Cerebral palsy: One mother's journey

Cerebral palsy: One mother's journey


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PERRY, Utah -- Melanie Grimaud straps on her running shoes and gets ready for her daily dose of self-therapy.

As a mother caring for a child who has a disability, running is her key to sanity. She uses each step, each mile and each marathon as a way to nurture herself so that she can stand ready to help her son day after day.

Her strength comes from endurance, and the endurance builds patience.

“He is our little miracle,” Grimaud says of her son, Crew. Seven years ago he suffered a traumatic birth in which he was deprived of precious and critical oxygen for an extended period of time, resulting in cerebral palsy.

Grimaud, who is from Perry, Utah, has three boys. Crew is the youngest.

“As I was expecting him, I planned to right every wrong I had made with the first two kids” she said. “This time around, I would make sure he was well taught educationally and well-mannered. Not that the other two weren’t, but I was really hard on myself and thought I could improve my mothering skills.”

From the moment Crew was born, Grimaud knew her son needed her in a way she never could have imagined before.

Cerebral palsy is caused by brain damage that affects a child's ability to control his or her muscles. The part of the brain that is damaged determines what parts of the body are affected. It is nonprogressive, which means that it does not get worse over time, though the exact symptoms can change over a person's lifetime.
  • 10,000 babies per year in the U.S. will develop cerebral palsy.
  • Children who are born prematurely or who are very low birth weight are more likely to have problems that might lead to cerebral palsy.
  • Some causes of cerebral palsy can be prevented. For example, bike helmets and car seats can prevent head injuries that might result in cerebral palsy

Crew is non-verbal, hard of hearing, has microcephaly, seizure disorder, and needs help sitting, standing and walking.

“Caring for Crew has empowered me. I never thought I would be the one in these shoes, and now that this is my life, I’ve had to learn and grow in ways I never thought possible,” Grimaud said. “This has taught me so much about people, life and most importantly myself.”

Grimaud is a mother who matters. Her days are spent lifting her son in and out of his wheelchair, making him comfortable and working with him over and over on alternative communication methods.

There are days filled with challenges as she tries to explain to him in a language he can understand that the legs he wants to use for running do not work. His little mind cannot yet comprehend the limitations of his body.

“The communication barrier is very frustrating, not only to Crew but to the entire family," Grimaud said.

An article, “The Health and Well-Being of Caregivers of Children with Cerebral Palsy,” published by the Pediatric Journal, says, “Although caregiving is a normal part of being the parent of a young child, this role takes on an entirely different significance when a child experiences functional limitations and possible long-term dependence. One of the main challenges for parents is to manage their child’s chronic health problems effectively and juggle this role with the requirements of everyday living.”

Beyond specific challenges, just the day-to-day reality of caring for a child with special needs can be exhausting.


Caring for Crew has empowered me. I never thought I would be the one in these shoes, and now that this is my life, I've had to learn and grow in ways I never thought possible.

–Melanie Grimaud


"Most of the time at home is spent caring for Crew, which can be very physically and emotionally draining,” Grimaud said. “If there was ever a time in this journey where I felt pushed beyond my limits, I would have to say those long winter months this past year were it. We started to feel like we lost our happy little boy, and it was very hard and exhausting to watch him change despite our efforts to do everything we could to make him comfortable and happy.”

Still, Grimaud said she came to terms with Crew’s disability a long time ago, and now her heart grows when she sees others help her son with acts of kindness.

“Those who care for Crew in any way are my best friends,” she said.

Family members, neighbors, speech pathologists and teachers have all become squares in the quilt of Crew’s life, but the thread that continues to hold him together is always his mother, who daily finds the silver lining.

“At the end of the day, regardless of whatever we’ve been through, I can always count on his arms around my neck, his hugs and kisses,” Grimaud says of her son, who has taught her so much about love.

“I always rock him to sleep, and holding his little sleeping body in my arms is priceless.”

Amy Wilde is a writer living in Brigham City, Utah. You can read her blog at http://amywildeatmosphere.blogspot.com/, follow her on twitter at wildeatmosphere or e-mail her at wilde.amy@gmail.com.

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