Meet Angela L.
Loving, and Being Loved, Unconditionally
by Angela Lowry-Sellers
lamellar ichthyosis
Being a parent with ichthyosis was scary in the beginning. When I had my first child in 1988, I was very concerned as to whether he would have ichthyosis. I often contemplated what it would be like to have someone, a baby of my own, that looked like me. But I also knew that living with ichthyosis can be an extremely difficult life to live. When my son was born, he was perfect – not because he didn’t have ichthyosis, but just because he was mine. Five years later, I gave birth to twins — healthy and perfect!
As a parent, I often worried about them going to school and having to explain their mother’s condition to their peers or teachers. What if someone asked them uncomfortable questions? What if they got teased or bullied? I didn’t let it deter me, however, because it was important to me to remain active with their school. I made sure I was at every game, performance, or activity that they were involved in. I had very few incidents where I had to explain my skin condition. My children were very happy and active, and they never once told me that they were being teased about how their mother looked. Although they learned the importance of having good manners in church, school and home, I also believe my children learned innately how to be more compassionate to strangers or those who are different from us.
I feel very blessed to be raised in an environment where I was accepted. My son and my twins, now adults, are so proud of me and have never felt ashamed that I was their mother. Not to mention my precious five grandchildren whose favorite term of endearment is “Mawmaw” — they are my prize possessions! The blessings of great parents and siblings, a loving husband, awesome children, and adorable grandchildren overshadow the unkindness of a world that I have to face daily living with ichthyosis. Their unconditional love is what keeps me afloat and brings such great joy to my life.
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