Today, I went for the monthly distribution of coupons that subsidize dialysis for people who cannot afford it by the Jain Dialysis Trust . These visits are truly humbling. When I see the work the trust is doing, my head simply bows down before them. It is not easy to save a human life. Yet, these people have saved at least a couple of hundred.
I happened to meet a young guy, on dialysis for a couple of months now. I introduced myself to him and chatted about his background and history with renal disease. I then asked him about a transplant. He said he was not told by his doctor about that option but had heard about it and was exploring it.
I wonder why he wasn't told about that option? Was any education given to him at all about his options? Was PD mentioned? Or was he simply condemned to a life of hemodialysis?
Who will educate patients if it is not for the doctors? Every patient does not have access to the internet. Even those who do may not be proactive enough or feel the necessity to look this up.
A simple talk about the different options doesn't take too long. Is that too much to ask? Tell me, someone please!