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Author Topic: How can I help without lecturing?  (Read 6256 times)
caringpct
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« on: July 20, 2010, 08:54:57 PM »

My FA and dietician keep telling me I have to remind my patients to take their binders and tell them what foods not to eat. I understand this is very important for their health, however most of these patients have been on D for years and know all this. I do educate new patients on foods and why we check potassium and phosphorus levels, but the ones that been there forever?? I always feel I am lecturing them or treating them like children, but if I don't say anything then I get "talked." How can I make things come across easier or even fun? I would love to play games but the ones I want to do I'm told are too difficult for patients.
Really?? My patients are not stupid, in fact they teach me a few things.
Anyway, sorry about that little rant.
Any suggestions would be appreciated. Thanks everyone. I love this site!!
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Riki
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« Reply #1 on: July 20, 2010, 09:20:05 PM »

I'm treated like a kid sometimes because I look like one, even though I'm in my 30s.  Best I can tell you is to level with them, be frank.  If their levels are off, just tell them that much.  If they've been doing it for a whle, they know what they need to do.  Maybe just ask, "you know what you need to do to fix that, right?"  For me, the answer is usually, "yeah, take the binders"  I have a high phosphorus level.  Always have had a high phosphorus level.  Don't lecture, just talk.. coversate.. *L*  and yeah, I know that's not a word.  You're likely to get a few rolled eyes, but you're doing your duty in letting them know.

Dumb question.  Why doesn't the dietitian tell the patients themselves.  Isn't that their job?  I've gotten phone calls from the dietitian telling me when my levels are off and what foods I should be avoiding
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RichardMEL
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« Reply #2 on: July 20, 2010, 11:56:12 PM »

Her's an idea I picked up from my football club. I was talking to some players (the football kind, not the other kind.. well actually I have no idea on that count!  :rofl;) and they have a system after every game they have to grade their own performance, and they then take that to the coaches - they have to be critical to point out things they did wrong as well as things they did right - rather than the coaches just saying "you did this wrong and that wrong" - a few of them said it works really well for them because they feel more empowered and trusted with their own output, and it can also show that they are learning what is expected of them based on what they do right, but also their ability to see, and hopefully learn from, what they did wrong.

So how does this translate to dialysis? Well, I like to play this little game with my team. Well more with myself than them, but most of them play along. I am one of the few who actually asks for my labs as soon as they are in the computer. Now some of them just say "it looks OK" or whatever, but usually they give me the lab printout hot off the press, and they ask *me* what I think of the results. So, I look down, and I know the reference ranges for the various important things like K, Ca, PO4, hemoglobin, albumin, etc and so they wait for ME to point out that oh PTH was elevated, and my Phos was a bit high(that pizza had more cheese than I thought !!  >:D) and so on.

Now I don't know if they allow that kind of thing where you work - I keep hearing about these awful sounding "report cards" and the like, but maybe with the longer term patients you could show them the labs(if they seem interested) and ask them if there's anything out of the ordinary that they can see(even if there isn't !) and if there is, to suggest why it might be. K up? drinking orange juice? had pineapple? etc.

I know when I get to look at my labs and show some understanding and appreciation for the issues that I feel empowered (and trusted), part of my treatment team, and not that I'm being lectured to, but being treated with respect.

I do sort of agree that why does the dietician expect you to do their work for them? I mean a long term D patient is probably pretty stable and knows what they need to do - just telling them again and again will piss them off, and if they have something abnormal, like a higher K or something, it is probably because they've decided they can live with the risk but they just love their potatoes, or tomato or whatever - I mean telling them stuff they already know will just piss them off. You could always try something like when they're getting ofdf say in a fun way "take it easy with that chocolate!" or "don't have too many at the bar tonight!" - maybe that will be less of a lecture, but still getting the point accross.

Anyway just a couple of ideas for you.
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« Reply #3 on: July 21, 2010, 04:23:26 AM »

No amount of talking or games will make people do things , they will either watch their diet or not ! Yes educate the newbies, but what is it they say ? ..you cant teach an old dog new tricks !  :rofl;
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RichardMEL
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« Reply #4 on: July 21, 2010, 04:44:57 AM »

tend to agree with that KS - but I think the problem that caringpct has is that if they doesn't make some sort of effort then THEY get in trouble! I personally think it's a bit unfair to do that with the longer term patients who, as you say, will do what they like and just resent more lectures. Caught beterrn a rock and a hard place in a way.
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3/1993: Diagnosed with Kidney Failure (FSGS)
25/7/2006: Started hemo 3x/week 5 hour sessions :(
27/11/2010: Cadaveric kidney transplant from my wonderful donor!!! "Danny" currently settling in and working better every day!!! :)

BE POSITIVE * BE INFORMED * BE PROACTIVE * BE IN CONTROL * LIVE LIFE!
caringpct
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« Reply #5 on: July 21, 2010, 06:29:54 AM »

Thank you all. The dietician does talk to the patients but she's bit of an airhead. And she lectures (trust me I have been on the receiving end of that one  :Kit n Stik;) I asked one of my patients what happens when her phosphorus goes high, best answer every, she replied, "I get griped at!" :rofl; :rofl; I loved it!! (of course she said it kiddingly) is that a word or am I just bad at spelling?
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« Reply #6 on: July 21, 2010, 07:31:00 AM »

*LOL*  that probably would have been my answer too.... although, I would have said that I get growled at.  The team leader in the unit came up to me a few weeks ago and mentioned to me that my phosphorus was high, and that if I didn't get it down, they could take me off the transplant list.  I know that it's true, because of the complications involved with high phosphorus, but I'm sick of that threat.

When I was a child, we couldn't make it to a clinic visit, because of a snowstorm, and the only way out of the province at the time was an ice breaking ferry that wasn't running due to high winds.  When Mom called to say that we weren't coming, she was told that not coming to clinic was considered noncompliance and that was grounds for taking me off the transplant list.  She gave that woman a blast so hard, I'll bet her ear is still sore.

it seems a threat they hold over your head. Do exactly as well tell you, or you're off the list

wow.. I went off on a tangent, didn't I.. *LOL*
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« Reply #7 on: July 21, 2010, 12:19:40 PM »

The games they tried to play annoyed my husband greatly.
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Stacy Without An E
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« Reply #8 on: July 21, 2010, 01:06:56 PM »

The only time anyone talks to me about my lab results is the nurse or the dietician.  For some reason, it seems like they want to pass their job duties on to you.  I believe I can speak for Dialysis veterans (6+ years) when I say:

1) No games!  It interrupts our TV, DVD, or music we're enjoying while trying to get through treatment.
2) After the first six months, most of us (except the crazies) know our routine and don't need to be lectured on our treatment.

Even asking the questions shows you're a conscientious and caring PCT.  It is my experience that is a rare gift in the Purgatory of Dialysis.
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Stacy Without An E

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Beth35
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« Reply #9 on: July 21, 2010, 03:55:52 PM »

I too hate being lectured about what I'm eating.  All I want to know is what my levels are and I'll go from there.  I want to know if my potassium is high as I really don't want to die but I'm still going to cheat once in a while and I'm a grown person so I hate the lectures from those who don't know what it's like to have such a strict diet and fluid restriction. 

Just give it to me straight and avoid the naughty girl lectures. 
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Quickfeet
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« Reply #10 on: July 21, 2010, 05:02:10 PM »

I still play innocent, when my labs are up. I'm like, really that's weird.

No games please. Milk = phosphorus Got it :2thumbsup;. Orange juice = potassium Got it.  :2thumbsup;
Give me a simple list of what I can and can't eat and why and that's all I need. Then I will decide what I will and wont eat. The games would be great for helping our children understand why we can't have certain foods.
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Riki
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« Reply #11 on: July 21, 2010, 05:16:00 PM »

what are these games you all talk about?  I think if one of the nurses or the dietitian tried to play a game about what foods I should eat, I'd look at them and tell them to take a look at my chart to see what year I was born

if that is what is it, it sounds rather degrading and condecending
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RichardMEL
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« Reply #12 on: July 21, 2010, 06:17:30 PM »

agree re the games.. sounds stupid and annoying.
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3/1993: Diagnosed with Kidney Failure (FSGS)
25/7/2006: Started hemo 3x/week 5 hour sessions :(
27/11/2010: Cadaveric kidney transplant from my wonderful donor!!! "Danny" currently settling in and working better every day!!! :)

BE POSITIVE * BE INFORMED * BE PROACTIVE * BE IN CONTROL * LIVE LIFE!
caringpct
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« Reply #13 on: July 22, 2010, 01:25:28 AM »

Even games that are not dialysis related? I just want to help pas the time for the patients.
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RichardMEL
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« Reply #14 on: July 22, 2010, 02:24:05 AM »

Even games that are not dialysis related? I just want to help pas the time for the patients.

Do patients not have enough entertainment options? Like TV's etc.. plus I am sure they can bring in their own - books, dvd players, ipods, whatever.

I think the problem is that doing something like that, as well intentioned as it is, is that playing games (of any sort) is likely going to be intrusive to others in the unit who are not interested. Our unit tries to keep a generally quiet atmosphere, tv use with headphones, no loud music etc and people are encouraged to not shout or yell or whatever (a bit hard for the deaf ones!).

I know if it was in my unit and someone wanted to do something like that to help pass the time, I would object if it made noise that distracted me. I have my laptop and watch movies. Others sleep etc. Now if, by games, you mean something more quiet, like perhaps playing a card game, or chess one on one or something, then hey I'm all for that because it wouldn't affect me. I don't quite see how that is very practical though.

Just a thought. Sorry - not trying to burst your bubble.. It's just an opinion.
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3/1993: Diagnosed with Kidney Failure (FSGS)
25/7/2006: Started hemo 3x/week 5 hour sessions :(
27/11/2010: Cadaveric kidney transplant from my wonderful donor!!! "Danny" currently settling in and working better every day!!! :)

BE POSITIVE * BE INFORMED * BE PROACTIVE * BE IN CONTROL * LIVE LIFE!
Quickfeet
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« Reply #15 on: July 22, 2010, 03:00:43 AM »

sorry I thought you meant just for education's sake. I don't do in center dialysis but if I did... If you mean card games, chess, etc. that would be ok If I didn't bring anything. But if I am enjoying a book the last thing I want to do is be is interupted. If they look bored out of their mind, it doesn't hurt to ask. Every person is different.

I think that many dialysis patients can be moody and what might offend one day, might brighten their day on another.
example 1
I feel like poop (translation: A feel like my whole body is dead weight and it's time to trade it in for a new model.). A healthy person comes up to me and tells me how much better I am looking. I say, "That's because my disease is on the inside." I don't say it in a mean way, because they mean well. But does make me grumpy.
example 2
I feel good (translation: I feel like a healthy person with the flu.) A healthy person comes up to me and tells me how much better I am looking. I say, "Thanks, I'm feeling pretty good." I feel just a little happier after that exchange.


The main thing is that you care. Being cheerful can be good but being too cheerful would just aggravate me, because I would be jealous that I wasn't as happy.
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Quickfeet
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« Reply #16 on: July 22, 2010, 03:14:52 AM »

Richard are you saying, you would not play games with a pretty Clinic worker because she made too much noise?  :(

My world has turned upside down.  :rofl;

Well I guess it makes since. Dialysis is probably the only time you can get away from all those women. :2thumbsup;

 :bow; :bow; :bow;
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RichardMEL
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« Reply #17 on: July 22, 2010, 05:27:59 AM »

haha quickfeet. Well those other sorts of games usually require the curtain be drawn.... and I'd prefer to have both arms free!!!  :rofl; :rofl; :rofl; :rofl;

good stuff. You got me good there!  :shy;
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3/1993: Diagnosed with Kidney Failure (FSGS)
25/7/2006: Started hemo 3x/week 5 hour sessions :(
27/11/2010: Cadaveric kidney transplant from my wonderful donor!!! "Danny" currently settling in and working better every day!!! :)

BE POSITIVE * BE INFORMED * BE PROACTIVE * BE IN CONTROL * LIVE LIFE!
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« Reply #18 on: July 22, 2010, 11:29:09 AM »

In the past they would bring in a PA system and try to play bingo.  Very few patients participated, and it was hard to hear my movie with someone yelling, "B-6!  Anyone have B-6!"

The most hilarious part though was the patients who don't speak English.  They kept staring at this woman and wondered why she was yelling at them over a speaker.
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Stacy Without An E

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« Reply #19 on: July 22, 2010, 01:55:53 PM »

wouldn't nurses have better things to do than be bingo callers??  I mean, mine are always so busy. They're charting, they're answering phones, they're doing up iv medications for those who need it, they're looking up lab results on the computer, they're responding to alarms, they're doing dressings and checking blood sugars.  They're putting people on and taking people off, they're cleaning chairs and machines.  They're always checking on people like me, who's bp can drop suddenly, or who can clot the dialyzer, and they're doing little tihngs like getting snacks for the diabetics, or ice chips or a warm blanket for somebody.  One fellow has a service dog with him, and they give the dog a bowl of ice halfway through his treatment.  They just wouldn't have time to play games.

I'm with Richard. if you want to play a quiet game with one of the patients, that's fine, but leave me alone.  I'm good with my ipod, my imagination, and my involuntary naps.
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caringpct
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« Reply #20 on: July 22, 2010, 04:24:31 PM »

Your nurses help take people off and on, dressing changes, and all that!!???? My nurses sit behind a desk and text message friends all day :banghead; Can I come work at your unit?

I see everyone's point. NO GAMES!!
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« Reply #21 on: July 22, 2010, 04:43:38 PM »

we don't have any techs. Just nurses and support workers.  Right now we have 12 nurses, 2 support workers, and 2 students.  There's also 2 nephrologists and a nutritionist, who I've only met once, and she's never been on the unit.  We're all monitored by the transplant centre, which is a different province, so we're quite happy that we have what we do, and it's close to home.  When I was a kid, I was the first child to do home dialysis in the province. There's been many since me, though.  I"m glad to have been a pioneer.
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RichardMEL
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« Reply #22 on: July 22, 2010, 09:30:08 PM »

wouldn't nurses have better things to do than be bingo callers??  I mean, mine are always so busy. They're charting, they're answering phones, they're doing up iv medications for those who need it, they're looking up lab results on the computer, they're responding to alarms, they're doing dressings and checking blood sugars.  They're putting people on and taking people off, they're cleaning chairs and machines.  They're always checking on people like me, who's bp can drop suddenly, or who can clot the dialyzer, and they're doing little tihngs like getting snacks for the diabetics, or ice chips or a warm blanket for somebody.  One fellow has a service dog with him, and they give the dog a bowl of ice halfway through his treatment.  They just wouldn't have time to play games.

Yep, my unit is like that too - always busy busy busy. A big thing yesterday was whtn a trainer or someone came in and got a bunch of them around for about 30 mins to explain calciulating Kt/V all that stuff in the machine. They did that with me (that was so cool!) but always had a couple of them monitoring the chairs, and running off to fix alarms or do obs or whatever.

I couldn't see anyone having the time for extra stuff like that, but I suppose every unit is different.

Quote
I'm with Richard. if you want to play a quiet game with one of the patients, that's fine, but leave me alone.  I'm good with my ipod, my imagination, and my involuntary naps.

Oh Riki if you were with me there wouldn't be in involuntary naps!!!  >:D >:D >:D >:D >:D >:D >:D >:D

 :shy;

(now that's a "game" I'd play!!!)
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3/1993: Diagnosed with Kidney Failure (FSGS)
25/7/2006: Started hemo 3x/week 5 hour sessions :(
27/11/2010: Cadaveric kidney transplant from my wonderful donor!!! "Danny" currently settling in and working better every day!!! :)

BE POSITIVE * BE INFORMED * BE PROACTIVE * BE IN CONTROL * LIVE LIFE!
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« Reply #23 on: July 22, 2010, 10:44:05 PM »

I get a piece paper from the dietitian, the PA comes in a tells me what us if, the doc comes in and tells me what is off, Now tell me, why do I need three people to telm me what I already know!
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« Reply #24 on: July 23, 2010, 05:41:23 AM »

When I found out 6 years ago that I had kidney problems, I did as much research as I could into how to protect them and myself.  Maybe I didn't look in the right places but I found it quite difficult to get specific information on what foods were high in Potassium etc. I knew the obvious ones like potatoes and bananas but it was a struggle at times finding out about other items.

I seem to have done a good job though because even though my kidneys failed and my creatine levels were through the roof, my years of avoiding Potassium had obviously worked because my K level was only 3.5 when I started dialysis. In fact, the highest my K level has ever been is 4.5.

How about creating a laminated fact sheet showing the levels of Potassium, Phosphorus etc in certain foods? Make it clear and concise so people can't find it confusing. You could then distribute it to every patient.  You could include common food substances and then recommend alternatives.  Example, 100g of Cheddar cheese has 512mg of Phosphorus whereas 100g of Feta has 337mg and 100g of Brie has 188mg.

If someone had given me a sheet like that, I'd have probably hugged them for a week.
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