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Author Topic: Delighted to Find This Blog  (Read 2234 times)
mallardduckling
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« on: August 22, 2011, 06:14:25 AM »

I'm merely a family member of a former dialysis patient, but am delighted to find this site since it encapsulates what was such a huge portion of my Mom's and my life for five years. Despite her physical suffering and all the attendant issues with hemodialysis, it became such a big part of our lives and we met such special people that in many ways, I miss the camaraderie and social interaction with so many fine people. My Mom actually thrived with that interaction, so the curse of the procedure actually became a blessing in many ways.

Despite starting at age 80, my Mom did well for 5 years. There was some misguided advice for her to NOT start dialysis...and if I can be an advocate for family members of older folks, who might require dialysis but are just hearing the negative aspects...I would like to encourage and support those folks.

You are a special bunch, my prayers for good treatment runs went out to you daily, although granted, in recent years I've forgotten some of those prayers, so I'll try to resume.

But I humbly ask you to bear with me if I try to interject my anecdotes to this blog. 
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Zach
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"Still crazy after all these years."

« Reply #1 on: August 22, 2011, 06:35:05 AM »

It's great to have you here!
Looking forward to your participation.
  :wine;
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Uninterrupted in-center (self-care) hemodialysis since 1982 -- 34 YEARS on March 3, 2016 !!
~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
No transplant.  Not yet, anyway.  Only decided to be listed on 11/9/06. Inactive at the moment.  ;)
I make films.

Just the facts: 70.0 kgs. (about 154 lbs.)
Treatment: Tue-Thur-Sat   5.5 hours, 2x/wk, 6 hours, 1x/wk
Dialysate flow (Qd)=600;  Blood pump speed(Qb)=315
Fresenius Optiflux-180 filter--without reuse
Fresenius 2008T dialysis machine
My KDOQI Nutrition (+/ -):  2,450 Calories, 84 grams Protein/day.

"Living a life, not an apology."
monrein
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Might as well smile

« Reply #2 on: August 22, 2011, 07:43:19 AM »

 :welcomesign;
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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
YLGuy
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« Reply #3 on: August 22, 2011, 08:33:11 AM »

 :welcomesign; Glad you found IHD.  I am sure you have valuable input and look forward to reading your posts.
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lmunchkin
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"There Is No Place Like Home!"

« Reply #4 on: August 22, 2011, 11:24:53 AM »

    :welcomesign;    and glad to have you!

God Bless,

lmunchkin

 :kickstart;
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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
jbeany
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Cattitude

« Reply #5 on: August 22, 2011, 12:13:38 PM »

 :welcomesign;

Love the name!  And we always welcome caregivers who are willing to share their experiences, too.

jbeany, Moderator
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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.

MooseMom
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« Reply #6 on: August 22, 2011, 01:01:34 PM »

The decision to initiate such an invasive treatment as dialysis on an elderly patient is fraught with special considerations.  The most important thing is that the patient him/herself should make that call.  Just because someone is elderly doesn't mean they can't make these important decisions for themselves.  If they CAN'T make such a decision, then maybe dialysis is more torture than treatment.
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"Eggs are so inadequate, don't you think?  I mean, they ought to be able to become anything, but instead you always get a chicken.  Or a duck.  Or whatever they're programmed to be.  You never get anything interesting, like regret, or the middle of last week."
boswife
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us and fam easter 2013

« Reply #7 on: August 22, 2011, 01:46:05 PM »

Great to see you and hope to see lots more.  This is a great place you've found and we'ed love to hear of your stories with this wonderful thing called Dialysis.  Thanks for comming to join us...  :welcomesign;
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im a california wife and cargiver to my hubby
He started dialysis April 09
We thank God for every day we are blessed to have together.
november 2010, patiently (ha!) waiting our turn for NxStage training
January 14,2011 home with NxStage
willowtreewren
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My two beautifull granddaughters

WWW
« Reply #8 on: August 22, 2011, 06:15:37 PM »

 :welcomesign;

Hi, Mallard!

Looking forward to hearing your stories!

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. :)
RichardMEL
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« Reply #9 on: August 22, 2011, 07:53:37 PM »

Welcome mallardduckling - I like duckings - so cute :)

Anyway I wanted to highlight something you wrote in your intro - about the great social benefits of doing dialysis. I couldn't agree more. It's a horrible situation and procedure, but when I was in the unit doing HD for overr 4 years, our little "family" was very special. I saw these folks often more than I saw members of my own family, and we were always asking after someone if they werre missing - be it staff or patient. When we had losses, we all mourned, when we had transplants we all cheered and kept fingers crossed for great news, Sometimes wives or family members of patients would visit and sit with the other patienrs, keeping them company etc.

Just yesterday I visited my old unit because I was at the hospital for transplant clinic. It's been 9 months. They were so happy to see me, and I them. We keep in touch and it's great to these people who *care* about you and you care about them.

I certainly feel I gained much from my time doing D in this respect. Don't get me wrong - I hate that machine, and I never want to be needled again, but I miss the patients and the staff, and when I visit it's really good to catch up with everyone(but I try to not "rub it in" to some of the patients that I'm off the machine and can lead a more normal life - i don't want to be cruel).

Anyway thank you for joining us, and we look fortward to your contributions!!

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!
Ang
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« Reply #10 on: August 24, 2011, 01:27:31 AM »

 :welcomesign;
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live  life  to  the  full  and you won't  die  wondering
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