posted
I forwarded the recent study (Persistence of Bb after antibiotics.....) to an ISDA-thinking doctor and thought some of you might like (or maybe not) to see her response to me.
At least it gives us an appreciation for maybe the other side of the fence? I do want to note that this doctor is really a nice person....just...sigh...
"I agree it's an interesting article and is in a respectable, peer-reviewed journal. It would be much more convincing if they could culture the organism--either from the treated subjects or from the ones who received material that came from the treated ones--and of course it would be helpful to know whether the organisms they identify actually cause symptoms and what happens to the host and the organisms they identify after more time passes beyond the end of the antibiotic course.
It sounds like they're planning to do some additional studies addressing these issues--hopefully they'll have more answers soon."
Posts: 561 | From mass | Registered: Jul 2007
| IP: Logged |
posted
So unless you drop a mountain of similar studies on her desk verifying the results no change in treatment will be forthcoming.
Not suprised -- just hope we all live long enough to see how long it takes this info to be accepted.
Posts: 590 | From Canada | Registered: Oct 2007
| IP: Logged |
Tincup
Honored Contributor (10K+ posts)
Member # 5829
posted
The ID doc said..
"It would be much more convincing if they could culture the organism--either from the treated subjects or from the ones who received material that came from the treated ones-"
Might you tell her that this study has once again proven the IDSA tests (their "gold standard" test as a matter of fact)- which are part of the Attorney General's investigation concerning fraud, antitrust, monopoly and exclusionary conduct related to the IDSA and their Lyme guidelines- is the problem.
NOT the spirochete situation. They were able to find the spirochetes... but like in Hopkins study.. they had to use multiple tests to do so... IF they could do it.
She said.. "-and of course it would be helpful to know whether the organisms they identify actually cause symptoms and what happens to the host"
If this study she mentions is done in mice... and they don't live long enough to carry it out further.. but IF they did this in an animal... the IDSA would say.. well that is in animals... not humans. Whimpy, whining excuses and more years of fighting.
In other words.. we are stuck by them insisting they have to PROVE everything to be able to give people something that has been shown over the years has helped. especially when they use horrible tests!
In the meantime.. millions are... and will suffer.
Plus.. if she could study this more throughly.. and put 2 and 2 together... BEFORE she gets Lyme... it sure would help! Waiting for the future "prison gang" to step up to the plate and do the right thing is not only harmful to so many... but criminal.
posted
I just keep laughing at the response. This doctor is affiliated with a Major teaching hospital in Boston and is willing to "humor" me so I keep in contact with her.....of course hoping I can get her to jump ship!
I will be following up with her regarding her 'concerns' with this study...honestly, I keep feeling like I'm on some sick Candid Camera show...
Posts: 561 | From mass | Registered: Jul 2007
| IP: Logged |
Geneal
Frequent Contributor (5K+ posts)
Member # 10375
posted
Blah, blah, blah..
A lot of words put together that don't mean anything....
Sometimes these ducks remind me of a cult....brainlessly following
Whatever the leader tells them. Yeah, go ahead....drink the grape kool-aid.
Hugs,
Geneal
Posts: 6250 | From Louisiana | Registered: Oct 2006
| IP: Logged |
CD57
Frequent Contributor (1K+ posts)
Member # 11749
posted
Her response just doesn't say.....anything! I am curious about her comment about it being from a "respected publication". Does that mean that anything that is not from one of the (probably few) publications that they read is not even considered in their day to day practice and way of thinking?
Cookbook medicine is still alive and well.
Posts: 3528 | From US | Registered: Apr 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/