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New CH.com Forum › Cluster Headache Help and Support › Cluster Headache Specific › RE:Initial US Cluster Headache Survey Data Avail..

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RE:Initial US Cluster Headache Survey Data Avail.. (Read 588 times)

JustNotRight

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CH version 15.0.8 member
since 2005 aka GingerS224

Posts: 1300
Wilkes-Barre, Pa (USA)
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RE:Initial US Cluster Headache Survey Data Avail..
Sep 12^th, 2009 at 9:55pm

Wow, this is sad and a bit shocking...

Quote:

Conclusions: In the United States many CH patients are not currently seeing a neurologist, are not being exposed to recognized acute and preventive therapies and are not finding treatment to be effective when prescribed. This is leading to job loss and disability. This survey will help define the clinical description of CH.

This is one way to see that our medical system is severely broken, people can't afford it, or that people have just plain lost faith it in.

<Edit>Someone may want to move this topic, my apologies, but I didn't see that one was already started.

« Last Edit: Sep 12^th, 2009 at 10:04pm by JustNotRight »

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Brew CH.com Sponsor CH.com Alumnus Offline Posts: 14163	Re: RE:Initial US Cluster Headache Survey Data Avail.. Reply #1 - Sep 12^th, 2009 at 11:26pm Those are three possible conclusions.
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