8 year old diagnosed with x link cerebral ALD march 16, 2018, 14.5 loes score. He has A LOT of energy but being almost blind hard to find outlets all day long. What are people out there doing for the “dad, what can i do now” and the total impatience. What medicines are people using to provide some calm?
Hi Ben. I’m so sorry that you and your son are going through this. I realize your posting was several months ago now . I’m guessing you’ve spent more time than I can imagine Googling, but if by chance you haven’t, I just Googled activities for blind/sight impaired children and found lots of possibilities for you and your son depending of course upon other circumstances. You’re in my heart as I type this. Many, many years ago I had a little brother with x-linked ALD.
Hello Matt and family! How are you and Ben doing these days? I checked out your site and was struck by the kindness and generosity of those in your circle of friends and in your community.
The people here would love to know how things are going. Have you found activities that Ben can do despite his limited vision? How about an update?