[ 02-13-2011, 06:24 PM: Message edited by: Lymetoo ]
Posts: 2675 | From ct, usa | Registered: Jan 2004
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Keebler
Honored Contributor (25K+ posts)
Member # 12673
posted
- Good point. Even if a "list" or a few names of LLMD are shared from here - one should do follow up to be sure those names ARE of real LLMDs. Since this lists are compiled from suggestions - sometimes, other names get on to referral lists, with non-LLMDs or a MD who is only marginally lyme literate. And the lists are not necessarily a complete listing.
By checking with local support groups - or in the area around where the doctor on the list works - one can get better first hand feedback. It's always good to check with many sources. -
[ 07-16-2010, 01:06 PM: Message edited by: Keebler ]
Posts: 48021 | From Tree House | Registered: Jul 2007
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California - Lyme Disease Association (CALDA) is a non-profit corporation acting as the central voice for all tick-borne disease issues.
When you get a doctor's name, be sure to check about their being what we call ILADS-educated or ILADS-minded. Talk to your local support groups, call the doctor's office and talk with the office manager about the doctor's affiliations and experience so that you might find a "good fit" for your particular case.
Topic: How to find an ILADS-educated lyme literate (LL) professionals in these areas:
Naturopathic doctor (ND); Acupuncturist (L. Ac.), a doctor of Oriental Medicine (O.M.D.), or a doctor of Ayurvedic Medicine (D.Ay.), certified herbalists or nutritionists, . . .
** Includes many professional links, articles and books on complementary / integrative methods - & RIFE links -- all by LL authors.
** Nutritional Supplements in Disseminated Lyme Disease **
J.J. Burrascano, Jr., MD (2008) - Four pages
===
It's very important to have this book as a reference tool for self-care and support measures. It answers so many questions in detail that is impossible here on the forum.
This book is based on interviews with 13 Lyme-Literate Health Care Practitioners. Each practitioner is given one chapter in which to share their healing strategies
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/