We continue to choose the road less traveled. Our stories started in New York and Michigan. We took an detour to New Jersey, and had a most excellent adventure to Ethiopia. In July, 2013 we moved our family from Detroit to Texas. People can say a lot about us, but they can't accuse us of being boring....
Saturday, October 20, 2007
afternoon update
talked to case manager today but she didn't have much to offer. She said to check back on monday and they should know more. mom's resting now. She's gone back and forth with being "with it" and she's showed signs of her sense of humor.
Mom's having a lot of
Mom's having a lot of pain today. she's likely going to have morphine at 11.30 today. hoping to talk to case mgr today.
Friday, October 19, 2007
Update from Nurse
Just talked to Courtney, Mom's nurse since this morning. She confirmed that the transfer to St. Luke's home had been cancelled, and she wasn't sure what the next step was. She said that Mom is resting comfortably now. She guesses that she got worked up earlier when going down for a test, and got short of breath. Her paid also escalated at that point, but once she got the morphine she felt better. Courtney said that the case manager will be there until noon tomorrow, and that we'll be able to talk to her more then.
No good news to report
Jennifer got Mom's phone charged up, so she was able to text me from the hospital. No big updates regarding hospice or other next steps. Her only immediate report was that she was crying because of how much pain she was in and utlimately got a dose of morphine. She was better once she had that.
Have I mentioned lately how much this SUCKS! I just hope she's able to manage the pain. I hate to think of her having to endure pain while having to comprehend what's to come..........
Have I mentioned lately how much this SUCKS! I just hope she's able to manage the pain. I hate to think of her having to endure pain while having to comprehend what's to come..........
Rehab is a no go
Well, I was wondering about this whole rehab thing, but it seemed like the signs pointed in a positive direction, but I guess within the last couple of days, the progress was temporary. As of last night, Mom is getting a higher level of oxygen than was previously necessary, and now we're starting to talk about hospice care rather than rehab.
I've already spoken with Dr. Hunsicker and Jennifer today, and they'll be looking more into this option later today. It just sounds like the only things left would be under the category of "heroic efforts" and Mom made it clear to me last year that she wanted to fight the good fight, but not be resussitated, on the vent, etc. I'm sure they'll be more news later today..........
I've already spoken with Dr. Hunsicker and Jennifer today, and they'll be looking more into this option later today. It just sounds like the only things left would be under the category of "heroic efforts" and Mom made it clear to me last year that she wanted to fight the good fight, but not be resussitated, on the vent, etc. I'm sure they'll be more news later today..........
Thursday, October 18, 2007
Ugly Betty
That's nothing against Mom, it's just what she was watching tonight on TV! It's hard to come up with snappy titles for these posts, so I do what I can..............
I talked to her for a few minutes, but I didn't catch her at a good time. She was not in a good position to talk and tried to get repositioned and couldn't catch her breath. She told me to call back in ten minutes, and I did, but she didn't sound a whole lot better. I talked to her for a few minutes more, but she was tired and let me go. She knows there's talk of transferring to the rehab, and I tried to reassure her that it would be good, and that if anything went wrong, they could get her back to the hospital ASAP. We'll see how she's doing this weekend, but my guess is that they won't try to move her until next week anyway.
I talked to her for a few minutes, but I didn't catch her at a good time. She was not in a good position to talk and tried to get repositioned and couldn't catch her breath. She told me to call back in ten minutes, and I did, but she didn't sound a whole lot better. I talked to her for a few minutes more, but she was tired and let me go. She knows there's talk of transferring to the rehab, and I tried to reassure her that it would be good, and that if anything went wrong, they could get her back to the hospital ASAP. We'll see how she's doing this weekend, but my guess is that they won't try to move her until next week anyway.
Rehab
Bill called me last night after arriving home, and he said that Mom had another decent day. She slept quite a bit, but was comfortable and able to manage pain well. She's not strong enough to be discharged, but she's at a point where the care of the hospital is really more than necessary, so Dr. Hunsicker is talking about having her go to a rehab facility for a while.
The case manager is going to be checking on available bed status today, and will be contacting my Mom's insurance carrier to see what's covered. I'm guessing that even if her medical insurance doesn't cover it, the cancer insurance she purchased from AFLAC might, so we'll have to check into all the angles. Speaking of which, if you ever have the opportunity to sign up for cancer insurance at work, do it. Mom paid just a couple dollars per pay for it, and it's paid out thousands already. It's a good thing that little voice told her to go for it because I'm sure this experience would have been much different without it.
The case manager is going to be checking on available bed status today, and will be contacting my Mom's insurance carrier to see what's covered. I'm guessing that even if her medical insurance doesn't cover it, the cancer insurance she purchased from AFLAC might, so we'll have to check into all the angles. Speaking of which, if you ever have the opportunity to sign up for cancer insurance at work, do it. Mom paid just a couple dollars per pay for it, and it's paid out thousands already. It's a good thing that little voice told her to go for it because I'm sure this experience would have been much different without it.
Wednesday, October 17, 2007
Update from Bill
As I mentioned previously, Mom's brother Bill and his wife Kathryn made the trip up to the valley yesterday. They'll be spending more time with Mom today before heading back down, and Bill said that he may try to make it back up to the valley this weekend.
He was able to get a wealth of information from the surgeon that placed the chest tube and the nurses on duty. The surgeon actually came to remove the chest tube from her right side. He said that the Pleurodesis seemed to do its job, and the amount of fluid being drained was minimal. He explained to Bill that there were two "pockets" of fluid that had collected, and they were evidently not connected which is why the chest tube had to be moved initially. (Still seems a little funny to me, but you can only know so much without performing some kind of invasive surgery........)
There is still some talk of putting the chest tube on the right side, but the amount of fluid there isn't at a dangerous level, so he's going to let her go without for a few days and re-evaluate the situation then.
The nurses communicated to Bill that Mom had been using morphine less and less frequently. She didn't need it at all yesterday, opting for a more moderate pain reliever. (Still more than the Excedrin in my desk drawer, but not like morphine.)
Bill said that she seemed very lucid and was able to have a substantial conversation. He said that there were quite the antics going on in the next bed, but Mom seemed to sleep through it anyway. I guess they had an overabundance of visitors, and even had a birthday party for a five year old girl in there! (Hello? These rooms are about 12' x 20' with two hospital beds and all the equipment around them.) Bill said that he avoided the confrontation and bit his tongue because it didn't seem to phase Mom.
There's evidently been some talk of moving Mom to the physical therapy center behind the hospital, but that wouldn't happen until they get the whole chest tube situation under control. The surgeon confirmed for Bill that they're not just going to kick Mom to the curb at some point if she's unable to care for herself at home, and if there's not some type of medical assistance available. I guess we'll find out more in the coming days, but for now, she still requires a substantial amount of care, and isn't going anywhere.
He was able to get a wealth of information from the surgeon that placed the chest tube and the nurses on duty. The surgeon actually came to remove the chest tube from her right side. He said that the Pleurodesis seemed to do its job, and the amount of fluid being drained was minimal. He explained to Bill that there were two "pockets" of fluid that had collected, and they were evidently not connected which is why the chest tube had to be moved initially. (Still seems a little funny to me, but you can only know so much without performing some kind of invasive surgery........)
There is still some talk of putting the chest tube on the right side, but the amount of fluid there isn't at a dangerous level, so he's going to let her go without for a few days and re-evaluate the situation then.
The nurses communicated to Bill that Mom had been using morphine less and less frequently. She didn't need it at all yesterday, opting for a more moderate pain reliever. (Still more than the Excedrin in my desk drawer, but not like morphine.)
Bill said that she seemed very lucid and was able to have a substantial conversation. He said that there were quite the antics going on in the next bed, but Mom seemed to sleep through it anyway. I guess they had an overabundance of visitors, and even had a birthday party for a five year old girl in there! (Hello? These rooms are about 12' x 20' with two hospital beds and all the equipment around them.) Bill said that he avoided the confrontation and bit his tongue because it didn't seem to phase Mom.
There's evidently been some talk of moving Mom to the physical therapy center behind the hospital, but that wouldn't happen until they get the whole chest tube situation under control. The surgeon confirmed for Bill that they're not just going to kick Mom to the curb at some point if she's unable to care for herself at home, and if there's not some type of medical assistance available. I guess we'll find out more in the coming days, but for now, she still requires a substantial amount of care, and isn't going anywhere.
Tuesday, October 16, 2007
No Update from Last Night
Well, I called the nurse's desk last night, but she was tied up with a patient and asked me to call back. It was getting pretty late, so I figured with Bill driving up today that he would likely get the latest on Mom's condition and call me later tonight or tomorrow.
Monday, October 15, 2007
Sunday Night Call
I called and talked to Mom last night. I think I woke her up, but she went ahead and talked to me for a few minutes anyway. She remembered that I was supposed to call at 8 "yesterday" and I reminded her that it was Friday, and that I had called but she was probably asleep. I was just glad that she recalled it at all and was half right!
Other than that she actually sounded stronger than she had in previous phone calls, so that was a positive sign. She wasn't clear on what was happening with the chest tube, so I think we need to primarily rely on the nurses and doctors for any official information at this point. I haven't bugged the nurses in a while, so I'll plan on checking in with them this evening to see what I can find out.
Mom's brother Bill is travelling up to the valley tomorrow with his wife, Kathryn. I'm sure we'll get some more news from that visit. Jennifer continues to visit prior to going to her job in the afternoon, and I'm planning to head out there this coming weekend.
Other than that she actually sounded stronger than she had in previous phone calls, so that was a positive sign. She wasn't clear on what was happening with the chest tube, so I think we need to primarily rely on the nurses and doctors for any official information at this point. I haven't bugged the nurses in a while, so I'll plan on checking in with them this evening to see what I can find out.
Mom's brother Bill is travelling up to the valley tomorrow with his wife, Kathryn. I'm sure we'll get some more news from that visit. Jennifer continues to visit prior to going to her job in the afternoon, and I'm planning to head out there this coming weekend.
Saturday, October 13, 2007
Good Day!
Wow! It sounds like Mom had a really great day today. She had a lot of visitors, and I got good reports all around. Her brother Bob came up from his job assignment in Pennsylvania, and his wife Mary, daughter Lauren, and son Daniel came up from Connecticut. Darlene also came with Kenny and her daughter, Lisa. My sister also came up with Conrad.
I got reports from Bob and Darlene, and they both said she had a really good day. She was awake, alert and coherent. She ate half her lunch while they were there, and Bob was really encouraged that she has backed off on using morphine, and is using a pill to manage her pain lately, he thought it was hydrocodone. Bob asked her about the plan to move the chest tube from the left side to the right side, and this was news to Mom, but that's not surprising as she was more out of it earlier in the week.
They both said that they had tired her out pretty well, and that she was resting after their visit. I may try to call later to see if she's up for talking for a few minutes.
I got reports from Bob and Darlene, and they both said she had a really good day. She was awake, alert and coherent. She ate half her lunch while they were there, and Bob was really encouraged that she has backed off on using morphine, and is using a pill to manage her pain lately, he thought it was hydrocodone. Bob asked her about the plan to move the chest tube from the left side to the right side, and this was news to Mom, but that's not surprising as she was more out of it earlier in the week.
They both said that they had tired her out pretty well, and that she was resting after their visit. I may try to call later to see if she's up for talking for a few minutes.
Friday, October 12, 2007
Hunsicker Returned the call
I did hear from Dr. Hunsicker toward the end of the business day yesterday, and just didn't have an opportunity to post anything. She provided me with the answers to my questions, but doesn't have a positive long-term prognosis at this point.
They did not perform the pleurodesis yesterday. With the amount of fluid that continues to drain, they're concerned that it will just wash out the agent. I didn't quite get it, but I believe that she just referred to it as talc. The talc is supposed to fuse the pleura to the chest wall and prevent the re-accumulation of fluid.
As for the fluid itself, it was tested and did not contain cancer cells, nor did it have signs of infection. She was pretty surprised at this, but the fact that it continues to re-accummulate and drain is a continuing problem. She's not one to offer a lot of additional information, so I tried to ask as pointed questions as possible to get the most I could.
She went on to discuss "end of life" issues and I told her that she had completed a DNR order some time ago. She said that it wasn't referenced in her electronic chart, but that it may be in the paper chart. I talked to Jennifer about this last night, and she confirmed that Mom did complete this, and that Jennifer has some amount of oversight in this matter. Jennifer believes that this was re-affirmed during the hospital admission, but also has another copy of a document outlining this wish. She'll make sure that these wishes are better known as we proceed.
Jennifer did also say that Mom had a pretty good day yesterday, and made a point of drinking some ensure, and even ate some solid food. She was able to have some coherent conversations with her which has been rare lately as she's been sleeping most of the time.
Mom will be getting some visitors soon with Darlene (long-time friend and former sister-in-law) visiting this weekend. Mom's brother Bill and his wife Kathryn will be heading up on Tuesday and spending a couple of days, and I'm planning to head out myself next weekend.
I certainly don't know that the future holds, but unless something dramatic happens, it sounds to me like the hospital is in "do what you can" mode to make her comfortable. They're not pushing the food issue and leaving this to Mom because for one, she can still choose to eat solid foods herself if she wants. Two, inserting a permament feeding tube would be a more aggressive life-prolonging action, and while Hunsicker didn't say this explicitly, that's the feeling I was left with. They want to take action on the most significant, pain-causing items, (i.e. chest-tube to drain fluid) but when it comes to the feeding tube and ultimately the ventilator, they're going to make every effort NOT to utilize those.
They did not perform the pleurodesis yesterday. With the amount of fluid that continues to drain, they're concerned that it will just wash out the agent. I didn't quite get it, but I believe that she just referred to it as talc. The talc is supposed to fuse the pleura to the chest wall and prevent the re-accumulation of fluid.
As for the fluid itself, it was tested and did not contain cancer cells, nor did it have signs of infection. She was pretty surprised at this, but the fact that it continues to re-accummulate and drain is a continuing problem. She's not one to offer a lot of additional information, so I tried to ask as pointed questions as possible to get the most I could.
She went on to discuss "end of life" issues and I told her that she had completed a DNR order some time ago. She said that it wasn't referenced in her electronic chart, but that it may be in the paper chart. I talked to Jennifer about this last night, and she confirmed that Mom did complete this, and that Jennifer has some amount of oversight in this matter. Jennifer believes that this was re-affirmed during the hospital admission, but also has another copy of a document outlining this wish. She'll make sure that these wishes are better known as we proceed.
Jennifer did also say that Mom had a pretty good day yesterday, and made a point of drinking some ensure, and even ate some solid food. She was able to have some coherent conversations with her which has been rare lately as she's been sleeping most of the time.
Mom will be getting some visitors soon with Darlene (long-time friend and former sister-in-law) visiting this weekend. Mom's brother Bill and his wife Kathryn will be heading up on Tuesday and spending a couple of days, and I'm planning to head out myself next weekend.
I certainly don't know that the future holds, but unless something dramatic happens, it sounds to me like the hospital is in "do what you can" mode to make her comfortable. They're not pushing the food issue and leaving this to Mom because for one, she can still choose to eat solid foods herself if she wants. Two, inserting a permament feeding tube would be a more aggressive life-prolonging action, and while Hunsicker didn't say this explicitly, that's the feeling I was left with. They want to take action on the most significant, pain-causing items, (i.e. chest-tube to drain fluid) but when it comes to the feeding tube and ultimately the ventilator, they're going to make every effort NOT to utilize those.
Wednesday, October 10, 2007
Pleurodesis Part Deux
I haven't heard back from Dr. Hunsicker yet. Hopefully tomorrow. I wonder if she reads this blog?
Anyway, I got to talk to Mom today for a few minutes. Jennifer was at the hospital, and we worked out a way for her to call the cell phone without needing a calling card. (It's a long story, but it works..........) Mom asked me where I was, and I told her that I was at the office, and she just said that she was a little unclear on time, which is understandable. She went on to some other conversation and then came back to me, and said, "I'm a little spacey, don't I deserve to be a little spacey?" (It may not be a direct quote, but the sarcasm was definitely there which means to me that the lights are still on inside.) I talked to her about family, and Pauline (mother of her childhood friend, Gail, whom she's been recently reacquainted), and she understood what I was talking about and knew that they were going to do the Pleurodesis again this afternoon. She confirmed that her pain was still manageable, and then signed off.
I still pressed her to eat more, but it's still unclear how well that's going. I'm hoping to convince Dr. Hunsicker that while a feeding tube may be out of line at this point, I think she should still use the IV solution that she or Lynn mentioned. Any kind of nutrition at this point has to be valuable.
Not that anyone wants to think about this, but I'm also going to be talking to Hunsicker to make sure that the hospital is aware of Mom's wishes. She told me after Dad died that she signed papers with a "do not resuscitate" order. It was nothing I pressed her for, it was just something she told me after I had to sign papers to authorize them not to put Dad on the vent on that last day. I'm assuming that whatever papers she signed were more explicit about what circumstances were to be considered. I don't know how legitimate these are in New York, but in Michigan with my Dad and Loretta, it seemed like the doctor's just followed the family's wishes, and it was much better to know the patient's wishes when they had a clear mind.
If I don't hear from Hunsicker tomorrow, I'll plan to call and speak to the nurse tomorrow evening to get the latest status.
Anyway, I got to talk to Mom today for a few minutes. Jennifer was at the hospital, and we worked out a way for her to call the cell phone without needing a calling card. (It's a long story, but it works..........) Mom asked me where I was, and I told her that I was at the office, and she just said that she was a little unclear on time, which is understandable. She went on to some other conversation and then came back to me, and said, "I'm a little spacey, don't I deserve to be a little spacey?" (It may not be a direct quote, but the sarcasm was definitely there which means to me that the lights are still on inside.) I talked to her about family, and Pauline (mother of her childhood friend, Gail, whom she's been recently reacquainted), and she understood what I was talking about and knew that they were going to do the Pleurodesis again this afternoon. She confirmed that her pain was still manageable, and then signed off.
I still pressed her to eat more, but it's still unclear how well that's going. I'm hoping to convince Dr. Hunsicker that while a feeding tube may be out of line at this point, I think she should still use the IV solution that she or Lynn mentioned. Any kind of nutrition at this point has to be valuable.
Not that anyone wants to think about this, but I'm also going to be talking to Hunsicker to make sure that the hospital is aware of Mom's wishes. She told me after Dad died that she signed papers with a "do not resuscitate" order. It was nothing I pressed her for, it was just something she told me after I had to sign papers to authorize them not to put Dad on the vent on that last day. I'm assuming that whatever papers she signed were more explicit about what circumstances were to be considered. I don't know how legitimate these are in New York, but in Michigan with my Dad and Loretta, it seemed like the doctor's just followed the family's wishes, and it was much better to know the patient's wishes when they had a clear mind.
If I don't hear from Hunsicker tomorrow, I'll plan to call and speak to the nurse tomorrow evening to get the latest status.
Message into Dr. Hunsicker
I left a message with the receptionist. Last week she was able to return my call at the end of the day, so hopefully I'll hear from her again at some point later today.
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