I Hate Dialysis Message Board
Welcome, Guest. Please login or register.
November 22, 2024, 12:45:23 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: Home Dialysis
| | |-+  PD and Caregiver Backup?
0 Members and 1 Guest are viewing this topic. « previous next »
Pages: [1] Go Down Print
Author Topic: PD and Caregiver Backup?  (Read 1884 times)
Marilee
Full Member
***
Offline Offline

Gender: Female
Posts: 278


Hubby was a PD Person - I was 'support'

WWW
« on: December 11, 2019, 10:31:14 AM »

My hubby, a PD patient, had to undergo extensive eye surgery 4 weeks ago and he did not spring back from the anesthesia readily. Actually, he was delirious for weeks, so I took over all aspects of PD to get through that rough patch. On Thanksgiving morning I woke to some weird flashes and new floaters in one eye, and fears of retinal tears or retinal detachment bubbled up. I thought, "Oh, no! What is my backup if I can't help with the PD?" So I contacted the VA - they have a caregiver respite program where someone comes to the house to help out. But they wouldn't do PD setups. I contacted other home health caregiver organizations but they also didn't do PD. All our extended family live out of this state, so I was more than relieved to learn that I was OK after all and didn't need a backup. This week at PD clinic, I brought this scenario up to find out what they recommend if indeed I were out of the picture for awhile, and they said they would do an emergency catheter for hemodialysis because caregivers can give a person a ride to hemo appointments. But that means that my poor hubby, reeling from the effects of surgery, would undergo yet another surgery. It seems like overkill when really I just need someone strong enough to carry 14 pound bags, connect per the machine instructions, wash their hands and hook a few tubes together.

Has anyone else traveled this road and come up with better solutions?
Logged

As my hubby would say, "Don't let what you can't do get in the way of what you can."
cassandra
Elite Member
*****
Offline Offline

Gender: Female
Posts: 4974


When all else fails run in circles, shout loudly

« Reply #1 on: December 12, 2019, 04:55:07 AM »

Maybe ask VA if you are okay to show a caregiver [size=78%]what to do with pd before your eyes go. [/size]
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
Marilee
Full Member
***
Offline Offline

Gender: Female
Posts: 278


Hubby was a PD Person - I was 'support'

WWW
« Reply #2 on: December 12, 2019, 05:22:56 AM »

LOL!

I actually wrote the VA a letter noting that PD is something that is being promoted from the White House on down, and it is in the VA's interest to make it possible for me to continue to be the 24/7 caregiver that I am. I said they have skilled nurses on staff that can train and that it doesn't require nursing skill to actually do (I am not a nurse)… haven't heard back yet :) .
Logged

As my hubby would say, "Don't let what you can't do get in the way of what you can."
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!