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Author Topic: Dialysis Administrator (Me)  (Read 4442 times)
Mr. B
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« on: October 05, 2007, 08:38:31 AM »

Where do I start? I am the administrator for a home health company. Our customers, clients & patients have all asked the owner, a pastor, to develop an independent patient-centered center. We realized that over 80% of dialysis centers are owned by large companies. Large companies NEVER deliver care thinking patient first--no matter what they say. I am on this forum to hear from you. I want to know what patients want. In our center, you guys will have more input than most. So let me have it!
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Sluff
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« Reply #1 on: October 05, 2007, 08:42:42 AM »

Welcome Mr.B to IHD.

I'm sure you will find all the answers you are looking for. Feel free to look around and post as often as you like.

I'm pre dialysis and really can not help you in this subject.

I commend you however for making your quest a priority.

Sluff/ Admin
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paris
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« Reply #2 on: October 05, 2007, 09:41:48 AM »

So glad you joined us! We need people like you on our side.  Take time to read through the threads, there are many opinions here!   :welcomesign;
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Joe Paul
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« Reply #3 on: October 05, 2007, 10:13:23 AM »

Welcome Mr. B, good to have you aboard.
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okarol
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« Reply #4 on: October 05, 2007, 10:17:40 AM »

Where do I start? I am the administrator for a home health company. Our customers, clients & patients have all asked the owner, a pastor, to develop an independent patient-centered center. We realized that over 80% of dialysis centers are owned by large companies. Large companies NEVER deliver care thinking patient first--no matter what they say. I am on this forum to hear from you. I want to know what patients want. In our center, you guys will have more input than most. So let me have it!

 :waving; Hi Mr. B!
Nice that you could join us. I hope to read more about what you have in mind under the other thread.
There's lots of good info here and many patient's with loads of experience. I am sure they will be glad to respond.
Welcome!


okarol/moderator
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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.
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Please watch her video: http://youtu.be/D9ZuVJ_s80Y
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MyssAnne
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« Reply #5 on: October 05, 2007, 10:41:25 AM »

Welcome, Mr. B! I'm a pd patient, so I can't really respond, but I will say, whatever you can do to make the patients comfortable (and sane!) :welcomesign;
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angellady07
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« Reply #6 on: October 05, 2007, 10:54:46 AM »

welcome.
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thegrammalady
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« Reply #7 on: October 05, 2007, 11:46:32 AM »

:welcomesign;  you are a brave man, most people here don't hold anything back. that said, we are a very caring, extremely loving family. welcome.
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« Reply #8 on: October 05, 2007, 01:34:16 PM »

 :welcomesign;
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goofynina
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« Reply #9 on: October 05, 2007, 01:38:36 PM »

Hi Mr. B, Welcome to ihatedialysis.com.   You have found a great group of people who are all willing to share their stories and give advice, support, encouragement and anything else that is needed to help our fellow members dealing with this disease.  Please feel free to post questions, comments and/or concerns of your own.  Looking forward to hearing from you.   :2thumbsup;
 

Goofynina/Admin.
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Mr. B
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« Reply #10 on: October 05, 2007, 01:41:05 PM »

What a great welcome! I really look forward to learning from you guys as the center project moves forward. I already have gotten a few ideas! Thanks again.
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« Reply #11 on: October 05, 2007, 10:44:47 PM »

Welcome to our community!  I am from the Caribbean, so our situation may not be the same as yours, but there are some things that should be priorities whenever dialysis patients come for care.
1. - nephrologists who spend time with patients
2. - nurses and techs who consider the patient's comfort as important, and not just getting the job done.
3. - clear explanation of everything to patients, or to their loved ones and caregivers.
These to me are the most important.
I think you have already shown that you are stepping in this direction.  I wish you great success in your project.


Bajanne, Moderator



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keefer51
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« Reply #12 on: October 06, 2007, 07:39:23 AM »

 :welcomesign;
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i am a 51 year old male on dialysis for 3 years now. This is my second time. My brother donated a kidney to me about 13 years ago. I found this site on another site. I had to laugh when i saw what it was called. I hope to meet people from all over to talk about dialysis.
paris
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« Reply #13 on: October 06, 2007, 06:37:03 PM »

 :welcomesign;  If you want honest opinions, you have come to the right place!  It is nice for someone to ask what we would like to see in the dialysis field.  Glad you found us. 
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« Reply #14 on: October 06, 2007, 06:55:44 PM »

 :welcomesign;
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Adam_W
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« Reply #15 on: October 06, 2007, 08:03:41 PM »

 :welcomesign;. It's good to have someone in the dialysis field who puts patients first. That seems to be becoming rare nowadays.

Adam
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-Diagnosed with ESRD (born with one kidney, hypertension killed it) Jan 21st, 2007
-Started dialysis four days later in hospital (Baxter 1550-I think, then Gambro Phoenix)
-Started in-centre dialysis Feb 6th 2007 (Fres. 2008H)
-Started home hemo June 5th 2007 (NxStage/Pureflow)
-PD catheter placed June 6th 2008 (Bye bye NxStage, at least for now)
-Started CAPD July 4th, 2008
-PD catheter removed Dec 2, 2008-PD just wouldn't work, so I'm back on NxStage
-Kidney function improved enough to go off dialysis, Feb. 2011!!!!!
-Back on dialysis (still NxStage) July 2011 :(
-In-centre self-care dialysis March 2012 (Fresenius 2008K)
-Not on transplant list yet.


"Don't live for dialysis, use dialysis to LIVE"
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« Reply #16 on: October 07, 2007, 03:29:04 AM »

 :welcomesign;
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Dialysis Sucks and Transplants Don't.................So Far Anyway !!!!!
angela515
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« Reply #17 on: October 07, 2007, 08:26:45 AM »

 :welcomesign;
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Black
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« Reply #18 on: October 07, 2007, 10:20:30 AM »

:welcomesign;  I am extremely pleased to find that there are still people striving to do what is best for dialysis patients.   :thx;

I had read and heard so many horrible things about dialysis centers that we looked at several, in two states, before my husband started dialysis.  We were ready to move to another state in order to get a NxStage, so my husband never had to do dialysis in a dialysis center.  Thankfully, our state got a center with NxStage training just a few weeks before he started dialysis.  We drove 200 miles and he stayed for three weeks of training.

Anyway, I can't really say anything about our first-hand experience inside a dialysis center, as we don't really have any, other than our three weeks of training in a room separate from the in-center patients.  But, based on what we saw during our tours of the clinics, there is much room for improvement and YOU will be very much in demand.

One thing I do recommend is trying to institute an education program for all patients who may one day need dialysis.  Patients need to be educated by those who see them way before you see them.  No one told us that there were things which could be done to prolong the life of his kidneys, no one recommended a consult with a renal dietitian, no one told him that he needed to protect his arm veins and exercise his hand/arm to increase the chances of getting a natural A/V fistula.  Even when we visited the dialysis center, not one person told us about ALL of the different kinds of dialysis available.  I know this isn't what you were asking for, but it directly affects the physical and mental condition of the patients when they finally come to you.

You have a great attitude and you will do well.  Thanks again for caring enough to ask.
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Lorelle

Husband Mike Diagnosed with PKD Fall of 2004
Fistula Surgery  1/06
Fistula Revision  11/06
Creatinine 6.9  1/07
Started diaysis 2/5/07 on NxStage
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« Reply #19 on: October 08, 2007, 11:15:53 AM »

 :welcomesign; Mr. B!  ;D Your name makes me smile because our dog is named Boomer and I call him Mr. B sometimes! Anyway, welcome!
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Mr. B
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« Reply #20 on: October 08, 2007, 07:21:18 PM »

Black,

I too have heard do many bad things about centers. I really think that this can be improved. My goal is not to make dialysis pleasurable, but dang it, a huge part of dealing with a chronic illness is cognative & emotional. If we haven't figure out how to be be human to sick people in our center, I'll just go home. I am not a very religious person (I tend to act more Christian than "devout" Christians) and I don't know where my empathy comes from, but in many ways it's clear with a simple question: how would you or a family wish to be treated? As someone in healthcare administration, I stop & ask myself & my staff that question when I have to make a tough call. I have a boss (and owner) that supports this.

On the physical side, I have not heard anyone on this board talk about palliative care. If someone has had a palliative consult, let me know. In the mean time I am hooking up our brand spanking new neph with our palliative doc. I am going to give them some cash to come up with a program. Dialysis folks complain about a lot of physical symptoms in connection with dialysis. I simply don't believe that some of these can't be palliated. Palliation combined with a supportive center that strives to meet psycho-social needs is a road I am going to try. Oh, yes I intend on getting excellent equipment too.
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Hawkeye
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« Reply #21 on: October 09, 2007, 06:47:42 AM »

Hello and  :welcomesign;
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