posted
seeking LLMD in Manhattan, NY, NY, preferably on the upper west side. I currently live in Maryland, but may move to Manhattan late summer to be with my husband. I've been living in Maryland with my parents because of my job in DC, but since I'm too sick to work, I am planning to move to New York. my parents took care of my children while I worked, but I don't want to be a burden on them to take care of me as well.
Thank you in advance for all the MAryland referrals. I will following up with a doctor in Maryland first since it will be a few months before we can move to NY, but I wanted to have a doctor lined up there as well.
Posts: 2 | From Bethesda, MD | Registered: Feb 2011
| IP: Logged |
Abxnomore
Frequent Contributor (5K+ posts)
Member # 18936
posted
PM sent.
Posts: 5191 | From Lyme Zone | Registered: Jan 2009
| IP: Logged |
posted
have a very good one I am seeing in NYC, if interested let me know and I will send you PM.
-------------------- Diagnosed with chronic neuro lyme 12/10 after 30 years of vertigo.2 tick bites in 3 yrs from upstate NY. Was on omincef for nine mths..zith and rifampin stopped.Remission~ All the pain and symptoms are back and I am not treating now with biaxin. Posts: 788 | From New york..queens | Registered: Nov 2010
| IP: Logged |
posted
Hi, I'm also Seeking an LLMD in the NYC area. I'm already seeing someone in NJ but I'd like to find someone closer to home. Also, I've developed a recurring pericardial effusion and have other Chronic Lyme persistent symptoms and believe my current treatment may need to be reassessed. Any help would be appreciated. Thanks.
Posts: 3 | From New York City | Registered: Mar 2011
| IP: Logged |
Abxnomore
Frequent Contributor (5K+ posts)
Member # 18936
It's best not to add onto another post. For your own benefit it's best to have a separate post as you initially started in the link above. Once a post is answered and you add on to it your request may not be seen or it can get lost in the sauce, if you will.
It's better to PM Aspark directly and see if he/she received any additional names that you did not receive.
Posts: 5191 | From Lyme Zone | Registered: Jan 2009
| IP: Logged |
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,
NJ08534USA http://www.lymenet.org/