The Infectious Diseases Society of America recently announced that it will finally be updating its Lyme disease guidelines. They have opened a 30-day window for the public to comment on their guideline development process. I’ve only had a few days to review their proposal, but I am deeply concerned by what I see. . . .
posted
If they chose a person who's not a Lyme patient to be a "patient representative," then I think their whole process is going to be a sham again, no matter what we say.
Posts: 13116 | From San Francisco | Registered: May 2006
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Rumigirl
Frequent Contributor (1K+ posts)
Member # 15091
posted
Everything about how they are doing this is yet again another sham.
To chose a patient, who knows absolutely nothing about Lyme is so blatant, it's unbelievable!! Not that the rest of it isn't just as blatant.
There is a time period for public comment throught April 9, if I remember the date right (it's listed above).
Posts: 3771 | From around | Registered: Mar 2008
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droid1226
Frequent Contributor (1K+ posts)
Member # 34930
posted
Doesn't mean we don't try. I posted to a few hundred people on twitter. I hope someone gets her name. Not to harass. To file a complaint about an imaginary person won't get too much traction.
poppy
Frequent Contributor (1K+ posts)
Member # 5355
posted
The name is known, and it is the fault of the IDSA crooks, not the patient they chose.
Posts: 2888 | From USA | Registered: Mar 2004
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droid1226
Frequent Contributor (1K+ posts)
Member # 34930
posted
Ok, what's the name? Of course it's the IDSA's fault. That doesn't mean we let this person believe lyme is cured after 3 weeks of antibiotics. Right? Not if she has some influence.
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