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| | |-+  How do you motivate and encourage to be pro active
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Author Topic: How do you motivate and encourage to be pro active  (Read 5569 times)
jessup
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Gemma - the tucker monster

« on: October 15, 2008, 01:58:25 PM »

I know that being positive and encouraging is the way to go but "you can take a horse to water but you can't make it drink".  Anyone got suggestions on how to motivate Dad.  I believe I should respect his decisions but WTF - it's hard to sit back and not "tell him" a few home truths.  I don't want to rattle him 
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flip
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« Reply #1 on: October 15, 2008, 02:37:29 PM »

Set some goals for him. Talk about things you want to do and places you want to go. Find some chores that he needs to do. Sometimes too much caregiving causes complacency.
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That which does not kill me only makes me stronger - Neitzsche
monrein
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« Reply #2 on: October 15, 2008, 03:00:03 PM »

Do you think your Dad is clinically depressed Jessup?  I mean more than "down" or "blue", I mean depressed.  Has he ever seen a doctor about this?  It's a fairly common feature of dialysis patients.
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Pyelonephritis (began at 8 mos old)
Home haemo 1980-1985 (self-cannulated with 15 gauge sharps)
Cadaveric transplant 1985
New upper-arm fistula April 2008
Uldall-Cook catheter inserted May 2008
Haemo-dialysis, self care unit June 2008
(2 1/2 hours X 5 weekly)
Self-cannulated, 15 gauge blunts, buttonholes.
Living donor transplant (sister-in law Kathy) Feb. 2009
First failed kidney transplant removed Apr.  2009
Second trx doing great so far...all lab values in normal ranges
jessup
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Gemma - the tucker monster

« Reply #3 on: October 15, 2008, 03:09:34 PM »

Yes I think he is but I'm not a medico
 his response is
"I'm not going to a psych "or" you don't take tablets .. you just have to get your head around it.."
"who wouldn't be depressed "
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willieandwinnie
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« Reply #4 on: October 15, 2008, 03:25:38 PM »

jessup  :cuddle; many dialysis patients go through depression or anxiety. My husband was put on Ativan for a few months and that seemed to help him. The doctor at the clinic can prescribe it or something similar. Good luck.
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"I know there's nothing to it, but I want to know what it is there's nothing to"
monrein
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« Reply #5 on: October 15, 2008, 03:32:20 PM »

OK.  He's right.  Who wouldn't be depressed is right on the money.  You can reassure him that he wouldn't need to see a shrink, just his family doctor.  You could also tell him that several of us on here take them because we tried ,just like him, to get our heads around it and had a tough time doing it so we're trying to take a tablet to make it easier to find our former selves again.  I'd also tell him that these meds don't have to be a long time commitment, if they don't help he can stop.   Without getting mad at him you can also tell him a few "home truths", like how much you care for him and how painful it is to see him not himself and how you'd do anything to get him back even just for short periods of time.

Here's a link to an Australian site that addresses the symptoms of anxiety and depression.   Hugs to you Jessup for your caring self which shines through so strongly, even in the face of your understandable frustration.  :cuddle;


http://www.anxietyaustralia.com.au/depression.shtml

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Pyelonephritis (began at 8 mos old)
Home haemo 1980-1985 (self-cannulated with 15 gauge sharps)
Cadaveric transplant 1985
New upper-arm fistula April 2008
Uldall-Cook catheter inserted May 2008
Haemo-dialysis, self care unit June 2008
(2 1/2 hours X 5 weekly)
Self-cannulated, 15 gauge blunts, buttonholes.
Living donor transplant (sister-in law Kathy) Feb. 2009
First failed kidney transplant removed Apr.  2009
Second trx doing great so far...all lab values in normal ranges
jessup
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Gemma - the tucker monster

« Reply #6 on: October 15, 2008, 03:56:18 PM »

jessup  :cuddle; many dialysis patients go through depression or anxiety. My husband was put on Ativan for a few months and that seemed to help him. The doctor at the clinic can prescribe it or something similar. Good luck.
You  are not going to believe this but IT IS TRUE ............ There is not Doc or Neph at the renal clinic.  He comes to the clinic once a month and checks the patients charts etc. But in four months of Dad receiving dialysis at this clinic he has never seen the Doc/Neph.  I finally was able to speak to the "man"(doc/Neph) and he told me on the phone that patients can't make appointments to see him - the "team" will make appointments to see the patient if "they" deem it necessary.
So to put it more clearly
whether you are a private or public patient you (the patient) can't make appointment
BLOODY UNBELIEVABLE - there is only one neph in the capital city where we live - YES A CAPITAL CITY IN AUSSIE
WTF !!!! :banghead; :banghead; :banghead; :banghead; :banghead;
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monrein
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« Reply #7 on: October 15, 2008, 04:34:56 PM »

Does your Dad have a family doc?
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Pyelonephritis (began at 8 mos old)
Home haemo 1980-1985 (self-cannulated with 15 gauge sharps)
Cadaveric transplant 1985
New upper-arm fistula April 2008
Uldall-Cook catheter inserted May 2008
Haemo-dialysis, self care unit June 2008
(2 1/2 hours X 5 weekly)
Self-cannulated, 15 gauge blunts, buttonholes.
Living donor transplant (sister-in law Kathy) Feb. 2009
First failed kidney transplant removed Apr.  2009
Second trx doing great so far...all lab values in normal ranges
jessup
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Gemma - the tucker monster

« Reply #8 on: October 15, 2008, 04:41:40 PM »

Does your Dad have a family doc?
Yes but he has said last two visits "I'll refer you to neph because I'm not up to speed on this dialysis stuff and medication" 
It is also worth noting that this doc is on the board of the AMA
But anyway Dad likes him and doesn't see a need to find a new doc
I think he (the doc) passes the buck and treats us like we are pathetic impiciles (?)
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monrein
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« Reply #9 on: October 15, 2008, 04:54:02 PM »

Jess, don't give up on this family doc.  Let him know of your frustrations with the clinic/neph situation and tell him you need his help to advocate for your Dad.  He will most likely not be able to give you info about your Dad because of patient confidentiality but you can give him your ideas and concerns about your Dad and also about the system.  Another possibility is to talk to the team, tell them your worries and ask them to schedule an appointment.  I know that it's you who deems it necessary but I'm hopeful you can convince them.  Talk to the charge nurse, head muckety muck or whatever you call her/him there.

BTW, all this stuff drives all of us nuts and you don't have to take any action at all until you feel really ready to.  I keep suggesting things and I know it feels hopeless to you right now but I'm stubborn and persistent and you can be too.  I just really wish you weren't having all this on you.
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Pyelonephritis (began at 8 mos old)
Home haemo 1980-1985 (self-cannulated with 15 gauge sharps)
Cadaveric transplant 1985
New upper-arm fistula April 2008
Uldall-Cook catheter inserted May 2008
Haemo-dialysis, self care unit June 2008
(2 1/2 hours X 5 weekly)
Self-cannulated, 15 gauge blunts, buttonholes.
Living donor transplant (sister-in law Kathy) Feb. 2009
First failed kidney transplant removed Apr.  2009
Second trx doing great so far...all lab values in normal ranges
jessup
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Posts: 773


Gemma - the tucker monster

« Reply #10 on: October 16, 2008, 12:39:05 PM »

Thanks everyone
NB - Monrein - I appreciate your honesty and forthrightness (is that even a word)
I will contine to be a pain in the bum to these so called "professionals"
I think they hope I will get sick of hum bugging them with questions and advocating
But I will continue to persist even if Dad is not proactive
Surely he can't stay in denial for ever!!!!!
 :thx; :thx; :thx; :thx;
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G-Ma
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« Reply #11 on: October 16, 2008, 02:57:33 PM »

jessup...you keep being a great family to dad and keep on persisting...I know sometimes you see things that dad doesn't see and it may feel like a long time of what he is feeling but please hang in there with him.  I know he appreciates it.
Ann
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Lost vision due to retinopathy 12/2005, 30 Laser Surg 2006
ESRD diagnosed 12/2006
03/2007 Fantastic Eye Surgeon in ND got my sight back and implanted lenses in both eyes, great distance & low reading.
Gortex 4/07.  Started dialysis in ND 5/4/2007
Gortex clotted off Thanksgiving Week of 2007, was unclotted and promptly clotted off 1/2 hour later so Permacath Rt chest.
3/2008 move to NC to be close to children.
2 Step fistula, 05/08-elevated 06/08, using mid August.
Aug 5, 08, trained NxStage and Home on 9/3/2008.
Fistulagram 09/2008. In hospital 10/30/08, Bowel Obstruction.
Back to RAI-Latrobe In Center. No home hemo at this time.
GOD IS GOOD
RichardMEL
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« Reply #12 on: October 17, 2008, 01:47:47 AM »

What the....??? One Neph in a capital city?? Are you sure?? Where are you guys? Perth? or come to think of it did you say Canberra?

That seems very odd.. but I can't believe the response you got that the neph doesn't let patients make appointments with him but the team does.. what the...?? I'd definitely kick up a stink there with the unit manager that your dad has been put on dialysis and the neph hasn't seen him AT ALL in that time? Who is managing his medication and checking his labs to make sure everything is stabalising and all that kind of thing? Sounds like a mess.

Although maybe what the neph is saying is that if there IS only one(?!!) then you'd think he'd be pretty busy so perhaps the idea is that the dialysis staff should be vetting things a little as in they should be handling more day to day things as opposed to bigger things.. still the mind does boggle somewhat. I can't imagine a situation like that at all.

At least I know in my unit there's 3-4 nephs on the staff so if mine is away (usually the case! LOL) or something I can see one of the others.. most of whom I know in one capacity or another - and they definitely know me!! LOL

Of course I'm attached to a hospital unit so I guess things are different since they're right there.

Anyway onto the motivation issue... 4 months is still pretty early in to dialysis to get settled into the life changes this brings about and it can be very depressing to find suddenly you're resitrcted in diet, drinks and of course the thrice weekly grind to get on the machine. Perhaps you should listen to where your dad is at and try and be there for him. I bet the last thing he wants is his daughter telling him "you HAVE to do this. You HAVE to do that" - I bet he gets enough of that from the dialysis people. Maybe an idea is to sit with him and ask him where he's at and what he'd like. If he's like "oh nothing it's all too much. I feel like crap" and that sort of thing or in denial and not wanting to know about what is going on get the unit manager to refer you to the social worker and/or a psychologist to try and work something out. It is a huge transition but it's also NOT the end of his life...

It's important to remember that dialysis is not the end of his life or anything and he can live quite well with it - even with the restrictions and stuff. It may not seem like it at first, but it is possible (we are all proof!! :) )... Does he talk at all with the other dialysis patients? Maybe there might be someone chatty at his unit that he can talk to who has done it for awhile and sort of show him through action they get out and do stuff and live still..

Not sure what else to suggest at this point...
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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!
jessup
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Gemma - the tucker monster

« Reply #13 on: October 17, 2008, 02:32:32 PM »

Thanks for the post RichardMEL
I have sent you a private message to let you know where we are
I am worried if I identify myself and Dad too much there might be consequences from the neph
He might or maybe a nurse read this website

He is an egotistical, self righteous f$%@k wit who has a reputation of being rude, arrogant etc with patients, staff and fellow docs

I can assure you my info is spot on
It's un bloody believable

Cheers
Jessup
 :boxing; :rant; :rant; :rant; :rant; :rant; :boxing; :boxing; :boxing; :boxing;


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