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Lyme Community Lyme Disease Support Forums General & Support Posting LLMD names and numbers, question
Posting LLMD names and numbers, question
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02/02/2008 15:57
Julie4848
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 I have a questions, who made the rule that no one can post doctors name.

And I don't want to hear that it is because we have to protect the LLMD, if there really doctors they should stand up for what they believe in. What is the difference between PM and posting it, is it not the same thing???

Julie

Lyme will not win, we will and we WILL…

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02/02/2008 16:17
bisja
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Post edited by: bisja, at: 04/28/2008 18:07
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02/02/2008 16:22
Julie4848
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 Good point bisja...I just never understood it and my husband asked me the other day when he saw Bettyg's post, he thought it was a little strange so I thought I would question it. And I would love to know WHY...We aren't here to hind anything, we are here to HELP people in need...

Julie

Lyme will not win, we will and we WILL…

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02/02/2008 16:43
bisja
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Post edited by: bisja, at: 04/28/2008 18:08
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02/02/2008 16:50
Clayton72
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 Sh*t - the CDC and rest of those jerks can get any info from us in other ways -- They can pull your bank account info, etc. and know exactly what doctor you are going to anyway... hiding the info isn't going to do much.. it'll just take them 4 minutes longer to get it.

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02/02/2008 16:58
Julie4848
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 This is my point, so why does everyone hide it...I guess I just don't understand it...The goverment knows more about us then we know about our selfs..lol

Julie

Lyme will not win, we will and we WILL…

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02/02/2008 17:02
Clayton72
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 Yep - I have noticed all sites ask people to not post them so I just don't. Oh well...
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02/02/2008 17:05
bisja
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Post edited by: bisja, at: 04/28/2008 18:10
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02/03/2008 04:50
jaime1978
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 I agree whole heartidly with this post. Most of these doctors have thier own websites, and aren't hiding anyhow. Many people have said they have asked thier doctors and they have said they don't care who knows. The government knows what doctors are treating what. They have access to our medical records. Some of us are lucky enough to have docs that accept insurance, ummmm.... records.... not to mention our records of drugs we have filled....

It's like Clayton said, it was stressed to me not to post them , so I don't. I think I know where that got started, and I think it's overly dramatic. But just my humble opinion.

Please do not take anything I say as medical advice. I am not a doctor.

~lyme disease support group leader~
please pm me with any special concerns
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02/03/2008 06:14
bisja
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Post edited by: bisja, at: 04/28/2008 18:11
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