Living with hidradenitis suppurativa (HS) has been one of the greatest challenges of my life. For many years, I suffered in silence as I began having flare-ups at a young age. I felt isolated and misunderstood while coping with the pain, drainages, scarring, surgeries, and the emotional toll that this disease can bring. 

I presently live with Hurley’s Stage III hidradenitis suppurativa, the most severe form of HS. My flares occur throughout my body, affecting not only my physical health but also my appearance, confidence, relationships, and daily activities. Over the years, I have been under the care of dermatologists and plastic surgeons, undergoing treatments and procedures in an ongoing effort to manage this chronic condition. 

This coloring book was created from a place of understanding, resilience and hope. It is for every person who has ever hidden their scars, canceled plans because of a flare, struggled to explain their pain, or felt alone in their journey with HS. 

Hidradenitis suppurativa is more than a skin condition- it is a lifelong disease and autoimmune condition that impacts every aspect of life. Yet despite the challenges, we continue to show incredible strength each day. We learn to adapt, advocate for ourselves, and keep moving forward, even during the hardest moments. 

My hope is that these pages provide a sense of comfort, creativity, and connection. Whether you yourself are living with HS, are supporting a loved one, or simply learning more about this condition, I want you to know that you are not alone. Your scars tell a story–not of weakness, but survival, perseverance, and courage. 

Thank you for allowing me to share a part of my journey with you. May this book also serve as a reminder to be gentle with yourself, celebrate your victories, and never lose hope. 

With love, understanding and solidarity,

Krystal Coleman

HS Warrior, Advocate, and Author