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Author Topic: hi im dean cank  (Read 2327 times)
deanocank
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« on: November 19, 2011, 01:50:15 AM »

hi my name is dean cank im a dialysis patient from Leicester England im 28 i have nephotic syndrome,polysistic kidney disease, anaemia, i have been living with kidney failure and receiving dialysis for just over 2 years im finding it very hard to cope with all the complications of life living with dialysis just looking for some Wright minded people that can help me through this its so hard for me and know 1 around me understands what im going through i used to do so much and now i dont leave the house cuz i just feel so ill all the time .
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iketchum
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« Reply #1 on: November 19, 2011, 03:19:35 AM »

Hello there. My name is Bill and I live in Warren, Maine in the USA. I do know how you feel, I have had most of the same issues. I used to work two jobs and still hunted and fished as much as I could. Now I do dialysis three days a week and struggle to hunt. I try to stay as active a s possible, makes me feel more in control I guess. I hope you hear from Darthvader, she is in Dublin and is very smart person, and allot of fun too. She is a care giver to her Mom and is a wonderful person. I am on in the mornings and evenings here, I know the time difference makes for short chats, but do anytime. Just know we are here and you are not really alone.
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CebuShan
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« Reply #2 on: November 19, 2011, 05:59:34 AM »

   :welcomesign;   to IHD! You are NOT alone! Many of us are going through similar circumstances and there are a lot of young people on here so settle in and make yourself at home. I understand how you feel about not wanting to in out because of feeling crappy. I walk every day but there are days that I have to force myself to get out. It does help that I have a dog who loves to walk. All I have to do is mention "walk" and if won't leave of alone until we in for at least a short walk. Best of luck to you and remember that you ARE NOT ALONE!!    :grouphug;
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Think GOD doesn't have a sense of humor?
HE created marriage and children.
Think about it! LOL!
willowtreewren
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My two beautifull granddaughters

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« Reply #3 on: November 19, 2011, 06:03:32 AM »

Hi, Dean.

We have many members in the UK! I hope you can connect with them. Welcome to IHD. Come here to vent, companionship and information!

Aleta
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Wife to Carl, who has PKD.
Mother to Meagan, who has PKD.
Partner for NxStage HD August 2008 - February 2011.
Carl transplanted with cadaveric kidney, February 3, 2011. :)
monrein
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« Reply #4 on: November 19, 2011, 08:57:02 AM »

  :welcomesign;  Dean...you're most definitely NOT alone. 
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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
MooseMom
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« Reply #5 on: November 19, 2011, 02:38:24 PM »

Hello, Dean Cank.

What's Gary Lineker doing these days?

Glad you've joined.  You will find many people here who know exactly what you are going through.

Could you possibly be a candidate for transplant?
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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."
Joe
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« Reply #6 on: November 19, 2011, 02:54:01 PM »

Dean, there are a lot of folks here that are more than willing to share their experiences with you. Ask questions, read, vent about this life we are living. just knowing there are other fokks oout there in the same boat helps a bunch. hope to see you around the boards.
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davecapper
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Authoring books for dialysis. Find them on Amazon.

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« Reply #7 on: November 19, 2011, 07:56:19 PM »

As you can see, you are not alone. All of the people here, caregivers included know what you are going through. it is not easy to be on dialysis and while diet is an important part of your life now, it takes more than eating right to get past all of these things. You are not alone and never give up are good words to offer to you now.

If there is anything I can do, let me know. I agree, if you want to vent or ask questions, people here can help.

Good luck to you.
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Silver Spoons Holiday Cooking with Renal Failure book is now available on Amazon or at your favorite bookstore.
Poppylicious
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« Reply #8 on: November 20, 2011, 01:48:45 PM »

 :welcomesign; Dean.  I'm in England too, in East Anglia.  My Blokey (just a few years older than you) was on dialysis for over two years but recently had a transplant.  Are you on 'the list' for a transplant?  I'm glad you've joined; there are so many people on here who can offer you support and advice.

 ;D
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- wife of kidney recepient (10/2011) -
venting myself online since 2003 (personal blog)
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Everything was beautiful, and nothing hurt.
lmunchkin
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"There Is No Place Like Home!"

« Reply #9 on: November 20, 2011, 02:41:11 PM »

Hi DC &  :welcomesign;

lmunch
 :kickstart;
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11/2004 Hubby diag. ESRD, Diabeties, Vascular Disease & High BP
12/2004 to 6/2009 Home PD
6/2009 Peritonitis , PD Cath removed
7/2009 Hemo Dialysis In-Center
2/2010 BKA rt leg & lt foot (all toes) amputated
6/2010 to present.  NxStage at home
Rerun
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Going through life tied to a chair!

« Reply #10 on: November 21, 2011, 06:03:05 PM »

Hi Deano,  That is what I call my friend Dean.  I'm so glad you joined us.  Make sure and stay through your whole session and learn about your dry weight.  If they take too much fluid off me I don't feel well until the next day. 

I hope you feel well enough to read this site.  It has lots of information.

Rerun, Moderator           :welcomesign;
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Ang
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« Reply #11 on: November 24, 2011, 11:52:20 PM »

 :welcomesign;
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Wenchie58
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« Reply #12 on: November 25, 2011, 03:36:08 PM »

 :welcomesign;
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Live your life in such a way that when your feet hit the floor in the morning Satan shudders and says "Oh s**t, she's awake!"

Right nephrectomy 1963
Diagnosed ESRD 2007
"Listed" summer 2007
Transplant 3/6 match  10/24/08
Cordelia
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« Reply #13 on: November 25, 2011, 03:48:55 PM »

 :welcomesign;   to you!
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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
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