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| | |-+  A new reality TV show: "Kidney Kings"!
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Author Topic: A new reality TV show: "Kidney Kings"!  (Read 6137 times)
chiawana
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« on: June 07, 2012, 08:58:06 PM »

So my husband and I came up with an idea for a new reality show. We were watching Hell's Kitchen tonight and I said they should have a competitive show about people learning to use the Nxstage hemodialysis system. The first person or team who can set it up and perform an alarm-free treatment wins . . . a free Nxstage system? Free supplies for life? Hey, it's no worse than some of the other tripe on TV.


EDITED - MOVED TO PROPER TOPIC -  Rerun, Moderator
« Last Edit: August 13, 2012, 08:37:09 PM by Rerun » Logged

My husband is represented in the avatar - he's a Capricorn, the Goat. He's been knocked off his mountaintop so many times by his health issues, but he continues to fight his way back to the top, a little worse for wear.
galvo
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« Reply #1 on: June 07, 2012, 10:06:36 PM »

Or, perhaps, The Big Kidney House - the winner gets a new kidney!
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Galvo
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« Reply #2 on: June 08, 2012, 12:13:09 AM »

Good thinking both of you!!!
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One day at a time, thats all I can do.
Poppylicious
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« Reply #3 on: June 08, 2012, 02:16:21 AM »

Or, perhaps, The Big Kidney House - the winner gets a new kidney!
:clap; ... Love this!
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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)
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Everything was beautiful, and nothing hurt.
boswife
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us and fam easter 2013

« Reply #4 on: June 09, 2012, 07:35:55 AM »

funny thing,,, i'd LOVE the show..hehe  Though since we're so good at NS, if we won we'ed be donating the kidney to one of you guys here  ;D  On the other hand..lol,  now that i think of it... we REALLY take our time at set up and all so would just be a big bore..lol
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im a california wife and cargiver to my hubby
He started dialysis April 09
We thank God for every day we are blessed to have together.
november 2010, patiently (ha!) waiting our turn for NxStage training
January 14,2011 home with NxStage
natnnnat
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« Reply #5 on: June 09, 2012, 07:59:53 AM »

I can so imagine that could work.  I can see it on Australian tv for sure!  And maybe there'd be more kidney donations?
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Natalya – Sydney, Australia
wife of Gregory, who is the kidney patient: 
1986: kidney failure at 19 years old, cause unknown
PD for a year, in-centre haemo for 4 years
Transplant 1 lasted 21 years (Lucy: 1991 - 2012), failed due to Transplant glomerulopathy
5 weeks Haemo 2012
Transplant 2 (Maggie) installed Feb 13, 2013, returned to work June 17, 2013 average crea was 130, now is 140.
Infections in June / July, hospital 1-4 Aug for infections.

Over the years:  skin cancer; thyroidectomy, pneumonia; CMV; BK; 14 surgeries
Generally glossy and happy.

2009 - 2013 PhD research student : How people make sense of renal failure in online discussion boards
Submitted February 2013 :: Graduated Sep 2013.   http://godbold.name/experiencingdialysis/
Heartfelt thanks to IHD, KK and ADB for your generosity and support.
jbeany
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« Reply #6 on: June 09, 2012, 11:47:36 AM »

I think the prize should be life time insurance coverage for the one on the nxstage, and for any possible living donor.   ;D
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"Asbestos Gelos"  (As-bes-tos yay-lohs) Greek. Literally, "fireproof laughter".  A term used by Homer for invincible laughter in the face of death and mortality.

deniferfer
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« Reply #7 on: June 09, 2012, 12:52:58 PM »

Hey how about just a general reality show where they follow our lives and get to see the up and down of kidney failure. To show how important it is to donate is and how it could change and save lives. I know in my life something is always going on and would make a great reality show. I often joke how that my life needs to be a sitcom and cuz it just doesn't seem real at times!!   
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1981-1995: Perfectly fine
1996: November, started feeling sick
1997: April, creatine at 17 and began dialysis    
1997: May Place on PD
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Poppylicious
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« Reply #8 on: June 10, 2012, 01:35:53 PM »

Hey how about just a general reality show where they follow our lives and get to see the up and down of kidney failure. To show how important it is to donate is and how it could change and save lives. I know in my life something is always going on and would make a great reality show. I often joke how that my life needs to be a sitcom and cuz it just doesn't seem real at times!!
I think this is a brilliant idea.  Not just a one-off documentary or interview but a real soul-baring follow in my footsteps for a year kind of show, with a variety of people (old, children, those holding down jobs and caring for a family, etc.) so that the general public really get to understand what it's like for everybody involved.  Maybe you should pitch an idea to a local channel?!

 ;D
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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.
Cordelia
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« Reply #9 on: June 10, 2012, 01:43:27 PM »

Love it!!!!!            :2thumbsup;
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Diagnosed with Polycystic Kidney Disease at age 19.
Renal Failure at age 38 (2010) came about 2 hrs close to dying. Central line put in an emergency.
Began dialysis on Aug 15, 2010.
Creatine @ time of dialysis: 27. I almost died.
History of High Blood Pressure
I have Neuropathy and Plantar Fasciitis in My Feet
AV Fistula created in Nov. 2011, still buzzing well!
Transplanted in April, 2013. My husband and I participated in the Living Donor paired exchange program. I nicknamed my kidney "April"
Married 18 yrs,  Mom to 3 kids to twin daughters (One that has PKD)  and a high-functioning Autistic son
galvo
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« Reply #10 on: June 10, 2012, 08:25:03 PM »

Yeah! We could call it: Days of our Kidneys[.
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Galvo
deniferfer
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« Reply #11 on: June 11, 2012, 07:03:23 PM »

I think this is a brilliant idea.  Not just a one-off documentary or interview but a real soul-baring follow in my footsteps for a year kind of show, with a variety of people (old, children, those holding down jobs and caring for a family, etc.) so that the general public really get to understand what it's like for everybody involved.  Maybe you should pitch an idea to a local channel?!

 ;D
[/quote]

Thanks, you got exactly what I was thinking and I also should what someone who donates gos thur. There are so many myths about donation and people don't understand the daily struggles that people with CKD go thur.... the question is how to write it to propose it to them and what channel...Also I think it would be cool to have people world wide tell their stories... 
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1981-1995: Perfectly fine
1996: November, started feeling sick
1997: April, creatine at 17 and began dialysis    
1997: May Place on PD
2006: Had to replace PD tube
smcd23
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The patient, the baby and the donor - October 2010

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« Reply #12 on: June 29, 2012, 09:36:22 PM »

Yeah! We could call it: Days of our Kidneys[.

I literally snorted and laughed out loud when I read that! I can just see the hour glass turning, or better yet, the little wheel thingie on the front of the hemo machine while they play that dreadful music like they do on Days of our Lives. Then the voice saying something like "Blood through the dialysis machine increases the Days of our Kidneys" I am giggling over here, must be from my lack of sleep and bordem. For some reason this mental image has me tickled!
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Caregiver to Husband with ESRD.

1995 - Diagnosed with vesicoureteral reflux and had surgery to repair at age 11. Post surgery left side still had Stage I VUR, right side was okay. Both sides were underdeveloped.
2005 - Discovered renal function was declining, causing HBP. Regular monitoring began.

March 2008 - Started transplant evaluation for preemptive transplant due to declining function.

September 16, 2008 - Transplanted with my kidney.
September 18, 2008 - Kidney was removed due to thrombosis in the vessels in and leading to the kidney.

October 2008 - Listed in Region I

May 2009 - Started in Center Hemo
January 2010 - Started CCPD on Liberty Cycler

June 15, 2012 - Kidney transplant from a 43 year old deceased donor
June 22, 2012 - Major acute rejection episode and hospitalization began
June 27, 2012 - Nephrectomy to remove kidney after complete HLA antibody rejection. Possibly not eligible for another transplant, ever again.

Now what?
AnnieB
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« Reply #13 on: August 13, 2012, 05:01:57 PM »

Yeah! We could call it: Days of our Kidneys[.

 :lol; :bandance;
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MightyMike
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Why do bad things always happen to good people?

« Reply #14 on: December 16, 2012, 09:33:57 AM »

I learned everything in 3 days but had to stay in training for 2 weeks to get back water samples and get supplies delivered.
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"The greatest pleasure in life is doing what people say you cannot do."
   -Walter Bagehot
==========================
December 2003 diagnosed with IgA Nephropathy 80% Function.
October 2004 started In-Center Hemo Dialysis Perma-Cath 5% Function.
September 2005 Living Related Donor (Mother) Transplant.
March 2009 Diagnosed CKD and IgA Nephropathy.
August 2009 Upper Left Arm Fistula.
November 2009 started In-Center Hemo Dialysis.
December 2010 started Home Hemo Dialysis.
January 2012 went back to In-Center Hemo Dialysis.
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