Anyone see Dr. P in CT

UBBFriend: Email this page to someone!

Author

Topic: Anyone see Dr. P in CT

Rubicon
Member
Member # 7919

posted

I have my first appt. with LLMD Dr. P in CT. Does anyone have any feedback on him?

I hope he treats based on symptoms because I no longer test positive. I only tested positive in 1993 and had a relapse in 97 & 05.

--------------------
I'm in the tunnel and I still don't see any light!!

Posts: 42 | From RI tick capitol of the world | Registered: Sep 2005 | IP: Logged |

beachcomber
Frequent Contributor (1K+ posts)
Member # 5320

posted

I don't see him but I do know that he treats very aggressively, so be careful. I know a few who do see him.

Also, check his credentials & track record. Just a suggestion.

You can contact the Wilton Support Group and ask for references from some of those folks.

Posts: 1452 | Registered: Feb 2004 | IP: Logged |

Rubicon
Member
Member # 7919

posted

DMC,
Thanks so much for the info. I was on 4 weeks of Rocephin and then my pcp stopped my meds and I was getting better... that was about 8 days ago. I see Dr. P in 7 days and i have gotten worse again now that I am off the abx. I'm hoping Dr. P will perscribe something after my first visit. I can't keep missing work!!!! Will he wait for blood work result to start treatment?

Thanks agian.

--------------------
I'm in the tunnel and I still don't see any light!!

Posts: 42 | From RI tick capitol of the world | Registered: Sep 2005 | IP: Logged |

sweet pea
LymeNet Contributor
Member # 6495

posted

Dr. P. in Ridgefield has been recommended to me by several people. I think he is a true LLMD, and will base treatment on a clinical diagnosis. (I was going to go to him, but when I was first looking for an LLMD, I was able to get an appt. with Dr. H. much sooner.)

Let us know how your appt. goes!

Posts: 449 | From Vermont | Registered: Nov 2004 | 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/