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Author Topic: I had a heart attack and A fib. Now I want to die  (Read 5809 times)
kickingandscreaming
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« on: July 23, 2019, 07:27:45 PM »

I've been in hospital, feeling utterly desolate deliberating how I want to die.  I don't want to die of a heart attack and I don't want to die during a cardiac ablation or during open heart surgery to repair my broken mitral valve.  I feel so hopeless and alone with this decision.   At least in hospice I can exercse some control on how I die.  What a very sad state I'm in.
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Diagnosed with Stage 2 ESRD 2009
Pneumonia 11/15
Began Hemo 11/15 @6%
Began PD 1/16 (manual)
Began PD (Cycler) 5/16
GA_DAWG
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« Reply #1 on: July 23, 2019, 09:49:55 PM »

I am so sorry kickingandscreaming. I really wish there was more I could say, but I've learned that sometimes all we can offer is to be there to listen, and I am sure there are many here who are willing to serve that use for you. You are a valued member of this community and I know we all wish the best for you. On many occasions you have offered valued advice and support to many, and I just wish we could do the same for  you.
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SooMK
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« Reply #2 on: July 24, 2019, 11:23:09 AM »

I am so sorry. You are showing so much courage.
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SooMK
Diagnosed with Uromodulin Kidney Disease (ADTKD/UMOD) 2009
Transplant from my wonderful friend, April 2014
Volunteering with Rare Kidney Disease Foundation 2022. rarekidney.org
Focused on treatment and cure for ADTKD/UMOD and MUC1 mutations.
lulu836
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« Reply #3 on: July 24, 2019, 12:03:38 PM »

I am sorry you are having to go through all of the troubles.  All any of us can do is offer to listen  if you need to vent.  I'm up at all hours of the night because of insomnia.  Please let us hear from you. 
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Of all the things I've lost, I miss my kidneys the most.
Brooklynite
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« Reply #4 on: July 24, 2019, 12:46:05 PM »

It breaks my heart to see someone going through so much where stay want to truly die.  This too shall pass.  :boxing; 

Kickingandscreaming take it one day at a time.  You will get through this.  It seems harder when you are going through it alone but you will get through it.   This is the downside of dialysis but don't let dialysis win.   You have to go at dialysis kicking and screaming until you put it back in its place. 

You started off right by expressing how you are feeling; a start to healing. 

Hang in there and take it one day at a time and you will feel better.

 :cuddle;
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On dialysis since 1999
In-Center 11 years
Home HD 8 years - still at home
One attempt for transplant - didn't get it due to clotted veins
Another attempt for transplant - testing done and same results | clotted veins
Been on dialysis for 20 years and still trying to live my life everyday
kickingandscreaming
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« Reply #5 on: July 24, 2019, 01:03:12 PM »

Thank you all for your kind words.  I'm still struggllng and working hard to deal with all this.
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Diagnosed with Stage 2 ESRD 2009
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Began Hemo 11/15 @6%
Began PD 1/16 (manual)
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MooseMom
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« Reply #6 on: July 24, 2019, 02:00:26 PM »

I feel very sad thinking about your situation.  I wish I could make your world happy and carefree again.

I know the value of just venting, knowing that there are people out there all too happy to listen, who will not judge and who will not try to solve all of your problems.  Sometimes there just are no answers.  So, it is with some trepidation that I offer one suggestion.  Have you looked into palliative care?  I confess to not knowing much about it; I don't know how one accesses it as perhaps it is regulated/licensed by each state separately.  I don't know how it is paid for.  I was speaking to a lady at the pool this morning, and she has a myriad of health problems.  While she has family around, they don't really seem to take much notice of her, so she is pretty much on her own.  She mentioned maybe speaking to her doctor(s) about palliative care, and as soon as she said those words, I thought of you.

We all care about you and will do whatever you think we might do for you to make your life a bit easier.  I'm just sorry that these words are having to be "said" on a computer screen.
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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."
kickingandscreaming
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« Reply #7 on: July 24, 2019, 06:03:35 PM »

I have made contact with a palliative care doctor.  Hospice s ONE of my options (besides staying alive).  It's my ace in a hole and I'm gratfeful it's there.  In the meantime, it's one foot after the other.
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Diagnosed with Stage 2 ESRD 2009
Pneumonia 11/15
Began Hemo 11/15 @6%
Began PD 1/16 (manual)
Began PD (Cycler) 5/16
lulu836
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« Reply #8 on: July 25, 2019, 06:09:38 AM »

Keep on keeping on!   :thumbup;
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Of all the things I've lost, I miss my kidneys the most.
MooseMom
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« Reply #9 on: July 25, 2019, 10:29:03 AM »

I have made contact with a palliative care doctor.  Hospice s ONE of my options (besides staying alive).  It's my ace in a hole and I'm gratfeful it's there.  In the meantime, it's one foot after the other.

I'm sure we'd all be interested in what the palliative care doctor has to say.   :grouphug;
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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."
kickingandscreaming
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« Reply #10 on: July 25, 2019, 11:12:26 AM »

I haven't got the energy now to recall and report on the conversation.  But it was a good one.  I felt quite good about how she thinks and about how she described the process.

On a more immediate note, I just had a Nuclear stress test to view the heart and blockages.  The test was pretty unpleasant, but the result is terrific.  NO BLOCKAGES, LOOKS PERFECT.  So that is great to know.  I still have A fib and a bad heart valve to deal with, ether of which could kill me or make my life Hell.  But one down. That's a relief.  I figured, with my luck my arteries would be blocked to the brink.  Fortunately. my healthy lifestyle did pay off.  The A fib is a congenital defect and the valve was damaged by my kidneys and old age.
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Diagnosed with Stage 2 ESRD 2009
Pneumonia 11/15
Began Hemo 11/15 @6%
Began PD 1/16 (manual)
Began PD (Cycler) 5/16
MooseMom
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« Reply #11 on: July 25, 2019, 12:15:46 PM »

I'm very glad you had a good conversation, and I'm relieved to hear that you got some good news at last!
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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."
lulu836
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« Reply #12 on: July 25, 2019, 01:01:58 PM »

That is terrific news!  Glad you had the conversation and you heard positive news.
« Last Edit: July 26, 2019, 08:23:28 AM by lulu836 » Logged

Of all the things I've lost, I miss my kidneys the most.
UkrainianTracksuit
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« Reply #13 on: July 25, 2019, 05:00:28 PM »

Very sorry to read of this awful situation, k&s. On the other hand, glad to read of no blockages. Here is hoping that you can stay stable for as long as you want and feel at peace otherwise. Have a whole team rooting for you here. Prayers and thoughts!  :grouphug;
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Michael Murphy
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« Reply #14 on: July 25, 2019, 07:42:51 PM »

October 2016 I suffered a major heart attack it left me with a injection fraction of 20%.  The normal injection fraction is close to 60%.  I laid in bed and heard the doctors discussing the fact I was probably going to die.  The next day I had a emergency angioplasty and was still in bad shape.  I was sent to another hospital for a high risk angioplasty, I was discharged at the end of the week.  On Monday next week I went back to my normal dialysis clinic after treatment I walked to my car and could not breathe, called cardiologist and his assistant told me to go to the medical group urgent care center. Was there for 9 hours when I had my 4 th episode of not being able to breathe.  A nurse was in my room at the time and started screaming I was in vtach.  Ambulance back to hospital where it was determined I needed to go to another hospital ambulance ride again to hospital electro physiologist was at.  Had 7.5 hour operation to implant icd and abalation.  It took a year before I began to feel good.  Today there are things I still can’t do but all in all I am happy.  I too was almost ready to pack it in but then I realized I am a Dialysys patient and if I didn’t like how I ended up I would just stop Dialysys.  Well while not perfect my recovery has returned enough functionality that my life is worth living, by the way not only vtach but afib was involved.  Nether has bothered me in the last 2 years.
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Charlie B53
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« Reply #15 on: July 26, 2019, 06:59:01 PM »


I don't really know anything about valves.  My by-pass was vessala only.

But I've heard valves are replaced daily.  Some actually done through the veins, not even splitting the chest.  Wow.

A-fib, one of the Nurses in Wife's Nursing Home had to take a trip to the ER a few months ago.  Seems she has a history of A-fib and her rhythm was getting seriously out of sync.  A bit of adjustment in her mes and she was back at worok the next week end.  She works weekend doubles Sat AND Sun.

Keeping that positive attitude that you have shown us for so long has to be the key.  Learning more about your conditions and how your behaviour, diet, fluids, everything that can have an effect, makeing those adjustments in order to minimize the effects of the condition.

You are far stronger than you think.

Take Care,

Charlie B53
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iolaire
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« Reply #16 on: July 26, 2019, 08:48:18 PM »

kickingandscreaming, I’ve been following  your posts and have no advice.  But I’m glad the heart attack didn’t get you. I hope you find comfort in your days ahead whatever path you choose for the near future.
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Transplant July 2017 from out of state deceased donor, waited three weeks the creatine to fall into expected range, dialysis December 2013 - July 2017.

Well on dialysis I traveled a lot and posted about international trips in the Dialysis: Traveling Tips and Stories section.
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« Reply #17 on: July 27, 2019, 07:14:47 AM »

Kicking and Screaming, after heart attack and vtach issues I was slated for release and the hospital sent some one to see if I could climb a set of stairs.  I realized I could walk about a 100 feet then I would need to sit for a few minutes to get my breath back.  Now in real life there are not chairs every 100 feet.  So I bought a rolling walker that had a seat.  Go 100 feet lock walker sit, wait a couple of minutes, get up go another 100 feet.  As time went on I began to go father.  I still have some limitations.  But I have adapted so I still do what I need to.  I was tempted to just give up, when I could not walk the 8 feet from my hospital bed to the toilet with out spending 10 minutes getting my breath back.  It was probably the exertion invoking vtach.  So looking back at the work involved in recovery it clearly was worth the effort.  Not only am I still alive but am looking forward for the future.  I know I will not live for ever and if I go soon so be it.  I do know every day I live is one more day at&t pays be to be alive.  Since they changed the rules and took half my pension, I enjoy knowing I am a net debit on their corporate books.
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kickingandscreaming
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« Reply #18 on: July 27, 2019, 08:04:16 AM »

I am now known as a "multi-morbid" patient.  I am sick on multiple levels--  under it all is my bad kidneys, then there's my heart which has at least 4 problems:  Heart Block (where my pulse goes way low and necessitated getting a pacemaker.  Then there's A fib that can stirike at any time and can cause a clot/stroke.   This heart attack I just had was caused by A fib.  Then there's the queen of my heart issuses, the regurgitating mitral valve which could only be repaired by open heart surgery (which would probably kill me at this age, etc.

Charlie-  this is a minimally invasive version of valve repair, but I am not a candidate for it since my kiidneys have deposited calcium on the valve, making it irreparable except with open heart surgery.

And now, on top of everythig else, my calves (on both legs) are swollen, engorged, hard as rocks, and in horrible pain.  I had them looked at but basically nothing was done except antibiotics.  but it's not an infection.  to walk is to feel agony.  I live totally alone so I have to walk even tho it is nightmarishly painful to do so.

So it is this WHOLE that drives me to consider going into hospice to put myself out of misery.  Add to this that I only have one familh  memeber ( a niece in a distant state), no children, not even a dog anymore.  I really have very little to live for.  And when you add to that my country, America, has been under constant assault by the delusional, malignat narcissist in the White House.-- there's a big part of me that is ready to chuck ip.
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Diagnosed with Stage 2 ESRD 2009
Pneumonia 11/15
Began Hemo 11/15 @6%
Began PD 1/16 (manual)
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MooseMom
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« Reply #19 on: July 27, 2019, 08:29:55 AM »

I personally think that the whole "positive attitude will help you live longer" is a load of old bollocks.  There is no evidence showing this is true.  When one has a medical condition (kidney failure) that cascades into multiple maladies, some of which are physically painful to the point of making every day life just excruciating, it is no wonder that you, k&s, feel the way you do.  You really are caught between the proverbial rock and hard place.

My husband's elderly father has had A-fib for many years and has been on many meds whose effectiveness has dwindled as time went on.  He's had that procedure where a nerve was cut, and surprisingly it did not work as well as his doctor had expected.  So I know that A-fib is not easy to treat, and the idea that it can strike and kill you at any time is a hard thing to live with.

Let's say that you did decide to have the open heart surgery to repair the mitral valve, and let's say that it was successful.  How much would that repair improve your life?  Would it improve your life to the point where you might think it would be worth the risk?

What in the world could be wrong with your calves?  I'm a bit disappointed that your doctor put you on antibiotics; this sounds rather dismissive to me.  "Oh, I don't know what this is, so I'll just throw some antibiotics at it and hope for the best."  That is probably an unfair assessment by me, but that's my gut reaction.  I hope I'm wrong. 

If it weren't for my kidneys and the expense of treatment, I'd seriously consider moving to another country.  I've considered going back to the UK, but they're going down the same road (maybe even a much rockier one) as we are.
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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."
kickingandscreaming
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« Reply #20 on: July 27, 2019, 11:16:33 AM »

MM-  I spent 3 days in the hospital being tested about my legs.  They did multiple blood and skin cultures, assuming it was a bacterium.  And I was on a series of antibiotic based on that assumption and the symptoms at the time--red, hot, swollen.  On some level they've improved:  less red, less bumpy and FAR less painful but still VERY painful.  Very hard to get around and since I'm alone, I have to get around on my own steam.  This new wrinkle is mystifying, since it had seemed to be improving and then BAM it's back in a slightly different form.   I have now seen 2 hospitals, one urgent care, and one PCP and I'm still in this boat.  I put in a call for a referral to a rheumatologist thinking it might be vasculitis and not cellulitis.  Still waiting for some real helpl

I think positive thinking (altho it feels good to true believers)  is a crock when it comes to serious health issues.  It doesn't hurt, but may keep a person in denial.
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Diagnosed with Stage 2 ESRD 2009
Pneumonia 11/15
Began Hemo 11/15 @6%
Began PD 1/16 (manual)
Began PD (Cycler) 5/16
MooseMom
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« Reply #21 on: July 27, 2019, 02:17:53 PM »

Oh, OK.  I didn't know you'd been in the hospital for 3 days about your legs, so I'm not quite so outraged.   :)  How very odd.  You're a real medical puzzle, k&s, you are! 

You must have been in so much pain.  I am so sorry this is happening.  I hope you can get a referral quickly and find out what is happening and what can be done for you.  It's just all so very odd.
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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."
Charlie B53
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« Reply #22 on: July 28, 2019, 04:37:27 PM »


Some like Trump, others, not so much.   I like to think he is upsetting the apple cart, the way Congress has been doing business as usual.

Even if re-elected you can look forward to his eventual end of term and the public will elect someone else.


Whether that new President will continue to upset the apple cart or join Congress in doing business as usual, driving up taxes and improving nothing but their own bank accounts, well, we will just have to wait and see.

I would very much like for you be be here with us to see for yourself.
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jambo101
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« Reply #23 on: July 31, 2019, 02:19:52 PM »

You could try calling the Kidney connection peer support program1-866 390-7337
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Jim
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Going through life tied to a chair!

« Reply #24 on: July 31, 2019, 02:25:04 PM »

Yes, what Charlie said. 

                  :thumbup;
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