I just got off the phone with the financial adviser for the transplant unit. They are taking me off the list.
She says my current insurance wont be enough to cover a transplant. OK! They told me at the evaluation everything was good but I can accept that since it is up at the end of the year anyways, and since I just got listed recently and have type O, I wouldn't need to worry about one any time soon any way and was planning on waiting to get a new policy starting Jan. 1st, as my social worker recommended due to already paying out of pocket max for this year.
Then while talking to her I got even more confused. First I made the mistake of saying that the AKF was covering my deductible and she told me that doesn't get looked at very well in regards to getting a transplant. I brought that up because I was confused when she mentioned about me needing to apply with the states KDP (kidney disease program) for any post transplant assistance. Me and my big mouth (I thought they were the same). My social worker never mentioned that. But it probably doesn't matter because I am already on there bad list because of using the AKF for helping with my current premiums. She didn't believe that I could afford my premiums post transplant if I don't qualify for the state's KDP because I'm having the AKF pay my current premiums which they stop doing once transplanted
So then I bring up that I was planning to call SS this week to start applying for medicare. I was planning to apply for part A, B, then get part D and a medigap policy in which due to my age (45) I only qualify for medigap part A level 1. She stated that the medigap policy part A won't cover part B. That any hospital stays (which there will be many post transplant) will require a high deductible EACH visit. So now it doesn't look like I would qualify for a transplant with medicare because the medigap doesn't cover anything. She also brought up how expensive the part D donought hole is (about $3000) and that most people would have other insurance for their prescriptions as they cost 5 to 6000/ month. She doesn't see how I can afford the donought hole. (of course she doesnt know my financial info so how would she know that?) I guess even with part D I'd be paying several grand/month for medication? I thought once I went through the donought hole all would be covered. Oh well, wrong again.
Then she wanted to check my claim since I stated that I applied for SSDI back in May. UH OH, another negative. It seems that since I applied for SSDI I wont be able to get medicare for 24 month's.
?? Huh? I thought haveing ESRD and being on dialysis (hemo starting may 1st and home PD for the past 1 1/2 month's) qualified me for mediacre and that it would start at home dialysis. Another notch against me.
Then the final blow was when she tried to check my current claim and I stated the number having an HA at the end. She said that was it, I only qualify for medicare hospital (part A) since my current SS claim number has those letters following it. Oh well.
I guess I have to study these new insurance plans that they came out with to see if I can decipher what they will cover since it doesn't seem medicare really covers anything in regards to a transplant.
Does this sound legit? I understand they want to make sure they'll be covered, but everything I read shows medicare covers this. Am I missing something? Is it best just to get a new policy if I can afford one and bypass medicare altogether?
The not qualifying for medicare part B even though I have ESRD, not being able to start medicare for 24 month's, and the medigap not covering anything and me still having to pay the 20% or so medicare doesn't cover really has me confused.
I'm also a little upset in that when I went to the transplant evaluation back in Aug they said everything looked real good with my insurance for now. That I should get on medicare with a medigap so I could get part D for prescriptions though. Today I was told that what they said doesn't matter because she is the one who is actually in charge of seeing if everything was OK.