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5 things to do after someone you love receives a special needs diagnosis

September 3, 2014 by Gillian Marchenko

Evie blue eyes

5 things you can do after a family you love receives a special needs diagnosis

I’ll never forget the moment I was told my baby had Down syndrome. I was sitting next to her incubator in a hospital, holding on to her heel. I remember being pleased because her eyes were open. She stared intently into mine. The doctor spoke and the words ‘Down syndrome’ crashed over me. Suddenly I was alone without a buoy, paddling like crazy in a sea of worry and grief.

When a parent first hears, ‘your child has a disability,’ it can be devastating. For friends and family, it can be a trying time too. Sometimes people end up doing nothing because they aren’t sure what they are supposed to do  or how to help.

If someone you love has recently been told about a special needs diagnosis, read on.

5 things friends and family can do to support a loved one with a new special needs diagnosis

  1. Show up: Sometimes friends and families stay away from loved ones with a new diagnosis because they don’t know what to do. Showing up and letting the family know you care makes a huge difference in their lives.
  2. Research the diagnosis: If you don’t know anything about the disability, do a little research. If you look on-line, make sure the resource is-to-date.
  3. Refrain from platitudes and pat advice: If a family is grieving a new diagnosis, the best thing to do is to let them know you care, and to listen. Don’t give them pat advice or minimize their situation with clichés or flippant memorized verses from the Bible.
  4. Talk to your children: Once you learn about the disability, if they are at an appropriate age, explain the diagnosis to your children. Stigma is broken with educated minds. Explain disability in a way that isn’t scary, and that tells kids that we all are made differently, and that is OK.
  5. Give tangible help: Bring a meal, watch other children, and visit them in the hospital. Offer gentle, tangible help.Everyone needs it, but especially families in crisis.

After our first special needs diagnosis, some of my friends and family didn’t know what to say or do. But one instance of incredible support stands out in my mind. I remember my brother calling me.  I can’t remember exactly what he said to me, but it went something like this: 

“I’m not going to pretend I know what you are going through right now, but I went on-line and found out some things I can do and say to help you.”

He told me that he loved me, and that he was there for me.

That phone call was one of the most precious moments of my life. He cared enough to show up however he could. He cared enough to learn about Down syndrome in order to better support our family. My prayer is that you love and support your loved ones like my brother supported me if you ever find yourself in that situation.

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Gillian Marchenko

Gillian Marchenko is the author of Sun Shine Down, a memoir about her daughter Polly's birth and diagnosis of Down syndrome while the family lived in Ukraine. She writes and speaks about special needs, depression, adoption, and deep belly laughs and lives in Chicago with her husband Sergei and their four daughters. Most Sundays, you’ll find Gillian in the back row of the church Sergei pastors, bouncing a toddler on her knee and giving the older girls the look. The world is full of people who seem to have it all together. Gillian speaks up for the rest of us. Check out her website at www.gillianmarchenko.com.
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Latest posts by Gillian Marchenko (see all)

  • For parents who aren’t ready to celebrate Down syndrome during Down syndrome Awareness Month - October 7, 2015
  • Love pushes us to the front of the crowd, reflecting on a dual diagnosis - April 1, 2015
  • Letting go of self-sabotage on the special needs journey - March 4, 2015

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Filed Under: Down Syndrome, Gillian Marchenko, Uncategorized Tagged With: 5 things to support a special needs diagnosis, Down syndrome, Gillian Marchenko, special needs diagnosis

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