Andy, I believe that we could find all the information that is out there through the Diabetes Foundation. I wouldn't know where to begin to get the funding to hire an individual to modify it and meet the needs of our children with CAH. This disorder is considered rare therefore the fame and glory are not there to peak the interest of any scientists. And as such, there wouldn't be much money to be made from sales with the relatively few people who would benefit from it's production, compared to diabetes that is anyway. Don't get me wrong, I am not saying that ALL scientists are without compassion, but if the funding isn't there there isn't much one person can do. Perhaps if we found the right place to call on and we all made a plea for help for our children's sake we could get somewhere. I will call the Diabetes Foundation and see what I can find out. Then maybe I can find out the name of the company that makes the "pager" type system for them and contact them. I am sure it would be necessary to have an endo involved in there somewhere guiding them through it. If we are successful, it would mean that we would have to finger stick our children a couple times a day, but the outcome could make a difference in their growth potential and, most importantly, the possibility of an adrenal crisis. If something like this was available to us two years ago we could have picked up on the fact that 18 out of 19 patients weren't getting the proper amount of Liquid Cortef during that time. Imagine what heart ache that would have saved. Perhaps this is wishful thinking, but it sure is worth a try. Anybody else with me or have any other ideas?