Hear from people taking SPEVIGO
Individuals featured here have been compensated for the time spent to share their stories.
Life on the dance floor
Jordan, whose choice is SPEVIGO
Prior to my GPP diagnosis, I was working on several things, like renovating a cabin, applying to grad school, and becoming a dance instructor. But then, in 2021, I started to feel lethargic and couldn’t move my body as much as I usually could. Symptoms came on suddenly and were severe. Pustules began to appear, and the skin along my scalp began to crack. They covered my scalp, chest, and nail beds. Once a dance instructor, I could barely move my body.
So, I began an extensive search for treatment options, going to the library to do research and reading as much as I could. I was focused on learning more about GPP and kept the faith that there had to be a medication that would help me.
When I heard about SPEVIGO, I felt hope.
I was so relieved to learn that there was a specific treatment for GPP.
My doctor and I discussed the pros and cons of treatment, and we both felt comfortable moving forward with SPEVIGO.
Sharing my experience could bring me to tears. Now, I look in the mirror, and I see more of myself. I’m so grateful.
GPP can be a challenging, painful journey. Don’t give up.
Individual results may vary based on many factors, including elements like the severity of your GPP, your treatment plan, and any other conditions you may have.
GPP=generalized pustular psoriasis.