Treatment for Kids with Spina Bifida | Testimonial
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- āđāļāļĒāđāļāļĢāđāđāļĄāļ·āđāļ 6 āļ.āļĒ. 2024
- 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.
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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.
Wow. That is a lot of progress! Hope she keeps progressing and getting stronger! âĪ
Hurray! I wish all is well with the beautiful girl and her family!
She very cuteðĨ°
More power to dear
Itâs a disorder. Letâs not call it a disease maâam. My son also suffers this. Iâd advice u watch alot of related videos on TH-cam so youâd be able to asist your don at home. I pray he gets better soon ð
ðĒMy son has the same disease, but it is to a greater degree than your daughter, and he suffers a lot because in my country he was not treated. This is a very painful thing. My son is not yet three years old.
With treatment, they will be able to deal with it much better. They will have to live with weakness or some degree of paralysis in the lower extremities. But they are just legs and many have lived through similar conditions. Your son will live through it fine with your support and the right medical guidances. Good luck and stay strong. Youâre a father. No matter what, you need to stay strong for your boy