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BobN
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« on: March 07, 2009, 07:02:15 AM »

My first post here.  OK my first post anywhere.

I'm new to the blog stuff.  Not new to dialysis. 

I'm an otherwise healthy (evidence later) 53 year old male (couldn't tell from the name, right?) on dialysis.

It's semantics, but it's important.  I don't define myself as a "dialysis patient".  I'm "on dialysis".  I feel better already.

I've been on dialysis for a total of 4.5 years.  I was on for a year in my 30's, then I got a transplant from my mother.  What a gift.

The kidney worked great for 16.5 years.  It finally petered out in August of 2006.  I've been back on the big D ever since.

I've always been on hemodialysis.  In center.  Is it a pain to burn 4 hrs three times a week?

Yep.  But from my perspective, it's the least of all evils.  I figure, I'd rather just get it done and then go on with a semi-normal life the rest of the time.

I treasure my Saturday-Sunday, and honestly rarely think about dialysis, other than the ever-present dietary restrictions.

I'm employed full-time.  I have an officer-level position at a Fortune 100 company.   

I could write an entire blog (and maybe will some day) on being in a high-visibility, high-responsibility position while being on dialysis.  It certainly presents its challenges that I'm sure are familiar to people visiting this site.

Oh yeah, before I forget, my evidence of being healthy.  My wife and I are in first place in a mixed-doubles tennis league in Texas.

OK, it's a beginners league, she's a top-notch player, and I'm a complete hack, but still, first place is first place, right?

Anyway, I try to stay active as part of my effort to keep dialysis from running my life.

Which brings me to what brings me to this site.

I have mixed feelings about the concept of Ihatedialysis. 

On the one hand, the actual process of dialysis is about as much fun as falling out of trees. 

But really, aside from the sticks, pain, dizziness, nausea, crampling, vomiting, fainting, and itching, what is there to complain about, right?

On the other hand, can we really complain too much about a medical-miracle process that, let's face it, keeps us alive.

If the good Lord were smiling on us differently and we were born, say around the times our parents were born, and dialysis were in it's infancy, and our kidney problems struck us at the same stage in our lives, it would more than likely be syonara.  (Don't know if I spelled that right, but you get the idea.)

So, there are times I hate it.  But more times than not, I'm very thankful for it.  I try to live life to the fullest when I'm not on dialysis.

Well, as much as you can live life to the fullest without pepperoni pizza and beer.

Anyway, I like the blogs.  Definite group therapy feel to them.  I'll try to stay in touch with feelings on worklife, diet, exercise and anything else that pops up.

I hope everyone out there stays healthy, stays active, and finds a reason to laugh every once in a while.

Thanks for reading.
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www.bobnortham.com
Author of The ABC's of the Big D: My Life on Dialysis
Bob's Prescription for Living With Dialysis:
Follow Your Recommended Diet and Especially Watch Your Potassium, Phosphorous, and Fluid.
Stay Active - Find a Form of Exercise You Like and DO IT!!
Laugh Every Chance You Get.
willieandwinnie
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« Reply #1 on: March 07, 2009, 07:13:11 AM »

 :welcomesign; Bob. Glad you joined us. We are great for sharing information and giving loads of support. Hope you post often.  :cuddle;
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"I know there's nothing to it, but I want to know what it is there's nothing to"
Wenchie58
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Always carrying the big silly grin!

« Reply #2 on: March 07, 2009, 07:34:38 AM »

 :welcomesign; Bob.  Glad you joined us.  Yes, first is first!  lol
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Live your life in such a way that when your feet hit the floor in the morning Satan shudders and says "Oh s**t, she's awake!"

Right nephrectomy 1963
Diagnosed ESRD 2007
"Listed" summer 2007
Transplant 3/6 match  10/24/08
Joe Paul
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« Reply #3 on: March 07, 2009, 07:45:42 AM »

Welcome Bob, 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
Zach
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"Still crazy after all these years."

« Reply #4 on: March 07, 2009, 08:13:46 AM »

What?  You mean you gave up pepperoni pizza and beer?
No way!  Just don't be a slob about it.  One slice and one beer.

Then later a good tennis workout till you sweat.

Great to have you here!
 :beer1;
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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."
paris
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« Reply #5 on: March 07, 2009, 01:06:26 PM »

Welcome Bob.  This is a great site, full of information and even more support.  We share good times and bad.  The ones with experience help the members dealing with a new problem.   I learn something from here everyday.  We all really do care about each other.  So glad you joined our family.   :2thumbsup;






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.
monrein
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Might as well smile

« Reply #6 on: March 07, 2009, 01:53:17 PM »

Nice intro and nice to meet you here.  I look forward to hearing more about you handle everything and stay plugged in to life despite the massive "inconvenience" that D presents.
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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
David13
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A meow massages the heart.

« Reply #7 on: March 07, 2009, 06:32:31 PM »

Welcome, Bob.  This is a great place to learn, to share, and to get support.  I am sure your perspective will be a welcome addition.
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“The first human being who hurled an insult instead of a stone was the founder of civilization” - Sigmund Freud
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« Reply #8 on: March 07, 2009, 07:20:05 PM »

Bob --
Like you, my husband Marvin (he's the patient) and I don't hate dialysis.  While we don't enjoy the process itself, we sure do enjoy what dialysis gives us (14 years of "extra" life for my Marvin, who started in 1995 -- that's 14 years and still counting...).  Marvin's also 53 years old and stays busy, busy, busy (doesn't work, but volunteers extensively in our community -- mostly coaching youth baseball teams).  Our life is good -- dialysis and all.

Marvin says he's not a "dialysis patient" -- he's a "dialysis survivor."

And, I know what you mean about being born now instead of when our parents were.  Marvin's dad died of "uremic poisoning" (official wording on his death certificate) after having multiple heart attacks (stress of a body full of toxins for so many years and no dialysis) in 1970.  Marvin was a teenager when his dad died.  Dialysis back then was not for the poor, working man.  Marvin says, "There's no telling how many more years Daddy could have had if dialysis had been an option for him like it is for me."

We're so lucky, and it sounds like you think you are, too.

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st789
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« Reply #9 on: March 07, 2009, 07:26:50 PM »

Welcome, you had a good run with your last transplant. 

Hope you will get another transplant in the near future.

Again, welcome to the site.
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Romona
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« Reply #10 on: March 07, 2009, 07:58:47 PM »

 :welcomesign;
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dwcrawford
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Getting the heck out of town.

« Reply #11 on: March 07, 2009, 08:03:04 PM »

Hi Bob... so we are the newbies???  I've not been considered a newbie for a long, long time. 

Thanks for your comments.  I'm on here looking for inspiration, motivation, etc.  I have one of the better Nephrologist  (I know that is not how to spell it but maybe the "spell checker" will fix it for me) in Houston along with an excellent Internist.  I've been doing so well with  my type 2 diabetes for such a long time that  this all came as a shock to me.  I've just attended a couple of classes presented by the DaVita group in the Medical Center.  It is associated with Methodist -- so more or less I'm in good hands.

I am trying to figure out how to do the home dialysis but it is out of my reach I suppose since I live alone, an really, really, really old and have no family, etc. to work with me.  Anyway, I'm still exploring this.  I'm supposed to  have a fistala (another spelling problem I'm sure) in a couple of months.  We shall see.

I feel fine except I'm a little tired.  I feel as if the old neuropathy from the diabetes is coming back but at this point I don't know what is real and what is imagined.

I suppose I'll just real these messages and try to learn the difference between threads and blogs and maybe pickup on a few ackronyms.  So many little faces.  Let me choose one!!! :Kit n Stik;
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Come to think of it, nothing is funny anymore.

Nothing that I post here is intended for fact but rather for exploration into my personal thought processes.  Any slight, use of words with multiple connotations or other percieved insults are totally unintended.  I reserve my insults for private.
G-Ma
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« Reply #12 on: March 07, 2009, 09:26:28 PM »

 :welcomesign;
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Lost vision due to retinopathy 12/2005, 30 Laser Surg 2006
ESRD diagnosed 12/2006
03/2007 Fantastic Eye Surgeon in ND got my sight back and implanted lenses in both eyes, great distance & low reading.
Gortex 4/07.  Started dialysis in ND 5/4/2007
Gortex clotted off Thanksgiving Week of 2007, was unclotted and promptly clotted off 1/2 hour later so Permacath Rt chest.
3/2008 move to NC to be close to children.
2 Step fistula, 05/08-elevated 06/08, using mid August.
Aug 5, 08, trained NxStage and Home on 9/3/2008.
Fistulagram 09/2008. In hospital 10/30/08, Bowel Obstruction.
Back to RAI-Latrobe In Center. No home hemo at this time.
GOD IS GOOD
TeenHatesDialysis
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« Reply #13 on: March 07, 2009, 10:07:17 PM »

 :welcomesign; Bob!

Thanks for joining the group! I think it is great the you have a successful career, go to hemo dialysis 3 x per week and stay active playing/winning tennis! :2thumbsup; Is there special vitamins that you take??? My teenager has a difficult time getting through 4 H.S. classes with hemo dialysis 3x/wk and maybe one social activity per week. I know that dialysis impacts people diffierently, but if you have the secret to getting energized while on dialysis, PLEASE LET US IN ON IT.   :thx; I hope that you post often. :flower;
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Susan, mom of Jaclyn, Deziree and Valerie

www.cotaforjaclynp.com
Jaclyn and Deziree diagnosed CKD 2/07; NPHP (type 1) 9/07
Jaclyn started dialysis 1/2/08
Successful Transplant 7/4/2009 at Lucile Packard Childrens Hospital @ Stanford, Palo Alto, CA
Deziree in denial
Jaclyn listed 5/08
Deziree listed 1/09 ("Inactive")
Jaclyn Cadaver kidney transplant 7/4/09 (Independence from dialysis day!)
BobN
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« Reply #14 on: March 08, 2009, 07:04:44 AM »

Thanks to everyone for the welcome messages from my introductory blog yesterday.

I also posted to the "Working While on Dialysis" blog yesterday.  You may find some of my work experiences interesting.

I'll try to keep in touch fairly regularly with other dialysis-life related issues.

Stay active.  Stay happy.  And stay in touch.





EDITED: Merged Topics - Sluff/Admin




« Last Edit: March 08, 2009, 04:49:27 PM by Sluff » Logged

www.bobnortham.com
Author of The ABC's of the Big D: My Life on Dialysis
Bob's Prescription for Living With Dialysis:
Follow Your Recommended Diet and Especially Watch Your Potassium, Phosphorous, and Fluid.
Stay Active - Find a Form of Exercise You Like and DO IT!!
Laugh Every Chance You Get.
Bajanne
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Goofynina and Epoman - Gone But Not Forgotten

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« Reply #15 on: March 08, 2009, 05:21:41 PM »

Welcome to our community, Bob!!  I am so glad that you found us and decided to join us.
I see that you understand the conflicting nature of the name of our website.  Epoman chose that name for shock value. I think you are going to like it here.  As they say 'You don't have to be crazy to be in the IHD family, but it certainly helps!' 
Seriously, this is an excellent place for information and for support.  That is why it is more than just a website - it is a genuine family  :grouphug;  Just keep reading and keep posting, and you will see. Please take advantage of all this site has to offer.
Looking forward to hearing from you.



Bajanne, Moderator
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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;
Dan.Larrabee
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Dialysis Dan

« Reply #16 on: March 10, 2009, 01:49:23 AM »

Welcome Bob.
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AKA Dialysis Dan
Feeling the best I can because of Home Hemo
Doing it the best way I can by making it Nocturnal
Sharing it to help everyone feel they best they can
www.youtube.com/dialysisdan
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