I am a girl with Cystic Fibrosis Related from the United Kingdom and have a lot of worries about understanding if it is possible or how I would ever potentially travel to United States either for a short holiday or longer duration. As I know that the United States has different costs for medical expenses and treatment.
I am wondering if anyone has any possible advice or information about this or personal experience with travelling properly.
I am wondering if anyone has any possible advice or information about this or personal experience with travelling properly.