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» LymeNet Flash » Questions and Discussion » General Support » if stupid reporters and doctos can constantly give bad advice, why can't we?

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Author Topic: if stupid reporters and doctos can constantly give bad advice, why can't we?
missing
LymeNet Contributor
Member # 22437

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on this board, we are always so careful to say that what we are saying is just our opinion.

I think we all deserve the right to give medical advice on this disease, if so many reporters and doctors are giving so many people bad advice.

Does that make sense?

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I am not a doctor. I have no clue.

Posts: 606 | From somewhere out there | Registered: Sep 2009  |  IP: Logged | Report this post to a Moderator
BoxerMom
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Oh my Gosh! I love your idea!!!

And we have no licenses to risk!!

I think we are very good at giving "cautious advice" here. We should keep it up.

[Big Grin]

--------------------
 - Must...find...BRAIN!!!

Posts: 2867 | From Pacific NW | Registered: Apr 2010  |  IP: Logged | Report this post to a Moderator
missing
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Of course, we need to be careful, because someone may not even have Lyme disease,

lets say they had cancer instead, and we wouldn't want to prevent them from getting proper treatment.

I have a huge admiration for doctors and nurses. How do they manage to get it right? I could never do their job.

But when I see bad reporting and bad doctors, I just get so frustrated.

I just look at how confused my mother-in-law is. So many people tell her that Lyme is no big deal, and the Usana people say they got cured taking their products.

My mother=in=law honestly believes these people. She tries so hard to figure it out, but she really can't.

So many people take advantage of her.

I could go on and on.

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I am not a doctor. I have no clue.

Posts: 606 | From somewhere out there | Registered: Sep 2009  |  IP: Logged | Report this post to a Moderator
onbam
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Liability issues, mostly. If something bad did come of what you said--you could get sued or it could get used against you in a variety of ways.
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map1131
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We don't have a license to practice and everyone knows we are just a crazy bunch of lulus.

If they come after us and our opinions, they would be busy busy people. Giving your experience is different than charging for your advice.

That'll be $1.00. Thank you.

Pam

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"Never, never, never, never, never give up" Winston Churchill

Posts: 6478 | From Louisville, Ky | Registered: Jan 2002  |  IP: Logged | Report this post to a Moderator
onlyflippin
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ha ha ha "that"ll be a $1.00 thank you" ha ha ha lol

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Help I am being forced against my will to learn medicine!!!

Posts: 164 | From WASHINGTON | Registered: Jun 2011  |  IP: Logged | Report this post to a Moderator
randibear
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that would be great. but what about if i tried something you said was ok and i ended up in the hospital.

then i sue lymenet and everyone.

it's a fantastic idea but not very practical.

there's always some joker in the box and you never know what they're going to do.

everyone is sue happy. look at my doc in denton. he had to go out of practice because some jerk husband didn't like his wife's treatment. so he sues, goes to the state, and has this doctor reprimanded.

there's too many people out there claiming this or that "cures" lyme and they have no liability.

it's just too risky.

the psychiatrist is in.

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do not look back when the only course is forward

Posts: 12262 | From texas | Registered: Mar 2007  |  IP: Logged | Report this post to a Moderator
Razzle
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If we make recommendations and someone decides to sue, we could go to jail for "practicing medicine without a license." So I agree we need to be careful (and I'm looking at myself in a mirror on this, too).

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-Razzle
Lyme IgM IGeneX Pos. 18+++, 23-25+, 30++, 31+, 34++, 39 IND, 83-93 IND; IgG IGeneX Neg. 30+, 39 IND; Mayo/CDC Pos. IgM 23+, 39+; IgG Mayo/CDC Neg. band 41+; Bart. (clinical dx; Fry Labs neg. for all coinfections), sx >30 yrs.

Posts: 4166 | From WA | Registered: Feb 2011  |  IP: Logged | Report this post to a Moderator
cjfrank
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And I want to thank all of you who gave me advice when I first came to this site. And I want to thank all of you who gave me advise who were not even aware of it.

I read everything, things that pertained to me and things that didn't. By the time I got to the doctor I knew more about Lyme than she did.

I don't know what I would have done without everyone here. Many of you are not even aware that you helped me, but you did, just by being here and knowing that I was not alone.

--------------------
cjfrank

IGG Western Blot - negative
IGG Bands Detected - p18
IGM Western Blot - positive
IGM Bands Detected - p23, p41

Posts: 49 | From Maine | Registered: Jul 2010  |  IP: Logged | Report this post to a Moderator
   

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