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Author Topic: Were you on dialysis during the Earthquake of 8/23/2011?  (Read 3560 times)
Meinuk
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« on: August 23, 2011, 12:30:13 PM »

First off, I hope that everyone is well, and this was just a scary inconvenience. A 5.9 earthquake hit Virginia this afternoon - prime in-center dialysis time, and it was felt all up the Eastern Seaboard.  (My office in NY was evacuated).

I'd like anyone who was on the machine, either at home or in center to please comment on: 

How did the earthquake affect you?  How did your facility react?  What could have been done better?  What worked? Did the facility staff talk to you about what was going on?  Were you taken off the machine?  Was it simply ignored?

Now is the time, while things are fresh in our thoughts to make a list of what worked, and what didn't work. This way, we can all be better prepared for the next time.

Thanks,

Anna

And just as a refresher, here is a link to:
Preparing for Emergencies: A Guide for People on Dialysis  (English)  http://www.ipro.org/index/cms-filesystem-action/esrd/preparing_for_emergencies.pdf

Prepárese para Emergencias: Una guía para personas en diálisis  (Spanish) http://www.ipro.org/index/cms-filesystem-action/esrd/preparese_para_emergencias.pdf

These booklets should have been mailed to you when you first started dialysis.  If you didn't get or don't remember getting the New Patient Orientation Packet (NEPOP), here is a link to the materials sent:  http://www.esrdncc.org/index/new-patient-orientation-packet

And here is a GREAT resource for Dialysis Emergencies:  KCER the Kidney Community Emergency Response Coalition:  http://www.kcercoalition.com/


« Last Edit: August 23, 2011, 12:41:49 PM by Meinuk » Logged

Research Dialysis Units:  http://projects.propublica.org/dialysis/

52 with PKD
deceased donor transplant 11/2/08
nxstage 10/07 - 11/08;  30LS/S; 20LT/W/R  @450
temp. permcath:  inserted 5/07 - removed 7/19/07
in-center hemo:  m/w/f 1/12/07
list: 6/05
a/v fistula: 5/05
NxStage training diary post (10/07):  http://ihatedialysis.com/forum/index.php?topic=5229.0
Newspaper article: Me dialyzing alone:  http://ihatedialysis.com/forum/index.php?topic=7332.0
Transplant post 11/08):  http://ihatedialysis.com/forum/index.php?topic=10893.msg187492#msg187492
Fistula removal post (7/10): http://ihatedialysis.com/forum/index.php?topic=18735.msg324217#msg324217
Post Transplant Skin Cancer (2/14): http://ihatedialysis.com/forum/index.php?topic=30659.msg476547#msg476547

“To doubt everything or to believe everything are two equally convenient solutions; both dispense with the necessity of thought.” - Henri Poincare
Willis
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« Reply #1 on: August 23, 2011, 12:42:11 PM »

Well, technically--since I'm on PD--I'm on dialysis ALL the time.  :lol;

I was at work and felt the quake at about 4.x level for about 10 seconds near Charlotte, NC. Caused a lot of talking but everyone soon returned to work. Nothing damaged except billable hours.  :P

 
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MooseMom
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« Reply #2 on: August 23, 2011, 01:27:02 PM »

Meinuk, I clicked onto the link re new patient info packets, and it brought a question to my mind.  If I understand correctly, new dialysis patients fill out some CMS form, and that information is entered into a database.  But what if that new patient (ie, me) has private insurance and so will not be on Medicare for 30 months?  At what point does the CMS or any other official entity (other than my insurance company) become informed that I am on dialysis?  Will I be getting one of these information packs?
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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."
Rerun
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« Reply #3 on: August 23, 2011, 02:12:17 PM »

Your social worker should give you one or a photocopy of emergency situation suggestions.  It is quite ridiculous what they expect you to keep in a backpack that you would need a mule to haul to a safe place.  You all know I like NePro the dialysis drink.  I just keep extra of those and I'd grab those and run.  It is a meal in a can and 8oz of fluid.  It would keep me alive for a few days and beyond that....

What do you say Anna????

I hope everyone made it through.  This earth is getting crazy.
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cattlekid
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« Reply #4 on: August 23, 2011, 02:15:44 PM »

MooseMom, I'm still on private insurance and I had to fill out the CMS form anyhow when I started D.  I got the big packet o' information from CMS not too long after that. 

Meinuk, I clicked onto the link re new patient info packets, and it brought a question to my mind.  If I understand correctly, new dialysis patients fill out some CMS form, and that information is entered into a database.  But what if that new patient (ie, me) has private insurance and so will not be on Medicare for 30 months?  At what point does the CMS or any other official entity (other than my insurance company) become informed that I am on dialysis?  Will I be getting one of these information packs?
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MooseMom
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« Reply #5 on: August 23, 2011, 02:34:10 PM »

MooseMom, I'm still on private insurance and I had to fill out the CMS form anyhow when I started D.  I got the big packet o' information from CMS not too long after that. 


Oh good...thanks for that!  I expect to be inundated with paper!
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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."
Meinuk
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« Reply #6 on: August 23, 2011, 02:38:20 PM »

There are many forms that are filled out once a person starts chronic outpatient dialysis.  They are filled out by the facility, and signed by the patient.  Many providers have many different contracts, but the form that has been mentioned here is the CMS 2728 form. This is an attestation that a person has started chronic dialysis, signed by both the MD and the patient, filled out by the facility (any facility that is covered my medicare - the majority in the USA are Medicare facilities), then submitted to the ESRD Network covering your area, and the person living on dialysis is entered into a database - a person on chronic hemodialysis is tracked from day one. No matter what the insurance.  The clock starts clicking on the 30 month coordination of benefits (plus 3 month wait if you are in-patient) at the first chronic outpatient dialysis treatment (the insurance lobbyists want to protect their profit).  But the data is really for many reasons, all having to do with Medicare.

The NEPOP mailings are sent out between two - three months after a person has started dialysis.

And as far as what to do during a disaster?  Rerun, I think that I am with you.  I grabbed my Sweet Potato Chips (the last of my lunch) and my phone, and I evacuated the building with all 100 of my co workers. I was kinda screwed anyway had it been a major earthquake in my area, as my car was on the lower 3rd level of the underground parking garage.

Speaking of "Go Bags".  When I was badly infiltrated at DaVita Life Care in NYC, they had to call an ambulance.  I was so annoyed that I couldn't just walk to the emergency room, and I was annoyed that they pumped saline into my already infiltrated arm.  When the ambulance attendant grabbed my dialysis bag (Large LL Bean Boat bag with a pillow, laptop, blanket, water, work paperwork and my handbag), he cracked "You don't travel light, do you?"  If I had had a good arm, I would have punched him.

My advice:  Think about what can save you in an emergency.  What you would need to get back home, if you are away from home, and keep it with you.  Don't go overboard.  Rerun, I have seen you go to dialysis, fly to Vegas and scurry under a table to sit with your friends. I think that with a bottle of Nepro, you could change the world.  (but have your cellphone charger, emergency numbers and dialysis prescription and med list in you handbag just in case!)   :)

(8/24/2011 edited to fix the COB by adding the wait period)
« Last Edit: August 24, 2011, 10:49:35 AM by Meinuk » Logged

Research Dialysis Units:  http://projects.propublica.org/dialysis/

52 with PKD
deceased donor transplant 11/2/08
nxstage 10/07 - 11/08;  30LS/S; 20LT/W/R  @450
temp. permcath:  inserted 5/07 - removed 7/19/07
in-center hemo:  m/w/f 1/12/07
list: 6/05
a/v fistula: 5/05
NxStage training diary post (10/07):  http://ihatedialysis.com/forum/index.php?topic=5229.0
Newspaper article: Me dialyzing alone:  http://ihatedialysis.com/forum/index.php?topic=7332.0
Transplant post 11/08):  http://ihatedialysis.com/forum/index.php?topic=10893.msg187492#msg187492
Fistula removal post (7/10): http://ihatedialysis.com/forum/index.php?topic=18735.msg324217#msg324217
Post Transplant Skin Cancer (2/14): http://ihatedialysis.com/forum/index.php?topic=30659.msg476547#msg476547

“To doubt everything or to believe everything are two equally convenient solutions; both dispense with the necessity of thought.” - Henri Poincare
MooseMom
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« Reply #7 on: August 23, 2011, 03:12:24 PM »

Can you tell me more about what sort of forms a new patient has to fill out?  I'm sure there's a shedload of them, but I confess to not knowing what they are.  I'm sure different facilities have their own nifty-neato forms but am also sure that there are lots of standard forms, too.  In case I'm really sick on that first day, I'd like to have some advance warning of what I am signing.
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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."
sullidog
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« Reply #8 on: August 23, 2011, 05:30:39 PM »

I'm glad you posted these, when I started at my center, I was given these but then they expected me to read these myself, well duh I'm blind so I can't but now that you posted them, I did. Basically though when I started I knew nothing about emergencies, etc. until last year when they finally showed me how to clamp.
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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
boswife
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us and fam easter 2013

« Reply #9 on: August 23, 2011, 07:20:37 PM »

I know our friend M3Riddler was ON dialysis when it happened.  He did disconnect and i hope he'll see this and come to share his eperence ...
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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
jbeany
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« Reply #10 on: August 23, 2011, 07:27:17 PM »

Whoops - they were talking on the radio about feeling it all the way here in Michigan.  I was having an insomniac bookworm night last night, staying up to finish a book, so I was still sleeping in when it hit here.  I bet that's exactly the time my cat started yowling and stomping all over me, though!

Poor baby - an earthquake in the morning and a massive thunderstorm tonight.  She's gonna need kitty prozac soon.
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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.

texasstyle
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« Reply #11 on: August 23, 2011, 08:00:18 PM »

they reported on the news that at our local hospital someones tracheotomy tube came out because the "machine" fell over.
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caregiver to husband using in-center dialysis 4 years
Meinuk
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« Reply #12 on: August 24, 2011, 04:35:36 AM »

Can you tell me more about what sort of forms a new patient has to fill out? 

You should direct your questions to the facility that will be providing your dialysis. Each provider varies in their patient intake forms.
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Research Dialysis Units:  http://projects.propublica.org/dialysis/

52 with PKD
deceased donor transplant 11/2/08
nxstage 10/07 - 11/08;  30LS/S; 20LT/W/R  @450
temp. permcath:  inserted 5/07 - removed 7/19/07
in-center hemo:  m/w/f 1/12/07
list: 6/05
a/v fistula: 5/05
NxStage training diary post (10/07):  http://ihatedialysis.com/forum/index.php?topic=5229.0
Newspaper article: Me dialyzing alone:  http://ihatedialysis.com/forum/index.php?topic=7332.0
Transplant post 11/08):  http://ihatedialysis.com/forum/index.php?topic=10893.msg187492#msg187492
Fistula removal post (7/10): http://ihatedialysis.com/forum/index.php?topic=18735.msg324217#msg324217
Post Transplant Skin Cancer (2/14): http://ihatedialysis.com/forum/index.php?topic=30659.msg476547#msg476547

“To doubt everything or to believe everything are two equally convenient solutions; both dispense with the necessity of thought.” - Henri Poincare
pagandialysis
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« Reply #13 on: August 24, 2011, 12:15:37 PM »

Nope, I was in bed asleep. I had no clue it happened until after I woke up.
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Dining on Dialysis - www.diningondialysis.com
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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)
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