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Author Topic: Hi! I'm a newbie here.  (Read 3937 times)
AutumWind
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« on: September 26, 2008, 01:18:40 PM »

Hello everyone. I am so glad to be referred to your site by the social worker at the dialysis center. I am new to dialysis and kidney disease and really need some place where people understand and for support, both to give and receive. My story.......

I had my first kidney failure on July 29th. I was in the hospital 10 days. I finally got to go home and thought all was okay. But on Friday, September 19th, I got very sick. I was admitted to the hospital with acute kidney failure and congestive heart failure.  >:( Two caths were put in my neck on Monday and received dialysis that day and every day since, except today. I go again in the morning.

I don't know how much to tell about myself here. I also have diabetes and copd. I am a single mom and a grandma of two precious granddaughters. I have tried to care for myself to avoid any kidney problems and kept my sugar under tight control. I want to live for my daughter and granddaughters as long as I can. This has really hit me hard and I guess I am still in shock.

For hobbies I crochet, read and like to play games online. I love to do puzzles online, too. I just received a Hoveround today and will attempt to learn to drive it when I do not feel so tired and weak. Is that normal?

I guess that is it for now. Thank you for letting me be part of your group. I look forward to getting to know you all.

Autumn

Edited: Changed print color to black, as required. Boxman, Moderator
« Last Edit: September 26, 2008, 04:45:25 PM by boxman55 » Logged
willieandwinnie
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« Reply #1 on: September 26, 2008, 01:26:07 PM »

:welcomesign; AutumWind. We are so glad that your Social Worker pointed you in our direction. We are a great group, lots of information and so much support. I'm a caregiver and I know about the shock when they came and told me my husbands kidneys were not working.  :cuddle; There's lots to read here and rant away when you feel the urge. Hope your treatment tomorrow goes well.  :grouphug;
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"I know there's nothing to it, but I want to know what it is there's nothing to"
peleroja
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« Reply #2 on: September 26, 2008, 02:50:31 PM »

Welcome to the group.  Tons of good information and lots of shoulders to cry on and lots of folks to cheer you on.  Come back and post often.
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Wayne
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Martin (the snorer) & Mack (cat w/renal failure)

« Reply #3 on: September 26, 2008, 03:06:12 PM »

 :welcomesign; aboard!
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Happily Married for 11 Wonderful Years!!! :-)
3/01 diagnosed with fsgs
7/07 listed
4/08 fistula surgery
10/08 pd catheter placed
12/08 started pd
2/09 started hemo
Rerun
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Going through life tied to a chair!

« Reply #4 on: September 26, 2008, 03:10:20 PM »

Welcome to IHD Autumn.  You will learn lots on this site and laugh again.

                                     :welcomesign;
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Zach
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"Still crazy after all these years."

« Reply #5 on: September 26, 2008, 03:14:11 PM »

It's real good to have you with us!

8)
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Uninterrupted in-center (self-care) hemodialysis since 1982 -- 34 YEARS on March 3, 2016 !!
~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
No transplant.  Not yet, anyway.  Only decided to be listed on 11/9/06. Inactive at the moment.  ;)
I make films.

Just the facts: 70.0 kgs. (about 154 lbs.)
Treatment: Tue-Thur-Sat   5.5 hours, 2x/wk, 6 hours, 1x/wk
Dialysate flow (Qd)=600;  Blood pump speed(Qb)=315
Fresenius Optiflux-180 filter--without reuse
Fresenius 2008T dialysis machine
My KDOQI Nutrition (+/ -):  2,450 Calories, 84 grams Protein/day.

"Living a life, not an apology."
Maggie and Jeff
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Life as a Pincushion

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« Reply #6 on: September 26, 2008, 03:46:32 PM »

:welcomesign; to the group
We have found that Maggie does not feel as tired when all of her labs are in the correct ranges.  We get a copy of the labs as soon as they are available so we can change things like how much cheese she is eating.  Protein and vitamin B are both important to having energy and of course your hemoglobin level (we Check weekly).  Iron stores, phosphorous, calcium and potassium also play a role.  If any of her meds need to be changed we e-mail the Doctor and ask what he thinks. 

The more infomed you are the better you will feel Because you will be able to work with your doctor by making suggestion as to what you think needs changed to feel better.

Knowing your option's like in-center (3 days per week) or home hemo (5-7 days per week) and making the chooses that are right for you.  The doctors and nurses work for you.  They are suppose to support your decisions and help you make the one's that will benefit you the best. 

Never be afraid to ask questions.  Hope this helps and you do well. 

Also you should read about fistulas and peritoneal dialysis
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The LORD is my light and my salvation--so why should I be afraid? The LORD is my fortress, protecting me from danger, so why should I tremble?

Jeff is the needle pusher Maggie is the pincushion.
kellyt
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« Reply #7 on: September 26, 2008, 03:53:52 PM »

 :waving;  Welcome to the Family, AutumnWind.  You will like it here.  The people on this website have forever changed my life.  I have learned so much in the last year and feel I'm ready for whatever this stupid disease throws at me!  Tell your Social Worker "Thanks" for the referral.     :cuddle;    :thumbup;
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1993 diagnosed with glomerulonephritis.
Oct 41, 2007 - Got fistula placed.
Feb 13, 2008 - Activated on "the list".
Nov 5, 2008 - Received living donor transplant from my sister-in-law, Etta.
Nov 5, 2011 - THREE YEARS POST TRANSPLANT!  :D
monrein
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« Reply #8 on: September 26, 2008, 04:30:24 PM »

Welcome and post often.  We'll always listen and give any tips or suggestions we can.  Together we have vast experience in the renal disease area.  Unfortunately, it's first hand experience.  :waving;
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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
paris
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« Reply #9 on: September 26, 2008, 04:35:06 PM »

Welcome AutumnWind.  What a lovely name!  We are so glad your social worker referred you here.  This is a great site with so much information.  If you need an answer, someone here can probably help you.  We are also a great support system for each other.  I depend on the members here for so much.  We share problems but we also share joys (like your two sweet granddaughers that we want to hear more about!).  Fatigue is very normal.  I think that is something most of us agree on. You have had a lot thrown at you in a very short time. We are here to help. Lean on us.  It will get better.  :grouphug;  





Paris,moderator
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It's not what you gather, but what you scatter that tells what kind of life you have lived.
boxman55
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« Reply #10 on: September 26, 2008, 04:50:46 PM »

Welcome Autumnwind, It is great to hear that a social worker made you aware of this site. That tells me she is doing her/his job.  ;D We are so glad you joined us. There is a lot of information here to help you understand a little more your kidney and for that matter your diabetes disease. We are hear to help and hope you have a little fun too

Boxman, Moderator
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"Be the change you wished to be"
Started Hemodialysis 8/14/06
Lost lower right leg 5/16/08 due to Diabetes
Sister was denied donation to me for medical reasons 1/2008
cookie2008
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« Reply #11 on: September 26, 2008, 06:30:43 PM »

 :welcomesign;
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Started PD in 11/07
Started Hemo in 7/08
Started NxStage 5/09
Joe Paul
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« Reply #12 on: September 27, 2008, 10:38:11 AM »

 Welcome AutumnWind, good to have you aboard.
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"The history of discovery is completed by those who don't follow rules"
Angels are with us, but don't take GOD for granted
Transplant Jan. 8, 2010
southyard
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« Reply #13 on: September 27, 2008, 02:36:29 PM »

Hi Autumn.  Welcome to IHD.

I came to have my kidney failure shortly after yours Abt aug 10th.  Tis after being told in May that it would be 2-3 years down the line b4 I'd neesd dialysis. But then Drs practice emdicine and are only guessing what our bodies will do.  I am pushing 85 so have decided I will give this a 6 months trial. So far I have not seen any graet improvement but then I have not been following the diet structure nto well.   I do over do on liquidsand certain foods  that I am used to eating and love.   Also I am diabetic

I suffer from tiredness most of the time and my breathing has not improved with hemo. 

This site if used to its fullest will make your life a lot easier.  While I do not follow the directives fully I intend to make my life in the ensuing months the best I have ever had. People say I am nutty but having seen people in nursing homes not enjoying the so called golden years I decided I would never be place in such positionI fully believe that I have the right to make my own decisions and wants.

Sorry for the rant but I feel both sides must be considered.  My family know of these and agrees they are mine to make

Southyard  (harold the old guy)
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Ang
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« Reply #14 on: September 27, 2008, 06:30:18 PM »

 :welcomesign; Autumn wind







EDITED:  Icon error corrected - Bajanne, Moderator
« Last Edit: September 29, 2008, 01:18:20 PM by bajanne2000 » Logged

live  life  to  the  full  and you won't  die  wondering
napala turki
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« Reply #15 on: September 28, 2008, 07:36:32 AM »

Welcome Autumn Wind,

Be with us, and share what you have too..... blast out of your heart.... :cuddle;
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G-Ma
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« Reply #16 on: September 28, 2008, 07:53:50 PM »

 :welcomesign;
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Lost vision due to retinopathy 12/2005, 30 Laser Surg 2006
ESRD diagnosed 12/2006
03/2007 Fantastic Eye Surgeon in ND got my sight back and implanted lenses in both eyes, great distance & low reading.
Gortex 4/07.  Started dialysis in ND 5/4/2007
Gortex clotted off Thanksgiving Week of 2007, was unclotted and promptly clotted off 1/2 hour later so Permacath Rt chest.
3/2008 move to NC to be close to children.
2 Step fistula, 05/08-elevated 06/08, using mid August.
Aug 5, 08, trained NxStage and Home on 9/3/2008.
Fistulagram 09/2008. In hospital 10/30/08, Bowel Obstruction.
Back to RAI-Latrobe In Center. No home hemo at this time.
GOD IS GOOD
Bajanne
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« Reply #17 on: September 29, 2008, 01:24:06 PM »

Welcome to our community, AutumnWind!  I am so upset that Paris upstaged me.  I wanted to tell you how lovely I found your name first! (just kidding)  This site is just the place for you to be.  Here you will find great support, lots of information, a place to vent when needed and loads of fun.  Just take advantage of all this site has to offer.
You sound so much like me.  I am a single parent with a grandson whom I want to see grow up (he is five).  I can promise you that it will all get better.  As your body gets accustomed to dialysis, you will start to feel better - I did. 
Please keep reading and keep posting.  We want to know how you are doing.  We're family now :grouphug;

Bajanne, Moderator
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"To be found in Him, not having a righteousness of my own ...but that which is based on faith"



I LOVE  my IHD family! :grouphug;
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