For Patients · CKVÖ

You live with
cluster headache.

The Cluster Kopfschmerzen Verein Österreich (Austrian Cluster Headache Association) is the first point of contact for patients in the German-speaking world. Community, information and support – from people who know it first-hand.

Numbers · Rarity

What you already know – in numbers

Cluster headache is one of the most intense forms of pain known to medicine. Its rarity makes diagnosis and understanding difficult – which makes a strong community all the more important.

~1 %
of the population affected
5–15 min
up to 3 h attack duration
3:1
men to women
avg. 7 yrs
until the correct diagnosis
Membership · What you get

What the association offers you

Membership means more than an annual fee. You become part of a community that actively works towards improvements for patients in Austria.

Self-Help

No longer alone

Cluster headache is rare – the chance of meeting someone in everyday life who knows what an attack feels like is small. In the association you meet people who know it from their own experience.

Awareness

Being heard

The association campaigns publicly for better awareness and faster diagnoses. As a member, you are part of this voice – towards doctors, the media and policymakers.

Counselling

Psychosocial support

Through our partner association clusterberatung.at, psychological support is available to you – for the time between attacks and during acute crisis periods.

Online Group

Digital exchange

In our moderated online group you can connect with other patients across Austria at any time – without geographical boundaries.

Membership

Become a member now

The membership application takes only a few minutes to complete. The annual fee goes directly into awareness work, self-help services and the running of the association.

Questions before joining? verein@clusterkopfschmerzen.at or reach us directly via our contact page.