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| | |-+  How to pay for life-long immunosuppressants
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Author Topic: How to pay for life-long immunosuppressants  (Read 22543 times)
monrein
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Might as well smile

« Reply #50 on: December 25, 2008, 02:42:31 PM »

Pretty much every day I'm grateful for our medical system Pelagia.  I think of it and my donors almost every day and thank my lucky stars.
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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
okarol
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Photo is Jenna - after Disneyland - 1988

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« Reply #51 on: March 03, 2011, 11:02:29 PM »


I worry about other young people who lose coverage at 3 years post-transplant. It's an issue that still has not been resolved.
We have coverage still, but others are not so lucky. Hopefully having pre-existing conditions removed with the healthcare bill will allow people to purchase policies (for a reasonable amount.)
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Admin for IHateDialysis 2008 - 2014, retired.
Jenna is our daughter, bad bladder damaged her kidneys.
Was on in-center hemodialysis 2003-2007.
7 yr transplant lost due to rejection.
She did PD Sept. 2013 - July 2017
Found a swap living donor using social media, friends, family.
New kidney in a paired donation swap July 26, 2017.
Her story ---> https://www.facebook.com/WantedKidneyDonor
Please watch her video: http://youtu.be/D9ZuVJ_s80Y
Living Donors Rock! http://www.livingdonorsonline.org -
News video: http://www.youtube.com/watch?v=J-7KvgQDWpU
rsudock
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will of the healthy makes up the fate of the sick.

« Reply #52 on: March 05, 2011, 09:40:02 AM »

I know I said it before on other post but I will say it again! Jenna is so lucky to have parents that are so involved in her healthcare!! Fighting for her and helping her. When I was graduating from college worried sick about how I was going to afford to pay for my health insurance my mother couldn't even give two rips that I was really in a tight bind. It wasn't her job to help me! Thank goodness everyday for caregivers who do care and sacrifice their own time to help their loves ones!! Thankfully I have a boyfriend who has stepped in to help me....

Great advice on here!!

xo,
R
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Born with autosomal recessive polycystic kidney disease
1995 - AV Fistula placed
Dec 7, 1999 cadaver transplant saved me from childhood dialysis!
10 transplant years = spleenectomy, gall bladder removed, liver biopsy, bone marrow aspiration.
July 27, 2010 Started dialysis for the first time ever.
June 21, 2011 2nd kidney nonrelated living donor
September 2013 Liver Cancer tumor.
October 2013 Ablation of liver tumor.
Now scans every 3 months to watch for new tumors.
Now Status 7 on the wait list for a liver.
How about another decade of solid health?
okarol
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Photo is Jenna - after Disneyland - 1988

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« Reply #53 on: July 24, 2011, 03:00:24 PM »


Supposedly anyone who gets a transplant now would be ok 3 years from now as the healthcare bill prohibits insurance companies from excluding patients due to a pre-existing condition. But no one says how much the health insurance will be, or what will happen if you cannot find employment or can't afford the premiums.
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Admin for IHateDialysis 2008 - 2014, retired.
Jenna is our daughter, bad bladder damaged her kidneys.
Was on in-center hemodialysis 2003-2007.
7 yr transplant lost due to rejection.
She did PD Sept. 2013 - July 2017
Found a swap living donor using social media, friends, family.
New kidney in a paired donation swap July 26, 2017.
Her story ---> https://www.facebook.com/WantedKidneyDonor
Please watch her video: http://youtu.be/D9ZuVJ_s80Y
Living Donors Rock! http://www.livingdonorsonline.org -
News video: http://www.youtube.com/watch?v=J-7KvgQDWpU
The Noob
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« Reply #54 on: July 24, 2011, 05:38:49 PM »

we wonder about this too. hubby was terminated from his employer of 26 yrs after 12 months of medical leave. he has medicare and NKF is paying the cobra, i think there was issue about it being 1 yr or 29 months?
so he gets a transplant soon, which is looking very likely, then what? he has a family member who's offered to get him a state job if we move there (which we would love to do). he'd never find work here, very depressed area.
what would you do?
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MooseMom
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« Reply #55 on: July 24, 2011, 06:37:42 PM »

What has the social worker at the transplant center had to say?  They won't list/transplant anyone unless they are satisfied that the patient's post-tx drugs can be paid for.
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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."
okarol
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Photo is Jenna - after Disneyland - 1988

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« Reply #56 on: October 25, 2011, 09:21:03 PM »

What has the social worker at the transplant center had to say?  They won't list/transplant anyone unless they are satisfied that the patient's post-tx drugs can be paid for.

Yes, if you cannot show a long term plan they can deny your being wait listed.
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Admin for IHateDialysis 2008 - 2014, retired.
Jenna is our daughter, bad bladder damaged her kidneys.
Was on in-center hemodialysis 2003-2007.
7 yr transplant lost due to rejection.
She did PD Sept. 2013 - July 2017
Found a swap living donor using social media, friends, family.
New kidney in a paired donation swap July 26, 2017.
Her story ---> https://www.facebook.com/WantedKidneyDonor
Please watch her video: http://youtu.be/D9ZuVJ_s80Y
Living Donors Rock! http://www.livingdonorsonline.org -
News video: http://www.youtube.com/watch?v=J-7KvgQDWpU
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