posted
And any other list of what tests to take, such as thyroid, CD57, for other protocols. I want to see where I stand now and what to do about this doggone brain fog. I have it somewhere....(Dr. B's list, not my brain.)
I think I have Dr. S's book somewhere....but maybe I checked it out of the library and it's back there now.
Thanks.
** moderator's note - edited to remove doctor's name **
[ 08-20-2010, 10:00 PM: Message edited by: sixgoofykids ]
Posts: 97 | From Great Lakes state | Registered: Jul 2008
| IP: Logged |
Keebler
Honored Contributor (25K+ posts)
Member # 12673
posted
- I can't say about tests but you asked for links. Personally, I would save your money on the CD57. It's not all that definitive regarding progress. How you feel and how you progress will tell you much more, in my experience. -----------------------
** 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.
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/