Cluster Headache Survey Results

SURVEY ON ACCESS TO HEALTHCARE FOR CLUSTER HEADACHE (CH) PATIENTS IN EUROPE

Project description

This survey is about the access to healthcare for Cluster Headache patients in EU countries.

The European Headache Alliance Cluster Headache Special Interest Group (EHA CHSIG) involved its member organizations into a survey to find out more about the experience of access to healthcare from the CH patients’ view across the EU.

On February 2018 a large-scale online survey was launched. The objective was to identify potential challenges in the area of access to healthcare for patients and to inform policy-making and ensure that future the advocacy actions are developed with consideration of the special need of CH patients

Related Events Calendar

CHAD

Cluster Headache Awareness Day 2018

From: 21/03/2018 14:00 to 21/03/2018 22:00 | Events |

This survey is about the access to healthcare for Cluster Headache patients in EU countries. The European Headache Alliance Cluster Headache Special Interest Group (EHA CHSIG) involved its member organizations into a survey to find out more about the experience of access to healthcare from the CH patients’ view across the EU. On February 2018 a large-scale online survey was launched. The objective was to identify potential challenges in the area of access to healthcare for patients and to inform policy-making and ensure that future the advocacy actions are developed with consideration of the special need of CH patients

Making visible the invisible

This survey is about the access to healthcare for Cluster Headache patients in EU countries. The European Headache Alliance Cluster Headache Special Interest Group (EHA CHSIG) involved its member organizations into a survey to find out more about the experience of access to healthcare from the CH patients’ view across the EU. On February 2018 a large-scale online survey was launched. The objective was to identify potential challenges in the area of access to healthcare for patients and to inform policy-making and ensure that future the advocacy actions are developed with consideration of the special need of CH patients

2018-05-02T17:47:33+00:00 13/03/2018|Tags: |

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