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AFcop
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« on: January 11, 2010, 02:03:14 PM »

Well my journey with ESRD started while I was on Active Duty as an AF Security Forces Chief of Police in Izmir, Turkey back in '06.   I had episodes of edema and what I thought was possibly lactose intolerance due to some unfortunate incidences.  Being that we only had a small clinic assigned, I was misdiagnosed (and sometimes ignored altogether).  After having blood tests done (and "lost") I just followed the military's regime of “take Motrin and you'll feel better” since that is all they would give me.  We used to call Motrin "Air Force Candy".  This continued until Feb 08 when I decided to retire after 22years in.  After coming home I was still sick, tired, and just felt beat down.  I went to Great Lakes naval facility to complete my retirement physical which the AF thought I really didn't need.  By May I was assigned a great PCM who didn't like my labs and ordered more. 
  On 8 May I was called at home by my PCM and my life changed forever.  I was told "get to the ER right now and tell them your creatinine level is 9.8 and they will get you in right away".  So off I went. My wife was at work so I had to call her and freak her out.  She made it to the hospital in record time.  The doctors took more blood and x-rays and confirmed the obvious; I had stage 5 kidney failure.  bp of 220/113 and they couldn't figure out how I was functioning normally.  To me, I felt fine.  I was admitted right away and had the neck catheter first with my first HD taking 5Lt out of me.  Boy was that fun.  The next day I had the catheter removed and a chest catheter installed.   So begins another fun journey, I was a mere two weeks from my official retirement and the military was scrambling with what to do.  In the end they extended me on active duty and sent me to WPAFB, OH for 9 months and I officially retired on 15 Feb 09 with full disability from the VA .
  While in Ohio I was able to come back home and get my evals done and get on the transplant list in Dec 08.  I also had my fistula placed in my left forearm which lasted until this last Dec.  I’m sure the vein looked like Swiss cheese after it was mangled so many times by people who were studying to interrogation specialists.  I would have told them anything at the level of pain they were bringing.  Guantanamo would be like a resort!!!  Well, we made it home from Ohio and set out to find a new home since living in my mother-in-law’s basement was NOT a long term option.  We found our dream home in June and promptly moved in the middle of the month.  My center for HD is only 3 miles away and alternates aren’t all that far off.   I haven’t worked since Jan 09 and it’s killing me.  I know I can’t be a police officer any more so I’m looking at alternatives and even a whole new direction.     
  I kind of feel like a train wreck.  I had a partial parathyroidectomy which brought my PTH level down from a disgustingly high 4400 to a reasonable 137.  My first fistula completely failed 1 Dec which led to a new chest catheter and a new fistula which was reconnected just a few inches up from the old one.  Looks rough with that big crossover lump but it seems to buzz just nicely.  You would think it should work like a champ but the Gestapo seems to like to get it to NOT work.  We’ve been using it for a week and it’s already having issues like the arterial wouldn’t work and I had some internal leakage leaving some wonderful swelling the last couple of days.  I know by reading some posts that I have it SO much better than it could be.  I like to hope beyond hope.  Sometimes you get let down.
  I should add that in no way would I have ever made it to this point without the support from my wife and family.  My wife has really adapted things like cooking to make life so much easier (and tasty!).  We went from not seeing each other much for almost two years while I was deployed to spending every waking moment (other than HD) together.  I don’t know how she puts up with me!!!    I couldn’t post anything about me without giving her credit for taking the very best care of me though all of this. She is my guardian angel.
  I’m sure there is more (and as you can see I like to talk!)but I am sure that will come out in the future.  As for my personal side, I like to fish, hunt, and generally be outdoors and ESRD hasn’t stopped me yet.  Slowed me down a bit but will not stop me.  Don’t hate me for being a Cubs fan and yes I’m still heartbroken over my beloved Packers loss.  I’m also a Blackhawks fan but love any level of hockey.  I’m hoping to get back into cycling but will re-evaluate my energy levels this spring. Ok, enough about me….
 :police:
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Zach
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"Still crazy after all these years."

« Reply #1 on: January 11, 2010, 02:28:21 PM »

Hey Dan,

Welcome to our community!

 :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."
galvo
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« Reply #2 on: January 11, 2010, 02:41:10 PM »

G'day Dan! A well-told story. You've arrived at a good spot here. Your experience will be valuable to others and I reckon you'll find lots of good stuff yourself. Stick around, post often, and have a ball.
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Galvo
monrein
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Might as well smile

« Reply #3 on: January 11, 2010, 03:29:32 PM »

 :welcomesign; and thanks for telling us enough about yourself to have a sense of how you got to this point.  This is a great site and I hope you find it as helpful as I have.
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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
cariad
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What's past is prologue

« Reply #4 on: January 11, 2010, 03:33:39 PM »

:welcomesign; to IHD, Dan. Glad you found us.

I, too, live in the Dairy State. Don't hate me for not caring about the Packers in the least. ;)

I look forward to reading more of your posts.
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Be kind, for everyone you meet is fighting a great battle. - Philo of Alexandria

People have hope in me. - John Bul Dau, Sudanese Lost Boy
Hanify
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Hadija, Athol, Me and Molly at Havelock North 09

« Reply #5 on: January 11, 2010, 03:47:01 PM »

Welcome
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Diagnosed Nov 2007 with Multiple Myeloma.
By Jan 2008 was in end stage renal failure and on haemodialysis.
Changed to CAPD in April 2008.  Now on PD with a cycler.  Working very part time - teaching music.  Love it.  Husband is Paul (we're both 46), daughter Molly is 13.
willowtreewren
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My two beautifull granddaughters

WWW
« Reply #6 on: January 11, 2010, 05:25:52 PM »

Welcome to IHD, Dan.

What an intro! This is a great site!

I'm looking forward to hearing more from you!

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. :)
looneytunes
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Wishin' I was Fishin'

« Reply #7 on: January 11, 2010, 05:38:54 PM »

Hey AFCop, welcome to IHD.  Great intro!
 :welcomesign;
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"The key to being patient is having something to do in the meantime" AU
HubbysPartner
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Our first New's Year's together - A new beginning

« Reply #8 on: January 11, 2010, 05:50:58 PM »

 :welcomesign; Welcome Dan!  Glad you found us.  This is a great site with great supportive people and lots of great information.  Come back and post often. 
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Caregiver to husband, Lou, diagnosed 2/2008
4/2009 - Fistula
10/2009 - Started NxStage training
112009 - Finished training; at home with nxstage

Our family - husband, Lou; me, Marge; sons, Marc & Keith; daughter, Liz
Be still and know that I am God. - Psalm 46:10
Jean
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« Reply #9 on: January 11, 2010, 06:34:40 PM »

 :welcomesign; to IHD Dan. Great intro you wrote. Glad to have you with us. This is a great site, you can learn a lot and help us a lot too. Look forward to more of your posts.  :welcomesign;
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One day at a time, thats all I can do.
silverhead
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« Reply #10 on: January 11, 2010, 07:57:35 PM »

Welcome Dan, We are transplanted Wisconsonites, and still have most of our relatives scattered about the state, Where are you located?
You will find lots of useful info here. And thank you (and your family), for your service.....
Tom
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Do not argue with an idiot. He will drag you down to his level and beat you with experience.
fc2821
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Just another hamster on the dialysis W.O.F.

« Reply #11 on: January 12, 2010, 04:43:58 AM »

 :welcomesign; Dan.   We seem to have a lot in common, I was in the Air Force (way back in the dinosaur age), was a deputy sheriff for 23 1/2 years, and came into dialysis and kidney failure suddenly as you have.   Good people here, don't be shy ask questions and get to know them they are a gret resource. 
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In center hemo dialysis since Feb 14, 2007. 

If I could type properly, I'd be dangerous!

You may be only one person in the universe but you may mean the the universe to someone else.
cloud393
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« Reply #12 on: January 12, 2010, 10:01:49 AM »

 :yahoo;  Welcome Dan.  Nice to meet you.
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May you live as long as you want and never want as long as you live.
AFcop
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« Reply #13 on: January 18, 2010, 04:28:45 PM »

Thanks everybody.  It's good to have a voice and know you all will listen(not necessarily the case during dialysis!).  I'm learning alot from you all and am sure I'll have alot of questions.  I'm almost on a second list for a kidney at UW-Madison.  I may be asking about the facility there in case anyone has any experience with them.
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