I Hate Dialysis Message Board
Welcome, Guest. Please login or register.
November 29, 2024, 12:33:20 AM

Login with username, password and session length
Search:     Advanced search
532606 Posts in 33561 Topics by 12678 Members
Latest Member: astrobridge
* Home Help Search Login Register
+  I Hate Dialysis Message Board
|-+  Dialysis Discussion
| |-+  Dialysis: Spouses and Caregivers
| | |-+  Thank you for letting me whine.
0 Members and 1 Guest are viewing this topic. « previous next »
Pages: [1] Go Down Print
Author Topic: Thank you for letting me whine.  (Read 4108 times)
KensGirl
Newbie
*
Offline Offline

Gender: Female
Posts: 4

« on: April 10, 2014, 04:02:46 PM »

Hi All,
I’ve only posted once, but I lurk a lot.  I am a wife/caregiver to my husband who has been doing HD for 22.5 years. He has developed co-morbidities over the last several years that include hyperparathyroidism (parathyroid now removed)  legal blindness due to ischemic stroke to the optic nerves in each eye, dialysis-related amyloidosis, polycystic bone disease, and the latest diagnosis of cystic renal cell carcinoma, inoperable.

We’ve been told he is dying and he has an appointment to see an in-clinic palliative care provider in about a week. Apparently, you cannot have home palliative care for cancer if you are on dialysis, because they (Medicare) don’t consider you homebound if you are transported to have your dialysis treatment.

I am a mess.  I’ve been working at holding it together, through all these years of supporting him, being the breadwinner, as he could no longer work after going into renal failure, we raised our kids through all of this, and now I’m falling apart.
We had to leave our lovely home in Alaska to be able to come to the States where there was better renal care than there was in Fairbanks 22 years ago. We grew up there, married, had our children there, and then the accident that put him into renal failure. We have been together for 33 years and I don’t know what I’m going to do without him.

I adjusted to being the spouse and helper of a dialysis patient years ago, but these newest issues are breaking my heart. He’s dying and you can look at him and know it’s true. He is in such pain from the amyloidosis and he’s lost so much weight that the dialysis crew has to keep lowering his dry weight every other week just to keep up. He runs fevers all the time in the 100 – 101 range. He cannot eat, but just a small amount, every couple of days.

I know I’m just venting, but I have nowhere else to go to vent and I have no one I can vent to because I have to be the strong one for him and the kids and grandkids.

Thank you for allowing me to be a part of your community. I appreciate you all.

KensGirl
Logged

Wife and Caregiver to Ken.
Ken started In-Center Hemodialysis in Nov. 1991
MooseMom
Member for Life
******
Offline Offline

Gender: Female
Posts: 11325


« Reply #1 on: April 10, 2014, 10:24:27 PM »

I cannot begin to know what the two of you have been through, but just reading your post has made me tear up.

We have quite a few noble souls on this site who have been wonderful caregivers for many years, and I am hoping they will be better equipped than I could ever be to give you well deserved support.  But those of us who have renal failure do know that it takes its toll on our families.

No one here would ever accuse you of whining.  I am glad you chose to share your feels with us.  We know that sharing these sorts of thoughts with family members can result in all kinds of difficulties.  You are safe with us.
Logged

"Eggs are so inadequate, don't you think?  I mean, they ought to be able to become anything, but instead you always get a chicken.  Or a duck.  Or whatever they're programmed to be.  You never get anything interesting, like regret, or the middle of last week."
galvo
Member for Life
******
Offline Offline

Gender: Male
Posts: 7252


« Reply #2 on: April 10, 2014, 11:16:04 PM »

My thoughts are with you.
Logged

Galvo
Jean
Member for Life
******
Offline Offline

Gender: Female
Posts: 6114


« Reply #3 on: April 11, 2014, 01:30:02 AM »

Oh Honey, you just come here and rant and scream and do whatever you need to do. It really is just not fair and you really do deserve a break. Get one when you can. Feel so sorry for your impending loss and the hard times. Hang tough!!!
Logged

One day at a time, thats all I can do.
Bambino_Bear
Full Member
***
Offline Offline

Gender: Female
Posts: 285


WWW
« Reply #4 on: April 13, 2014, 12:47:58 AM »

 :grouphug; :grouphug; :grouphug;

So sorry KensGirl. 
Logged

I am a caregiver to my wonderful husband,  He is 4p and started PD October 2013. We have several living donors waiting to be tested for a transplant. Dialysis is a bridge to get us where we need to go. 
He had a transplant in November 2019.
cassandra
Elite Member
*****
Offline Offline

Gender: Female
Posts: 4974


When all else fails run in circles, shout loudly

« Reply #5 on: April 13, 2014, 12:40:51 PM »

I'm so sorry for you, and your family

       :grouphug;   :grouphug;   :grouphug;

Lots of love, and lots of strength to you all, Cas
Logged

I started out with nothing and I still have most of it left

1983 high proteinloss in urine, chemo, stroke,coma, dialysis
1984 double nephrectomy
1985 transplant from dad
1998 lost dads kidney, start PD
2003 peritineum burst, back to hemo
2012 start Nxstage home hemo
2020 start Gambro AK96

       still on waitinglist, still ok I think
Pages: [1] Go Up Print 
« previous next »
 

Powered by MySQL Powered by PHP SMF 2.0.17 | SMF © 2019, Simple Machines | Terms and Policies Valid XHTML 1.0! Valid CSS!