Anyhow, I hope you keep us updated on his journey with it . Getting a diagnosis for a child with complex medical issues isn't always easy.

I feeld very scared, too, but am hopeful.

The views of these organizations are their own and do not reflect the official position of CDC. Because microcephaly can range from mild to severe, treatment options can range as well. During pregnancy, microcephaly can sometimes be diagnosed with an ultrasound test (which creates pictures of the body).

Because it is difficult to predict at birth what problems a baby will have from microcephaly, babies with microcephaly often need close follow-up through regular check-ups with a healthcare provider to monitor their growth and development. He also has hypoplasia or partial agenesis of the corpus callosum. Some children with microcephaly will have normal intelligence and a head that will grow bigger, but they will track below the normal growth curves for head circumference. just to name a few. I was just hoping for a positive story of someone who defied the odds. Nope.

Have you tried the micro board on yahoo? I don't think anything will paint the whole picture, honestly. Babies with mild microcephaly often don’t experience any other problems besides small head size. Get the latest public health information from CDC: https://www.coronavirus.gov I believe it's only microcephaly if your child's head is 2 standard deviations below the growth curve at all. Anyway, although we also know we can't predict his future, so far he has met all his milestones (he crawled at 6 months and is cruising now), except for speech but I think that is b/c of his hearing loss. .

These services, known as early interventionexternal icon, can include speech, occupational, and physical therapies. Download slidespdf icon | Download transcriptpdf icon. First of all-- both of your kids are adorable! Thank for for the positive story! Microcephaly is a lifelong condition. Microcephaly is a condition where a baby’s head is much smaller than expected.

The National Institute of Neurological Disorders and Stroke (NINDS), one of several institutes of the National Institutes of Health (NIH), conducts and funds research aimed at understanding normal brain development, as well … Why do you think I'm on the special needs board and not her age board? She's very small for her age, so if you look just at her size, she's microcephalic. The measurement value also may be designated as less than the 3rd percentile. That is it and at 2 yo cannot talk,walk, sit, roll or feed herself. CDC scientists announced that enough evidence has accumulated to conclude that Zika virus infection during pregnancy is a cause of microcephaly and other severe fetal brain defects. . The EEG showed abnormal activity, but DD is deafblind and very very sensory seeking (constantly rocking and banging her head) so we're not sure if that was what was abnormal or there were actually abnormal waves. Major birth defects data from population-based birth defects surveillance programs in the United States, 2006-2010. . Saving Lives, Protecting People, National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, 5 Ways to Lower the Risk of Neural Tube Defects, Birth Defects are Common, Costly, and Critical, U.S. Department of Health & Human Services, Developmental delay, such as problems with speech or other, Intellectual disability (decreased ability to learn and function in daily life), Feeding problems, such as difficulty swallowing, Certain infections during pregnancy, such as, Severe malnutrition, meaning a lack of nutrients or not getting enough food, Exposure to harmful substances, such as alcohol, certain drugs, or toxic chemicals, Interruption of the blood supply to the baby’s brain during development. National Birth Defects Prevention Network. To learn what it’s like to live with a birth defect and how these conditions affect people’s lives, read these real stories from people living with birth defects and families with children affected by birth defects.



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