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heapy
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« on: August 14, 2013, 01:35:51 AM »

Hi everyone, I am 38 years old and crashed with stage 5 end stage renal failure 4 months ago. Obviously this came as a massive shock as I had no warning whatsoever, I was rushed into hospital with breathing difficulties. Turns out my kidneys had failed due to long term undiagnosed high blood pressure (hypertension). I am now on nightly eight hour PD dialysis at home. I have joined this forum as I am struggling to come to terms with what has happened and find it difficult to open up to family and friends as they all see me as being strong and to be able to easily cope (not that easy though is it!!).

Heapy
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Poppylicious
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« Reply #1 on: August 14, 2013, 02:26:08 AM »

 :welcomesign; Heapy! 

... not that easy though is it!!

Nope.   ;D  (And I say this as the non-patient; it's my Blokey who was on haemoD, but he's fortunately now had a transplant.)
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- wife of kidney recepient (10/2011) -
venting myself online since 2003 (personal blog)
grumbles of a dialysis wife-y (kidney blog)
sometimes i take pictures (me, on flickr)

Everything was beautiful, and nothing hurt.
obsidianom
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« Reply #2 on: August 14, 2013, 02:42:11 AM »

Welcome. we are here to help. Just ask.
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My wife is the most important person in my life. Dialysis is an honor to do for her.
NxStage since June 2012 .
When not doing dialysis I am a physician ,for over 25 years now(not a nephrologist)

Any posting here should be used for informational purposes only . Talk to your own doctor about treatment decisions.
Genlando
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« Reply #3 on: August 14, 2013, 05:40:27 AM »

I have joined this forum as I am struggling to come to terms with what has happened and find it difficult to open up to family and friends as they all see me as being strong and to be able to easily cope (not that easy though is it!!).

Heapy

Welcome to the IHD Forum!

I discovered that I had Stage 5 kidney failure without any warning.  Sure, I knew I had high blood pressure; however, I never expected things to deteriorate so quickly: on Monday, I worked a 12-hour day, and drove over 300 miles; the next day, I was in ICU with ESRD and congestive heart failure.  My employer found out that I was severely sick, and they terminated me over the phone while I was still in the ICU.

It took me several months to get over the loss of my previous life.  Eventually, however, I realized that things would've been a lot worse: I would've ended up with cancer, or a heart attack.  Really, as long as you keep up with your treatments and watch your diet, you can live a LONG time on dialysis.  Sure, my life without dialysis may be over; however, my life now isn't so bad.  Just give yourself a little time, and you'll see what I mean. 

And above all else, don't hesitate to talk about your problems and frustrations here on IHD. 
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3/9/2010--Diagnosed with ESRD
3/24/2010--Fitted with catheter, and began hemodialysis
4/2010--First fistula attempt--clotted up and failed
6/2010--Second fistula attempt--didn't clot, but slow development
11/2010--3rd fistula surgery--fistula now developing
1/2011--fistula ready for H/D!
6/2011--Started using NxStage at home
8/2012--Switched to PD using Liberty Cycler
Angiepkd
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« Reply #4 on: August 14, 2013, 07:55:08 AM »

 :welcomesign; heapy!  You have found a great place to vent and ask questions!  We have all been through those same emotions as we entered the wonderful world of D.  Hang in there!  It does get better over time as you get into a routine.  Letting your family and friends know how hard it is can be very difficult.  I keep the smile on my face as I lie and say I am doing great.  Truth is, I am angry that I am dealing with all this.  I am sad for the life I have lost to the D machine.  I feel guilty and ashamed about the stress I have put on my husband.  I have learned that no one wants to hear it.  They want me to be strong and fine with everything, so that is what I tell them.  That is what makes this site so wonderful.  Real people who know how you feel and give you permission to let it out!  I have been doing home hemo for 6 months, and it really isn't that bad.  I feel better than before I started.  I have more energy.  I can deal with the hours on the machine, because it beats the alternative!  While my current life isn't what I expected, I still get to spend time with my friends and family, and I am willing to do whatever it takes to continue that.  All things considered, I am alive and able to do most of the things I did before.  For that, I am thankful!  Hope you do great on PD!  Looking forward to hearing more from you!
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PKD diagnosis at 17
Cancer May 2011, surgery and no further treatment but placed on 2 year wait for transplant
October 2011 first fistula in left wrist
April 2012 second fistula in upper arm, disconnect of wrist
January 2013, stage 5 ESRD
March 2013 training with NxStage home hemo
April 2013 at home with NxStage
April 2013 fistula revision to reduce flow
May 2013 advised to have double nephrectomy, liver cyst ablation and hernia repair. Awaiting insurance approval to begin transplant testing. Surgery in June.
June 2013 bilateral nephrectomy.
August 2013 finishing testing for transplant, 4 potential donors being tissue typed.
January 2014 husband approved to donate kidney for me
March 4th 2014 received transplant from awesome hubby. Named the new bean FK (fat kidney) lol!  So far we are doing great!
UkrainianTracksuit
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« Reply #5 on: August 14, 2013, 08:53:52 AM »

 :welcomesign;
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