I'm in need of an LLMD that uses both antibiotic and natural methods in the NJ, NY, PA area. I'd prefer to go completely natural, but an open to antibiotics if need be (this is a relapse I am dealing with).
Please PM me any reviews, they are greatly appreciated!
Posts: 4 | From NJ | Registered: May 2012
| IP: Logged |
Keebler
Honored Contributor (25K+ posts)
Member # 12673
posted
- I hope you get some specific suggestions.
In the meantime, links below should help.
It's important to know that not all states license NDs (some do so with various restrictions). Of the states that do license NDs, only some states also allow NDs to prescribe pharmaceuticals.
(What ILADS is) . . . WHY you need an ILADS-educated, Lyme Literate Doctor
===============================
It's best to consult with an ILADS-educated LL (lyme literate) doctor who has completed four years of post-graduate medical education in the field of herbal and nutritional medicine -
- and someone who is current with ILADS' research & presentations, past and present. -----
Integrative / Holistic M.D., etc. (Be aware that those in this category can have various levels of formal herbal &/or nutritional education, perhaps even just a short course. Do ask first.)
Links to many articles and books by holistic-minded LL doctors of various degrees who all have this basic approach in common:
Understanding of the importance of addressing the infection(s) fully head-on with specific measures;
Knowing that support supplements are important, but NEVER enough alone. And knowing which supplements have direct impact, which are only support and which are both.
You can compare and contrast many approaches.
BASIC HERBAL EDUCATIONAL links, and
BODY WORK links with safety tailored to lyme patients,
RIFE links (you might consider this but be sure to get professional guidance)
BIONIC 880 (& PE-1) links, and
LOW HEAT INFRARED SAUNA detail. -
Posts: 48021 | From Tree House | Registered: Jul 2007
| IP: Logged |
You might want to click on "Support Groups" in the upper left-hand corner of the Lymenet page, then the states you are looking for. Contact information will come up. Maybe they can help you.
Posts: 9020 | From Illinois | Registered: May 2006
| IP: Logged |
Dekrator48
Frequent Contributor (5K+ posts)
Member # 18239
posted
I sent you a private message with LLMD info for PA.
-------------------- The fibromyalgia I've had for 32 years was an undiagnosed Lyme symptom.
"For I know the plans I have for you", declares the Lord, "plans to prosper you and not to harm you, plans to give you hope and a future". -Jeremiah 29:11 Posts: 6076 | From Pennsylvania, USA | Registered: Nov 2008
| 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/
UBBFriend: Email this page to someone!
Printer-friendly view of this topic