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Author Topic: Just had my tunnel catheter put in.  (Read 2909 times)
komomai
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« on: August 14, 2013, 05:09:16 AM »

Was posting on the home PD, home dialysis page, but since I'm doing my dialysis at the hospital, felt it should go here.

Well after 2 hours of shots, cuts and pushing and pulling, my tunnel catheter is in, procedure was done on a Monday and now it's Wednesday and I've completed a 4 hour 20 minute session.  Which is good, as I've never completed one before.  I would start to get leg cramps and tell them to shut the machine.  This time it was different because at the 3 hour mark, the signs of a leg cramp was starting up, I asked the technician to please crank the pressure back from 800 ml of water draw to 400 ml and that did the trick no signs of cramping.

The coolest part was the hook up so quick and no needles,  blood flow was good.

The other good news is that after 6 weeks of being in the hospital, I'm going home on Friday, and will try to be back at work on Monday.  2 infections are gone. :bandance;
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Angiepkd
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« Reply #1 on: August 14, 2013, 08:02:44 AM »

Glad you got some good news!  I can't imagine how hard it would be to stay in the hospital that long!  Bet you can't wait to sleep in your own bed again!  Hope everything continues to go smoothly with the neck cath and D.  Sounds like you are on the right track and will be back to normal in no time!  Remember to rest when you can.  Six weeks in the hospital probably zapped some of your energy.  Keep us posted on your progress!   :cheer:
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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!
obsidianom
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« Reply #2 on: August 14, 2013, 10:03:22 AM »

Are you going to consider home hemo now? My wife uses her catheter at home on Nxstage now that her fistula is not working well. The catheter is quite easy to work with as you can see. Can you do Nxstage in Japan?  It is shorter treatments done more frequently. It tends to improve how you feel during and after dialysis.  If you want info on it or on home hemo, just ask. There are many of us here doing it.
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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.
rocker
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« Reply #3 on: August 14, 2013, 02:46:17 PM »

There are definitely good aspects to having a catheter along with the bad.  It does make the hookup/detach of dialysis about a thousand times easier.
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komomai
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« Reply #4 on: August 17, 2013, 05:23:05 PM »

Mahalo for the words of encouragement.  On my 2nd session with the tunnel I was running a fever of 38.1 but the doctor said I was in good condition to do hemo, I did the same thing asking the technician to please dial down the amount water being taken out. 

I have asked about doing home dialysis and I would be the first one in Okinawa Japan to do so.  Also since it is Japan the machine would be like the ones they use in the hospital the brand name is Nippro, training would be provided by the hospital.  I think this would be an option to consider. :thx;
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rocker
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« Reply #5 on: August 17, 2013, 09:06:57 PM »

There is so much to recommend home dialysis. You can do the treatment when you want, no more being tied to the center's schedule. You can control your treatment, and do the things you would normally do at home.  If you feel you need a treatment sooner, or longer, you can do it.

I wish you very much luck in this.  It is a big responsibility, but there is so much more freedom.
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Sugarlump
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10 years on and off dialysis

« Reply #6 on: August 24, 2013, 09:09:37 AM »

Interested to know what dialysis is like in Japan.
Do you have lots of dialysis units?
Is it easy to obtain dialysis?
Do you have a transplant list too?
 :welcomesign;
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10 years of half a life
3 years HD 1st transplant Feb 08 failed after 3 months
Back to HD 2nd transplant Dec 10 failed after 11 months
Difficult times with a femoral line and catching MSSA (Thank you Plymouth Hospital)
Back on HD (not easy to do that third time around)
Fighting hard (two years on) to do home HD ... watch this space!
Oh and I am am getting married 1/08/15 to my wonderful partner Drew!!!
The power of optimism over common sense :)
komomai
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« Reply #7 on: August 25, 2013, 03:28:34 AM »

Aloha Sugarlump, the hospital that I go to is one of the major ones for Okinawa, it's called Chubu Hospital.  They have 24 beds/dialysis stations.  They don't use chairs(boo), all the dialysis nurses speak Japanese, although a few understand a little English, enough so that I can tell them to dial back the amount of water to be taken off before I go into the cramp/shitty mode.

Yes, there a quite a few hospitals that will treat end stage renal failure and provide hemodialysis treatments.

Unfortunately since I'm not Japanese and I  don't have the Japanese national health insurance I can't go on their transplant list.  However my wonderful wife has said she will donate a kidney for me, hope to do the transplant within a year, just need to lose a little more weight.  Since starting hemodialysis and eating the bland hospital food for 40 days I've lost 15 kilos.  Also debating if we will do it here in Okinawa, Japan or get it done in Hawaii.  :bump;
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Sugarlump
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10 years on and off dialysis

« Reply #8 on: August 25, 2013, 07:00:38 AM »

My closest major hospital (about 70 miles away) Addenbrookes Hospital in Cambridge actually uses japanese dialysis machines now!!!!
That's the fist time I have seen them in this country (or anywhere else actually!) :boxing;
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10 years of half a life
3 years HD 1st transplant Feb 08 failed after 3 months
Back to HD 2nd transplant Dec 10 failed after 11 months
Difficult times with a femoral line and catching MSSA (Thank you Plymouth Hospital)
Back on HD (not easy to do that third time around)
Fighting hard (two years on) to do home HD ... watch this space!
Oh and I am am getting married 1/08/15 to my wonderful partner Drew!!!
The power of optimism over common sense :)
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