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Author Topic: I'm a dialysis wife  (Read 4887 times)
petey
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« on: January 08, 2008, 04:34:49 PM »

Hey, all!  I'm Marvin's wife and his dialysis partner.  Marvin found this site a couple of months ago, and he's been reading/sharing stuff from here with me.  I saw there was a section for spouses/partners, and Marvin said I should get my own login for this site so I could put my  :twocents; in.  It took a while (and the brains of Hawkeye, willieandwinnie, and that mastermind Sluff  :bow; to get me in), but I'm now in!

We've been married for 22 years, but Marvin and I have been together on his ESRD journey for the last 13 years.  He started on hemo (in center) in 1995.  He tried PD, and I trained with him for that, but it didn't work for him (one kinked cath and then peritonitis).  He stayed on in-center hemo for 5 and a half years.  I gave him one of my kidneys (open surgery -- big scar) the day before our 14th wedding anniversary.  That lasted for three years and three months before the transplanted kidney caught the same disease that destroyed his original kidneys (IGA nephropathy).  He went back on in-center hemo in October of 2003 and back on the waiting list.  We trained for home hemo this past summer, and we're currently using NxStage.  We both like it a lot, but it does take a lot of time.  We think it's worth it.

I know the whole ESRD and dialysis thing is rough on the patients, but sometimes it gets tough on the spouses/partners, too.  I always try to be brave and optimistic in front of Marvin (I never, never cry in front of him in times of crisis -- no matter how bad it seems), but sometimes when I get by myself, I do break down a little.  I hope this site will be a place where I can share, cry, and vent because most of my friends and family really have no idea what we're going through.  Oh, they're attentive, interested, concerned, loving, and all that stuff, but you never really know what's it like until you've "walked a mile in our shoes."  You guys know what I'm talking about!

I'm so glad to be in a place (IHD) where I feel like I belong.
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boxman55
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« Reply #1 on: January 08, 2008, 04:39:44 PM »

Welcome petey, God bless you for being there...Boxman
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"Be the change you wished to be"
Started Hemodialysis 8/14/06
Lost lower right leg 5/16/08 due to Diabetes
Sister was denied donation to me for medical reasons 1/2008
willieandwinnie
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« Reply #2 on: January 08, 2008, 04:44:57 PM »

:welcomesign; petey,

So glad you joined us. I am/was the caregiver. My husband got a transplant 9/7. I know what you mean about crying, I use to get in the shower and bawl. I never wanted to let Len know that some days I was just upset. You have a lot of reading to do. IHD is better then family. Everyone here understands what everyone is going through and offers support and opinions. Take care and Welcome aboard.
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"I know there's nothing to it, but I want to know what it is there's nothing to"
bolta72
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my best friend

« Reply #3 on: January 08, 2008, 04:45:16 PM »

Glad to see you made it in    :welcomesign;
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gotta do what I gotta do.. 2 yrs in ctr hemo
Sluff
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« Reply #4 on: January 08, 2008, 05:34:31 PM »

Welcome Petey,

That was pretty painless now wasn't it? Glad you made it and I hope you enjoy your visits and gain friendships, knowledge and above all the best way to help and you and Marvin understand things from both point of views.

Sluff/ Admin
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Romona
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« Reply #5 on: January 08, 2008, 08:38:40 PM »

 :welcomesign;
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Joe Paul
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« Reply #6 on: January 08, 2008, 11:55:38 PM »

Welcome  Petey, good to have you aboard.
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"The history of discovery is completed by those who don't follow rules"
Angels are with us, but don't take GOD for granted
Transplant Jan. 8, 2010
kitkatz
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« Reply #7 on: January 09, 2008, 09:35:31 PM »

Welcome. Great to have you aboard.



kitkatz,moderator
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lifenotonthelist.com

Ivanova: "Old Egyptian blessing: May God stand between you and harm in all the empty places you must walk." Babylon 5

Remember your present situation is not your final destination.

Take it one day, one hour, one minute, one second at a time.

"If we don't find a way out of this soon, I'm gonna lose it. Lose it... It means go crazy, nuts, insane, bonzo, no longer in possession of ones faculties, three fries short of a Happy Meal, wacko!" Jack O'Neill - SG-1
goofynina
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He is the love of my life......

« Reply #8 on: January 09, 2008, 09:41:54 PM »

Hi Petey, Welcome to ihatedialysis.com  :waving;  Looking forward to all you can share with us. :)  You've come to a great place for information and support  :grouphug;  Looking foward to hearing more from you.  :2thumbsup;


Goofynina/Admin.
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....and i think to myself, what a wonderful world....

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Goofynina and Epoman - Gone But Not Forgotten

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« Reply #9 on: January 10, 2008, 02:31:10 AM »

Welcome to our community!  it is always a very precious sign when a loved one joins us.  As you have learnt, IHD is now a genuine family, so we are always open to new members.  Please continue to post and take advantage of all the site has to offer.  :grouphug;
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"To be found in Him, not having a righteousness of my own ...but that which is based on faith"



I LOVE  my IHD family! :grouphug;
MyssAnne
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« Reply #10 on: January 10, 2008, 02:48:55 AM »

Welcome, Petey!!

SO glad you finally got in!!! 

You caregivers mean so much to us.  I am single, but my fiancee takes care of me when
I need it, and I do have a family I report to every day. Or else!!  I don't take it as being
dominated, all they want is a quick email, yes I am at work, and am okay. That's it!  If I don't
I get emails/calls...WHERE ARE YOU????

So, you caregivers can be obtrustive and pushy, but WE LOVE YOU!!!!!!!
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2_DallasCowboys
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« Reply #11 on: January 10, 2008, 03:06:46 AM »

Hi,Petey!  Welcome!

I am also a "dialysis  wife" - my
husband Les has been on dialysis
since 3/31/06.  His kidney failure
happened quickly, resulting from
heart bypass surgery the month
before.
This site is  wonderful-the best people,
and so much helpful information- and
most of all, I think,  a very strong support
system.   
Please visit often and let us know how everything
is going.
Anne
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Ken Shelmerdine
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Life's a bitch and then you go on dialysis!

« Reply #12 on: January 10, 2008, 07:45:57 AM »

 :welcomesign;
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Ken
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Home hemodialysis since May 07

« Reply #13 on: January 10, 2008, 08:14:49 AM »

 :welcomesign;
Marvin is lucky to have you as many of us are lucky to have amazing spouses as well.
The journey is hard...but it's worth it if you're with someone you love!
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Not giving up...thanks to Susan.
keefer51
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« Reply #14 on: January 11, 2008, 01:47:18 AM »

 :welcomesign;
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i am a 51 year old male on dialysis for 3 years now. This is my second time. My brother donated a kidney to me about 13 years ago. I found this site on another site. I had to laugh when i saw what it was called. I hope to meet people from all over to talk about dialysis.
Hawkeye
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« Reply #15 on: January 11, 2008, 12:31:28 PM »

Hello and  :welcomesign;

Glad you got into the site ok.
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del
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del and willowtreewren meet

« Reply #16 on: January 11, 2008, 04:38:43 PM »

Welcome I am a dialysis wife too.  Hubby has been on dialysis since Aug. 1997.  We trained for home hemo in Oct. 06.  It is a whole lot better than having to travel to in center.  We use a fresenius machine. Nxstage is not available in Canada
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Don't take your organs to heaven.  Heaven knows we need them here.
Ang
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« Reply #17 on: January 11, 2008, 08:35:41 PM »

welcome  aboard,glad  to  hear  you  got  in  ok
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live  life  to  the  full  and you won't  die  wondering
oswald
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« Reply #18 on: January 11, 2008, 09:00:00 PM »

 :welcomesign;
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ESRD 11/95
1st Transplant 7/1996 (failed; Nephrectomy 12/1996)
2nd Transplant 3/1999 (lasted 6 years)
3rd Transplant 5/2007 (lasted 4 years)
kimcanada
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WWW
« Reply #19 on: January 12, 2008, 11:35:22 AM »

 :welcomesign; :2thumbsup;
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donnia
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me and my donor Joyce

« Reply #20 on: January 12, 2008, 04:18:33 PM »

Welcome Petey!
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Born with one kidney 1972
Ureter re-constructured 1975 (reflux had already damaged the kidney)
Diagnosed and treated for high blood pressure 2000
Diagnosed ESRF October 2006
Started dialysis September 2007
Last dialysis June 4, 2008
Transplant from my hero, Joyce, June 5, 2008
Black
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« Reply #21 on: January 12, 2008, 11:54:50 PM »

Welcome from another NxStage wife.  I can soooo identify with you.  There are days that all I can do is, just get through it, and then I feel guilty because I know it's worse for him because he's the one on dialysis
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Lorelle

Husband Mike Diagnosed with PKD Fall of 2004
Fistula Surgery  1/06
Fistula Revision  11/06
Creatinine 6.9  1/07
Started diaysis 2/5/07 on NxStage
lola
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I can fly!!!

« Reply #22 on: January 13, 2008, 06:19:06 AM »

 :welcomesign; IHD and the shower are my God send I to am a wife of pt and IHD has gotten me through some pretty dark days
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Lori1851
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This is me Lori , Dustin's mom

« Reply #23 on: January 13, 2008, 02:16:56 PM »

 :welcomesign;
Glad to have you aboard!! Know what ya mean about not crying in front of them. I have a son 22 on dialysis due to FSGS. I found myself crying today driving to go see my aunt in the hospital. I have days just like you so you are not alone ;)
Lori/Indiana
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paris
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« Reply #24 on: January 13, 2008, 05:07:39 PM »

 :welcomesign; This is the best place for you to be. It is a wonderful group and I lean on everyone here for so much support.  I am the one with kidney failure, but I also the one who never--never cries in front of anyone.  Late at night, when I am all alone- that is when I cry.   So, come here and we will all cry together!! And then we will laugh together!  Glad you joined our family :cuddle;
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It's not what you gather, but what you scatter that tells what kind of life you have lived.
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