Pete in MI
New member
And more pain.
Posted 23 hours ago
It hasn't let up all day and he is miserable. We have increased his doses of pain meds to every 2 hours from four hours and it doesn't seem to help. Brian is getting very frustrated.
He takes a medicine designed to minimize nerve pain every 8 hours. His pediatrician has increased each dose from 5 mils to 8 mils to see if that will help.
It looks like we're in for a long night.
We heard from the National Institute of Health today. They diagnosed and named Brian's disorder (gnathodiaphyseal dysplasia) back in 2001 from his case study. I asked how the research was going and they said that "...regretfully, little has been done." They've pretty much hit a brick wall.
We watched Left Behind together last night and plan on watching part II tonight if he can. He really struggled last night, he hurt so bad.
Thanks, as always, for your thoughts and prayers!
Doug, Carol and Brian
Posted 23 hours ago
It hasn't let up all day and he is miserable. We have increased his doses of pain meds to every 2 hours from four hours and it doesn't seem to help. Brian is getting very frustrated.
He takes a medicine designed to minimize nerve pain every 8 hours. His pediatrician has increased each dose from 5 mils to 8 mils to see if that will help.
It looks like we're in for a long night.
We heard from the National Institute of Health today. They diagnosed and named Brian's disorder (gnathodiaphyseal dysplasia) back in 2001 from his case study. I asked how the research was going and they said that "...regretfully, little has been done." They've pretty much hit a brick wall.
We watched Left Behind together last night and plan on watching part II tonight if he can. He really struggled last night, he hurt so bad.
Thanks, as always, for your thoughts and prayers!
Doug, Carol and Brian
Love in Christ, Ma & Gamma Betty