OSKALOOSA, Iowa – World Down Syndrome Day is Sunday. It falls on March 21 as a result of Down syndrome is attributable to having three of the twenty first chromosome.
Seems that additional chromosome in a single little lady is making up for what her mom is lacking.
Like all 8-year-old, Khia loves watching her pill and consuming sweets. She’s the youngest of Lynette Gordon’s 5 children, children she wasn’t positive she’d be capable of have after being recognized with Turner syndrome as a teen.
“Turner syndrome is a situation the place the lady is lacking one of many intercourse chromosomes. And if that’s lacking in all the cells, then it’s extremely unlikely that she’s going to be capable of reproduce,” Dr. Neil Mandsager, maternal-fetal drugs doctor at MercyOne, mentioned, “but when it’s solely lacking in a number of the cells, what we name a Mosaic Turner, then it’s potential that she will have kids.
Lynette remembers Dr. Mandsager consulting when she was pregnant together with her twin boys, and once more when she had superior maternal age when pregnant with Khia. She mentioned her ultrasounds indicated every little thing was high-quality.
“It’s so true once they say a mom’s instinct as a result of, all through my entire being pregnant, I felt like there was one thing unsuitable.”
It was Nov. 16, 2012 when Khia was born. It was additionally then once they observed she was displaying traits of Down syndrome.
“About three hours after she was born, our physician got here in,” Lynette recollects, “and as quickly as he walked via that door, I may simply inform one thing was not proper.”
As a single mom with 4 children at dwelling, Lynette was overwhelmed and uncertain if this was one thing she may tackle by herself.
“I felt responsible. I felt like possibly she can be higher off with a two-parent household,” Lynette mentioned, “however then when she would smile at me, I used to be like there’s no method. She’s right here, she’s mine, she was meant to be right here with me.”
Lynette quickly realized Khia accomplished her household in additional methods than one.
“I’m lacking a chromosome and he or she has the additional.”
As we strategy a day that brings consciousness to a dysfunction that impacts so many households, Lynette has a message.
“I don’t even take into consideration Down syndrome after I have a look at her. I don’t deal with her any completely different. I would like individuals to see her skill and never her incapacity, and to see how extra alike she is than completely different as a result of she undoubtedly is.
Khia is blissful and wholesome, with no main well being issues associated to her analysis. She’s going to high school the place she’s studying the way to learn, and conserving her mother and siblings on their toes at dwelling.