posted
I came across a great new website full of Lyme information articles this a.m.
All published articles. I was researching for info on link between Interstitial Cytitis an Lyme Disease. Since I know I do NOT have Spastic Bladder. It is ICS. I am going to tell the Urologist that today. I have the proof to back up my claim.
I'm going to tell him he can PUT that in my records.
Go to there and just type in Lyme Disease. You will be AMAZED at the amount of articles that pop up. I'm sure you can plug in sphirocetes or Bb, neuroboriliosis or any other thing related to Lyme and it will come up.
Let me know what you think.
[ 25. July 2008, 07:57 PM: Message edited by: Nora DeBoard ]
Posts: 109 | From San Antonio,Tx | Registered: May 2008
| IP: Logged |
bettyg
Unregistered
posted
hi nora,
pubmed; this site knows it well.
member, california lyme/sarah, used to post daily any updates on lyme here.
she has taken a leave here since she was harrassed by BAD guys! when things settle up somewhere in future, she will be back.
may i suggest you edit, click on 2 people standing together, and change your subject to:
found pubmed; great lyme web site!
click edit send when done. now everyone knows at a glance which site you are talking about nora! big thanks!
IP: Logged |
METALLlC BLUE
Frequent Contributor (1K+ posts)
Member # 6628
posted
That's where I do a lot of my research.
-------------------- I am not a physician, so do your own research to confirm any ideas given and then speak with a health care provider you trust.
In searching for lyme, be sure to use other names. And, just adding an "s" can sometimes bring up a different number of abstracts.
And, be aware that not all the abstracts contain correct information. Many that say long term treatment does not work - well, they did the wrong treatments (usually mono therapy; too short of treatment time; wrong dose or method). And, usually such studies do not consider co-infections.
Always look to see who the authors are. Soon you will learn the IDSA authors who always try to minimize lyme and its danger.
The really cool thing about PubMed, too, is that you get abstracts from all over the world.
The IDSA's influence has reached to parts of Europe, but there are a few other scientists and doctors around the world who can understand that the IDSA approach is sorely inadequate and PubMed offers enough abstracts for a variety of views.
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/
UBBFriend: Email this page to someone!
![[Big Grin]](biggrin.gif)
![[Smile]](smile.gif)
![[Eek!]](eek.gif)
I'm sure you can plug in sphirocetes or Bb, neuroboriliosis or any other thing related to Lyme and it will come up.![[group hug]](graemlins/grouphug.gif)
![[bow]](graemlins/bow.gif)
....... ![[Wink]](wink.gif)
Printer-friendly view of this topic