I Hate Dialysis Message Board
Dialysis Discussion => Dialysis: General Discussion => Topic started by: Maker on November 07, 2009, 10:13:43 AM
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I just got lab results yesterday after 1 full month on dialysis.
Day one GFR = 11, Creatinine = 6.2, BUN = 17
Current GFR = 18, Creatinine = 3.4, BUN = 8
This seems like an incredible improvement to me, and I feel really good!! I was feeling pretty crappy when I started dialysis. I would be interested to hear what some of the rest of you think about this type of change in function?
I know it may be wishful thinking but I am still praying that I can quit dialysis and make it to transplant without starting it again. Has anyone done something like this? If so, what would be good enough numbers to justify quitting? :thx;
Edited: Fixed error in subject line - okarol/admin
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That sounds absolutely exciting!
I wish you all the best and good luck, Kristina.
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Maker , it is the dialysis that is making those numbers so good. Try stopping dialysis for a few days and the numbers will more than likely be back to where they were before you started dialysis. My husband's bloodwork results are really good to but he wouldn't be long getting sick if he gave up dialysis!! If dialysis is working your bloodwork results will really improve.
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Ditto to what Del said! Dialysis is doing it's job, that's all. Your creatinine at 3.4 is still very far from normal. The main point, and it's very very good news too, is that you're feeling better and by keeping your lab values within acceptable ranges you will be preventing longer-term damage to your body, damage that can be irreversible sometimes.
As lovely a dream as it may be, don't consider stopping dialysis or you will start feeling crappy again in short order.
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Yeah , sorry to burst your bubble but we all improve WITH dialysis. I wish i could tell you different :(
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Yep, shows D is doing its thing and that's half the reason for doing it - to make you well enough to get on with life (and to keep living it).
I remember a couple of years ago at my unit there was a girl who came in one day all excited! Her results were so great that they were saying she didn't have to come back to the next dialysis! There was real hope and some excitement. It *is* very rare, but it does happen that kidneys can recover some function. Well she skipped that next session.... .... and was back the session afterwards - they'd tested her again and sure enough the labs were back down in the dumps. Poor thing was so crestfallen. She didn't skip any more sessions.
So yeah Maker sounds good but I think you should focus on how good you're feeling and that those labs are very good rather than "can I stop dialysis?" - it's great you ARE doing so well!!! :2thumbsup;
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Ok, thanks guys, I get the picture...
I didn't know what to expect when I started dialysis, so I was really surprised to see such a big improvement. I will focus on being thankful that I feel good and I won't try to quit! :)
I definitely don't want to start feeling sick again.
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oh goodness maker,,,, I'm still in a bit of denial (i guess) that my hubby is really going to have to stay on dialysis.. See, for him, his GFR stayed at about 20-27 "unless" he got his bronchitis and then his GFR would be 18 or 19..(still too high for dialysis i thought) So, when this last time he went in coughing, and it was low and his hemoglobin was low, they gave him transfusions and started his dialysis. Back up came his GFR so i say, give him a try without dialysis.. They're reluctant to do this but boy oh boy do i feel your desire to try. All his numbers are good, but :'( he does retain water now so i guess thats the reason we probably HAVE to keep at it... It's really not too bad or anything, i just really want to know that we're doing the right thing and not doing it prematurely.. Gesh, sorry to go on about 'us'.... i just know how it feels to want to try, but as these good people here say,,,,, keep at it.. Im so glad you have a 'kidney' in your future..that will surely be a happy day :2thumbsup;
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Acute kidney failure (due to sudden blockage of the ureters or infection of the kidneys) is known to be reversible in many cases.
Reversibility of chronic kidney disease is much rarer (though it has happened). We had one patient in my dialysis unit whose kidneys recovered enough to get off dialysis. But that's just one patient, out of the scores of patients being dialyzed.
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When my husband started dialysis he felt so good for the first few months. Unfortunately he started slacking off with taking care of himself on the off days. Enjoy your life now that your feeling better. Dialysis is a treatment that needs to be continued with proper diet and a pro-active stance with your health. Do your best so that you can BE at your best!
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Hi,
I'm glad your results are coming back positive, you must be feeling heaps better. I've got my fingers crossed for you for the transplant and fistula (and prayers). Don't stop D though becuase it is working, you are feeling so good because hemo is really efficient at removing toxins from the body.
Alll the best, Jenny
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oh goodness maker,,,, I'm still in a bit of denial (i guess) that my hubby is really going to have to stay on dialysis.. See, for him, his GFR stayed at about 20-27 "unless" he got his bronchitis and then his GFR would be 18 or 19..(still too high for dialysis i thought) So, when this last time he went in coughing, and it was low and his hemoglobin was low, they gave him transfusions and started his dialysis. Back up came his GFR so i say, give him a try without dialysis.. They're reluctant to do this but boy oh boy do i feel your desire to try. All his numbers are good, but :'( he does retain water now so i guess thats the reason we probably HAVE to keep at it... It's really not too bad or anything, i just really want to know that we're doing the right thing and not doing it prematurely.. Gesh, sorry to go on about 'us'.... i just know how it feels to want to try, but as these good people here say,,,,, keep at it.. Im so glad you have a 'kidney' in your future..that will surely be a happy day :2thumbsup;
20-27 GFR does sound a bit high - but it also sounds like your hubby is seeing some other symptoms of ESRF so perhaps the decision to start, while surprising and a bit early, was made because of that. In the end stuff like eGFR is just a number - the important issue is how the patient is feeling and what physical symptoms they are having. You mentioned fluid retention which is clearly one issue that needs to be dealt with (note the numbers of threads dealing with fluids here!) so while getting off D sounds like a great idea, that won't solve the fluid issue, and you do NOT want fluids building up in hubby.
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Hey Maker! Congrats on the readings. I go back to the nephrologist next week andI'm looking forward to an improvement. I hope I can match yours. I'll let you know. Keep smiling.
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"""""[20-27 GFR does sound a bit high - but it also sounds like your hubby is seeing some other symptoms of ESRF so perhaps the decision to start, while surprising and a bit early, was made because of that. In the end stuff like eGFR is just a number - the important issue is how the patient is feeling and what physical symptoms they are having. You mentioned fluid retention which is clearly one issue that needs to be dealt with (note the numbers of threads dealing with fluids here!) so while getting off D sounds like a great idea, that won't solve the fluid issue, and you do NOT want fluids building up in hubby.
[/quote]""""
edited to say :oops; Dont know what i did or how to "quote" so that above me is a quote from RichardMEL
Thank you so much.. We're going to his reg neph tomorrow, and im not even sure what questions to ask anymore.. I feel like i've gotton so much info here already... I do think that his main reason for 'D' is because of fluid. His potasium and all that stuff is always right on (without meds etc) and sometimes they even question why he started d in the first place............and then he comes in with swolen feet and say ahhhhha... Again, thanks!
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Hey
I know you want to get off of dilalysis. And boy, you know from reading my most recent post, I do too. You really should look at the Kt/v. If that is high you can discuss it with your doctors. I see if your creatinine level is 3.4 the you have a lot, I mean a lot of kidney function left. Are you on any binders? Just curious.
Actually, I am writing my book. I have permission from a nearby nocturnal unit to talk to patients about being on nocturnal hemo dialysis. One of the guys that i am interviewing went 15 months without dialysis after being on dialysis for awhile.
I personally wont count on it. I am hearing stories that people after being on dialysis so long their kidneys kicked back in. My nurse was telling me that she had a few people that went off of dialysis because they didnt need it anymore, they are being watched. A issue of one the Davita, National Kidney Foundation or AAKP had a article way back about a guy who no longer needed dialysis for awhile.
I guess it has happned, I just wish i didnt hear about it. lol
Its too bad that you cant go on PD. Your levels would look good like this for a longer time then they are on hemo.
Lisa
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I wouldn't want to give you false hope Lori, but this can happen.
My Neph told me he had had a patient regain enough function to get off dialysis.
This lady was on the waiting list for a kidney and all.
I have read that the aim of "D" is to give you around 20% function.
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Hey
I know you want to get off of dilalysis. And boy, you know from reading my most recent post, I do too. You really should look at the Kt/v. If that is high you can discuss it with your doctors. I see if your creatinine level is 3.4 the you have a lot, I mean a lot of kidney function left. Are you on any binders? Just curious.
Actually, I am writing my book. I have permission from a nearby nocturnal unit to talk to patients about being on nocturnal hemo dialysis. One of the guys that i am interviewing went 15 months without dialysis after being on dialysis for awhile.
I personally wont count on it. I am hearing stories that people after being on dialysis so long their kidneys kicked back in. My nurse was telling me that she had a few people that went off of dialysis because they didnt need it anymore, they are being watched. A issue of one the Davita, National Kidney Foundation or AAKP had a article way back about a guy who no longer needed dialysis for awhile.
I guess it has happned, I just wish i didnt hear about it. lol
Its too bad that you cant go on PD. Your levels would look good like this for a longer time then they are on hemo.
Lisa
Yes Lisa, I am on binders. 800mg Renvela with meals & snacks. Seems to be working, my phosphorus went from 5.1 to 3.4 :2thumbsup;
Kt/V 1.8, URR 75
Peeing good right now without any swelling or edema. Woke up this morning with a full bladder :bandance;
I really don't think I want to do PD, but I really want to do home hemo if I can't get a living donor transplant fairly soon. I'm just trying to find out if its even an option without a "partner".
Hey Maker! Congrats on the readings. I go back to the nephrologist next week andI'm looking forward to an improvement. I hope I can match yours. I'll let you know. Keep smiling.
Yes Galvo, please let us know what you find out! How are you feeling since starting D?
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Ok, I go to what is reported to be the largest Davita in the world and my tech had 20 years experience there. She tells me that ONE man was able to get off dialysis since she's been there (alive I mean). Odds not that good!
Home vs. In Center: In Texas your are required to have A partner. I fought like heck to do home even finding different people who would come stay during my treatment but they would not approve. Didn't really think it was worth getting married. I am SO GLAD. I couldn't have handled all the responsibility alone. A nurse, a tech and myself get it all done three times a week. Also glad that they are responsible for all the required equipment, chemicals, helping make decision, etc. I now know I wouldn't want supplies it in the house as a constant reminder. All that and I get to visit three times per weeks, complain if I feel the need three times per week, watch movies, catch up on e-maiil (though one handed), read a lot of your posts plus a few other perks I shouldn't tell about.
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hey Im jealous that your center has internet. If it is so large, how many patients are there? My center in Detroit has 180. (I only do hemo when i get a hernia and have to heal after surgery).
Lisa
Ok, I go to what is reported to be the largest Davita in the world and my tech had 20 years experience there. She tells me that ONE man was able to get off dialysis since she's been there (alive I mean). Odds not that good!
Home vs. In Center: In Texas your are required to have A partner. I fought like heck to do home even finding different people who would come stay during my treatment but they would not approve. Didn't really think it was worth getting married. I am SO GLAD. I couldn't have handled all the responsibility alone. A nurse, a tech and myself get it all done three times a week. Also glad that they are responsible for all the required equipment, chemicals, helping make decision, etc. I now know I wouldn't want supplies it in the house as a constant reminder. All that and I get to visit three times per weeks, complain if I feel the need three times per week, watch movies, catch up on e-maiil (though one handed), read a lot of your posts plus a few other perks I shouldn't tell about.
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Ok, I go to what is reported to be the largest Davita in the world and my tech had 20 years experience there. She tells me that ONE man was able to get off dialysis since she's been there (alive I mean). Odds not that good!
Home vs. In Center: In Texas your are required to have A partner. I fought like heck to do home even finding different people who would come stay during my treatment but they would not approve. Didn't really think it was worth getting married. I am SO GLAD. I couldn't have handled all the responsibility alone. A nurse, a tech and myself get it all done three times a week. Also glad that they are responsible for all the required equipment, chemicals, helping make decision, etc. I now know I wouldn't want supplies it in the house as a constant reminder. All that and I get to visit three times per weeks, complain if I feel the need three times per week, watch movies, catch up on e-maiil (though one handed), read a lot of your posts plus a few other perks I shouldn't tell about.
You make some great points! I love the staff at dialysis and always look forward to seeing them. We have wi-fi so the 3 1/2 hours flies by, I'm never bored. And it is nice not to have all the supplies at my house. But I hear results are so much better when you get more hours and more FIRST hours of dialysis at home. Guess I'm doing pretty good for now though ;D
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In all my years as a Dialysis nurse, never heard of that. Until now. I had a patient on HD for years. She swas from a previous clinic. She called me the other day and said she hadn't been to HD in months. I congratulated her on her transplant, and she said "no, she just wasn't needing HD any more". She said her labs are grood, and that she feels great, and has gone back to work". This is of course a very rare instance, but I guess we can never say never. :cheer:
But everyone is right, you feel better and your labs are improved because HD is doing it's job!!!!!! :bandance;
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Maker, I've had the vasc cath in my neck removedand a chest one installed. 6 bouts of D, am now on 4 hours per session and I feel GOOD!!!!! As I said, I'm looking forward to my pathology figures next week. I hope I can match yours. Back to you, girl, how are YOU feeling?
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Maker, I've had the vasc cath in my neck removedand a chest one installed. 6 bouts of D, am now on 4 hours per session and I feel GOOD!!!!! As I said, I'm looking forward to my pathology figures next week. I hope I can match yours. Back to you, girl, how are YOU feeling?
Galvo, that's great :clap; I'm glad you are feeling good. I feel like a million bucks! Best I have felt in quite a while.
Post your lab results when you get them next week if you would like, and I really hope they are good. The fact that you are feeling better must be a good sign. Its exciting to see the results of our hard work - especially when we follow our diet and blood work shows it :)
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I've been wondering this lately as well... my labs have been really good:
Createnine - 3.2
Kt/v - 3.5
Phosphorus - 4.0 (no binders in 2 months)
hemoglobin - 13.9 (no Epo in 4 months)
I'm doing less dialysis and have still been doing great... I'd like to see what happens if I stopped dialysis but I'm too scared to try it :/ I just try to focus on the fact that I am feeling so much better than before and to be thankful for that.
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Wow that is awesomeSavemeimdtba!
What was your creatinine level when you started dialysis? 3.2 is quite low IMO. My nurse did tell me if someone's Kt/v is 4 or 5, you have enough residual kidney function to not need dialysis anymore.
Lisa
I've been wondering this lately as well... my labs have been really good:
Createnine - 3.2
Kt/v - 3.5
Phosphorus - 4.0 (no binders in 2 months)
hemoglobin - 13.9 (no Epo in 4 months)
I'm doing less dialysis and have still been doing great... I'd like to see what happens if I stopped dialysis but I'm too scared to try it :/ I just try to focus on the fact that I am feeling so much better than before and to be thankful for that.
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Great results! seems to me that you doing so well on dialysis and it's really filtering those toxins out well.. and all your RRF is kicking in too. Why don't you speak to your neph about it? Doing less is great so even if nothing else changes you're clearly feeling better and your labs are great - something to be very happy about I think!
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Good news Maker! My 1-month blood work is November 30th and I hope my numbers look as good as yours. Only difference for me is I'm on PD.
Effie
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Lill - my creatanine before dialysis was 11.0, then I started hemo and it hovered around 8 for those three months, once I started PD it's been steadily coming down. It appears to be pretty much staying around 3.0-3.5.
I will talk to my nephrologist, Richard. It's been pretty hectic there lately so we haven't been able to address any issues. My nurse left about 3 months ago and they haven't replaced her yet... so it's people in and out all the time who don't know me and my Dr. is running around in a panic. I don't even have the card that goes in my machine that records the dialysis data! So, they're really not giving much care to what's going on with me at all... hopefully it'll get back to normal soon. Luckily, I'm doing well, cause it would suck to have no nurse and having problems.
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My neph told me that patients with PD tend to have high creatinine values. My creatinine tends to increase over time after starting PD. Your creatinine can come down so much, maybe something happens to your kidneys.