Hi everyone,
I am new here.
I am a Thalassemia patient, 28 years old, female, living in Switzerland. I plan to have a scholar visit for my studies in the United States (probably in California) for a duration of 6. Since, my biggest concern is my treatment during the stay in the United States, I would like to get some information about health care system and expenses for Thalassemia patients there. I have B-Thalassemia Major, on monthly transfusion (3 packs every 4 weeks) and Exjade (1750 mg per day).
I would like to know whether or to what extent the treatment expenses of patients, similar to my case, are usually covered by insurance companies within the United States. If yes, how can I apply for such an insurance? Is it possible to get insurance for only 6 months? Shall I be employed in the US in order to get a health insurance? How much usually does a health insurance cost for my case? And finally, how can I find a medical center and a doctor for the duration of my stay in the US?
I would be very grateful if you could give me those information,
Best regards
Som