poppy
Frequent Contributor (1K+ posts)
Member # 5355
posted
The trolls that left comments seem to hunt up places where they can distribute their misinformation, spend a lot of time at it. Wondering if they can actually hold down jobs doing this, or maybe this is their job.
Posts: 2888 | From USA | Registered: Mar 2004
| IP: Logged |
Ellen101
Frequent Contributor (1K+ posts)
Member # 35432
posted
This is an old thread, but I was wondering if anyone knows of any updates to this story or how I could get in touch with Barbara Macleod.
Posts: 1748 | From United States | Registered: Dec 2011
| IP: Logged |
Keebler
Honored Contributor (25K+ posts)
Member # 12673
posted
- From Google Advanced Search of lyme + "her name" (in the URL), the most recent search results appear to be from the same time as that link, 2012.
There are others with the same name with a basic search, though, so that did not get me far.
You could contact her closest lyme support group - Kittery Point, Maine mentioned in the article - and see if they "are in the position to perhaps comment on how she's doing now?" and "if flagyl did turn out to be the turning point after all"
Of course, they may not be able to comment but it might be worth a try if she has been open and shares within that meeting circle. Anything beyond that would feel to me as intrusion.
FWIW, I've also heard of others for whom flagyl seemed to be an excellent help. -
Posts: 48021 | From Tree House | Registered: Jul 2007
| 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/