Does your transplant coordinator keep in touch with you?
I am curious know how does one manage the post transplant journey, specially those who are now transplanted 3-4 years back, who is your primary care provider? Do you get to talk to your transplant surgeon or the team that looked after you in the initial months before and after the transplant.
Who takes care of your when you face side effects from the medicines?
In different countries there are different care models, but all transplant patients face this challenge of life long management of Tac dose and the need to take of their new organ.