Hello . I should probably start with the basics; I'm Jonathan, I'm 27, I've had Crohn's Disease since about age 12 and I live in Norfolk in the UK .
I recently got engaged, though as my fiancee lives in New England, we've been looking into which of us should move country; her to the UK or me to the US. There's pros and cons of each, but what could make a big difference is how much healthcare might cost for me over in the US. I'm aware that's not an easy question to answer and is further complicated by the current talks of healthcare reform in the US, but I have got a couple of questions that I hope someone on here can help me with, please .
Is it generally possible [and advisable?] to find an insurance policy that recognises and covers things related to Crohn's Disease? Would it be a case of easy to find one that will, but would cost considerably more or is it more common that you'd find policies would specifically exclude things related to existing conditions like Crohn's and you'd have to look harder for one that would cover it? I gather a big factor could be what's available through your employer.
I'm currently lucky in that my condition is stable and rarely troubles me, I don't require regular trips to healthcare professionals for it, etc, but I do have my daily medication of Pentasa, along with suppliments like a folic acid tablet and an iron tablet. Would I be advised to be getting such medication through insurance [assuming that's possible] and just pay the co-pay or is it better to not factor those in and just pay "over the counter" type prices once I have a prescription for them?
I'm not trying to pry by asking for exact figures people have been paying, just trying to get my head around the system for the moment and finding out what would be the best/most sensible/usual way things are done for people with Crohn's in the US .
Thank you!
I recently got engaged, though as my fiancee lives in New England, we've been looking into which of us should move country; her to the UK or me to the US. There's pros and cons of each, but what could make a big difference is how much healthcare might cost for me over in the US. I'm aware that's not an easy question to answer and is further complicated by the current talks of healthcare reform in the US, but I have got a couple of questions that I hope someone on here can help me with, please .
Is it generally possible [and advisable?] to find an insurance policy that recognises and covers things related to Crohn's Disease? Would it be a case of easy to find one that will, but would cost considerably more or is it more common that you'd find policies would specifically exclude things related to existing conditions like Crohn's and you'd have to look harder for one that would cover it? I gather a big factor could be what's available through your employer.
I'm currently lucky in that my condition is stable and rarely troubles me, I don't require regular trips to healthcare professionals for it, etc, but I do have my daily medication of Pentasa, along with suppliments like a folic acid tablet and an iron tablet. Would I be advised to be getting such medication through insurance [assuming that's possible] and just pay the co-pay or is it better to not factor those in and just pay "over the counter" type prices once I have a prescription for them?
I'm not trying to pry by asking for exact figures people have been paying, just trying to get my head around the system for the moment and finding out what would be the best/most sensible/usual way things are done for people with Crohn's in the US .
Thank you!