A speech bubble highlighting the Pso logo above the words In America, surrounded by a fainter word cloud of logos for other Health Union websites.

In America: What’s That?

Last updated: January 2023

Whether you're newly diagnosed or have lived with psoriasis for years, managing the physical and emotional symptoms of this chronic condition is far from easy. In fact, at times, it can be pretty overwhelming.

How do I find a treatment that is going to work? Why are there so many options? What if my treatment stops working? Well, exactly what are my triggers? Why don't strangers or loved ones know it's so much more than simply moisturizing? Soon enough, psoriasis has become a big part of your identity.

To learn more about the challenges of living with psoriasis, we are conducting our In America survey. By taking our survey, you can bring awareness to the realities of life with psoriasis and help others feel less alone.

What is the survey about?

The survey covers “basics” like your diagnosis and treatment experiences but also dives into the nuances of psoriasis, like the emotional impact and day-to-day challenges. In addition, you’ll have the opportunity to not only tell us about psoriasis but also any other conditions you are living with and how each impacts your life.

Why should you take the survey?

Each person who takes the In America survey contributes to a better understanding of psoriasis as well as other health conditions. With better knowledge, we can help others who are navigating health challenges feel less alone.

We hope to capture a full picture of all aspects of your health experiences and bring greater awareness to conditions that may be misunderstood. Sharing your experiences through the survey can reveal how similar each person’s journey is, as well as the differences that make each journey unique.

What will the survey ask me?

The survey will ask about different moments of your journey with psoriasis, including:

  • Diagnosis
  • Symptoms and symptom management
  • Quality of life
  • Treatment awareness and experience
  • Other diagnosed conditions

We do not require your name, address, or other personal information for you to participate. You also do not have to take the survey all at once. Feel free to bookmark the survey in your Internet browser and return when you are able. You may continue where you left off.

How do we use the In America survey data?

Survey responses help us and our partners better understand the psoriasis community. All survey responses remain confidential, reported only in total. This means your specific responses will not be reported individually. All information will become property of Health Union, LLC.

What happens after I take the survey?

After the survey closes each year, PlaquePsoriasis.com will share the responses back to the community and highlight important findings from the survey. You can read the latest In America survey findings in Shattering Psoriasis Stigma: An Eye-Opening Quiz.

But that is not all. Throughout the year, we publish articles and videos based on what we learned from the survey. We hope this survey-driven content contributes to the information available to those affected by psoriasis and helps you all connect with others who walk the same path.

Sharing your story can make a difference, and we believe each story can change how others understand life with psoriasis.

Still have questions? Comment below, or email us at contact@plaquepsoriasis.com for more information.

By providing your email address, you are agreeing to our privacy policy.


Join the conversation

Please read our rules before commenting.

Community Poll

Do you anxiously anticipate a psoriasis relapse?