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denise
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« on: February 15, 2011, 06:08:19 AM »

Anyone who's willing to chat who understands being tired of the same scene...a chair 3 times a week just to stay alive...please hit me up.I could use the company
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paris
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« Reply #1 on: February 15, 2011, 08:03:49 AM »

 :welcomesign;   I think you have found the right place to find friends who truly understand.   This site was created so everyone could speak freely and share their experiences.  There is a lot of information here. And the support is incredible.    We also have a chat room where people can set up times to meet and talk there.   Glad you found us and we look forward to getting to know you.   Welcome to IHD.




paris, Moderator
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It's not what you gather, but what you scatter that tells what kind of life you have lived.
Rerun
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Going through life tied to a chair!

« Reply #2 on: February 15, 2011, 09:03:07 AM »

Hey Denise, welcome to IHD.  I'm so glad you found us.  You can come here anytime to vent and talk to people who know what you are going through.

I hope you post often.

Rerun, Moderator         :welcomesign;
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galvo
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« Reply #3 on: February 15, 2011, 01:22:34 PM »

G'day, Denise, and  :welcomesign;. Tell us a bit about yourself.
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Galvo
Hazmat35
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« Reply #4 on: February 15, 2011, 01:27:28 PM »

Join the club, Denise!  Dialysis SUCKS!!!!!

It's no fun in sunny Florida, when you have to look at it through the window in your chair 3x / week!!!!!! 
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Brother Passed away - 1990 - Liver Disease
Diagnosed w/ Polycystic Kidney Disease - 1998
Mother passed away - Feb. 1999 - PKD
Sister passed away - Feb. 2006 - PKD
AV Fistula / Upper Left Arm - September 2009
Father passed away - September 2009
In-Center Hemo Dialysis - April 2010
Broken Knee Cap - January 2015
Diagnosed w/ A-Fib October 2017
Surgery to repair Hiatal Hernia 2018
Multiple Fistula Grams / Angioplasty's since then!


Hating Dialysis since Day 1 and everyday since then!!!!  :)
RichardMEL
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« Reply #5 on: February 15, 2011, 05:00:53 PM »

Welcome Denise! You are totally in the right place. All of us who have been there (or are there) know exactly what you mean. This is the place to vent and share!!

Tell us more about yourself - where you are, what your experiences have been etc. Our community is very supportive and hopefully we can help you on your journey!

RichardMEL, Moderator
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3/1993: Diagnosed with Kidney Failure (FSGS)
25/7/2006: Started hemo 3x/week 5 hour sessions :(
27/11/2010: Cadaveric kidney transplant from my wonderful donor!!! "Danny" currently settling in and working better every day!!! :)

BE POSITIVE * BE INFORMED * BE PROACTIVE * BE IN CONTROL * LIVE LIFE!
sumalee
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« Reply #6 on: February 15, 2011, 08:06:29 PM »

Hi  :welcomesign; you come to the right place. I am alone and feel the same I am happy to chat with everyone.
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found out have kidney disease 1989
start PD November 2008
On a waiting list for transplant active December 2008
Ang
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« Reply #7 on: February 19, 2011, 07:26:17 PM »

 :welcomesign; Denise

                                    theres always someone around to chat to,we are all  at different  stages in this journey.

somebody will offer there experiences of what they've been through

come back often to say gidday, then we know your doing ok
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live  life  to  the  full  and you won't  die  wondering
dialysisinsider
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WWW
« Reply #8 on: February 21, 2011, 12:00:51 PM »

MouseMom - In terms of dialysis companies doing what's in the best interest of doing what is best for the patient and what is best for the bottom line... there are many factors going on here, and yes, money has something to do with it.

The concern of another patient here that DaVita might shut down nocturnal once it completes acquisition of her facility is welll founded. Any of the dialysis companies would do this because it is a business of making money... yes I said it. The companies will not be legally doing anything wrong because they would still offer dialysis, just not nocturnal. The patient could go somewhere else (perhaps farther away at her own expense) to get nocturnal, and she could still be treated during the day - that is the mindset.

In terms of nocturnal home, I don't know the answer. But many, many of the dialysis decisions made at the dialysis providers are financially driven. Even the outcomes of a facility are, in my humble opinion, really pushed to be better so that one provider can say, "we are the best" in terms of outcome, some come dialysis with us. This is not all bad in reality since this drives for better outcomes, it just doesn't always work out in the favor of patients.
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I used to be a Director for one of the two largest dialysis providers in the US. That means I managed more than 10 dialysis centers, some PD and some Home Hemo Programs. I'm here to answer any questions that you have about dialysis care. I have some interesting things to share with all.

http://terryforsyth.com/
karrye
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If Life give you Limes, make lemonade instead.

« Reply #9 on: February 23, 2011, 09:24:05 AM »

Welcome Denise!!  I sit in the lobby 4 to 5 hours a week, while Lee is having dialysis next door.  So, it isn't as bad as y'all having to watch your blood whirl around the machine or listening to all those blessed bleeping machines!!!  I go wild just listening from the lobby!! LOL  So, hang in there!
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Caregiver to husband:
Had surgery April 25, 2011 to bring fistula nearer to top of the skin.
Had staples removed from surgery on fistula May 3, 2011
Who started dialysis 1st week of December 2010.
Complete kidney failure November 30, 2010.
Surgery for 95% blockages in his right carotid and jugular February 22, 2011
Heart attack -- January 24, 2011
Chemotherapy -- September 2009 to April 2010
Colon Cancer -- April 2009
Colon removed --August 2009
Diagnosed with diabetes, Summer of 1996.
Brightsky69
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« Reply #10 on: February 23, 2011, 03:00:58 PM »

Welcome Denise... :cuddle; :grouphug;
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Transplant June 11, 1991 (1st time) my mom's kidney
Received my 2nd kidney transplant Oct. 19th 2010.
Des
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« Reply #11 on: February 24, 2011, 04:00:46 AM »

 :welcomesign;
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Please note: I am no expert. Advise given is not medical advise but from my own experience or research. Or just a feeling...

South Africa
PKD
Jan 2010 Nephrectomy (left kidney)
Jan 2010 Fistula
Started April 2010 Hemo Dialysis(hate every second of it)
Nov 2012 Placed on disalibity (loving it)
KrazeeBrod
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« Reply #12 on: May 28, 2011, 06:16:19 PM »

 :welcomesign;

I, too, hate this whole process.  In fact, my doctor was worried about me back in Jan/Feb because I was terribly depressed and nearly suicidal about the whole thing.  But several things happened that helped bring me out of it.

First, I met a really nice gal who sat next to me in dialysis, who had been on dialysis for two years... and she was only 28!  She does her own sticking, knows the machine interface backward and forwards, and she was very nice about telling me what was going on and, better yet, what to expect.  That, I realized, was part of the problem... they don't give you enough information on what to expect, so things seem to come at you quick and hard.  Before you have time to absorb one issue, another is coming at you.  Do you find that happening to you?

If you do, then get aggressive about knowing exactly what to expect, what is going on, and asking questions about what the techs/doctors are doing to YOUR body!  I am not an aggressive person normally, kind of quiet and somewhat reserved, but I learned to get aggressive about knowing what was going on.  This is YOUR life and YOUR body.  Take possession of it, hon.

If you need someone to talk to on the phone, send me a private message and I will be happy to talk to you at any time of the day or night.
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