Well, it is going to be a lovely sunny day so I’m going to enjoy that. Our yard is looking so pretty with daffodils, and the lawns turning bright green. Here’s the flowering cherry which is the prettiest bloom I’ve seen in a few years. Last year these trees were hit with a late frost and all the blooms died.
In the far background you can see some of the hoarders stuff across the fence! More daffodils.
Today is a gym day and B has platelets. I’m going to drop him off and then go over to the gym.
Sunday is sheet day so I’m doing those and since it’s so nice out, I thought I’d do our comforter as well.
There’s not a lot on the agenda for today so I guess that does make it a simple day.
I’m reading a new release in ‘home organizing’ called’The Home Edit’. It’s nicely presented with lovely pictures. So far I’ve gleaned a few ideas about organizing stuff. Nice book, if you’re needing some help putting things together. I’m going to pull everything out of the refrigerator today and give it a good clean.
This week we are in the Entryway, dining room(which we don’t really have) and porches. I’m planning to wash windows sometime this week as well.
We went to town. I went to the gym and then was going to pick B up but he had a reaction(second time) to the platelets. So he had to stay and then they sent him to the ER.
He’s home now and all seems ok.
Dinner is roast chicken.
Well, it has been a very involved week.
From last Monday when we decided to switch to UCD because it will be in network for the transplant to today when I went to Trader Joe’s.
I haven’t been to TJ’s in a while and there were some specific things I wanted. I read that their mahi-mahi burgers were very good, so I got some of those and lots of other things I’d been keeping a list of.
B had a platelet transfusion and my daughter went and picked him up as I was still down the hill as they say.
It’s supposed to rain off and on all week. I hope that changes as I’m completely done with rainy weather.
This week is the living room zone for those of you following Flylady. I did most everything in about 10 minutes. Last week I had washed the couch covers so they are fresh. I vacuumed yesterday so I’ll do that tomorrow. I like to vacuum every other day.
Dinner is a new recipe of green chile chicken. I’ll bake that not use the IP and have coleslaw on the side.
One of my favorite quotes!
So I talked with the bone marrow transplant coordinator for UHC this week to find out the actual numbers of our co-pay. She didn’t really know that but said that since Sutter was out of network, there could be unexpected bills that will show up. So I asked if we switch to in-network that won’t happen and she said yes. So I went hmmm….
So then I called UHC line and spoke to an agent and she was very helpful. As of right now till June 1st Barclay has met the $6,000 deductible so transplant is 100% covered. With that information, I came home and we discussed that it would be just easier and best for us to go in- network which will be UCD in Sacramento. Stanford or UcSF is just too far. Because we are less than 50 miles away( we are 40) no lodging or gas will be given. But that’s what we did the GoFundMe for.
So I called the nurse coordinator for Dr. Kiwan and told them we decided we needed to go with in-network. She spoke with Kiwan later and we canceled the appt for today. Then Barclay called his local oncologist and she is the one to send the referral to UCD. I think it’ll set us back a bit but the testing is done for his brother and he is a match. For some reason, they were going to mail us the results of the genetic breakdown to take to UCD. Not sure why they wouldn’t just send it with all his other test results. Anyway, we’ll need to meet with a transplant team all over but that’s ok.
I am 100% sure this is the right course of action. Even if we go past June 1st, we can make payments on the $6000. We will be sure they are aware of the deadline for this calendar year.
Hopefully, we will hear tomorrow or early next week.
But at least we know exactly where we stand.
I’m taking this idea from over at the blog ‘a smaller and simpler life’
written by Sue from Wales. She is a wonderful writer and is truly living what she aspires to be.
I’ve always been an introvert but in my earlier years just ignored what I needed. I don’t do that anymore. I don’t like crowds, parties, concerts etc. It’s just not what I’m interested in.
I am truly in a place where I like being alone/or with B who’s generally outside doing something so I have time to do what I want. When he was traveling for work I had many days where I was alone all day till either my daughter or son came home later in the evening. I was perfectly happy doing my own thing whatever that may have been.
I am embracing this as I get older and don’t feel the need at all to ‘fit’ in.
Having embraced minimalism and loving the simplicity of things, I don’t need to overextend or keep busy. I do my daily routines and enjoy the day. I may work on a project or plan something that might need to be done.
Now that we’re in ‘treatment’ mode, there’s no traveling about and as a matter of fact, I just canceled our spring trip to New Brighton beach because another round of chemo will start. That’s okay because I believe you must live the season you’re in and not fight it. We’ll go traveling again when this is over and it will be delightful.
Ha, it is a miracle!!!
Just when I sent a priority letter to NYC Corrections the next day, my documents were in the priority envelope I had paid for from before. So I now have in hand my brand new birth certificate, my original marriage license and the court documents for my legal name change. What a miracle!!! All in all, it only took 8 months. Now I can get a passport and the new real ID from California.
Today B has a transfusion early. He needs both blood and platelets but it’s been 18 days for the blood so that is an improvement. Like I said we see the transplant doctor Thursday but we know he has tentatively scheduled him for another chemo in April. I also, did not quite register the co-pay issue or maybe I was in denial but 20% of 500,000 is $100,000. I just can’t get it in my head that we would be responsible for that. I mean we don’t even have any retirement money to speak of so WHAT ARE WE GOING TO DO??? I hope this is wrong and I’m going to have B call UHC and talk to the coordinator to find out. Somehow it just doesn’t seem right.
I’m heading to Costco this morning too. I need some greens, avocados, almond milk and a few other things which I’m sure will morph into a bigger shop. Oh, and I need to return 2 items. One is the Instant Pot Cookbook which is, in my opinion, a waste. I’ve never returned a book and feel kinda weird about it. Like what read the book and then give it back. Heck, I may not do it after all.
Here’s a few pictures of the snow in Tahoe:
Well, off to do laundry. It’s sheet day!
It’s going to be another nice spring day. We didn’t walk this morning but will tomorrow. Sunday is my favorite day for walking as usually, no one is there. But this Sunday, B has his transfusion scheduled for 8 am. He doesn’t get labs till tomorrow at 3pm so we won’t know what he needs till after that. So getting out the door will be too rushed if we try and walk at 7am.
Today is going to be a fun day as we are driving up to Tahoe, actually, Incline to go to the Marijuana store for B to get some edibles and may the oil. He can’t smoke anything as he signed an agreement not to while undergoing the transplant. So just the chocolates and something else.
Then we’ll go to Truckee for lunch.
The dogs will be home outside so we need to time it so they’re not out for too long. I think we’ll be gone for about 5 hours.
Here’s a couple of pictures of the Ikea cabinet we got for the bathroom. Funny, it’s really the only thing that would have fit there so I guess I was spot on.
I’m planning on painting the tub black and we’re hoping to replace the floor this summer or fall depending on if B will be well enough or we may hire someone to do it.
This is one of my most favorite prints. I found this at a garage sale many years ago.
It’s been another frustrating week with NYC corrections not answering my emails about our original marriage license and then LLS (leukemia lymphoma society) denied my insurance claim because the breakdown in the forms we have doesn’t have B as the Assoc. alone. It shows him plus one. So that was not good enough for them even though that’s how I’ve been doing it since last June. Go figure. I resubmitted everything again with an additional form we found that shows his health credits but it still only shows him plus one. So I’m not going to sweat it although I was pretty nasty on the phone saying that was all we had to show it.
Since I’ll be switching to Medicare by June 1st I can just wait till then as they do cover Medicare. I did speak to an insurance agent and actually got MORE info. Wow, It’s amazing anyone figures this stuff out. So I need to get a form from B’s HR stating I won’t be on his insurance and then go into SS office for them to process. Then I add the plan F and Part D. He was helpful in that he said to go with the less expensive drug coverage as right now I don’t need the chemo drugs. And actually, in the future, I would ask for only infusions so that would be covered by Part B. I can’t see me going back on Revlimid since I became refractory to it. But if that does happen I can change the plan in January ( I think that’s what he said).
So at least I know the next step.
Dinner is some kind of pizza. I’m not making one so it may be a frozen one.