Ciao Ragazzi,
Ho giusto ora ricevuto questa mail che posto qui,dai fratelli USA;mi ero iscritto anni fa.
Sembra sia un'indagine sondaggio ,solo per americani,che servira' per le compagnie assicurative (Ramo medico-mutua/inps) e servira' sembra a pubblicizzare e riconoscere CH come malattia .
Il sondaggio necessita di 30-40 minuti; appena ho un po' di tempo gli do' un'occhiata .
Suiggerimenti per ns. uso e consumo?
Ciao
Giuly
Dear Giuliano,
Invitation to Participate in the Most Extensive and In-Depth On-Line Survey of U.S. Cluster Headache Sufferers Ever Conducted
As you know, there is a lack of comprehensive survey information concerning the U.S. cluster headache sufferer population.
This has been a key issue affecting awareness among physicians and the attitudes of insurance companies about cluster headache therapy.
The data from this survey will be used by a leading neurologist and cluster headache specialist, to prepare a paper for submission to a major medical journal, for presentations at neurology and headache specialist medical meetings and to educate medical insurance companies.
Only U.S. residents whose cluster headache condition has been diagnosed by a neurologist should participate.
The survey will not request your name or other personal identifying information.
We encourage you to participate in this in-depth ground breaking survey that will greatly benefit the welfare of the cluster headache community. The survey will require 30-40 minutes, and, you can return to finish it as many times as necessary within 2 weeks of starting it.
For full information and to participate in the survey, click on
http://chsurvey.infosurv.com The survey will run from October 13, 2008 through January 30, 2009.