I Hate Dialysis Message Board
Welcome, Guest. Please login or register.
November 23, 2024, 02:09:57 PM

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: General Discussion
| | |-+  Question		 0 Members and 1 Guest are viewing this topic. « previous next »
Pages: [1] Go Down Print
Author Topic: Question  (Read 2971 times)
tiredandthirsty
Full Member
***
Offline Offline

Gender: Male
Posts: 247
« on: April 10, 2012, 12:41:17 PM »
Hi all,

i have a rather embarrassing question for the learned and experienced folks in here.  I get really gassy sometimes after the treatment.  i mean it HURTS!  i do eat lunch before i go to the clinic.  so it's not like i am on empty stomach.  after a LOT of involuntary (sort of) air release from the front orifice as well as the back, it finally starts to feel normal. after quite a while.  and i am miserable until this happens.

anyone else have this issue?  anything i can do?  sorry if this is tmi.  but it is the truth after all :-)
Logged
iketchum
Full Member
***
Offline Offline

Gender: Male
Posts: 356
« Reply #1 on: April 10, 2012, 12:52:47 PM »
I have been doing dialysis for 4 years and, between the meds and treatment, have bad gas. Quick trip to the restroom before leaving the center gets me home okay.  :2thumbsup;
Logged
Cordelia
Elite Member
*****
Offline Offline

Gender: Female
Posts: 2012
« Reply #2 on: April 10, 2012, 12:53:00 PM »
What form of dialysis are you doing? 

I know when I get out of the chair after 3 and 3/4 of an hour, I am pretty gassy. I burp immediately when my chair comes forward. And, afterwards, I toot a lot.  It's like all that gas is pent up in me when I'm reclined in that stupid chair. Once I stand, oh boy, I have to be careful. It's embarrassing!         :sir ken;

I think its also medication. Lots of different kinds of meds can make you gassy. Renagel and my high blood pressure med causes a lot of gas.

Check your meds.....you could be on some meds that might make you gassy.
« Last Edit: April 10, 2012, 12:54:56 PM by Cordelia » Logged
Diagnosed with Polycystic Kidney Disease at age 19.
Renal Failure at age 38 (2010) came about 2 hrs close to dying. Central line put in an emergency.
Began dialysis on Aug 15, 2010.
Creatine @ time of dialysis: 27. I almost died.
History of High Blood Pressure
I have Neuropathy and Plantar Fasciitis in My Feet
AV Fistula created in Nov. 2011, still buzzing well!
Transplanted in April, 2013. My husband and I participated in the Living Donor paired exchange program. I nicknamed my kidney "April"
Married 18 yrs,  Mom to 3 kids to twin daughters (One that has PKD)  and a high-functioning Autistic son
tiredandthirsty
Full Member
***
Offline Offline

Gender: Male
Posts: 247
« Reply #3 on: April 10, 2012, 12:59:07 PM »
hi thanks for the prompt responses.

i am on in centre hemo.  week and a half old now.  so pretty new to dialysis. 

i am pretty much on the same meds as i have been for most of my life.  except for phos lo, which i started taking a while before i started d.  before dialysis, i was not having this issue.  but it has cropped up now.  do you lot think eating something mid way might help?  i don't do any snacking or anything while on the machine.  i don't even feel like taking a sip of water they keep it so cold in there. 
Logged
iketchum
Full Member
***
Offline Offline

Gender: Male
Posts: 356
« Reply #4 on: April 10, 2012, 01:06:26 PM »
     I am on phos binders as well, I need to use Doucosate to help 'unbind' me from the binder.
Logged
Cordelia
Elite Member
*****
Offline Offline

Gender: Female
Posts: 2012
« Reply #5 on: April 10, 2012, 01:11:22 PM »
I snack half way through my treatment and it doesn't make a difference at all.
Logged
Diagnosed with Polycystic Kidney Disease at age 19.
Renal Failure at age 38 (2010) came about 2 hrs close to dying. Central line put in an emergency.
Began dialysis on Aug 15, 2010.
Creatine @ time of dialysis: 27. I almost died.
History of High Blood Pressure
I have Neuropathy and Plantar Fasciitis in My Feet
AV Fistula created in Nov. 2011, still buzzing well!
Transplanted in April, 2013. My husband and I participated in the Living Donor paired exchange program. I nicknamed my kidney "April"
Married 18 yrs,  Mom to 3 kids to twin daughters (One that has PKD)  and a high-functioning Autistic son
tiredandthirsty
Full Member
***
Offline Offline

Gender: Male
Posts: 247
« Reply #6 on: April 10, 2012, 04:06:58 PM »
hmm..seems like this "airy" gift is inevitable.  bloody heclll.
Logged
Cordelia
Elite Member
*****
Offline Offline

Gender: Female
Posts: 2012
« Reply #7 on: April 10, 2012, 05:01:14 PM »
I know      :(
Logged
Diagnosed with Polycystic Kidney Disease at age 19.
Renal Failure at age 38 (2010) came about 2 hrs close to dying. Central line put in an emergency.
Began dialysis on Aug 15, 2010.
Creatine @ time of dialysis: 27. I almost died.
History of High Blood Pressure
I have Neuropathy and Plantar Fasciitis in My Feet
AV Fistula created in Nov. 2011, still buzzing well!
Transplanted in April, 2013. My husband and I participated in the Living Donor paired exchange program. I nicknamed my kidney "April"
Married 18 yrs,  Mom to 3 kids to twin daughters (One that has PKD)  and a high-functioning Autistic son
galvo
Member for Life
******
Offline Offline

Gender: Male
Posts: 7252
« Reply #8 on: April 10, 2012, 09:01:06 PM »
Me, I fart like a clydesdale!
Logged
Galvo
Whamo
Elite Member
*****
Offline Offline

Posts: 1028
« Reply #9 on: April 11, 2012, 09:08:34 AM »
My wife calls me stinkbug.
Logged
Cordelia
Elite Member
*****
Offline Offline

Gender: Female
Posts: 2012
« Reply #10 on: April 11, 2012, 10:05:18 AM »
You guys crack me up pun intended!       :rofl;        :sir ken;
Logged
Diagnosed with Polycystic Kidney Disease at age 19.
Renal Failure at age 38 (2010) came about 2 hrs close to dying. Central line put in an emergency.
Began dialysis on Aug 15, 2010.
Creatine @ time of dialysis: 27. I almost died.
History of High Blood Pressure
I have Neuropathy and Plantar Fasciitis in My Feet
AV Fistula created in Nov. 2011, still buzzing well!
Transplanted in April, 2013. My husband and I participated in the Living Donor paired exchange program. I nicknamed my kidney "April"
Married 18 yrs,  Mom to 3 kids to twin daughters (One that has PKD)  and a high-functioning Autistic son
tiredandthirsty
Full Member
***
Offline Offline

Gender: Male
Posts: 247
« Reply #11 on: April 11, 2012, 02:11:16 PM »
HAH...this thread is taking an entertaining direction.   ;D
Logged
Cordelia
Elite Member
*****
Offline Offline

Gender: Female
Posts: 2012
« Reply #12 on: April 11, 2012, 02:51:55 PM »
I agree.

I love a good laugh      :rofl;       :rofl;    God knows today I sure needed one!         ;D
« Last Edit: April 11, 2012, 03:03:14 PM by Cordelia » Logged
Diagnosed with Polycystic Kidney Disease at age 19.
Renal Failure at age 38 (2010) came about 2 hrs close to dying. Central line put in an emergency.
Began dialysis on Aug 15, 2010.
Creatine @ time of dialysis: 27. I almost died.
History of High Blood Pressure
I have Neuropathy and Plantar Fasciitis in My Feet
AV Fistula created in Nov. 2011, still buzzing well!
Transplanted in April, 2013. My husband and I participated in the Living Donor paired exchange program. I nicknamed my kidney "April"
Married 18 yrs,  Mom to 3 kids to twin daughters (One that has PKD)  and a high-functioning Autistic son
tiredandthirsty
Full Member
***
Offline Offline

Gender: Male
Posts: 247
« Reply #13 on: April 11, 2012, 03:07:15 PM »
i am on the machine right now and i have already let off a few good ones.  hopefully no one has heard anything.  it helps that i am kept in a separate room by myself.  but its a double edged sword because if it is a stinker, the bloody thing lingers forever....
Logged
Cordelia
Elite Member
*****
Offline Offline

Gender: Female
Posts: 2012
« Reply #14 on: April 11, 2012, 03:18:40 PM »
 :rofl;     :rofl;     :rofl;    You kill me.   I'm laughin' my     :sir ken;      off here.     I'm in  a private room when I'm on D too.  Thank God.    That's just ONE of the reasons why I chose to be in a private room so that I don't have to worry about er hum 'others' hearing my gassiness.         :secret;

I love that my room has a toilet station too.    When I need to pee, they just lower my pump speed on the machine and push my machine over so that I can get up and use the facilities      :rofl;
I'm the only one in my unit that stays attached to the machine when using the toilet!

I wouldn't trade my room for anything!!!!       ;D    I may be isolated from others but at least I don't have to worry about people hearing my bodily noises!     :rofl;
« Last Edit: April 11, 2012, 03:20:45 PM by Cordelia » Logged
Diagnosed with Polycystic Kidney Disease at age 19.
Renal Failure at age 38 (2010) came about 2 hrs close to dying. Central line put in an emergency.
Began dialysis on Aug 15, 2010.
Creatine @ time of dialysis: 27. I almost died.
History of High Blood Pressure
I have Neuropathy and Plantar Fasciitis in My Feet
AV Fistula created in Nov. 2011, still buzzing well!
Transplanted in April, 2013. My husband and I participated in the Living Donor paired exchange program. I nicknamed my kidney "April"
Married 18 yrs,  Mom to 3 kids to twin daughters (One that has PKD)  and a high-functioning Autistic son
Joe
Elite Member
*****
Offline Offline

Gender: Male
Posts: 1166
« Reply #15 on: April 12, 2012, 07:48:00 AM »
I don't have the issue of farts on PD, but I certainly do belch a lot! I guess I'm fortunate that all my gas seems to be in the upper end of the GI tract  :rofl;
Logged
Live simply. Love generously. Care deeply. Speak kindly.
Leave the rest to God...
tiredandthirsty
Full Member
***
Offline Offline

Gender: Male
Posts: 247
« Reply #16 on: April 12, 2012, 08:08:50 AM »
Cordelia:  toilet station in the room!!! you are lucky.  i have no such thing in this glass room i am kept in.  i am quarantined in this room.  i even get the older tv.  everyone outside has a newer, bigger tv whereas i get stuck with a box.  i should be grateful that it works.
Logged
Cordelia
Elite Member
*****
Offline Offline

Gender: Female
Posts: 2012
« Reply #17 on: April 12, 2012, 10:05:02 AM »
LOL on the belching Joe. I'm covering my mouth hiding a burp when my chair comes up from the reclining position. I often wonder if a lot of the gas is from being reclined in the dialysis chair     :rofl;

LMAO! TAT, hehehe yes, I'm super lucky I have a toilet in my room.      ;D     Luckily too, I've only been kicked out once when someone came back from a trip away from the unit and had to be quaranteened, they kicked me out for two days. I hated not being in my room.  They put me in another room with a bed and I must admit, I cannot lie down for dialysis. I have to sit, its too hard on my back if I'm lying down for my treatment. Drove me nuts! LOL     
Logged
Diagnosed with Polycystic Kidney Disease at age 19.
Renal Failure at age 38 (2010) came about 2 hrs close to dying. Central line put in an emergency.
Began dialysis on Aug 15, 2010.
Creatine @ time of dialysis: 27. I almost died.
History of High Blood Pressure
I have Neuropathy and Plantar Fasciitis in My Feet
AV Fistula created in Nov. 2011, still buzzing well!
Transplanted in April, 2013. My husband and I participated in the Living Donor paired exchange program. I nicknamed my kidney "April"
Married 18 yrs,  Mom to 3 kids to twin daughters (One that has PKD)  and a high-functioning Autistic son
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!