Cri du Chat Awareness Week – May 1 to 7 2016 (Day 6)

Cri du Chat Syndrome is a big unknown for many doctors and therapists out there.  Although we (the parents) know that this is a spectrum and that the diagnosis we receive is worst case scenario, many doctors still believe that our kids will accomplish nothing.

If you’ve been following Lessons from my Daughter for awhile, you know Emily is doing lots.  She is her own person and regardless of the challenges, she continues to move forward, she continues to learn and grow!

Here is what you can find about the development of kids with Cri du Chat Syndrome on the  5p- Society website

Development

Here’s some things to look for when it comes to development with 5P- syndrome.

  • Gross and fine motor skills
  • Expressive speech and language delays
  • Communicate by sign language, communication devices, gestures and a few basic words
  • Poor muscle tone (hypotonia)
  • Slow growth associated with failure to thrive
  • Constipation
  • Low Birth weight
  • Normal Life expectancy
  • Young adults may have premature graying
  • Most children walk, although at a slower pace and with a guarded gait.
  • Majority of children do not achieve toilet training.
  • Many children and adults have sleep issues.
  • Some have visual problems.
  • 80% of children have a hearing condition known as hyperacusis (hypersensitivity to noise).
  • Children with CdCS undergo typical changes in puberty at the appropriate age
  • Many children have seizures ranging from Grand Mal to silent.
  • Very few adults are able to work with supervision.
  • Even fewer adults are able to live independently.
  • Most children with CdCS have behavioral issues
  • Attention Deficit Hyperactivity Disorder (ADHD).
  • Poor concentration.
  • Impulsiveness and OCD.
  • Biting, hair pulling, pinching and hitting.
  • Temper tantrums, stubbornness, frustration, self-biting, head banging and skin picking.
  • Autistic-like characteristics- some are dually diagnosed with Autisim.
  • Hand flapping, string twirling and rocking.

As you can see, there is a wide range of challenges, not all kids face the same struggles but all of them do face some struggles.

Our kids have faced more challenges in their young life that many people will face in their whole life.

Regardless of the struggles, issues and challenges…

Emily is still smiling and laughing!

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Emily continues to learn and grow!

Emily will not let her syndrome define her and all the kids I have met with Cri du Chat Syndrome are the same…

They define Cri du Chat Syndrome!

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We have a facebook page: If you want short updates and timely pictures of the little things that are happening in our life, please like and follow Lessons from my daughterβ€˜s page.

You can also find me on Twitter at @plebrass

I am on Pinterest too: Lessons from my Daughter

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#CruduChatSyndrome

That happened!

For 6 years now, we drive Emily to and from school every day as we had her move into a school of our choosing, outside of our neighborhood.

When the forms are signed for this kind of transfer, you (as a parent) agree to be responsible for transportation.

We have juggled our schedules and made many adjustments here and there to be able to do this but here we are, nearing the end of Grade 11, only one more year to go on this “driver” plan we have with the school district.

This morning on the way to Emily’s school, I forgot to go to her school!

Yes, that happened!

We were chatting along and as I pulled in my work parking lot I realized that Emily was still with me πŸ™‚

I looked at her and said: “What am I doing?”

To which she answered by bursting out laughing.

When I asked her why she didn’t say anything, she laughed harder…

Lucky for me, the school isn’t far from my work so off we went to school and I was just in time for my Thursday morning 9am meeting.

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