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Author
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Topic: WARNING to ALL who post information
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ElizabethP Flash Member Posts: 27 From: Registered: Jan 2005
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posted 03 February 2005 19:53
duhhh...I'm a goofus.Never been in a discussion forum, didn't realize I shouldn't be myself. IP: Logged |
pattiecake Frequent Contributor Posts: 513 From: PA Registered: Oct 2004
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posted 03 February 2005 20:09
Dont feel dumb, I still cant figure out who the trolls are. pattiecakeIP: Logged |
Lymetoo Frequent Contributor Posts: 16145 From: Missouri Texan Registered: Feb 2001
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posted 03 February 2005 22:09
Some of you may want to do a little editing, just in case. http://flash.lymenet.org/ubb/Forum1/HTML/031276.html IP: Logged |
James H Frequent Contributor Posts: 388 From: Central Texas Registered: Oct 2004
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posted 03 February 2005 22:18
...And the troll just moves on to the next question... 'What do you take for pain'... and people are answering that one.This stuff does screw up our brains! IP: Logged |
snowboarder Frequent Contributor Posts: 525 From: Colorado Registered: Oct 2004
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posted 03 February 2005 22:23
Thank you Tincup! I've only been on this board since October and someone stands out in my mind. This person is asking for way too much information! Why would someone want to spend time on this board if they weren't sick is beyond me. It's draining enough just getting through a day. IP: Logged |
Mathias Frequent Contributor Posts: 644 From: NJ, USA Registered: Feb 2004
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posted 04 February 2005 10:01
http://flash.lymenet.org/ubb/Forum1/HTML/031158.html Don't forget about this one. IP: Logged |
troutscout Frequent Contributor Posts: 4496 From: North East, Iowa Registered: Sep 2002
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posted 04 February 2005 10:28
I recently recieved a request from someone who posts here frequently...stating they knew someone in my area with Lyme from a different board that needed help...I...against my better judgement replied...and got no answer. And, yes...I gave them my phone number. Only time will tell. But...then again my phone number is posted here on this website and is always available to those that need it. (They just have to look for it.) Trout  ------------------ Now is the time in your life to find the "tiger" within. Let the claws be bared, and Lyme BEWARE!!! Iowa Lyme Disease Assoc. www.ildf.info IP: Logged |
virginia/anez Frequent Contributor Posts: 49 From: greenacres,Florida,USA Registered: Nov 2004
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posted 04 February 2005 11:19
Thanks tincup!!IP: Logged |
cmichaelo Frequent Contributor Posts: 550 From: NY Registered: Jul 2004
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posted 04 February 2005 11:43
quote: Originally posted by snowboarder: Why would someone want to spend time on this board if they weren't sick is beyond me.
IMO, we, or rather the knowledge we have about the "truth" about Lyme, is viewed as a threat to "them". ...the "truth" about Lyme being the answer to the question: "Why is Lyme and other key infectious diseases not being researched, diagnosed and treated properly by the mainstream medical society when it's obviously such an epidemic and when it's obviously costing society mega-dollars due to loss of productivity and due to medical expenses?" Well, the truth is that we don't really KNOW the truth. We can only speculate as to the answer. But what we do know is that it makes NO sense that mainstream doctors 1) are unable to properly diagnose Lyme disease, 2) are unwilling to accept the disease, 3) are unwilling to treat the disease with proper dosages and long-term antibiotics, 4) would rather diagnose MS, fibromyalgia, CFS, and other just-as-little-understood-illnesses-as-Lyme, just to have an excuse to NOT diagnose/treat Lyme. And that alone is a threat, cause MDs just can't give good answers to why they don't wanna treat Lyme. They hide behind statements such as, "I don't think you have Lyme because .""I can't treat you for more than two weeks cause abx is bad for you and you may foster super-bacteria if exposed to long-term abx." "I don't think chronic Lyme disease is an actual disease." So who is "them"? Who's watching us? IMO, a whole lot of people: doctors, insurance companies, CDC, and... most importantly the drug companies who have the most to loose here...by far. I hope you guys can see that, no? So let's make it difficult for these folks, ok? Let's not mention any names, and keep your personal information to a minimum, and don't give out ANY personal information to anyone you don't trust 100%. I've been contacted several times where someone asked for my phone number. And they even gave me theirs. Some even wanted to meet. I can understand that some people may really want this kind of contact, and I try to be as sensitive as possible. But it's just not safe to be too naive. To this day, I still don't know if these people were legit. I replied with an email to their questions but didn't include my phone #. I NEVER heard from them again. So in all likelyhood, they were not legit. But for sure they sounded legit. But there was always something suspecious about the emails, not that I can put my finger on it. Michael [This message has been edited by cmichaelo (edited 04 February 2005).] IP: Logged |
SteveInMinnesota Frequent Contributor Posts: 125 From: Rocheser, MN, USA Registered: Dec 2004
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posted 04 February 2005 15:01
quote: Originally posted by cmichaelo: Well, the truth is that we don't really KNOW the truth. We can only speculate as to the answer.
Wow, of everything I've read here and other places, that is the one sentence that I believe 100%. IP: Logged |
daniella Frequent Contributor Posts: 462 From: connecticut Registered: Jan 2005
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posted 04 February 2005 16:02
Sometimes I feel like we are all guinie pigs in some bizzare experiment. ...Alright this might be a bit cruel but I just have to say it...forgive me all... As for camp A and the insurance Co.s One should never judge something if you don't have all the facts.( a good Md. Or scientist would know this) If someone wanted to do some REAL research as to what late stage or chronic Lyme... does, feels like, how painful it is, how it progresses, how it's effects your mind and emotions, how it affects your bank account, and finally how to cure it(or not) they could do it very easily. Now camp A and the ins. Co.s take notes. All they would need to do is have someone volunteer to be bitten by an infected tick... Then treatment would be purposely delayed three years. Just to solidify that LATE STAGE LYME disease diagnosis. When treatment is started it is only 21 days of doxy. No other tretament given and no testing for coinfections would be done. To me this would be the true test of a dedicated Dr. or Scientist. http://216.152.71.145/films/garland/kotnis.html This link is a Dr. who infected himself with a disease he was trying to cure. There is a more well known case but I can't think of it off hand. Anyway if you were a Dr., Scientist, or Insurance Co. who claimed to be REALLY interested in Lyme disease, wouldn't you want to do some REAL research and not just pussy foot around it asking odd semi-lame questions? A REAL man would do REAL research!... LOL But really come on already.... daniella
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Lymetoo Frequent Contributor Posts: 16145 From: Missouri Texan Registered: Feb 2001
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posted 04 February 2005 16:16
quote: Originally posted by daniella:
All they would need to do is have someone volunteer to be bitten by an infected tick... Then treatment would be purposely delayed three years. Just to solidify that LATE STAGE LYME disease diagnosis. When treatment is started it is only 21 days of doxy. No other tretament given and no testing for coinfections would be done. To me this would be the true test of a dedicated Dr. or Scientist. A REAL man would do REAL research!...
Yeah, this has been mentioned a few times before. It's always been my favorite solution to our problem of stupid "researchers" and proponents of 3wks of treatment for Lyme.Thanks for bringing this up again. It always makes me smile!  ------------------ oops! Lymetutu IP: Logged |
MADDOG Frequent Contributor Posts: 2004 From: Ohio Registered: Oct 2000
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posted 04 February 2005 18:26
I still wan't their names and addreses. I can allways change my vacation plans to a hunting trip. Here little troll here little troll . MADDOGIP: Logged |
TheCrimeOfLyme Frequent Contributor Posts: 2547 From: Greensburg, Pennsylvania Registered: Jun 2003
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posted 04 February 2005 20:32
I just wanted to point out that this was caught two weeks back also by RecipeGirl. I hae not seen her since. Has anyone checked on her? IP: Logged |
TheCrimeOfLyme Frequent Contributor Posts: 2547 From: Greensburg, Pennsylvania Registered: Jun 2003
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posted 04 February 2005 20:42
Check the profile. Research assistant  IP: Logged |
cmichaelo Frequent Contributor Posts: 550 From: NY Registered: Jul 2004
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posted 04 February 2005 21:05
quote: Originally posted by daniella: If someone wanted to do some REAL research as to what late stage or chronic Lyme... does, feels like, how painful it is, how it progresses, how it's effects your mind and emotions, how it affects your bank account, and finally how to cure it(or not) they could do it very easily.Now camp A and the ins. Co.s take notes. All they would need to do is have someone volunteer to be bitten by an infected tick... Then treatment would be purposely delayed three years. Just to solidify that LATE STAGE LYME disease diagnosis. When treatment is started it is only 21 days of doxy. No other tretament given and no testing for coinfections would be done. Anyway if you were a Dr., Scientist, or Insurance Co. who claimed to be REALLY interested in Lyme disease, wouldn't you want to do some REAL research and not just pussy foot around it asking odd semi-lame questions?
Holy moly! You ARE serious, are you not? Cause if this is a joke, I don't get it. What you're suggesting is a far cry from REAL research. And then you make it sound like it is all up to an individual scientist to decide if he/she wants to do real research. Well, there are precious few scientists who can decide for themselves what they want to research. And I'm quite confident that those who are blessed with such freedom, have other topics besides Lyme in the number 1,2 and 3 spots. And even if a scientist did your REAL research, who's to say that he/she would even develop significant symptoms after 3 years? And even if he/she did develop symptoms, how do we know the symptoms are due to Lyme, and not due to some other common infectious disease? Remember, a false negative for Babesia doesn't mean the scientist doesn't have Babs. Your REAL research won't work with Lyme because it just way too complicated a disease to do a single experiment with. Noone in the medical society is gonna pay any attention to a single data point when it's wrt Lyme. Not to mention that the poor researchers impartiality will be questioned. To do your REAL research, you'd need at least 20 impartial people so you can do some statistics. Good luck finding 20 totally healthy people who do not already have Lyme, coinfections, mycoplasma, Brucella, heavy metal problems, etc AND who are willing to get seriously sick to the extent that they loose their jobs and ruin the quality of their family lives for years? It just ain't that easy! Michael
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daniella Frequent Contributor Posts: 462 From: connecticut Registered: Jan 2005
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posted 04 February 2005 21:08
Relax..Micheal it was just a thought.... i think I'll take a break for a while till everyone chills a little... see ya... IP: Logged |
cmichaelo Frequent Contributor Posts: 550 From: NY Registered: Jul 2004
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posted 04 February 2005 21:22
quote: Originally posted by daniella: Relax..Micheal it was just a thought.... i think I'll take a break for a while till everyone chills a little... see ya...
Puh! Glad it was just a thought. Cause you sounded so serious, and it took my breath away... but it doesn't take much to take my breath away today... I'm popping 17.5g/day Amox, 200mg Mino, Plaquenil, Artemisinin, supplements and I'm coming down with some flu like crap... So pardon me if I was a bit harsh... Peace Daniella  Michael IP: Logged |
kam Frequent Contributor Posts: 2661 From: CA USA Registered: Dec 2002
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posted 04 February 2005 23:18
OK. It is February. May I suggest we attack the lack of educated doctor's in regards to lyme disease.Under general is a post for a conference this month in California on lyme disease with some excellent speakers. I have contacted some of the local papers and plan on contacting some of the better known papers in San Francisco, Los Angeles, perhaps Las Vegas, the Fresno Bee..help me out here guys. Please start posting email addresses so we can send requests to have this conference advertised in the Southwest papers. There is a press release that we can copy and paste onto our email on the post. Thanks. Think of the people you might just be helping NOT go through what you went through. A friend also copied and hand carried the flyer for the conference to her doctor here in California. The doctor's comment was that they may get one person with lyme a year but they would try to send someone from their office to the conference. I think that if they were more educated about lyme they might just find that there are really more of their patients walking around with lyme than they thought. IP: Logged |
kam Frequent Contributor Posts: 2661 From: CA USA Registered: Dec 2002
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posted 04 February 2005 23:23
HA! I just posted what I thought was a new topic. But, when I was through this post showed up and my post is no where to be found.I am assuming I hit reply instead of new topic and that it has not shown up yet. So, if you see it will you post it under new topic for me. Thanks. I'll check back again in the morning if I am able and if I am not too feeble.  IP: Logged |
groovy2 Frequent Contributor Posts: 353 From: Austin tx USA Registered: Oct 2004
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posted 05 February 2005 02:26
I am not scared- I just made a 20 minute TV show on Lyme Disease featuring Me and my story that will show here in Austin and will air over 50 times over the next year, I did shoot it in silhouette tho because I dont want to become the lyme guy here in town. I just think its good to get info out to help others--A friend of mine saw the show today and said they new it was me - by my Sexie Deep Radio voice-- that comment made me feel good. ---Jay-- IP: Logged |
tequeslady Frequent Contributor Posts: 84 From: Registered: Jan 2005
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posted 05 February 2005 08:04
quote: Originally posted by groovy2: I am not scared- I just made a 20 minute TV show on Lyme Disease featuring Me and my story that will show here in Austin and will air over 50 times over the next year, I did shoot it in silhouette tho because I dont want to become the lyme guy here in town. I just think its good to get info out to help others--A friend of mine saw the show today and said they new it was me - by my Sexie Deep Radio voice-- that comment made me feel good. ---Jay--
Jay, what network (and/or what program) is this showing on? I would love to see it. Congrats... this is a great thing you've done.
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