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Author Topic: What do you wish your family understood about kidney disease?  (Read 42499 times)
devon
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« Reply #50 on: September 12, 2008, 11:02:36 AM »

Catears,

YES! good point! Very well said!

Devon
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Sunny
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Sunny

« Reply #51 on: September 12, 2008, 02:34:34 PM »

I wish my family really understood what I go through when I contemplate the issues of:
1. What kind of dialysis should I do when I have to start?
2. Should I have a pre-emptive transplant and take my 59 yr old sister's kidney with High blood pressure?
3. Could I take a cadaver transplant knowing it requires me to think,in tha back of my mind, someone out there has to die young and healthy for me to get one?
4. Maybe I'll die first and these decision will never be made?

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Sunny, 49 year old female
 pre-dialysis with GoodPastures
kitkatz
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« Reply #52 on: September 12, 2008, 04:03:47 PM »

I wish my family would listen to me when I tell them what I want for my funeral and wake.  I tell them but they do not want to even think about it.  My mother will get one heck of a surprise when there is a party going on instead of a funeral service.
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lifenotonthelist.com

Ivanova: "Old Egyptian blessing: May God stand between you and harm in all the empty places you must walk." Babylon 5

Remember your present situation is not your final destination.

Take it one day, one hour, one minute, one second at a time.

"If we don't find a way out of this soon, I'm gonna lose it. Lose it... It means go crazy, nuts, insane, bonzo, no longer in possession of ones faculties, three fries short of a Happy Meal, wacko!" Jack O'Neill - SG-1
okarol
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« Reply #53 on: September 12, 2008, 04:49:41 PM »

I wish my family would listen to me when I tell them what I want for my funeral and wake.  I tell them but they do not want to even think about it.  My mother will get one heck of a surprise when there is a party going on instead of a funeral service.

Write it down and seal it an envelope marked "Open only in the event of death."
That's what my mother in law did - and inside it said she wanted to be buried, not cremated; and she wanted me to have her jewelry.
Shocked me. She didn't feel they were big enough things to add to her will, but she wanted to be sure her 4 sons knew what she wanted.





« Last Edit: September 19, 2008, 11:21:10 AM by okarol » Logged


Admin for IHateDialysis 2008 - 2014, retired.
Jenna is our daughter, bad bladder damaged her kidneys.
Was on in-center hemodialysis 2003-2007.
7 yr transplant lost due to rejection.
She did PD Sept. 2013 - July 2017
Found a swap living donor using social media, friends, family.
New kidney in a paired donation swap July 26, 2017.
Her story ---> https://www.facebook.com/WantedKidneyDonor
Please watch her video: http://youtu.be/D9ZuVJ_s80Y
Living Donors Rock! http://www.livingdonorsonline.org -
News video: http://www.youtube.com/watch?v=J-7KvgQDWpU
Mizar
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« Reply #54 on: September 12, 2008, 05:30:48 PM »

Done Wishing, I do Praying now........
I Pray that when People call and ask Where He Is and I say " Dialysis " they don't Sigh.
I Pray that when they call back later and ask for Him and I say " Sleeping " they don't Sigh.
I Pray that when they call on His off days and ask for him and I say " Sleeping " they don't Sigh.
I Pray, that when He does have a Good Day and I ask him to do something with me, He does not say " I'm too Tired " I Pray that alot.
This is Our Life Now. It is what it is. We enjoy all the Good Moments of every Good Day.
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cherpep
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« Reply #55 on: September 12, 2008, 08:24:57 PM »

I Pray, that when He does have a Good Day and I ask him to do something with me, He does not say " I'm too Tired " I Pray that alot.
This is Our Life Now. It is what it is. We enjoy all the Good Moments of every Good Day.


That was pretty good.  I would like my husband to know how much I appreciate everything about him - his never-failing understanding of my condition, his willingness to dedicate a good portion of his life to helping me with my treatments, his tender kisses on my forehead during the treatments, but mostly his devotion and love.  I am blessed.
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TynyWonder
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Calvin

« Reply #56 on: September 12, 2008, 08:28:01 PM »

aaaawwww those are blessings for sure cherpep!  You truly are one blessed lady!!!   I am happy for you!!!   :cuddle;

~Tammy~   :bandance;
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Diagnosed with ESRD-November 2006
I have had 2 fistuals-neither one worked
I have had 2 grafts the last one finally "took"
I had 3 different catheters from Nov. 06 - Dec. 08
Got on the transplant list - Halloween Day 2008

You can easily judge the character of others by how they treat those who they think can do nothing for them.    I BELIEVE THIS TO BE SOOOOO TRUE!
kitkatz
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« Reply #57 on: September 13, 2008, 08:53:37 PM »

I Pray, that when He does have a Good Day and I ask him to do something with me, He does not say " I'm too Tired " I Pray that alot.
This is Our Life Now. It is what it is. We enjoy all the Good Moments of every Good Day.


That was pretty good.  I would like my husband to know how much I appreciate everything about him - his never-failing understanding of my condition, his willingness to dedicate a good portion of his life to helping me with my treatments, his tender kisses on my forehead during the treatments, but mostly his devotion and love.  I am blessed.


Same to my hubby. God bless the lot of them for putting up with us!
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lifenotonthelist.com

Ivanova: "Old Egyptian blessing: May God stand between you and harm in all the empty places you must walk." Babylon 5

Remember your present situation is not your final destination.

Take it one day, one hour, one minute, one second at a time.

"If we don't find a way out of this soon, I'm gonna lose it. Lose it... It means go crazy, nuts, insane, bonzo, no longer in possession of ones faculties, three fries short of a Happy Meal, wacko!" Jack O'Neill - SG-1
G-Ma
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« Reply #58 on: September 13, 2008, 09:24:56 PM »

Thanks okarol..that is what I will do since no one wants to know.
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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
paris
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« Reply #59 on: September 14, 2008, 12:03:07 PM »

You are right, Kitkatz, no one wants to talk about "plans".  I finally wrote things down, because I just needed to put things in order for my own peace of mind.  Once I did that, I could forget about it.   
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It's not what you gather, but what you scatter that tells what kind of life you have lived.
okarol
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« Reply #60 on: October 23, 2008, 04:12:40 PM »


 :thx; Related thread - thanks to the members who agreed to be quoted. http://ihatedialysis.com/forum/index.php?topic=10719.0
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Admin for IHateDialysis 2008 - 2014, retired.
Jenna is our daughter, bad bladder damaged her kidneys.
Was on in-center hemodialysis 2003-2007.
7 yr transplant lost due to rejection.
She did PD Sept. 2013 - July 2017
Found a swap living donor using social media, friends, family.
New kidney in a paired donation swap July 26, 2017.
Her story ---> https://www.facebook.com/WantedKidneyDonor
Please watch her video: http://youtu.be/D9ZuVJ_s80Y
Living Donors Rock! http://www.livingdonorsonline.org -
News video: http://www.youtube.com/watch?v=J-7KvgQDWpU
thegrammalady
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« Reply #61 on: October 23, 2008, 04:22:32 PM »

i wish the uncle who thinks he knows all about it wourld realize that he doesn't and leave my mother alone!!!!
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If you can smile when things go wrong, you have someone in mind to blame.

Lead me not into temptation, I can find it myself.

Life isn't about waiting for the storm to pass, it's about learning how to dance in the rain.

Some mistakes are too much fun to only make once.

Meddle Not In The Affairs Of Dragons
For You Are Crunchy And Taste Good With Ketchup
kellyt
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« Reply #62 on: October 24, 2008, 08:49:25 PM »

I just wish they understood that just because I don't "look' sick and/or "act" sick doesn't mean that I'm not sick.  Same goes for scared, depressed, sad, anxious, etc.  I have found that I can hide those feelings pretty good even though I suck at hiding other feelings and emotions.
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1993 diagnosed with glomerulonephritis.
Oct 41, 2007 - Got fistula placed.
Feb 13, 2008 - Activated on "the list".
Nov 5, 2008 - Received living donor transplant from my sister-in-law, Etta.
Nov 5, 2011 - THREE YEARS POST TRANSPLANT!  :D
G-Ma
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« Reply #63 on: October 24, 2008, 09:28:12 PM »

Don't you think we are all becoming good actors?
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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
idahospud
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« Reply #64 on: October 24, 2008, 09:40:57 PM »

all tho I'm not on dialess yet . i wish my family and Friends would just let me tock . it's like if I even think of my CKD or thy ask where I'm going and i say the kidnes dr. thy freek out I'm not diying today nor am i going to be healed ether. i  wish  thy got it CKD JUST IS good days and bad days .
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cherpep
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« Reply #65 on: November 03, 2008, 02:14:48 PM »

okarol - thanks for this thread and your summary.  I printed your quotes on my caringbridge site, and have received several comments from my family.  It was very informative to many of them - simple and informative.  Thanks!
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okarol
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« Reply #66 on: November 03, 2008, 02:21:40 PM »

okarol - thanks for this thread and your summary.  I printed your quotes on my caringbridge site, and have received several comments from my family.  It was very informative to many of them - simple and informative.  Thanks!

That's great! i would love to visit your caringbridge page, would you PM it to me if you don't want to post it? Thanks.
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Admin for IHateDialysis 2008 - 2014, retired.
Jenna is our daughter, bad bladder damaged her kidneys.
Was on in-center hemodialysis 2003-2007.
7 yr transplant lost due to rejection.
She did PD Sept. 2013 - July 2017
Found a swap living donor using social media, friends, family.
New kidney in a paired donation swap July 26, 2017.
Her story ---> https://www.facebook.com/WantedKidneyDonor
Please watch her video: http://youtu.be/D9ZuVJ_s80Y
Living Donors Rock! http://www.livingdonorsonline.org -
News video: http://www.youtube.com/watch?v=J-7KvgQDWpU
okarol
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Photo is Jenna - after Disneyland - 1988

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« Reply #67 on: March 22, 2009, 11:22:49 AM »

 :bump;
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Admin for IHateDialysis 2008 - 2014, retired.
Jenna is our daughter, bad bladder damaged her kidneys.
Was on in-center hemodialysis 2003-2007.
7 yr transplant lost due to rejection.
She did PD Sept. 2013 - July 2017
Found a swap living donor using social media, friends, family.
New kidney in a paired donation swap July 26, 2017.
Her story ---> https://www.facebook.com/WantedKidneyDonor
Please watch her video: http://youtu.be/D9ZuVJ_s80Y
Living Donors Rock! http://www.livingdonorsonline.org -
News video: http://www.youtube.com/watch?v=J-7KvgQDWpU
Beth35
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« Reply #68 on: March 22, 2009, 11:49:33 AM »

I think people not understanding the extreme tiredness is one of the hardest things to deal with.  When I say I'm tired, I'm REALLY tired.  Even now, as I'm getting closer to dialysis again, I am SO tired.  I have a hard time getting everything done.  I am a single mom to two toddlers and to work all day with children and then come home and clean, and do baths and playtime and then when it's time to put them down I'm done for the day.  It gets harder and harder to keep up with it all.

I had an Aunt once tell me, "Gosh you were so lazy as a kid.  All you ever did was sleep your life away.  If you come visit me, you're not going to sleep all day!"  :o  I could have slapped her.  I said, "Well let's see, I was in kidney failure."  Duh!

People just really don't get that and it sucks!
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Found out I had kidney disease when I was 15.
Started dialysis when I was 20.
Got a kidney transplant when I was 25.
Kidney failed at 37 and I began my second journey on dialysis.
monrein
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Might as well smile

« Reply #69 on: March 23, 2009, 04:43:12 AM »

I think people not understanding the extreme tiredness is one of the hardest things to deal with.  When I say I'm tired, I'm REALLY tired.  Even now, as I'm getting closer to dialysis again, I am SO tired.  I have a hard time getting everything done.  I am a single mom to two toddlers and to work all day with children and then come home and clean, and do baths and playtime and then when it's time to put them down I'm done for the day.  It gets harder and harder to keep up with it all.

I had an Aunt once tell me, "Gosh you were so lazy as a kid.  All you ever did was sleep your life away.  If you come visit me, you're not going to sleep all day!"  :o  I could have slapped her.  I said, "Well let's see, I was in kidney failure."  Duh!

People just really don't get that and it sucks!

Beth, people don't understand often because they are not informed.  As hard as it is, we must teach them about kidney disease.  A long time ago, I used to give   printed info (there's lots on this site) about the symptoms and effects of this illness.  We should'nt HAVE to educate them but it's in our own best interest and I've often been surprised by the turn around in some people's attitudes once they "get it".   Next thing you know, the formerly ignorant are explaining things to others. 
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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
Neo
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Dont let dialysis stop you...

« Reply #70 on: March 31, 2009, 08:04:06 PM »

I wish they all understood the concept of limited energy.  Yes, I can spend a day at work, or cleaning the house - but only if I have a day to rest before and after.  When I say I'm tired, if means that if I keep going, I'm going to be fine while I'm with you, but I'm going to spend the next day puking.
Couldnt agree more people just dont get it, one day i can have energy and than the next minute im tired as hell. I hate feeling like people are doubting me or even think im lying becasue Im young and i quote"look healthy'
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G-Ma
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« Reply #71 on: March 31, 2009, 08:28:47 PM »

jbeany and neo..you are both very right..I try to look like I can run a marathon and clean 10 houses in 10 minutes but that is just it...."""look"""..the minute someone looks away I am on the couch resting for the next """look"""     :rofl;
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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
Wattle
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« Reply #72 on: April 01, 2009, 04:16:25 AM »

I just wish they understood that just because I don't "look' sick and/or "act" sick doesn't mean that I'm not sick.  Same goes for scared, depressed, sad, anxious, etc.  I have found that I can hide those feelings pretty good even though I suck at hiding other feelings and emotions.

Kelly .... this is sooo me. I wish my friends and family could live in my skin for just a day. I am sure they would then understand the crap I live with on a daily basis.

I just feel spent.   :stressed;
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PKD
June 2005 Commenced PD Dialysis
July 13th 2009 Cadaveric 5/6 Antigen Match Transplant from my Special Angel
msleeter
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« Reply #73 on: April 01, 2009, 08:53:20 AM »

I wish they all understood the concept of limited energy.  Yes, I can spend a day at work, or cleaning the house - but only if I have a day to rest before and after.  When I say I'm tired, if means that if I keep going, I'm going to be fine while I'm with you, but I'm going to spend the next day puking.

I couldn't agree more about the limited energy! I also wish folks would understand the emotional effects. I'm so thankful my wife understands me!
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Hospitalized October 6, 2008 (kidney biopsy October 9)
Diagnosed with Goodpastures Syndrome October 13, 2008
Started on chemotherapy & plasmapheresis October 13, 2008
Started on hemodialysis October 18, 2008 in hospital
Hemodialysis in center October 31, 2008
Re-hospitalized November 19, 2008 for more plasmapheresis treatments
Re-re-hospitalized December 3, 2008 - 2nd kidney biopsy done
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« Reply #74 on: April 04, 2009, 06:51:01 PM »

I wish my husband understood that I feel like crap and/or am very tired a great deal of the time, so I am going to be "bitchy" sometimes.
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Diagnosed type 1 diabetic at age 6, CKD (stage 3) diagnosed at 28 after hospital error a year before, started dialysis February '09. Listed for kidney/pancreas transplant at Ohio State & Univ. of Cincinnati.
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