Tincup
Honored Contributor (10K+ posts)
Member # 5829
posted
Just got this request....
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Subject: Video on Lyme
If you could spread the word in your area about this program produced in Houston, and ask as many people as possible to access this link, both ILADS folks and anyone else you know with an interest in chronic Lyme, this would be helpful. The more people that access this link
And watch the program of the interview with Kathleen Zabawa on Lyme, the more our local PBS affiliate, KUHT, will know there is a community of interest in this programming, so, that perhaps, if they get enough hits, this program will be passed on to the National PBS network and be distributed to other PBS affiliates across the nation.
This is just one small effort, but I'm glad that we did get this done, even if it's not the ultimate information program that perhaps I envisioned. It's a first step.
JillF
Frequent Contributor (1K+ posts)
Member # 5553
posted
Done and sent out via everyone on my email list and asked them to pass it on also
Good video/interview
But there is no Lyme in Texas! (sigh)
Posts: 1485 | From USA | Registered: Apr 2004
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dmc
Frequent Contributor (1K+ posts)
Member # 5102
posted
great find, sent link on to my email list of lymies and non-lymies. Getting favorable feed back.
I think seeing it's from a PBS station gave it creditability to those not savvy. Some think that those internet news sources (non mainstream) are questionable.
Posts: 2675 | From ct, usa | Registered: Jan 2004
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posted
Thanks to those whom have shown their thanks to this PBS station.
Up for the weekend Lymenetters who MUST see this video & follow suit!
Hugs &
-------------------- DR. Wiseass NOT a real doc - just a real wise Posts: 792 | From USA | Registered: Jan 2005
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klutzo
Frequent Contributor (1K+ posts)
Member # 5701
posted
I clicked on the link and got a page saying the video you want is not available, click here to see more, so I clicked, and got a page full of pop music videos. I'd like to see it. Any ideas?
Klutzo
OOPS! After using their search engine, I found it and watched it. There were a couple things about it that I found very upsetting, but at least we are getting some press.
[ 11. November 2006, 05:05 PM: Message edited by: klutzo ]
Posts: 1269 | From Clearwater, Florida, USA | Registered: May 2004
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JillF
Frequent Contributor (1K+ posts)
Member # 5553
posted
Email addresses for those of you who like to follow up with these types of things:
good video - some of the key messages about LLMDs and the controversies. I really like the part about how lymes is spread. that should scare some folks in to doing something
thanks mags Posts: 259 | From California | Registered: Mar 2006
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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!
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I clicked on the link and got a page saying the video you want is not available, click here to see more, so I clicked, and got a page full of pop music videos.![[Smile]](smile.gif)
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