Opinions on Florida and living with CF; Doctors, Clinics, Medicaid, etc.

[65RosesMomof2]

My daughter is almost 18 and has CF. She has been on disability for almost a year. I am considering moving to Florida from Ohio. She is trying to decide whether or not to come. I believe the more stable weather will be a benefit to her. She has been seen at Rainbow in Cleveland her entire life. I need info on the clinics in Florida. How they stand up if a lung transplant is ever required. And insurance matters. She is currently covered under her Dad's private insurance (but not sure how long) and medicaid because of her disability. This is a scary move and decision to change providers after all this time so any info would be very helpful.

 

[Oboe]

Here's a similar thread from a few months back. My post in it is still pretty relevant. If you have any questions feel free to ask.

http://forum.cysticfibrosis.com/thr...osis-and-Florida-Live-in-Florida-Please-Reply!