I Hate Dialysis Message Board
Welcome,
Guest
. Please
login
or
register
.
November 21, 2024, 07:05:05 AM
1 Hour
1 Day
1 Week
1 Month
Forever
Login with username, password and session length
Search:
Advanced search
532606
Posts in
33561
Topics by
12678
Members
Latest Member:
astrobridge
I Hate Dialysis Message Board
Dialysis Discussion
Dialysis: Pre-Dialysis
COPD and dialysis
0 Members and 1 Guest are viewing this topic.
« previous
next »
Pages:
[
1
]
Author
Topic: COPD and dialysis (Read 4248 times)
myporkchop
Full Member
Offline
Gender:
Posts: 129
COPD and dialysis
«
on:
July 10, 2016, 03:11:19 AM »
Hi all,
Two specialists have concerns about my mum starting dialysis given she has difficulties with COPD. She has recurrent chest infections. They are concerned that she might not be able to cope with dialysis. We went and saw the specialist last Thursday as they wanted her to have made a decision about starting dialysis or not. After joining this site and reading all of your comments etc she felt encouraged and made a decision to give it a go. They are looking at peritoneal dialysis as she hemo may be difficult for her to access veins etc. They said they could do the operation for the catheter under local anesthetic. They said they would have to be creative at it as putting her to sleep may be too risky "as may not wake up".
We are so dam worried. I feel so sorry for her going through this, and I don't know how to make this any easier for her
Logged
21st April 2016 - mum got told she had only a few months to live. Doctor's did not support dialysis treatment for her due to many other health complications. They didn't think she could cope and recommended conservative care. Our family was devastated. She is only 64 years old.
19th June 2016 - joined IHD. The support from all of you gave my mum the confidence to give dialysis a go.
26th September 2016 - started PD dialysis at home (CAPD). The first week has wrecked havoc with her blood sugar levels and diabetes, she has been in hospital twice within the week. Dialysis is going well though.
kickingandscreaming
Elite Member
Offline
Gender:
Posts: 2268
Re: COPD and dialysis
«
Reply #1 on:
July 10, 2016, 05:53:36 AM »
So sorry, MPC. Sometimes conservative care is the best way to go. Especially with so many bodily systems under duress. Going through with surgery/dialysis is a big gamble in your mother's case. But the alternative is perhaps more of a known-- but not a very comforting known. Sadly, we all reach a point where our issues get the better of us. Some of us are closer to that point than others. The most important thing is to go forward with your eyes open. I'm sorry there are so few options left.
Logged
Diagnosed with Stage 2 ESRD 2009
Pneumonia 11/15
Began Hemo 11/15 @6%
Began PD 1/16 (manual)
Began PD (Cycler) 5/16
myporkchop
Full Member
Offline
Gender:
Posts: 129
Re: COPD and dialysis
«
Reply #2 on:
July 10, 2016, 06:35:49 AM »
Thanku for that. It is very difficult decision for her. I don't want her to suffer but don't want to loose her so soon either. She wants to live but is so worried about her other health conditions. She is still young 64 and has fought thro many health complications. Although we thought we might have lost her years ago she kept fighting and got thru it. This time feels so unreal
Logged
21st April 2016 - mum got told she had only a few months to live. Doctor's did not support dialysis treatment for her due to many other health complications. They didn't think she could cope and recommended conservative care. Our family was devastated. She is only 64 years old.
19th June 2016 - joined IHD. The support from all of you gave my mum the confidence to give dialysis a go.
26th September 2016 - started PD dialysis at home (CAPD). The first week has wrecked havoc with her blood sugar levels and diabetes, she has been in hospital twice within the week. Dialysis is going well though.
DayaraLee
Full Member
Offline
Gender:
Posts: 239
Re: COPD and dialysis
«
Reply #3 on:
July 10, 2016, 08:14:46 AM »
Nothing helpful to add, Myporkchop. But I will be praying for you, mom, and family.
Logged
Husband Dx - CKD Stage 3, Diabetes Type II, Hypertensive, Stubborn...
"What is love? Love is the absence of judgment." ~Dalai Lama
myporkchop
Full Member
Offline
Gender:
Posts: 129
Re: COPD and dialysis
«
Reply #4 on:
July 10, 2016, 02:19:06 PM »
Thanku dayarlee
Logged
21st April 2016 - mum got told she had only a few months to live. Doctor's did not support dialysis treatment for her due to many other health complications. They didn't think she could cope and recommended conservative care. Our family was devastated. She is only 64 years old.
19th June 2016 - joined IHD. The support from all of you gave my mum the confidence to give dialysis a go.
26th September 2016 - started PD dialysis at home (CAPD). The first week has wrecked havoc with her blood sugar levels and diabetes, she has been in hospital twice within the week. Dialysis is going well though.
Charlie B53
Elite Member
Offline
Gender:
Posts: 3440
Re: COPD and dialysis
«
Reply #5 on:
July 10, 2016, 06:48:21 PM »
I have the early stages of COPD. I don't really know anything about it. I have a chronic cough, mostly mornings bringing up that yuck from almost a lifetime of smoking.
Recently I took 50 MG of benadril nightly, not to clear my sinus' but for the aide to falling asleep. I was having a bad time with a change in pain meds.
The benadril caused me serious distress during the daytime as it not only dried the mucus membranes it also dried the yuck somewhat, making it very difficult to clear my lungs. What I used to clear first thing in the morning now took almost ALL DAY.
You bet I quit taking benadril.
If your Mother has a productive cough be very wary with any new meds. She does not need anything to cause drying. Other than dialysis to remove the excess water. Possibly water pills to help any remaining kidney function to keep shedding watrer. Your Neph will be your best source for medication information.
Will be hoping to hear how she does.
Take Care,
Charlie B53
Logged
myporkchop
Full Member
Offline
Gender:
Posts: 129
Re: COPD and dialysis
«
Reply #6 on:
July 10, 2016, 11:48:16 PM »
Thank you Charlie. She smoked cigarettes from a very young age (approx. 45 years). She has been in and out of hospital for the last 8 years in the respiratory ward (usually around winter, but not always). She gets fluid on the lungs, chest infections and gets really short of breath. They prescribed her water pills which helped a lot. She always has a back up course of antibiotics to start as soon as she is noticing symptoms of COPD. I spoke to her GP today to inform him that she has made the decision to give dialysis a go. He seemed really pleased that a decision has been made so we can start with the process. I mentioned that we were worried about whether or not she is doing the right thing (having dialysis or not), he said there is not right or wrong answer. I mentioned to him that the surgeon said they can operate and the anesthetist said they would just need to be a bit creative in how they do the procedure (i.e under local anesthetic), but can do it. The G.P thought this sounded very positive. Which then gave us some hope, if he is positive about it.
Thanks again I will keep you all updated
Regards
Logged
21st April 2016 - mum got told she had only a few months to live. Doctor's did not support dialysis treatment for her due to many other health complications. They didn't think she could cope and recommended conservative care. Our family was devastated. She is only 64 years old.
19th June 2016 - joined IHD. The support from all of you gave my mum the confidence to give dialysis a go.
26th September 2016 - started PD dialysis at home (CAPD). The first week has wrecked havoc with her blood sugar levels and diabetes, she has been in hospital twice within the week. Dialysis is going well though.
cassandra
Elite Member
Offline
Gender:
Posts: 4974
When all else fails run in circles, shout loudly
Re: COPD and dialysis
«
Reply #7 on:
July 11, 2016, 02:57:55 AM »
Thanx for the update. Good luck to you, your mum and family
Love and strength, 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
Charlie B53
Elite Member
Offline
Gender:
Posts: 3440
Re: COPD and dialysis
«
Reply #8 on:
July 11, 2016, 12:41:43 PM »
Don't quote me, but I thought I heard that spinal block may be used in some cases a general anesthetic deemed to risky.
Some people are total paranoid about anyone poking into their spine. I myself have mixed feelings having both good and not so good experiences.
It may be an alternative worth asking questions about. although I would definitely want to be certain to make SURE the one doing the poking is very well experienced, NOT a recent beginner.
Logged
myporkchop
Full Member
Offline
Gender:
Posts: 129
Re: COPD and dialysis
«
Reply #9 on:
July 18, 2016, 03:01:54 AM »
Sorry Charlie, I thought I had responded and thanked you for your reply, but I hadn't...so thank you. I will ask about the spinal block.
Thanks again
Logged
21st April 2016 - mum got told she had only a few months to live. Doctor's did not support dialysis treatment for her due to many other health complications. They didn't think she could cope and recommended conservative care. Our family was devastated. She is only 64 years old.
19th June 2016 - joined IHD. The support from all of you gave my mum the confidence to give dialysis a go.
26th September 2016 - started PD dialysis at home (CAPD). The first week has wrecked havoc with her blood sugar levels and diabetes, she has been in hospital twice within the week. Dialysis is going well though.
Pages:
[
1
]
« previous
next »
Loading...