I went to a hospital like this myself when I was 2-18 in Texas for scoliosis. I was placed in multiple types of braces and then eventually had surgery once I turned 10 and then continued to see the doctors there until I turned 18 and are no longer eligible. It was a childrens hospital that you had to be referred to by your doctor and it was completely free, everything was taken care of by donations, however this particular hospital is not affiliated w/ Shriners childrens hospitals. Although my parents had insurance, they were never even asked to show an insurance card from what they told me. My parents told me they asked how much the surgery cost and all they were told is "it is well over $100,000...but its nothing you need to worry about".
I just pulled up the hospitals website and they still have the same practices. No cost of any kind to the families.
Was it Texas Scottish Rite? My son has been a patient there since he was 6 days old. We went for a visit Friday and they collected insurance information. They told us that they would be begin billing at some time in the near future.
I know that someone else asked if many children who were patients at Shriner's had insurance. I can only speak for our experience at Scottish Rite, which is also supported by the masons. The answer is YES!! We have insurance, and were referred by his pediatrician while still in the hospital.
We went to several other doctors to get second, third, fourth opinions. All of them not only recommended the same treatment, they recommended that Scottish Rite treat him. We are in the Dallas area also, so it isn't a small town. When you are dealing with a rare condition, you go where the experts are.
I have no problem paying co-pays etc... because the quality of care that he recieves is phenomenal. He is 10 years old now and I will say that several years ago, those co-pays, deductibles, etc... would have been pretty painful.
My bigger concern with this new policy is that our insurance has limitations. Our insurance will only cover a new prosthesis every 24 months. My son is on his 8th leg in 10 years. They do everything possible to extend the life of the limb, but eventually, it is just outgrown. I do have some fear that by accepting insurance, they will have to follow the insurance limitations. Hopefully, they will find a way to make it work. Kids grow and prosthetics don't!