Extra Effort Brings Extra Blessings
Building Ben's Brain is a blog documenting the trials and victories experienced with a comprehensive neurological program for a teenager with severe autism.
Second Chances
Building Ben's Brain is a blog documenting the trials and victories experienced with a comprehensive neurological program for a teenager with severe autism.
Brain-Injured Children Improve with Gillespie Approach–Craniosacral Fascial Therapy
Hi. I’m Dr. Barry Gillespie. I practice in the King of Prussia Medical Center in King of Prussia, Pennsylvania, in the United States of America. Today I’m going to talk about Gillespie Approach–Craniosacral Fascial Therapy and brain-injured children.
Child Struggling with Bedwetting, Back Pain, and Strabismus
For Gillespie Approach practitioners, I had a very interesting visit with the young boy from the October 4, 2018, post connecting his lower body issues to his strabismus.
‘Programme of hope’ for parents of children with special needs coming to Wexford
Matthew Newell and his Family Hope Centre (FHC), from Philadelphia, will present the first of two training lectures and introductory programs for parents.
An Update From Mom on the Toddler Struggling to Breathe
A seventeen-month-old boy is at the Family Hope Center (FHC) this week from the South. His doctors say that he needs throat surgery. The child cannot open his tight mouth and is on a feeding tube.
Hypotonicity in Babies with Special Needs
When you are working with a special-needs baby/child, s(he) may be very loose at the extremities, but the core of the body can be very tight.
The CFT Web of a Toddler with a Brain Injury
A seventeen-month-old boy is at the Family Hope Center (FHC) this week from the South. His doctors say that he needs throat surgery. The child cannot open his tight mouth and is on a feeding tube.
Brain Injuries, Birth and CFT/IDM
Seeing children with “birth defects” at the Family Hope Center, I only can think how their lives may have been better with the BBS/CFT/IDM model at birth.
Our Journey of Hope–Six Month Reevaluation
At our first visit in November 2014, it was verified that Aaron was neurologically 45.4 months (3 years 9 months), resulting in functionality of 54% with a severe brain injury. Â We received a robust therapy program that we were charged with leading him through at home.