The Good, The Bad, & the Nuts! ...ANYONE GOING MAY 8-15?

I also want to apologize for not replying direct to anyone. I have the iPad a either can't highlight, or can't figure out how to highlight. I also try to keep the posts small because if go back to edit after I see how terribly typoed it is, I can't scroll down through a long message. I love the size, and how portable it is, but it does have it's downfalls.
 
Today's news, up and walking twice.....very much easier than it was last night. Much....pretty soon I will advance to:banana::cool1:
Had the drug button removed. I am on a regular regimen if tylonel, more as a fever preventers, but I'm sure it's keeping the edge off on any pain too. Had the catheter removed, and took my first trip to the bathroom (tmi?). I left a larger contribution after just those couple hours off the catheter than I could work up in a whole day just last week.

I have a cath port(?) in my chest that they use for squirting in meds, and for drawing blood if need be. That is the only thing still stuck in me. When I take walks they attach a pulse ox monitor to make sure the walking isn't too much for me. I get short of breath quickly. Last night I walked to rthe end of the hall and back. Today I walked that then down the next hall. Last one was just a little further. She said next time maybe instead of backtracking I could circle around.

Pre op I was told I'd be here possibly 6 days. Post op after winding up in icu they said it would probably be longer. This morning my dr said possibly Sunday, probably Monday, which is 6 days! I'll have 2 - 3 dr visits and labs for a few weeks, which will gradually get less frequent.

Knock on wood I am off to a real good start!
 
Today's news, up and walking twice.....very much easier than it was last night. Much....pretty soon I will advance to:banana::cool1:
Had the drug button removed. I am on a regular regimen if tylonel, more as a fever preventers, but I'm sure it's keeping the edge off on any pain too. Had the catheter removed, and took my first trip to the bathroom (tmi?). I left a larger contribution after just those couple hours off the catheter than I could work up in a whole day just last week.

I have a cath port(?) in my chest that they use for squirting in meds, and for drawing blood if need be. That is the only thing still stuck in me. When I take walks they attach a pulse ox monitor to make sure the walking isn't too much for me. I get short of breath quickly. Last night I walked to rthe end of the hall and back. Today I walked that then down the next hall. Last one was just a little further. She said next time maybe instead of backtracking I could circle around.

Pre op I was told I'd be here possibly 6 days. Post op after winding up in icu they said it would probably be longer. This morning my dr said possibly Sunday, probably Monday, which is 6 days! I'll have 2 - 3 dr visits and labs for a few weeks, which will gradually get less frequent.

Knock on wood I am off to a real good start!


Tanya, I'd say that is an AWESOME start. Before you know it, you'll be doing this: :dancer::dancer::dancer:
 
My goal is that little leprechaun jig! But I'm saving that for when they officially clear me for my Disney trip.
 

Hey, Dan, I think you are cooler than Marv and he is on FB. :rotfl::rotfl::rotfl:
here that marv.
:listen:
I was a facebook holdout, then the aol disney boards were combined with general travel and were no longer Disney specific. We tried a yahoo group, but it was full of hassles, they eventually decided to friend each other on fb.....which meant I had to join up to stay in touch.....so like so much in my life.....it's disneys fault!
disney the cause of and solution to all of lifes problems.
:laughing:
Tanya, I'd say that is an AWESOME start. Before you know it, you'll be doing this: :dancer::dancer::dancer:
i hope she is dancing like that soon except she might want to go tanning first, no one likes a yellow face like that.
:laughing:
 
Tanya, it is so wonderful to read your little reports about how you are progressing!! :goodvibes

Don't worry about typos, not quoting etc. I think it is a treat that you are sharing your story with us in whatever form it is. :thumbsup2 It really sounds like they are very happy with you if they might release you after 6 days. I hope that this will be a good sign for the future.
 
No real new news. Still peeing like a big girl.....last week I would produce some piddly little bit when I'd get up in the morning and pretty much call it a day. Now it's every hour and a half to two hours. My bladder needs to relearn " holding it". It hasn't had to do that for quite some time! I know, I know tmi......but it is what it is!

My sil and her husband visited for an hour or so tonite.


I'm getting sent home on 11 medications. They called in to see what the Medicare and insurance folate would be. For a total of 10 I will owe $69. I have to buy proposed over the counter....so how much extra that will be. Very excited about that!

Had a lot of medical personell in and out nonstop, so wasn't on here as much.

All news is good, though!
 
Tanya, I'm still just tickled pink (I'll bet you just read that as tinkled) that you are taking us on your journey to recovery with you! Thanks for sharing!! Have a GREAT night's rest- we'll "see" you tomorrow!
 
The latest and GREATEST news....the dr is sending me home tomorrow - Sunday. Thats only 5 days, pre-op estimate was 6. Your prayers and picked dust must be doing their jobs. Thanks so very much! :love::cheer2::grouphug:
 
So Glad you are doing so well !!:hug:One of my consumers is gonna have to start dialysis in the near future !!I can see how tired she is looking over the last few months so am not surprised !! She has been on restriced fluids for a LONG time and is very good about it !!She already has the shunt in her arm so that;s one less thing to do!!:sad2:
 
I take it since she has thev shunt she is planning to do hemo? I lucked out and never had to go that route. I imagine peritoneal puts a lot more of the responsibilities on the patient, though. I wish her all the luck in the world. It sucks.....but it sure is a wonderful thing to have available!
 
I'M HOME!!!!! And I'm going to bed! Who'd have thought it - last week at this time I was going to bed with a follow-up appoint for the repair on my fistula, a week later I am going to bed with my brand new, fully functioning kidney! God is Good!
 
Tireder than I thought I would be so I am sooooooo far behind on boards it will be forever before I even dream of catching up. Know I am thinking of all of you and can't wait to have the energy to enjoy your adventures some more.

Once I got home my "output" had slacked way off. I had my first labs and follow up appt tuesday. I was feeling a little bummed Monday night, Tuesday morning, but after my appointment and they put things in perspective a little better. One of the anti rejection drugs is apparently very touchy on the kidney. I I was sent home on 2 in the morn and 2 in the evening. After my labs came back they told me to skip the next night and morning, then cut it to 1 each. Plus to increase the lasix. So since they were acknowledging the problem and offering some solutions, I feel a little better. This is my first time, and a countless one for them, I think I just want it to work so bad, I worry over every little thing.
 
I think I just want it to work so bad, I worry over every little thing.

Of course you are tired!! And of course you are worried about every little thing!! so glad they were able to put things into perspective for you and put your mind at ease some! Get the rest you need and you'll be feeling better soon- I KNOW IT!:hug:
 
I updated my facebook, but just getting around to here. Tuesday thus week I had my first follow up and labs. My output was dropping so they adjusted some of my medications. While at that appt the nurse commented that there was some fluid seeping from my incision and since I am up and moving more that can happen.

Wednesday I called in because my output was even less and I told her it looked like I spilled water on my pants, but sure didn't remember doing that and that by getting mirrors involved ;) I could see that there was dripping at the bottom of my incision. She said to put some gauze on it and not to worry as long as it was clear. If it became red, or had an odor to let her know. Well it got to the point that gauze was futile so (cover your eyes guys) I started laying a maxi pad over it to soak it up. And it did, they would be saturated within a couple hours.

Thursday was my next labs. Still very low output, still soaking through pads at a ridiculous rate. Came over, did labs, got home, phone rang. First they said something about adjusting the meds some more. About 15 minutes later they called and wanted me at the hospital they had a room for me. :scared1:

AT the hospital they sonogramed my kidney, then took me down to do my very first round of hemodialysis. When I got back to the room they tried to "collect" some of the fluid that was coming out. While I was lying down she didn't have much luck, when she stood me up it just ran out. It was like I was peeing down my leg, only I was doing it through my incision instead of "normal" places. :rolleyes1

They sent that in to be tested and discovered that it was in fact urine, and I was in fact peeing down my leg through my incision.:confused3. Once that was determined, that scheduled me for surgery.

In " my language" my understanding is one of the tubes connecting the kidney to the bladder had a pinhole leak in it. That is why there was "seeping" on Tuesday. By Thursday, that pinhole had burst and was filling my cavity around the kidney with urine instead of transporting it o the bladder so it was coming out through the incision.

So Thursday night they took me back in and fixed the leak. :thumbsup2. They have a small stent in there for about a month or so to help support it while it heals, then that will be removed at an office visit. I am on a bladder catheter because she wants my bladder to rest and heal after the repair surgery. But the good news is, the kidney itself has been waking up and making itself at home while the bladder and connecting tubes were giving me fits. So now that everything is hooked up and patched up I am "outputting" like crazy again. I won't share the numbers of "buckets" they have drained out of my catheter bag....but a term involving race horses comes to mind.:laughing:

Don't know when they plan to send me home, one doctor early this morning said that tomorrow is on the table. The other doctor mentioned leaving the catheter in a few days. I want to stay until the catheter is removed, and I don't want the catheter removed until they are sure it is ok to do so. So I'm not sure what's up there.

I feel fantastic. I went for a walk around the hall yesterday and my husband said I hadn't walked that good in years. I still have some diet restrictions that are hard to follow.....phosphorous is the big one and it seems to be in everything!

My creatinine level is in th 4 s......that's something in your blood and in your urine that helps gauge how well thebkidneys are doing their job. 1 is good, 6 is bad in a normal person, I had been in the teens. I haven't been in the 4s in many years.....so that is more goodnews.


As always your prayers and pixie dust are very much appreciated!:grouphug:
 
Tanya, good to hear from you! When I read your report I became very worried that things had gone horribly wrong! But it seems like it was just a "small" hiccup (within the scale of things, normally I would consider a leak in the tubes from kidney to bladder rather major).

I hope your recovery will continue and lots of output sounds just wonderful!
 
Hey, Dan, I think you are cooler than Marv and he is on FB. :rotfl::rotfl::rotfl:
:sad1:
If your posts start sounding more like Marv's :stir: we'll know why. ;)
Hey! She said the guy was younger than her...... :headache:
here that marv.
:listen:
What Kathy said is neither HERE nor there! :sad2:
No real new news. Still peeing like a big girl.....last week I would produce some piddly little bit when I'd get up in the morning and pretty much call it a day. Now it's every hour and a half to two hours. My bladder needs to relearn " holding it". It hasn't had to do that for quite some time! I know, I know tmi......but it is what it is!
So proud of my big girl!!!
I'M HOME!!!!! And I'm going to bed! Who'd have thought it - last week at this time I was going to bed with a follow-up appoint for the repair on my fistula, a week later I am going to bed with my brand new, fully functioning kidney! God is Good!
ALL the TIME!

So glad you made it home! Sorry for the little setback, but glad they found what was wrong and got you all fixed back up! Hope you will be back home soon and continue to improve! :hug:
 




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