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Be the Voice for Those Living with Chronic Urticaria

Offering guidance, resources, and a supportive community for those living with chronic urticaria. We see you. Find hope, strength, and a home on your journey with us.

Patient Advocacy

For many people with chronic conditions, including chronic urticaria, barriers can create considerable roadblocks to optimal care and outcomes. Advocacy helps to call attention to these obstacles and offers solutions, amplifying the voices of patients and families and highlighting systemic gaps in care that might otherwise go unaddressed.

Our advocacy efforts focus on: 

  • Improving access to specialists, diagnostics, and treatments
  • Increasing public awareness
  • Fostering better understanding of CU among policy makers, the general public, and health care providers 

By raising these issues at local and national levels, we strive to break down these obstacles and promote equitable access to evidence-based, patient-centered care for all impacted by CU.  

We also support self-advocacy, equipping people with CU and their families with urticaria education and tools. We encourage learning about your rights as a patient, engaging in shared decision-making with your healthcare team, and sharing your CU story. Every action contributes to a stronger, more empowered community and a future where CU is better understood, appreciated, and treated. 

Patient Advocacy

For many with chronic conditions, including chronic urticaria, barriers can create considerable roadblocks to optimal care and outcomes. Advocacy helps to call attention to these obstacles and offers solutions, amplifying the voices of patients and families and highlighting systemic gaps in care that might otherwise go unaddressed.

Our advocacy efforts focus on: 

  • Improving access to specialists, diagnostics, and treatments.
  • Increasing public awareness.
  • Fostering better understanding of CU among policy makers, the general public, and healthcare providers. 

By raising these issues at local and national levels, we strive to break down these obstacles and promote equitable access to evidence-based, patient-centered care for all impacted by CU.  

We also support self-advocacy, equipping people with CU and their families with urticaria education and tools. We encourage learning about your rights as a patient, engaging in shared decision-making with your healthcare team, and sharing your CU story. Every action contributes to a stronger, more empowered community and a future where CU is better understood, appreciated, and treated. 

Share Your CU Story

Discover inspiring stories from individuals whose lives have been touched by CU. Together, we are building a stronger, more connected community for those living with chronic urticaria.

Get in Touch with Us!

We’re here to answer your questions, hear your feedback, and work together to make a difference.

Send us a message!