October is Rett Syndrome Awareness Month


Makayla was diagnosed with Rett Syndrome in April of 2015 at the age of two.

At about 18 months, we noticed she had started some repetitive hand motions, and her pediatrician was a little concerned that she did not have many words.
She had learned some sign language, and was saying ‘mama’ and ‘dada’, but that was it. Then she suddenly stopped all of that. At her 2 year old check-up,
the pediatrician referred us to BabyNet, SC’s early intervention program.
Our BabyNet caseworker recommended that she be evaluated by the Greenwood Genetic Center.

We met with Dr. Mike Lyons at GGC’s North Charleston office. He evaluated Makayla and suggested some genetic testing. A few weeks later, he broke the difficult
news of Makalya’s diagnosis in a most gracious way. He also immediately recommended we meet with Dr. Steve Skinner in the Greenwood office, who is
an expert in Rett syndrome. Though we were overwhelmed at all we needed to know, Dr. Skinner, Fran Annese, and the whole staff were wonderful at that
first meeting, giving us all the time we needed to ask questions. Their compassion for families like ours really showed through that day and continues
to this day. They have remained accessible and informative, staying up to date on any changes or developments related to Rett syndrome and sharing
those as appropriate. They have been so encouraging for our family as we navigate through what, for us, are uncharted and scary waters. We have also
enrolled in the Rett Syndrome Natural History Study through GGC.

But, Rett Syndrome does not define Makayla.

Despite her diagnosis of Rett syndrome, Makayla is a happy little girl. We are blessed that she can do the things she can do! She can still walk, unlike
so many girls with Rett syndrome, but she also skips and runs in short distances when she is excited. She loves being outside, and her favorite thing
to do is play in water, at the pool, the beach, and even in the bathtub. Close behind that is riding her rocking horse, which she would stay on for
hours if we let her.

She also loves to watch sports, particularly basketball and football. With four older brothers, she has had many opportunities to watch games! And, she
loves to dance, especially to Michael Jackson and Johnny Cash!

Makayla’s diagnosis has been an incredible challenge for our family, but learning about and dealing with Makayla’s condition has done a couple of amazing
things. First, it has drawn us closer together as a family. Second, it has brought out a love in each of us that we just did not know was there. I
do not think there is any sweeter sound than when Makayla gets tickled and laughs and laughs. Our boys at times even vie for a turn at holding her,
and often we have to kick them out of her room at bedtime! She has and continues to bless our family in so many ways.

Thanks to Gov. Henry McMaster, SC is officially joining with the Rett syndrome community in honoring those families who face these challenges every month of the year. Join with us in supporting families like the Gunns, whose story is below. Learn a little about Rett syndrome and be a part of advancing research toward a cure!


To learn more about Rett syndrome visit rettsyndrome.org

By Hollis Gunn, Mt. Pleasant, SC
Mother and son

A Rare Beauty

The lobby of the JC Self Research Institute at GGC was transformed into a garden – of sorts. The art exhibit titled ‘Rare Roses’ consisted of 12 paintings that depict real roses with genetic variations. The series was created by Nicole Shannon, an artist from Greenville. Nicole was inspired by her son, who has a rare genetic disorder, and other individuals with genetic differences. Quinn, now 4, was born with a myriad of health issues and ...

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