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Author Topic: Working and Gov Insurance  (Read 4743 times)
pagandialysis
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« on: February 15, 2012, 02:52:47 PM »

I can't find a simple answer so I thought I would ask someone here.

If I go back to work I am sure I will lose my SSI but how would that affect my Medicaid and Medicare? And no I can not ask my social worker.
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Dining on Dialysis - www.diningondialysis.com
-------------------------------------------------------------
Kidney Transplant (December 31, 2014),
Dialysis-Hemo (Started May 17, 2011. Ended December 29, 2014),
AV Fistula #2 (This one is a Basilic Transposition),
CKD (IgA Nephropathy) Stage 5,
Hypertension (Under Control)
KarenInWA
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« Reply #1 on: February 15, 2012, 03:08:33 PM »

I work FT and have insurance through my employer, and I have Medicare. So I know that won't go anywhere. Don't know about the other 2. I know for SSI or SSDI, you are limited to the amount of money you can make in a month. If you do a search on here for SSI, SSDI, or Social Security, you should find a few threads about it.

KarenInWA
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1996 - Diagnosed with Proteinuria
2000 - Started seeing nephrologist on regular basis
Mar 2010 - Started Aranesp shots - well into CKD4
Dec 1, 2010 - Transplant Eval Appt - Listed on Feb 10, 2012
Apr 18, 2011 - Had fistula placed at GFR 8
April 20, 2011 - Had chest cath placed, GFR 6
April 22, 2011 - Started in-center HD. Continued to work FT and still went out and did things: live theater, concerts, spend time with friends, dine out, etc
May 2011 - My Wonderful Donor offered to get tested!
Oct 2011  - My Wonderful Donor was approved for surgery!
November 23, 2011 - Live-Donor Transplant (Lynette the Kidney gets a new home!)
April 3, 2012 - Routine Post-Tx Biopsy (creatinine went up just a little, from 1.4 to 1.7)
April 7, 2012 - ER admit to hospital, emergency surgery to remove large hematoma caused by biopsy
April 8, 2012 - In hospital dialysis with 2 units of blood
Now: On the mend, getting better! New Goal: No more in-patient hospital stays! More travel and life adventures!
pagandialysis
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« Reply #2 on: February 15, 2012, 03:11:05 PM »

I'm not worried about the money. I HAVE to have both Medicaid and Medicare for my transplant. If I lose either of them I am just dead... literally.
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Dining on Dialysis - www.diningondialysis.com
-------------------------------------------------------------
Kidney Transplant (December 31, 2014),
Dialysis-Hemo (Started May 17, 2011. Ended December 29, 2014),
AV Fistula #2 (This one is a Basilic Transposition),
CKD (IgA Nephropathy) Stage 5,
Hypertension (Under Control)
KarenInWA
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« Reply #3 on: February 15, 2012, 03:20:01 PM »

Medicaid depends on the state that you live in. Some make you live at such a level of poverty to have it, others let working people buy in to it.

rsudock started a thread about the Medicaid buy-in.  http://ihatedialysis.com/forum/index.php?topic=24031.0

I hope this helps!

KarenInWA
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1996 - Diagnosed with Proteinuria
2000 - Started seeing nephrologist on regular basis
Mar 2010 - Started Aranesp shots - well into CKD4
Dec 1, 2010 - Transplant Eval Appt - Listed on Feb 10, 2012
Apr 18, 2011 - Had fistula placed at GFR 8
April 20, 2011 - Had chest cath placed, GFR 6
April 22, 2011 - Started in-center HD. Continued to work FT and still went out and did things: live theater, concerts, spend time with friends, dine out, etc
May 2011 - My Wonderful Donor offered to get tested!
Oct 2011  - My Wonderful Donor was approved for surgery!
November 23, 2011 - Live-Donor Transplant (Lynette the Kidney gets a new home!)
April 3, 2012 - Routine Post-Tx Biopsy (creatinine went up just a little, from 1.4 to 1.7)
April 7, 2012 - ER admit to hospital, emergency surgery to remove large hematoma caused by biopsy
April 8, 2012 - In hospital dialysis with 2 units of blood
Now: On the mend, getting better! New Goal: No more in-patient hospital stays! More travel and life adventures!
tbarrett2533
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Me licking my kidneys from my birthday kidney cake

« Reply #4 on: February 28, 2012, 10:43:05 AM »

if you get SSD then you can work and earn under $1000 a month SSI you can earn $67 a month and not loose your SSI, as far as medicaid I know that you have certain income limitations unless you are in a special program (which I am in) medicaid spend down program for the working disabled, I can earn 75K a year and still keep my medicaid and they (DSS) even pay my $500 a month deductable and my Medicare bill as well

so I have medicaid, medicare and blue/cross blue shield which I pay no out of pocket expense for

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CKD since: 1981
9.22.10: Catheter surgery
9.23.10: Started in center Hemo
10.06.10: Fistula surgery
12.02.10: Started using right upper arm Fistula (15 gauge)
12.30.10: Catheter Removed
07.01.11: Laparoscopic CAPD Catheter insertion
07.29.11: Started CAPD, 2000ml, 4 exchanges (Baxter)
08.15.11: Started filling with 1500ml (instead of 2000ml), 4 exchanges
08.21.11: Back to 2000ml fills, 4 exchanges (3-2.5% & 1-1.5%)
10.12.11: 2000ml fills, 4 exchanges (3 1.5% & 1-2.5% overnight)
11.08.11: Transplant list

Dialysis works for me, I don't work for dialysis!
It's my body, my health!!
sullidog
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« Reply #5 on: March 03, 2012, 08:21:21 PM »

You shouldn't lose medicare since you are a dialysis patient.
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May 13, 2009, went to urgent care with shortness of breath
May 19, 2009, went to doctor for severe nausea
May 20, 2009, admited to hospital for kidney failure
May 20, 2009, started dialysis with a groin cath
May 25, 2009, permacath was placed
august 24, 2009, was suppose to have access placement but instead was admited to hospital for low potassium
august 25, 2009, access placement
January 16, 2010 thrombectomy was done on access
Annig83
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« Reply #6 on: April 10, 2012, 08:24:39 PM »

Pagan- I am on Medicare and Medicaid as well.  I live in Indiana, and when I was pre-D, since I had a preexisting condition I was eligible for Medicaid.  When I started working, I had my employers' insurance as my primary, and Medicaid as my secondary insurance.  I had to pay a copay for me to keep my Medicaid as secondary.  I believe that you can opt to not have your employers insurance, and keep both Medicare and Medicaid.  You may have to pay a premium (if you don't already), but you shouldn't lose either since you are a dialysis patient.  Hope that helps a bit?
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*~Annie~*
Any change, even a change for the better, is always accompanied by drawbacks and discomforts.
Arnold Bennett
Even though I have gone through so much with ESRD, my son is my inspiration to keep going.  He was delievered at 28 weeks weighing 1 lb 12 oz and today he is a fun-loving 1 year old, whom I love with all my heart!

Diagnosed with Nephrotic Syndrome Age 13- 1996 Unknown Cause. 35% functioning of both kidneys.
Stable until Age 27; complications with pregnancy, loss of 25% function. (Current functioning is between 5-7%).
December 3, 2010- PD Catheter Placed on Left Side
March 2011- PD Catheter Removal (Due to malfunction)
April 2011- PD Catheter Placement on Right Side
April 2011- Surgery to adjust Catheter and "tacking of fatty tissue"
May 2011- CCPD Started
October 2012- Infection of PD catheter.  PD Cath. removal surgery. Perma-Cath. Placed for Hemodialysis.
Hemodialysis started October 12, 2012.
January 16 2013- First Fistula
On Transplant List in Indiana, awaiting 1st Transplant at IU Health in Indianapolis.
Grumpy-1
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Make me the person my dog thinks I am

« Reply #7 on: April 11, 2012, 03:27:44 AM »

Working FT, I have insurance through work and after 3 months on D, I qualified for Medicare.  So between my health insurance and Medicare, I only have a small co-pay at times.
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Make me the person my dog thinks I am
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