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Take part in the Chronic Spontaneous Urticaria (CSU) Survey: Your Experience Can Make a Difference

  • Associazione Arco
  • 8 hours ago
  • 2 min read


If you are living with Chronic Spontaneous Urticaria (CSU) or care for someone affected by it, your experience is valuable.

The ARCO Association (Association for Research and Care of Urticaria), in collaboration with the Center for Economic and International Studies at the University of Rome “Tor Vergata”, has launched an anonymous survey to collect real, concrete data on how this condition impacts the daily lives of patients.


Why your participation in the CSU survey matters

Chronic Spontaneous Urticaria is not just a skin condition — it can have a significant impact on mental health, work life, social interactions, and everyday expenses.

Unfortunately, there is still no clear picture of how deeply CSU affects people’s lives on an economic and organizational level. Your input will help us:

  • Measure the indirect costs of CSU (missed work or school days, out-of-pocket expenses, etc.)

  • Gain a better understanding of patients’ real needs

  • Advocate for fairer and more effective healthcare policies

  • Make visible what is often invisible


How to take the CSU survey

The survey is online and completely anonymous.

It takes about 10–15 minutes to complete. It’s open to:

  • Individuals affected by CSU

  • Family members or caregivers actively involved in managing CSU


Click here to participate now: 



What will the survey ask?

You’ll be asked to share information about:

  • Your diagnosis and treatment journey

  • Any barriers or difficulties accessing treatment

  • The direct and indirect costs associated with CSU

  • How the condition impacts your work, studies, and daily life

All answers will be handled anonymously and aggregated, with full respect for your privacy.


Your voice matters

Giving a voice to those living with chronic urticaria is essential to promote a more inclusive, informed, and fair healthcare system. Your contribution is an act of responsibility and solidarity—for yourself and for others living with CSU.


Join now: your experience has value

Don’t miss the chance to make your voice heard and support scientific research on Chronic Spontaneous Urticaria.

Complete the survey now by clicking here: 



Share this initiative with others you know—every response matters!

 
 
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