Mikenh and Surgery
Comments
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I'll do a writeup for today
I'll do a writeup for today in the next 48 hours but I'm home now. The 75 minute ride home was uneventful and I'm home with my favorite computer. I have to go to the pharmacy (should I drive?) to get the Lovenex, Imodium, Fiber Packets. No pain in the wheelchair, walking to the car, the ride home or sitting at my desk at home. Not lifting more than 5 pounds for a week is going to be really tough. Also figuring out what to eat. At the moment, I actually feel great. Rather an amazing week. Cheering for Darcher next.
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A trading friend sent me anBRHMichigan said:Not for the weak
My hospital food & care was amazing. I did not want to leave until 100% ready. Glad you are getting the same!
Not sure what type of ostomy you are dealing with, but I found Coloplast to be far superior to Hollister. Interestingly, much of my pain was around and under my stoma. A burning pain. Oxycodone made me feel mentally out of it and didn't help the pain. I used Norco at home and still use it on occasion to help me sleep. My incision never hurt much. Lots of staples!! But not really sore. Also I was given choice of belly or thigh for heparin shots. No pain when administered to thigh.
I hope to be back at the gym next week. Need to get my legs back in shape and improve endurance before going back to work on the 13th.
Mike you are a great inspiration. And, Jim, I love the poker game analogy! I feel the same. Quality of life is so important.
Best wishes to all from Beth
A trading friend sent me an article on hospitals do the billing with Medicare and insurance companies and it appears that it's often a price per procedure as opposed to per stay night in the past. Given this, if they can get you out earlier, then it helps their profits. The problem is the incentive to discharge early. So Medicare penalized hospitals for readmits. I think that we all have an idea as to when we should go home. For me, it was my anxiety over pain. Once I had a sufficient explanation and sufficient confidence that I'd be fine, I was ready to go.
I think that a readmit is a tough thing because the situation has to be bad enough that you'd travel, and get out of your planned routine to be in the hospital, likely in a lot of pain.
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I would say...Mikenh said:I'll do a writeup for today
I'll do a writeup for today in the next 48 hours but I'm home now. The 75 minute ride home was uneventful and I'm home with my favorite computer. I have to go to the pharmacy (should I drive?) to get the Lovenex, Imodium, Fiber Packets. No pain in the wheelchair, walking to the car, the ride home or sitting at my desk at home. Not lifting more than 5 pounds for a week is going to be really tough. Also figuring out what to eat. At the moment, I actually feel great. Rather an amazing week. Cheering for Darcher next.
No, don't drive. Even with an automatic, your foot has to be on and off the gas pedal, and that all ties in with your tummy.
Just my opinion, and nothing near medical advice.
Tru
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Son drove and that was a goodTrubrit said:I would say...
No, don't drive. Even with an automatic, your foot has to be on and off the gas pedal, and that all ties in with your tummy.
Just my opinion, and nothing near medical advice.
Tru
Son drove and that was a good idea. I felt rather drained in the pharmacy (took forever to get my package of shots). I left the Oxy prescription with them asking if they could hold it. I'll decide next week whether or not I want the stuff. Had a nice home-cooked dinner (chicken porridge - chicken balls with super-boiled rice, soy sauce, ginger and garlic pieces - might be a staple with me with or without the chicken). VNA called and is coming over. Took a few Benefiber packets. My stoma is to watery - I think that I need to take the Imodium as well. I don't think that I need to drive for a while. I do need to sleep and I do need to transcribe all of the stuff from hospital discharge into my phone. I just realized how dependent I am on iCloud Notes and Reminders for getting all my stuff done.
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Welcome home!!
So glad to hear your pain is minimal and you're able to eat some decent food.
Interesting info about length of stay and billing. I hope your hone care nurse is helpful.
I agree with the others - don't push yourself too hard. Driving can wait. Of course, you are a great example of someone who isn't going to let this disease slow you down much!!
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I overdid it today. Yesterday
I overdid it today. Yesterday I walked 1/2 mile. No problems. Today I've walked close to a mile but I tried using a powerwalking approach to alleviate the dull ache. It did alleviate the dull ache but I had blood in my urine afterwards. So no more powerwalking. BTW, powerwalking is a technique - I wasn're really going any faster than before. I'll go back to my regular walking, dial it back down to no more than 1/2 mile a day and then work up from there.
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Just looking at some of the
Just looking at some of the lab results and my Glucose indicates that I'm pre-diabetic. What? Then I looked at the history of results. I was fine on 10/24 and it rose on the day of surgery but still within normal levels. Then the day after surgery it really spiked and came down the next two days though still a little above normal. They must have been pumping in D5W into my veins. My sodium and chloride levels were low as well and I noticed that they were declining with my hospital stay despite me adding two packets of sale to meals (I only ate once or twice a day though). So the surgery and hospital stay can really mess with your lab results.
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I'lll be getting lab results
I'lll be getting lab results tomorrow. Nearly forgot that they do pathology and so forth. Im not too worried since everything else has gone well except hamburgers on the day of surgery. That wasnt too bright.. There was no mention of home care follow up by anyone yet. Then again, I dont think I need it. I keep being told how great Im doing blah blah but Im sure they do that with everyone.
im trying to eat 3 meals although Im not really hungry and haven't pooped yet. Im getting close though with rumbling and gas. My wife and kids spent the night here last night which was nice for a change. The room is big enough to hold 20 people. Im on my 3rd pair of hospital walk around socks. They call them slippers but they are socks. These are the same type they had me wear for the ultrasound. I notice they have a lot of signs about preventing falls. These socks have rubber treads, like a car tire so there must be a connection. They dont wear out but do get dirty after walking a while. .
Waiting on dinner to show up. Had salmon for lunch which wasnt too bad although it was a tad dry. Trying pot roast now along with cheese cake which just arrived. It tastes quite good. Not what youd expect for hospital food.
The pain killer they have me on is an opiode yet I dont feel loopy or anything like that. But since it is that means this is going to hurt like hell when it wears off. That comes tomorrow too. Oh well, this is what I signed up for.
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It sounds like you're havingdarcher said:I'lll be getting lab results
I'lll be getting lab results tomorrow. Nearly forgot that they do pathology and so forth. Im not too worried since everything else has gone well except hamburgers on the day of surgery. That wasnt too bright.. There was no mention of home care follow up by anyone yet. Then again, I dont think I need it. I keep being told how great Im doing blah blah but Im sure they do that with everyone.
im trying to eat 3 meals although Im not really hungry and haven't pooped yet. Im getting close though with rumbling and gas. My wife and kids spent the night here last night which was nice for a change. The room is big enough to hold 20 people. Im on my 3rd pair of hospital walk around socks. They call them slippers but they are socks. These are the same type they had me wear for the ultrasound. I notice they have a lot of signs about preventing falls. These socks have rubber treads, like a car tire so there must be a connection. They dont wear out but do get dirty after walking a while. .
Waiting on dinner to show up. Had salmon for lunch which wasnt too bad although it was a tad dry. Trying pot roast now along with cheese cake which just arrived. It tastes quite good. Not what youd expect for hospital food.
The pain killer they have me on is an opiode yet I dont feel loopy or anything like that. But since it is that means this is going to hurt like hell when it wears off. That comes tomorrow too. Oh well, this is what I signed up for.
It sounds like you're having a great time there. Are you getting a temp ileostomy? You'd already have one now if you were. If not, then I'd guess that the you were reconnected up and will poop the old-fashioned way and you wouln't need any training for that. If you had a temp, then you'd have had training on it already. Did you try the chewing gum thing for waking up the bowels? My room had fall risk information as well. I was probably high-risk on day one and I think that they lowered me to low risk after they saw me meet goals on day two. Beth said that her hospital food was good too - maybe hospital food has a bad rap?
If I were able to walk as well as you are, then I would have put on my running shoes (that's what I wore to the surgery). I put them on the day I was discharged and it was moderately more comfortable than walking in the socks on the floor as the cushioning and stability on those things is really good. I suppose I should have worn them as soon as I was able to get up and walk.
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Friday
Friday
One of the things that overshadowed my hospital stay was my roommate who had some kind of infection. He had a lot of doctors in his room including a few people from the infectious disease department and he had been on a bunch of different antibiotics. They apparently figured out what he had (might have been more than one thing) and that morning, the doctors and nurses treating him were wearing gowns. There was a notice on the door of the room about contact precautions added. I also overheard them asking him to take precautions because of the possibility of passing something on to me. I had been careful from Wednesday using the public toilet instead of the shared one in the room when it was easy to do. My roommate had immune system issues which is why he caught this thing. A normal immune system shouldn't catch this and should be able to deal with it if it did. I just didn't need to be sick while recovering. I felt like I was in pretty good shape and ready to leave anyways.
I had a very good sleep last night as they didn't do vitals every few hours on us and they didn't need to come and change his medications. The pain thing was still an issue and I took some Tylenol. Additional rest cleared it up. Also peeing helped. I'm pretty sure that it's a bladder pressure issue.
6:20 AM Doctors' Rounds: they looked at the wounds and I described the pain situation and he said that it's probably a muscular thing and that it was a good sign. I indicated that maybe I was doing too much. I did squats, tree pose, warrior pose and a bunch of other stretches and range of motion exercises yesterday. He wants to dial back the Imodium to one or two and make it algorithmic instead of fixed. He wants me to keep up with the fiber packets as well.
I asked about removing the staples and that could be done at the post-op appointment. I also asked about driving and he said anytime, as long as not on medication.
I really wanted to take a shower but I was afraid to use the bathroom so I did I washed up with a towel as best I could. I also changed underwear and pads. I saw the mucous that leaked out and it didn't smell or anything. Just black-colored. Some had got on the bed protector too.
8:00 AM Ordered scrambled egg and whole wheat toast. I did not want to eat much before the long ride home so that I wouldn't have to change the bag along the way.
8:53 AM The IV Nurse took out one of th elines and redressed the other one. I had an Imodium, Tylenol, Ibuprofin and fiber packet. The Nurse went to assemble a team for discharge. I kept my ride informed via email. One note: flat pushups, fist pushups and dips are good exercises for working the arms and shoulders for getting out of bed when you can't use your abs.
9:30 AM Got out clothes for trip home and packed up.
11:00 AM An intern came in and removed the tubular loop that held the stoma outside the body. The intern had to push the bag back onto the body attachment and asked me to brace myself. I just tightened my abs and there were no problems.
11:15 AM Stoma change education. It's in another note (the description) but it took quite some time because my stoma was so active. The nurse was very patient. I think that I will do this first thing in the morning in the future so that I won't have to deal with stuff coming out while I'm changing the bag.
Discharge stuff was next. A list of documentation and directions and a form to sign. Then injecting myself with Lovenox. I got an ETA from my ride and the nurse called for a wheelchair and brought me to the valet area where I was picked up.
The trip home was uneventful. Zero pain on the ride home.
My son drove me to the pharmacy to pick up the first box of injections. I left the Oxy prescription with them but didn't get it filled. I'll decide on the Oxy next week.
I was weak and revenous and asked my wife for toast but she gave me a large bowl of chicken balls, rice porridge and soy sauce instead. Very good stuff.
I contacted the Visiting Nurse service and set up an appointment for a visit.
11:00 PM Had three packets of Benefiber and emptied the bag and the consistency was thick. It's more comfortable changing the bag at home where then enviroment is controlled.
Total walking for the day was about 1/2 mile.0 -
You're doing so well
Great transition to home! I must say, I was on a post-op floor in the hospital where everyone had a private room. I askked about it, and they said the surgeons all required it for their patients. Was heaven. You were ar a more sought after hospital, so maybe they have to double up?
I cannot believe how wonderfully active you are. I see my surgeon today for second followup. Can't wait to get the ok to go back to the gym. My incision is finally healed.
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The general standard of careBRHMichigan said:You're doing so well
Great transition to home! I must say, I was on a post-op floor in the hospital where everyone had a private room. I askked about it, and they said the surgeons all required it for their patients. Was heaven. You were ar a more sought after hospital, so maybe they have to double up?
I cannot believe how wonderfully active you are. I see my surgeon today for second followup. Can't wait to get the ok to go back to the gym. My incision is finally healed.
The general standard of care is determined mainly by the insurance companies. I had the option for going for a private room for $375/night extra and I considered it but the benefits of the private room would mostly be lost on me (gourmet food, hotel-style room, furniture for guests to sleep over and other amenities). I couldn't really eat much of anything for a few days. The hospital was very crowded. I think that the administrators were trying to get me out early as they had more patients to bring in.
I think that you'll love the gym. Remember, start out slowly. I actually do this myself when I start out from a break on a particular exercise as it is very easy to injure yourself using barbells, dumbbells and weight machines. My postop is only 8 days away and I look forward to getting the staples out, and driving. I could likely drive right now but there's no need to try.
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Becareful with Abdominal/Core Activities
My surgeon and oncologist have been very supportive of walking and running (did 5 mile run today!) but cautioning against abdominal or core activities for fear of getting a hernia which can be very complicated to fix. I had my reversal July 28 and they are still saying no abdominal or core training until January. It's been almost a year since my LAR. Do find that my gut has not been the same since all these surgeries. Kind of like a beach ball. Looks like I have 3 belly buttons too; real one plus two surgical ones. Hard to tell them a part. TMI! Anyway, good luck getting stamina back and daily lives in order to those on the surgery recovery roster....
Cindy
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Post-op Activity
Thanks, Cindy & Mike. I mentioned in another post that I visited my surgeon today. Although my incision is healed, no swimmimg for 3 months! Walking and stationery bike only. He fears hernia could result from too strenuous of activities. I am so disappointed. Can't use resistance equipment either. Welp, I am certainly learning patience.
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Thank-you for the data pointCindy225 said:Becareful with Abdominal/Core Activities
My surgeon and oncologist have been very supportive of walking and running (did 5 mile run today!) but cautioning against abdominal or core activities for fear of getting a hernia which can be very complicated to fix. I had my reversal July 28 and they are still saying no abdominal or core training until January. It's been almost a year since my LAR. Do find that my gut has not been the same since all these surgeries. Kind of like a beach ball. Looks like I have 3 belly buttons too; real one plus two surgical ones. Hard to tell them a part. TMI! Anyway, good luck getting stamina back and daily lives in order to those on the surgery recovery roster....
Cindy
Thank-you for the data point. I don’t expect to play tennis for six months out as it is a high stressor of abs. I may spend some time to see if there’s a sports specialist at Dana Farmer as this is a big part of my life.
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I can feel daily improvement
I can feel daily improvement but it’s slow. Walked 1.5 miles today and that’s the most since surgery. My rear end gets sore sitting for a while. Maybe related to all of the cutting down there. Good excuse to go for a walk. We get freez temps soon so I need five pounds of clothes to go out.
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It was nice and cool here in Ct today!Mikenh said:I can feel daily improvement
I can feel daily improvement but it’s slow. Walked 1.5 miles today and that’s the most since surgery. My rear end gets sore sitting for a while. Maybe related to all of the cutting down there. Good excuse to go for a walk. We get freez temps soon so I need five pounds of clothes to go out.
even colder the rest of the week so bundle up. I know different surgery but with my husband's liver resection surgery he got an enormous hernia, you could see it no matter what he wore because he went way too fast. So be careful!
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Walking
Mike, I think a mile and a half is amazing! I pushed myself to do a lot of activity today and feel much better for it. Need to spend our days LIVING. I go back to work Monday and am really looking forward to concentrating on work rather than cancer!
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The distance is the total for
The distance is the total for the day and is broken up into many short walks throughout the day. The limiting factor is the dwindling amount of daylight. I am walking about 3 MPH which is quite a bit faster than the 2 MPH from last week. My top walking speed is 4.5 MPH and top running speed is about 12 MPH.
The ache on on the left side is gone. It’s been replaced by a little aches to the right and in the middle. Both are likely due to increased activity. I’m monitoring both. Getting out of bed still takes a moderate amount of effort and care to avoid using abs musckes. And I have no desire to use any painkillers. There may be a little soreness due to sleeping with the bag. There was quite a bit of material in the bag this morning. I tend to let it fill up more than the recommended 1/3rd. I've been experimenting with the amount of fiber. The prescribed amount was 9 grams per day but I was doing 12 for a few days and went up to 15 yesterday because the bag contents were too watery. The discharge directions recommended four Imodium tablets but I'm trying to avoid them and use fiber to control thickness and absorbtion. The directions said that it may take a week or two for things to firm up so I'm just adjusting with the fiber. I'm getting about 12 grams of fiber in my regular diet as well. Typical is more like 30 grams but I don't want to crank it up to something like that all at once.
im debating my return to work date. Recovery has been slower than I expected but I was overly optimistic about this. My Short-Term Disability company suggested a return to work date of November 15. This is based on me getting approval for that on November 14 when I meet with the Surgeon. I'm also debating driving. I have the feeling that those that returned to driving, say within a week of surgery, may have not had the open surgery that I had. So a week after surgery was unrealistic for me. We're at 9 days now and I still don't think that I should drive. I will reassess every day though. If I'm not ready by Tuesday, then this complicates things as I won't be able to pick up my other car at my mother's house when I planned to. It would mean getting to my mother's house (I'd take a cab if I wasn't up to walking two miles, and taking two trains to get there), and then at least a one hour drive, likely with some traffic, on the first-ring highway. I could use the self-driving mode in the car - I just haven't used it enough to trust it completely.
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Humble PieMikenh said:Fir bag change took me an
First bag change took me an hour. One screwup cost me a wafer and redo. I’m going to have to get much better at this.
Changing the wafer is my greatest challenge and dread. I am tempted to just coordinate and pay for a home health care nurse to do it for me, but that is escapism and silly. I can do this - not well, but I can do this.
I finally had some minor leakage and a small area of my skin became irritated. Obviously, I need to change more often and do a better job of it.
I can identify with your concern over wasting a wafer. Insurance will only pay for 20 per month and the turn around time for resupply is slow and out of my control. I do not like that situation, so I have located local outlets where I can pay out of pocket for additional supplies.
If I could have one do-over, it would be to have the WOC nurse conduct another tutorial AND have me do it all while she observed and critiqued my performance.
Jim
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