LymeNet Flash: Hitting IDSA without hitting IDSA

LymeNet on Facebook

LymeNet on Twitter

Follow @LymeDiseaseNet

The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive

The Lyme Disease Network is a non-profit organization funded by individual donations.

»	LymeNet Flash » Questions and Discussion » Medical Questions » Hitting IDSA without hitting IDSA

UBBFriend: Email this page to someone!

Author

Topic: Hitting IDSA without hitting IDSA

lymeit
Member
Member # 5018

posted

Here is what the Canadian Lyme Disease Foundation is doing on their website.

www.canlyme.com/phys.html

Posts: 43 | From Canada | Registered: Dec 2003 | IP: Logged |

Truthfinder
Frequent Contributor (1K+ posts)
Member # 8512

posted

Thanks!

Wow! I spent an hour over there and barely scratched the surface of the information available. Much of it we already know, but it is great to have so much available through just one webpage.

This is a great resource page. It is titled "For Physicians", but all of us patients need to be aware, too.

Tracy

--------------------
Tracy
.... Prayers for the Lyme Community - every day at 6 p.m. Pacific Time and 9 p.m. Eastern Time � just take a few moments to say a prayer wherever you are�.

Posts: 2966 | From Colorado | Registered: Dec 2005 | IP: Logged |

Carol B
Unregistered

posted

Thanks I hope I hve the time this afternoon for some exploration ! Meanwhile I got so discouraged last night because I ran into an old friend from a few years back- who of, course, asked how I was doing-so I said "Truth?- I have Lyme Disease."

He just wrinkled his brow ad responded like "so what? I thought lyme disease was just some little bacteria that you treated with antibiotics for a couple weeks and it was gone."

Then he proceeded to talk about himself for half an hour-and all his travels and adventures. He's a professor at a local University-but I think he still needs a lot of "educating" Oh Well.

Carol

IP: Logged |

Printer-friendly view of this topic

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, NJ 08534 USA
http://www.lymenet.org/