Jealousy. It’s a feeling that we, as the siblings of those who are terminally ill, must hide… yet we go through it all the time. When your sibling is diagnosed, you become second. Your parents stop checking your homework, what TV shows you’re watching, who your friends are. Your needs are just not as significant as your sibling’s. As your parents attend doctor’s appointments, try new medications, and strive to make your sibling as comfortable as possible… you are overlooked. You must put your siblings needs in front of your own, and accept that others will too. As this occurs, you can easily become jealous of your sibling. They get more attention. They get to watch more TV. They get more toys. But they are also your best friend, so you learn to ignore all the little things and focus on them. Focus on making them laugh. Focus on being their sister. On being their brother. Because they are the bravest, most amazing person you know. So that jealousy slowly fades away.

Home is not the only place that we must hide our jealousy. “Normal” siblings are everywhere. At school, in stores, on social media. All of my friends have siblings. Siblings who can talk and walk. Everyone’s brothers and sisters are such a big part of their lives, so obviously other kids talk about their siblings all the time.

“My sister drove me to school today!”

“My brother and I are going to lunch together.”

“My sister watched a movie with me last night.”

“My brother made a hilarious joke this morning.”

All these little things, that everyone takes for granted, would mean the world to kids like me. Everytime someone mentions their sibling, my heart drops. There are so many things that I will never experience. When people complain about something that their sibling did, I stay quiet because I wish that those things could happen to me. I’d give everything to have my sister make fun of me. To have her steal my toys, or tattle-tale to my parents about something that I did. I wish that she would borrow my clothes and never give them back. Or yell at me for saying something embarrassing. My friends will never have to watch their sibling digress. They will never wonder if a word their sibling says will be the last. Or how long it will be until they laugh again. Yet they will also never get to watch their brother or sister be as strong and courageous as mine. They will never be able to say that their sibling did the impossible, and smiled through the challenges of a life-threatening disease. And most importantly, they don’t have an angel watching over them everyday.

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Finding the Unity in Disability

If I don’t have a topic in mind when it’s time to write a column, I read articles. I look into the lives of other siblings of special needs individuals, delving into the struggles, pains, and joys of their respective experiences. From this, I usually find something that I can relate to in my own life, and I let the writing guide me to my own ideas. Read More

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Running Out of Pictures

Now that my sister is gone, photos are one of the main ways I feel that I can connect with her. Whenever I’m missing Blair, I look through old photos and memories. I find it healing to edit photos of us creatively to be symbolic and make it feel new. Here are some of those edits. Read More

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