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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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My Patient Story: Amanda
My son was diagnosed with Spinal Muscular Atrophy (SMA) at about two months of age. He wasn’t hitting milestones and when I mentioned it at this one month check up, his pediatrician pushed it off as he was a lazy baby. I thought his issues may have been related to complications during birth.
I had a high risk pregnancy and his delivery was troubling, forceps had to be used. Looking back I know that was due to his muscle weakness. This is my second child and he completed our family.
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