Our 36-year-old special needs son that is non-verbal was born with a very rare syndrome what we now know to be Pitt Hopkins Syndrome. For most of his life he has suffered from horribly stomach pain and constipation. He would drop to the ground unexpected anywhere at anytime and just start flailing his arms and legs screaming in pain. Randy had an attack every 1-2 weeks. The pain would last 2-4 days. We have now done 40 hours in the EESystem and we have seen a huge reduction with his pain attacks. Now he has 1 small attack per month and lasting a few hours and he has healthy bowel movements. We’ve noticed he is using his tongue more and hear him trying to verbalize with new sounds and words.