NY/NJ Lymies: Dr. B in Morristown NJ

New Topic Post Reply Printable Version
[ << Previous Thread | Next Thread >> ]

MarriedtoLymeinNJ
Regular Member


Date Joined Sep 2007
Total Posts : 273
   Posted 7/18/2010 6:18 AM (GMT -6)   
http://ht.ly/2cRuA

The NJ Depression and Bipolar Support Alliance is having a lecture on July 28 with Dr B.

Robert C. Bransfield, MD

"Late Stage Lyme Disease as a Cause for Depression and Bipolar Disorder". Lyme can take years to diagnose. Often is undertreated or mistaken for something else. It can have brain involvement. Dr. Bransfield is an international expert. He is president of ILADS (International Lyme & Associated Disease Society). He will be the President of the NJ Psychiatric Association next year. He is a clinical psychiatrist and psychopharmacologist with an emphasis on treatment resistant cases. He earned his medical degree from the George Washington U. School of Medicine, residency in psychiatry at Sheppard and Enoch Pratt Hospital. He has done ground-breaking research, treats many patients who have Lyme Disease and has authored many articles also in medical books. His practice is in Red Bank.

I spoke to the man running this and he said to please pass the info along. A small donation ($3) is appreciated, no registration needed.
I am definitely going to be there even though is is past my bedtime :D
Chris: Diagnosed Lyme, Chronic Mono
Married to Lyme in NJ aka Gary: Lyme, Bartonella
Mom to Scott: Lyme, Babesia, Bartonella
Mom to Caitlyn: Lyme, Bartonella
My Blog: http://faerywings.wordpress.com/


Tallison
Regular Member


Date Joined Jun 2007
Total Posts : 417
   Posted 7/18/2010 7:29 PM (GMT -6)   
Hi!  Thanks for posting this.  Perhaps I will see you there.
I heard there is a lyme spt group in Morristown.  Anyone here heard of it or have links to it?  Anyone on here in the area?
Tracy

MarriedtoLymeinNJ
Regular Member


Date Joined Sep 2007
Total Posts : 273
   Posted 7/19/2010 8:05 AM (GMT -6)   
T- let me know if you are going, Gary, kids and I will be there as well as my MIL (did you meet her at the Lymapalloza?)

Don't know of a Mo-town support group, but will keep my eyes open
Chris: Diagnosed Lyme, Chronic Mono
Married to Lyme in NJ aka Gary: Lyme, Bartonella
Mom to Scott: Lyme, Babesia, Bartonella
Mom to Caitlyn: Lyme, Bartonella
My Blog: http://faerywings.wordpress.com/

New Topic Post Reply Printable Version
Forum Information
Currently it is Monday, October 23, 2017 9:27 AM (GMT -6)
There are a total of 2,886,011 posts in 316,665 threads.
View Active Threads


Who's Online
This forum has 157768 registered members. Please welcome our newest member, mariegonz995.
948 Guest(s), 18 Registered Member(s) are currently online.  Details
PeteZa, Celie, scifigal2k, NancyG457, mattamx, Surfer22, tickbite666, JNF, Michael_T, NiceCupOfTea, Dmc695, gabybee, PA_grandma, quincy, MacroMan, ZoeUK1989, mcloud, iPoop


Follow HealingWell.com on Facebook  Follow HealingWell.com on Twitter  Follow HealingWell.com on Pinterest
Advertisement
Advertisement

©1996-2017 HealingWell.com LLC  All rights reserved.

Advertise | Privacy Policy & Disclaimer