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The information and materials accessed through or made available for use on any of our Sites, including, any information about diseases, conditions, treatments, or medicines, are for informational purposes only. The Content is not intended to be and is not a substitute for professional medical advice, diagnosis, or treatment, and your participation on our Sites does not create a healthcare professional-patient relationship. You should consult a doctor or other qualified health care professional regarding any questions you have about your health or before making any decisions related to your health or wellness. Call your doctor or 911 immediately if you think you may have a medical emergency.message sent
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Girl Born With Progressive Disease SMA on the Mend, Has Big Plans for the Future
As four-year-old Celine practiced her half turn, her mother, Amber Joi-Watkins, said she was just an infant, she and her husband Tom Domalski felt something wasn’t quite right with their baby girl.
“When she was about three months old, I noticed that she wasn’t rolling or kicking. We were just doing some of the things that I saw other kids doing at my ‘Mommy and Me’ yoga class,” said Watkins.
At first, Watkins’ pediatrician told her Celine was just fine. But she could tell something was off. A few months later she was told to find a neurologist right away. The diagnosis was spinal muscular atrophy or SMA.


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