myelomeningocele - #17357
I recently learned that my baby has been diagnosed with myelomeningocele, a form of spina bifida, which is a neural tube defect. This news came as a shock, and I’ve been trying to understand what this condition means for my baby’s health and development. I understand that myelomeningocele is when the spinal cord and nerves are exposed due to a gap in the spine, but I’m still unclear about the long-term effects and how it can be treated or managed. I know that early intervention is key, and some treatments can be done soon after birth to close the gap, but I wonder if there are any natural or complementary therapies that can support the treatment process. I’ve heard of physical therapy and surgery, but I’m hoping there might be other options that can help with mobility, strength, and overall development. What are the risks associated with myelomeningocele, and how can it affect a child’s motor skills, bladder function, and cognitive development? Is there a way to prevent complications, or are these risks inevitable? I’ve also been researching how to best support a child with myelomeningocele using holistic and natural methods. Are there Ayurvedic treatments, such as specific herbs or therapies like massage, that can improve circulation and nerve health in children with this condition? Has anyone here had experience with myelomeningocele or known someone who has? What treatments or therapies were most helpful, and how did you manage the emotional and physical challenges of this diagnosis?
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