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» LymeNet Flash » Questions and Discussion » Medical Questions » Press conference on CFS/ME

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Author Topic: Press conference on CFS/ME
timaca
Frequent Contributor (1K+ posts)
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Sept 18th 10:30 a.m. EDT

http://cii.yewda.com/Blog.aspx?LOfRcb

Best, Timaca

Posts: 2872 | From above 7,000 ft in a pine forest | Registered: Feb 2005  |  IP: Logged | Report this post to a Moderator
Keebler
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Thanks so much, Timaca. That certainly looks interesting.

The ILADS conference is later in the Autumn.

Good to get this dates onto our calendars NOW to be sure we catch every minute we can.

Glad to see it starts at a fairly reasonable time for those on the West Coast (7:30 am) - well, compared to the 5:30 am ones for ILADS last year.

For those in different time zones, it's especially helpful to know well in advance of very early video conferences.

Last year I just couldn't get up at 5:30 am (my time) for start of ILADS because I did not realize it until the day before.

From now on, I'll look ahead for all video conference schedule and even figure out when to plan lunch (that will be all ready), scoot a recliner by computer, etc.

It's so wonderful when we can get these opportunities.
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Posts: 48021 | From Tree House | Registered: Jul 2007  |  IP: Logged | Report this post to a Moderator
Keebler
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Sending up so folks can mark their calendars for this coming TUESDAY, 9-18

7:30 am PT; 10:30 am ET

Even if some of us have "moved on" from the CFS diagnosis once lyme & co. became clearer, there is still much to learn from the researchers, doctors and patients in the CFS/ME circle.

So much overlaps, especially regarding self care habits or new medicines to treat symptoms (or causes) or support supplements that can help those in either diagnosis "zip code".

The kinds of chronic stealth infections that concern the CFS/ME researchers are also some that can plague those with lyme and other TBD.
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Posts: 48021 | From Tree House | Registered: Jul 2007  |  IP: Logged | Report this post to a Moderator
   

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