Foundation for Ichthyosis & Related Skin Types® (FIRST) member Cynthia carries a message so full of hope, it transcends the label of ichthyosis—offering inspiration to anyone who is challenged with a physical difference. Ichthyosis is a family of genetic mutations of the skin characterized by dry, scaling skin that may be thickened or very thin, and most forms of the disorder are rare. Each year, more than 16,000 babies are born with some form of ichthyosis and it affects people of all ages, races, and gender. Cynthia’s belief: relationships, compassion, and her laugh are among the many things that define her. Not her skin. Read Cynthia’s story.
One of the challenges in learning to live with skin that is affected by lamellar ichthyosis has been to develop an understanding that I am not innately a flawed person. Because ichthyosis is so visible, it can feel like a brand of some deeper disorder. But it is not. It is simply a disorder of the skin and probably only a failure of an enzyme or two.
When I was born in 1950, lamellar ichthyosis was poorly understood. I endured many painful experiences. I was hospitalized for a month of treatment trials as an infant. I had all my hair cut off as a third grader to try a treatment on a nearly bare scalp. As a grade-schooler, I was kicked out of a public swimming pool while taking lessons with my neighborhood friends. As a teenager, a hair dresser with whom I had an appointment refused to cut my hair once she saw my scalp.
Nearly everywhere I went people asked “What’s wrong with you? What happened to you? Were you burned?” I remember well the sense of embarrassment and shame that I was different. I assumed that the something wrong with me was way more than skin deep.
Thankfully I was also around people who knew that there was much more to me and to life than my skin. My family, nuclear and extended, my teachers, and others loved me for the normal, complete person that I was and helped me put ichthyosis in its proper place in my life. My healing continued as I got married, had wonderful children, worked in and out of our home, pursued my hobbies and developed a relationship with God through Jesus Christ.
It was God who showed me it’s never too late to have your dreams come true when He brought me my first horse at age 52, satisfying a lifelong longing for a horse of my own. My husband and I cherish our relationships with each other, our sons and their beloveds, our friends, our horse and cats, and other animals we come in contact with. We enjoy physical activity and being out in nature. I also love to sing and to paint in watercolor.
I understand the courage it takes for anyone with a visible difference to leave the house and participate fully in life, and I admire them. A person is interesting when they engage wholeheartedly in activities and relationships that they value. Having a skin condition is irrelevant to most of that.
Recently I was talking with a surgeon a couple days before he was going to operate on my spine. I wanted to alert him to the condition of the skin on my back so he wouldn’t be surprised at the time of the surgery. I was pleased that without thinking too much I said, “The skin on my back is affected with lamellar ichthyosis. You won’t have to do anything special with it during surgery.” To me that’s different than saying “I have ichthyosis,” or “I was born with ichthyosis” or some other way of saying “I’m ashamed of my skin.”
So, it was a triumph, when without a sense of shame, I put ichthyosis in its place, as a condition of my skin. My sense of myself as a valuable person was intact. My interests, my relationships, my compassion, my laugh are among the many things that define me. My skin does not.
The Foundation for Ichthyosis & Related Skin Types, Inc.® (FIRST) is invited as a guest blogger and does not endorse or serve as a product representative for Coolibar.