Treatment for Children with Spina Bifida | Testimonial

The mother of a child with spina bifida shares her experience using electrical stimulation as part of the physical therapy program. They have been doing electrical stimulation for about five months, and she has made incredible progress with her motor skills. Now, she is rolling, crawling with assistance, and pulling up by herself. In physical therapy, we use electrical stimulation to activate muscles during transitions from sitting to standing, standing up with/without support, and walking. Her mom is highly dedicated to the home program using e-stim and has compiled a fantastic team to help her child get stronger and thrive.
What is spina bifida? Spina bifida is the most common defect of the neural tube. It is a congenital spinal defect in which the spine does not close completely. Usually, at the end of the first month of pregnancy, the neural tube begins to close, and it develops into the brain, spinal cord, and nervous system.
Myelomeningocele is the most severe type of spina bifida. It develops into a fluid-filled sac containing part of the spinal cord and nerves and protrudes from the baby's back. Electrical stimulation is used as part of the physical therapy program for children with neurological diagnoses such as spina bifida and cerebral palsy. There are several ways to use e-stim depending on the functional goal, such as rolling, crawling, standing up, or walking. For spinal stimulation, the electrodes are located on the spinal muscles (the baby's back) to facilitate an upright posture and increase the sensation pathways between the spine and the brain.
Another type of electrical stimulation called Functional Electrical Stimulation can be used on specific muscle groups like the abdominals, gluteus, and legs for facilitating activities such as standing up and walking.
For more information about electrical stimulation, read the blog:
www.solshinept.com/blog/elect...
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Lorena Vargas is a physical therapist with 15 years of experience educating families and helping children get stronger. At Sol Shine Physical Therapy, we encourage the development of motor skills and independence in daily life activities through play and functional activities while combining innovative therapies recognized in the United States and internationally. Lorena is passionate about helping children with low muscle tone, spasticity, coordination and balance challenges, disabilities, and diagnoses such as cerebral palsy, brachial plexus damage, down syndrome, spina bifida, delayed motor development, and neuromuscular conditions.
This content is not intended as a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your doctor or another qualified healthcare provider with any questions you may have regarding a medical condition. All information provided by Sol Shine Physical Therapy and associated videos is strictly for informational and educational purposes. It is not intended to replace the advice of your healthcare provider. The information is not advice and should not be treated as such. The information in this video is provided "as is" without any representation or warranty, expressed or implied.

[@gardenvistas]

So good to see her making incredible progress with the physical therapy and electrical stimulation treatment.

[@muneirahmed5075]

What is electrical stimulation

[@salongeschild]

Thanks for sharing. I am a Mom of a SB Warrior. These videos help. My daughter is 2.

[@SolShinePhysicalTherapy]

I am happy it is helpful! Kids are so resilient and strong! I have seen huge progress with electrical stimulation to activate their muscles and improve sensation in their legs. Thanks for watching the video!

[@odelyflores3376]

Mi hija también tiene spina bífida 🥺

[@SolShinePhysicalTherapy]

Hola Odely, por favor no dudes en escribirnos a [e-mail] para enviarte información de estimulación eléctrica para hacerle a tu hija con espina bífida. Muchas gracias!

[@zahidasaif261]

My son born with spina bifida miningocele .doctor told me we will see after four months😢