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Author Topic: Soooo tired of this....wish someone would shoot me and put me out of my misery  (Read 6667 times)
Lillupie
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« on: February 04, 2012, 05:29:40 PM »

 :rant;
 Im soooooooo sick and tired of this dialysis bullshit. Im sick and tired of people getting a transplants and i have yet to get one. I have been doing this bs for over 4 years now. Im sick of hte time consumption that this takes. Im tired of not being abe to have more kids, but yet i cant get on birth control. Im sick and tired of the diet and having to strave myself to prevent from cheating. Im tired of all the damn meat every  day. Im tired of being called in the clinic at the last minute to retake a lab that stupid Davita labs made too high and when I go and get the test retested my lab(s) come back normal. Im tired of all the threats my center likes to tell people. They tell us if we are late on kt/v, dont turn in the log sheets, miss a clinic Medicare isnt going to pay. I understand/get that the logs, going to clinic, kt/v is important but do they have to threaten us or black mail us?

Lisa
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Check out my Facebook profile for CKD "Help Lisa Spread Awareness for Kidney Disease"

It is my utmost dream and desire to reach out to other kidney patients for them to know that they are not alone in this, also to reach out to those who one day have to go on dialysis though my book i am writing!

dx with lupus nephritis 5/99'
daughter born 11/2005
stage IV CKD 11/2005-6/2007
8/2007- PD cathater inserted
9/2007- revision of PD Cathater
10/2007 started PD
willowtreewren
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My two beautifull granddaughters

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« Reply #1 on: February 04, 2012, 05:34:35 PM »

 :grouphug;

Oh, Lisa. I know that it can be overwhelming. I'm sorry.

 :grouphug;

Aleta
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Wife to Carl, who has PKD.
Mother to Meagan, who has PKD.
Partner for NxStage HD August 2008 - February 2011.
Carl transplanted with cadaveric kidney, February 3, 2011. :)
jbeany
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Cattitude

« Reply #2 on: February 04, 2012, 06:05:29 PM »

 :grouphug;
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"Asbestos Gelos"  (As-bes-tos yay-lohs) Greek. Literally, "fireproof laughter".  A term used by Homer for invincible laughter in the face of death and mortality.

Gerald Lively
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« Reply #3 on: February 04, 2012, 06:50:23 PM »

Bang!
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Hodgkin's Lymphoma - 1993
Prostate Cancer - 1994
Gall Bladder - 1995
Prostate Cancer return - 2000
Radiated Prostate 
Cataract Surgery 2010
Hodgkin's Lymphoma return - 2011 - Chemo
Renal Failure - 2011
Renal Function returned after eight months of dialysis - 2012
Hodgkin's Lymphoma returned 2012 - Lifetime Chemo


Human hopes and human creeds
have their roots in human needs.

                          Eugene Fitch Ware
texasstyle
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« Reply #4 on: February 04, 2012, 06:59:58 PM »

how about a hug instead?  Aww... I see at home as a care taker how you must feel.  Oh by the way, you sure are pretty!  Hope tomorrow you feel a little better physcially and emotinally.
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caregiver to husband using in-center dialysis 4 years
YLGuy
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« Reply #5 on: February 04, 2012, 07:00:26 PM »

I am sorry.  I know.  :grouphug;
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lmunchkin
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"There Is No Place Like Home!"

« Reply #6 on: February 04, 2012, 07:14:22 PM »

Lisa, nothing I can say is gonna help take your pain away!  Im so sorry. I wish I had a magic wand!

lmunchkin
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11/2004 Hubby diag. ESRD, Diabeties, Vascular Disease & High BP
12/2004 to 6/2009 Home PD
6/2009 Peritonitis , PD Cath removed
7/2009 Hemo Dialysis In-Center
2/2010 BKA rt leg & lt foot (all toes) amputated
6/2010 to present.  NxStage at home
CebuShan
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« Reply #7 on: February 04, 2012, 07:34:09 PM »

    :cuddle;    Wish I could make it all go away. I understand. You're not alone.    :grouphug;
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Think GOD doesn't have a sense of humor?
HE created marriage and children.
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glitter
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« Reply #8 on: February 04, 2012, 08:04:14 PM »

I am sorry too, I hope this is your year to get a kidney, but vent away! sometimes it may help a bit?  :grouphug; :grouphug; :grouphug;
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Jack A Adams July 2, 1957--Feb. 28, 2009
I will miss him- FOREVER

caregiver to Jack (he was on dialysis)
RCC
nephrectomy april13,2006
dialysis april 14,2006
galvo
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« Reply #9 on: February 04, 2012, 10:49:37 PM »

 :flower;
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Galvo
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« Reply #10 on: February 05, 2012, 12:54:58 AM »

I'm sorry Lisa.  I feel the same f*****g way.  I only feel better when I'm somehow able to forget about the past and the future at the same time and find something pleasant right now and try to make it last. 

And I've gained comfort from the people here too.

 :grouphug;
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billybags
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« Reply #11 on: February 05, 2012, 03:37:25 AM »

Lisa it is a shitter but what can you do. This is the hand you have been given. I really feel for you, hope to-morrow is better for you. I send you lots of hugs.
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Poppylicious
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« Reply #12 on: February 05, 2012, 04:00:15 AM »

Awww, Lisa.  Sending you many *huggles*.  I know they're absolutely no use to you at all, but it's the best I can do I'm afraid.

 :grouphug;
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- wife of kidney recepient (10/2011) -
venting myself online since 2003 (personal blog)
grumbles of a dialysis wife-y (kidney blog)
sometimes i take pictures (me, on flickr)

Everything was beautiful, and nothing hurt.
Jean
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« Reply #13 on: February 05, 2012, 05:32:24 AM »

Lisa, I am not even "there" yet and know how you feel. This sucks!!!!   :grouphug; :grouphug;
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One day at a time, thats all I can do.
Riverwhispering
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« Reply #14 on: February 05, 2012, 05:48:49 AM »

Lisa I know your depression,  I'm not "there" (dialysis) yet but will soon be and seem to be depressed at least 80% of the time.  It's freaking me out since I've never been a depressed person. 

I wish there was a silver lining to this dark cloud   :grouphug;

River

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It's only one step from the Jungle to the Zoo
kellyt
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« Reply #15 on: February 05, 2012, 06:20:50 AM »

Four years is a long time to have to deal with all this.  :cuddle;   You're time is coming!  Don't give up or let anyone get you further down.  Fight through this and you will come out on top!  We are here for you always!  Rant away if needed!  There are so many people here who are either where you are, have been where you are, or will be where you are. 
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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
monrein
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Might as well smile

« Reply #16 on: February 05, 2012, 06:24:34 AM »

Sorry this is getting to you so bad Lisa...it does suck!!!  I hope your call comes soon.   :grouphug; :grouphug; :grouphug;
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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
plugger
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« Reply #17 on: February 05, 2012, 06:28:26 AM »

I think you are doing the right thing blowing off some steam, I'm praying you will find the good and the strength in your life to get you through this.  You remind me a lot of my own daughter.   :grouphug;
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Proud member of DialysisEthics since 2000

DE responsible for:

*2000 US Senate hearings

*Verified statistics on "Dialysis Facility Compare"

*Doctors have to review charts before they can be reimbursed

*2000 and 2003 Office of Inspector General (OIG) reports on the conditions in dialysis

*2007 - Members of DialysisEthics worked for certification of hemodialysis
technicians in Colorado - bill passed, renewed in 2012 and 2019

*1999 to present - nonviolent dismissed patients returned to their
clinics or placed in other clinics or hospitals over the years

On my tombstone: He was a good kind of crazy

www.dialysisethics2.org
Whamo
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« Reply #18 on: February 05, 2012, 08:22:02 AM »

Hey, girl, go on FACEBOOK, and tell your story, and ask for a new kidney.  It's a numbers game.  Somewhere someone would like to help you.  It's your job to go find them.  I do feel sorry for young people I see with kidney problems.  Especially young, attractive people, in the prime of their lives, missing out on a lot of things I took for granted at the same age.  I've worn out most of my body organs through living hard, but at least I got to live it up.  And, even with dialysis, I feel great.  You might try Mind Aerobics to get your mind in a deep, relaxed state.  A half hour on the headphones and my mind is at rest.  Do a search on the internet for multisync "Mind Aerobics" and you can check it out.
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jshabanian
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« Reply #19 on: February 05, 2012, 08:34:28 AM »

I can't even tell you how many times I thought the same thing...someone please just shoot me and get this over with.  Then I remember my family and how sad they would be if I weren't here.  I too am sick and tired of thinking about my health 24/7.  What helps me is this:

I know this sounds trite but when I start to feel sorry for myself I remember all the little kids that go through worse than I do.  The kids with leukemia or cancers or other terrible painful diseases.  They spend their whole childhood in terrible pain, undergoing painful surgeries and procedures.  Some live most of their lives in the hospital.  Yet they always seem to have a smile on their face. They find joy where they can. My suffering pales in comparison.

None of this makes my suffering go away but it puts it in perspective.

The nurses at your center sound like real jerks.  They should be supportive of you and be there to help you along this path. At my center the nurses and wonderful and so helpful.  Can you switch centers? 

I am so sorry you are having such a terrible time right now.  Hang in there and hopefully things will level out and become tolerable.  Since you hate the meat so much why don't you eat more eggs and protein shakes?  Hide your meat in yummy things like soft tacos with lots of salsa and lettuce.

Good luck!

Janet
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ToddB0130
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« Reply #20 on: February 05, 2012, 12:09:20 PM »

I am sorry you are so down right now and that dialysis causes so much unheaval in your life.  I too hope that you get your call soon and get some semblence of normalcy back in your life.  Sorry people at your center are not more compassionate.   Your transplant will come .... and until it does,  remember your child and the times you are with her when you're not on dialysis.  It does suck, but for now, it's helping you to have time with loved ones and for them to be with you too.
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No day but today
kyshiag
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« Reply #21 on: February 05, 2012, 12:23:15 PM »

You are so strong for even being willing to state your feelings out loud.  I'm praying for your strength to continue
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Dannyboy
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« Reply #22 on: February 05, 2012, 01:06:42 PM »

Lisa,
I want to add my note as another who can identify with your feelings.
--Dan
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ESRD Summer 2011
Started using NxStage September, 2011
"Everything is funny as long as it is happening to Somebody Else"--Will Rogers

Alcoa and Reynolds are in a bidding war to buy my serum Aluminum.
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I only look like a sheep - but I ain't

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« Reply #23 on: February 06, 2012, 04:38:50 AM »

I found Karol's old article on living donors: http://kidneytimes.com/article.php?id=20090730163148
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Proud member of DialysisEthics since 2000

DE responsible for:

*2000 US Senate hearings

*Verified statistics on "Dialysis Facility Compare"

*Doctors have to review charts before they can be reimbursed

*2000 and 2003 Office of Inspector General (OIG) reports on the conditions in dialysis

*2007 - Members of DialysisEthics worked for certification of hemodialysis
technicians in Colorado - bill passed, renewed in 2012 and 2019

*1999 to present - nonviolent dismissed patients returned to their
clinics or placed in other clinics or hospitals over the years

On my tombstone: He was a good kind of crazy

www.dialysisethics2.org
HSM
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« Reply #24 on: February 12, 2012, 04:48:06 PM »

Hey Lisa, I've been on for over 4 years too, all I know is, you never know what's around the corner in life, for better of for worse! Keep your head up, things can get better in the blink of an eye.

I know the diet can be annoying, I'm a vegetarian/ vegan, it's difficult while on dialysis, but I have plenty to live for. It's about ability not disability.

You've got a whole family of people on here you can chat to when you feel down, never give up!

"It is my utmost dream and desire to reach out to other kidney patients for them to know that they are not alone in this"!

Those words ring a lot of truth. If you need a dose of positivity, bite my ear off! That goes to all of you!
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The only reason I attend dialysis is for the tea and the biscuits!

Dialysis wasn't the end, it was just the beginning!

It's about ability, NOT disability!
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