Late Mylanization Syndrome

Another Story Blind & Mentally Disabled - "sees and reads, walks with assistance,  and is developing language."

This testimony of Emily Papin will truly encourage any parent who has a child facing Late Mylanization Syndrome.  There's still hope for a future.

Emily Papin

"Emily was diagnosed with "Late Mylanization Syndrome' and it was suspected that she was autistic. She had tried many different programs in France and Italy, but was falling further behind. She could walk only a few meters, was not independent in any task, did not talk, could not understand well and drooled all day. We were told to put her in an institution and not distress our family. We were deeply depressed as we were told she would never get well. We began her new program with great hope 5 years ago, as we now knew where she was injured and was given a specific program for her problem.

“For six years Matthew Newell was somebody very important in our work with our daughter Emily. She can read beautifully, she runs 5 km. nonstop, her language is improving all the time, her self-awareness and independence continues to always progress. Matthew was one of the most humane people that we met during our visit, and at the same time the one person who explained to us our physical program with great skill. He always gave us very difficult programs, but very interesting and according to what our child needs for her development that he helped in her pathway to success. We will always thank him for his kindness and his understanding and we have a high respect for the work that he and his wife Carol are doing and we will continue trusting him.“

J. P. & Florence Papin, Daughter Emily, 11 years old
France

Learn more about Late Mylanization Syndrome