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, December 29, 2007
Friday, November 23, 2007
Sunday, November 18, 2007
Nate sees Santa
Thursday, November 01, 2007
Wednesday, October 31, 2007
Tuesday, October 30, 2007
Saturday, October 27, 2007
Elizabeth A. Backus
ILION - Elizabeth A. Backus, 58, of 519 Doty Drive, Ilion, passed away on Friday, Oct. 26, 2007 at the Abraham House in Utica.
She was born March 12, 1949 in Herkimer, N.Y., the daughter of the late Alton and Inita (Sexton) Pelletier, and received her education in the Ilion Central School system.
Elizabeth was employed as a customer service representative with ConMed in Utica and also was employed at Weiser's Jewelers in Herkimer.
Elizabeth was a member of the Red Hat Society and enjoyed spending time with her family and friends.
Elizabeth is survived by one son and daughter-in-law, Craig and Gail Backus of Redford, Mich., one daughter and son-in-law, Jennifer and Conrad Bottorff of Ilion; two brothers, William Pelletier of Brewster, N.Y. and Robert Pelletier of Naugatuck, Conn.; and two grandchildren, Timothy Eric Farmer, Jr. and Nathaniel Craig Backus, as well as several nieces and nephews.
Funeral services will be held on Monday, Oct. 29 at 11 a.m. at the Ilion Presbyterian Church, with Rev. Victor McKusick officiating. Interment to follow at the Fort Plain Cemetery.
Friends may call on Sunday, Oct. 28 from 4-7 p.m. at the Whiter-Hendrix Funeral Home, Inc., 100 Otsego St., Ilion.
Friends are asked to consider memorials in Elizabeth's memory to the Abraham House. Envelopes are available at the funeral home.
Online condolences may be left by goig to http://www.whiter-hendrix.com/.
The Evening Telegram, Oct. 27, 2007
Observer-Dispatch, Oct. 27, 2007
Friday, October 26, 2007
Funeral Arrangements
I asked about visitation at the church, but the church will not allow it, so the only visitation will be Sunday evening.
Visitation, Sunday, October 28 4p to 7p
Whiter-Hendrix Funeral Home, Inc.
100 Otsego St
Ilion, NY 13357
315.894.3781
Funeral Service, Monday, October 29, 11a
First Presbyterian Church of Ilion
90 Morgan St
Ilion, NY 13357
315.894.2070
Internment, Monday, October 29, immediately following funeral
Ft. Plain Cemetery
Luncheon, Monday, October 29, 2p
Elks BPOE
8 West St
Ilion, NY 13357
315.894.1444
If you're so inclined, Donations can be sent in care of Elizabeth Backus to
Abraham House
1203 KEMBLE ST
UTICA, NY 13501
Thursday, October 25, 2007
Mom's at Abraham House
Wednesday, October 24, 2007
Visitors Today
As noted in previous posts, Mom's moving to the Abraham post after tomorrow. The address there is:
1203 KEMBLE ST.
UTICA, NY 13501
Exchanged some more text messages with Jennifer today. She told Mom about the transfer tomorrow, but she's still pretty confused overall. However, Mom had some visitors from her workplace, Conmed, and Victor, her pastor from the Ilion Presbyterian Church. She did recognize them and had a fairly coherent conversation, so at least she knows there are lots of people who care about her and have come to visit.
Not sure what the number is there, and I'm not sure if Mom is going to be up for talking on the phone anyway. I'm going to be there this weekend, so if anyone wants a direct update, call me on my cell phone: 313.300.8452.
Abraham House is a go!
Mom is doing better than yesterday, but is still confused. She's at least communicative with Mom, but was wanting to get up to go to the bathroom and that's no longer necessary as she's been outfitted with a catheter. She was also trying to unscrew her IV. Perhaps the fentynol has lingering effects and it may not have completely warn off yet.
On another note, I got an e-mail from NWA that there's a fare sale to select cities, and I can use 15,000 frequent flyer miles instead of the usual 25,000. I started reserving something for next weekend, and I thought, well maybe something could work out for this weekend. It did! I'm able to fly in and out of Syracuse for the 15,000 miles arriving late on Friday, and leaving first thing Monday morning again. I'm a big believer in coincidences that happen for a reason, so at least if God isn't going to wash away Mom's cancer, perhaps he's at least pushing some other buttons for once!
Tuesday, October 23, 2007
Abraham House
I did some more googling about the Abraham House tonight, and it seems like a good thing. It's supported by a number of charities in the area including the First Presbyterian Church of Utica, and Hamilton College. There were many positive references to it, and I didn't see anything that jumped out as "don't bring a loved one here."
Jennifer said that the Case Manager was still working with the insurance company to get the transfer and on-going doctor visits approved, but I have to believe that it's meant to be. Think about it, a place with only two beds has one open at the exact time that Mom needs it? I really can't imagine anything going wrong at this point. Just trying to think positive didn't cure Mom's cancer, but hopefully positive thinking can at least get this one victory for her!
Hmmm I'm not sure what to think!
However, Jennifer said that Mom was sleeping, and that Hunsicker reported that Mom was delirious earlier today. The last note I received from Jen was that she would open her eyes but otherwise completely unresponsive to Jennifer. However, if she was delirious earlier today, they may have given her a sedative or something.
Monday, October 22, 2007
St. Luke's Home
This is the same facility that Anne Tanguay was in last year and it seemed pretty nice the couple of times I visited her there. There were a couple of cats that wandered around, but hopefully they won't jump into bed with Mom!
Next Steps
Sunday, October 21, 2007
BTW anyone reading this blog
added a Fentanyl patch today
not a great day. lots
Saturday, October 20, 2007
Saturday Night in the Valley
I guess the next step is to work with the case manager next week to see what we can set up for hospice care. There's really not a lot of room at the homestead, but there seems to be a number of places around that sound like they have the right philosophy.
I'm not really sure what the future holds from here, but I'm going to plan on heading back to Michigan Monday morning as planned, and then we'll just play it by ear from here.
afternoon update
Mom's having a lot of
Friday, October 19, 2007
Update from Nurse
No good news to report
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
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
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
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
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
Monday, October 15, 2007
Sunday Night Call
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!
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
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
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
Tuesday, October 09, 2007
Another Pleurodesis
The other thing that has me really worried is the fact that she still hasn't eaten much. They started giving her Megace last week to hopefully stimulate her appetite but she's just been very tired and sleeping a lot. She's also pretty disoriented when she awakes and is getting more and more confused. However, I think I would be pretty confused to if I hadn't eaten in 2+ weeks!
I don't really understand the theory here. Are the doctors taking care of the most significant problems, and then letting the things that are up to choice to Mom? Are they presuming that if she's not eating then she's given up? If she's confused now, is it really appropriate to presume that, or do they assume that a person's innate will to survive will override the confusion?
I think I'm going to try to connect with Dr. Hunsicker again tomorrow and pose these questions.
Sunday, October 07, 2007
And the hits keep coming!
Anyone have any GOOD news?
Today being October 7 also means that it's been one year since Dad passed away. We took Nate to the cemetery today to go see "sick papa" and he wondered where he was, and we told him this is where we come to remember him.
So all in all, let's chalk this up to a pretty crappy day!
I just wish Mom could catch a break because being cooped up in the hospital hooked up to all sorts of tubes can't be much fun. Is this what being on all these prayer lists gets you? The "wonder and mystery" of God seems downright cruel to me sometimes.
Saturday, October 06, 2007
Cat Scan today
Friday, October 05, 2007
Hunsicker Called
The doctor said that the "infections" expert is also going to be looking at things to make any recommendations for next steps. She said that she would keep track of my phone number and get in touch with me as necessary.
I did talk to Mom directly and she was a little confused at first, but then did get oriented and confirmed that the chest tube remained. She said that she's been eating somewhat, but that she was very tired and was going to lay back down.
Hunsicker not Huntzinger!
Update from Stella
The short of it is that the chest tube was not removed as of 9p last night. Mom was very uncomfortable from the Pleurodesis on Wednesday and didn't have a good day at all. She was very tired on Thursday and likely was sleeping or had turned off the ringer. Stella (nurse on shift) also answered my questions on eating and confirmed that she hadn't eaten much, and I asked when the doctors would step in and take more aggressive action, and she said that they would when they felt it was necessary. Mom has been getting a lot of IV fluids, so there's no risk of dehydration, but at some point she's going to need to get a more steady flow of nutrition.
Hopefully she'll get the chest tube removed today, and then they can consider whatever's next in the process. I'm guessing at some point we should hear if there are any results back from whatever testing they did on the fluid that was removed over last weekend.
I had put a message into Dr. Razia last week, but she never responded, so I think I may try to pin down Dr. Huntsinger's number (GP) to see what information I can get from her.
Wednesday, October 03, 2007
Pleurodesis
Here's some more info on it from Wikipedia: http://en.wikipedia.org/wiki/Pleurodesis. I realize this isn't the most authoritative resource on the Web, but the information I've found there is generally the type that helps me understand the basics. Anyway.................
Dr. Jezioro explained Saturday that this is what was planned, and it was done today. The chest tube is still in to drain whatever fluid remains, but they're hoping that the Pleurodesis will prevent any additional fluid from accumulating.
I asked if she's eaten anything, and she said not much, but they did give her a drug that would hopefully increase her appetite. Lynn said she has consumed some type of fortified milkshake, and will hopefully eat more tomorrow.
I asked about a feeding tube, or when it would be critical to do something more, and she said that while that's an option, there's a lot more they can do in the meantime. She said there's even some type of nutrition they can introduce through the IV, so one way or another they'll make sure she gets some nourishment.
Tuesday, October 02, 2007
Chest Tube Remains........
I asked her about eating, and she said that she's been trying some type of nutrition drink today and that's been working out better. She's going to ask if it's available in the grocery store. I'm guessing it must be Ensure or something similar. Anything at this point is better than nothing at all.
I did manage to get her to laugh tonight. I went out with Nate for a little while in the car, and forgot to bring his pacifier. (I know he's too old, but we pick our battles......) Anyway our name for it is the "paci," so when he asked for it tonight, I told him that I didn't have one. He said, "Daddy go home and get me a paci or you're fired!" And once I didn't turn around he just said, "Daddy, you're fired!" I'm not sure where he got that from, but it was pretty comical, and he was lots of entertainment for people in line at the post office...........
Monday, October 01, 2007
Back in Michigan
I told her I'd call in a couple of days to see how she was doing, and she said that she'd call me first if she got out of the hospital. I think she's going to have to come a long way before getting out of the hospital. She's been so tired, and her system just isn't reacting right, but if she works to build up her strength this week, she might possibly have a chance of getting out by week's end. I think it's more likely that she'll end up with a stint at a rehab facility to help her build up the strength to get home. We've seen this before with my Dad, and Gail's Grandma, and they were really able to make a big difference. In the hospital, they're really trying to treat the biggest problems, but they don't really focus on getting people ready to go home. This is all rampant speculation on my part, but we'll see how it goes.
Sunday, September 30, 2007
Sunday Update
We didn't end up seeing Jennifer today as she was still dealing with the after effects of the bug or whatever she's dealing with. She discovered today that there is some leak under the bathroom so she's put a call in with the local handy man to hopefully get this fixed in the near future.
We plan to head back to Michigan tomorrow, but we'll be stopping in at the hospital before we leave.
I just hope she's able to eat something soon. Gail said that she was down to 107 upon entering the hospital, and I'm sure she's lost more weight this week. I guess we'll just have to wait and see and hope for the best.
Saturday, September 29, 2007
Saturday Update
Mom's general practitioner made the first stop about 9.30a, and she seemed to think that while this was a bit of a set back, that mom will likely rebound pretty well and be able to continue her chemo treatments and return home relatively soon. She wasn't too sure about the chest tube, but another doctor stopped by later and had the drain continue, and there was a total of more than 2 liters of fluid by the time we left. We talked to her pulminary specialist, and she felt that the chest tube would remain in until Monday, and then they were going to try a drug that will coat the lining that protects the lung, and hopefully prevent further fluid from building up.
She's still having quite a bit of pain, and looks for the morphine every two hours on the dot, but the biggest pain right now is the chest tube, so once that's out, she'll hopefully have much less pain.
Another new thing for mom was a nebulized breathing treatment. They must have heard a little crackle in her lungs, and want to prevent pneumonia, so they started that tonight. She also has a "lung exerciser" which she needs to use to do deep breathing exercises and that should help to cough up the extra fluid.
One really good sign was that she asked for a fishamajig sandwich from Friendly's. She hasn't eaten a whole lot this week, but she seemed really interested in this, so we went out to dinner there and brought it back. She hadn't started it by the time we left, but I'm hoping she'll eat at least half of it.
I guess Jennifer has caught some kind of bug, as she's not been feeling well, and now Conrad has the same symptoms. (No need for a big description, let's just say "stomach problems.") He drank out of one of her glasses, so hopefully she didn't transfer the bug to Mom, but needless to say, we'll likely not be connecting with them tomorrow.
We'll probably head up there a little later tomorrow, and try to get Mom out of bed, and at least into the chair next to it. She's likely not going to be able to go far with the chest tube in, but she's got to move around somewhat.
More news tomorrow.................
Friday, September 28, 2007
Reporting Live from Happy Valley!
Thursday, September 27, 2007
Fluid Removal Delayed
Wednesday, September 26, 2007
Wednesday Update
Today, they're going to drain some fluid from her lung. I hope that goes well. I guess they just use some novacaine, and do a small incision to insert the tube and allow it to drain. I know one time for Dad it didn't seal up right, and it allowed air to leak in all over his body. His skin felt like bubble wrap and it started to close off his windpipe! They were able to act quickly and got him squared away, but it was a little freaky. (This happened 3 or 4 years ago.) Needless to say, I didn't share this little story with Mom, but I am hoping that it goes better for her today. I'm pretty sure they did the same thing last year when she first went into the hospital, and she didn't have any problems.
Tuesday, September 25, 2007
Update from Nurse
I also called into Dr. Razia's office, and left a message hoping to find out more about why there's an increase in pain in the last couple of weeks. I posed a couple of ideas to the nurse, and she said that it would be inappropriate for her to speculate about it and that I should try to connect with the doctor.
The nurse didn't indicate that there were any plans to discharge Mom, so It's likely she'll be there until her status improves. Razia should be back to the office by Friday, and may check in with Mom over the weekend.
Gail, Nate and I plan to head to the valley this weekend. I'm not sure if we're heading out Thursday evening, or Friday, but we'll likely be there by Friday evening, and plan to head back to Detroit on Monday. I'll bring my laptop with me, and should be able to post updates while we're there.
Sunday, September 23, 2007
Hospital Update
Thursday, September 20, 2007
Mom in Hospital
Sunday, September 09, 2007
Wilcox Wedding Pictures have been posted!
I got the official word last night that I can post these to the site! Enjoy!
Friday, August 03, 2007
Wedding News!
It's official! Doug is set to marry Mary Wyka on August 31! We're looking forward to it!
Monday, July 09, 2007
Nate's Third Birthday
Tuesday, July 03, 2007
New Pictures
I thought I would see what I could figure out with the Multiply site. I determined that I could set up certain folders to be viewed by everyone, so I uploaded some recent photos, and I also found a video on the PC from last Easter. I'll see how much more I can add in my 'spare' time.
Wednesday, April 25, 2007
Jennifer's Blog
It sounds like Mom is going to be in the hospital for a few more days dealing with the chest tube and recovering from the surgery overall. No word yet on when they might reschedule the other procedure that was supposed to be completed this week.
Saturday, April 21, 2007
Mom in the Hospital
This stay at the hospital has postponed one procedure that was supposed to be this week, so hopefully that will get rescheduled so that she can continue her chemotherapy routine and keep the existing cancers at bay.
She's very anxious for us to firm up our trip to Vegas as we're hoping to go before it gets too hot there, but we may just have to plan lots of indoor activities once we do get things finalized.
Please keep her in your prayers, and we'll hope for the best.