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Author Topic: Hello from Texas  (Read 3154 times)
Beckahboo62
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« on: January 17, 2012, 08:17:11 AM »

Im 49,and in stage 4 of CKD,my Drs been going over my options on dialysis,and getting prepared. This has been a scary,and depressing time for me. Id just like to talk to people going through this,or people that have been through this.....its all still confusing for me.
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willowtreewren
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My two beautifull granddaughters

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« Reply #1 on: January 17, 2012, 09:27:59 AM »

Hi, Becka!

Well, you have come to the right place. No matter what you are going through, there are others here who understand and can hold your hand every step of the way.

Renal failure can be scary, but there are so many options these days, from PD to in-center and even home hemo.

Read through the boards and ask questions! We are here to help!

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. :)
Joe
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« Reply #2 on: January 17, 2012, 09:37:01 AM »

You cerainly are in a good place to ask questions Beckah. Hope we can answer some things for you here.
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Live simply. Love generously. Care deeply. Speak kindly.
Leave the rest to God...
Poppylicious
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« Reply #3 on: January 17, 2012, 01:11:29 PM »

 :welcomesign; Beckah!  Hope you find us useful!
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- wife of kidney recepient (10/2011) -
venting myself online since 2003 (personal blog)
grumbles of a dialysis wife-y (kidney blog)
sometimes i take pictures (me, on flickr)

Everything was beautiful, and nothing hurt.
Traveller1947
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« Reply #4 on: January 17, 2012, 02:33:40 PM »

Hi, Beckah and welcome!  You've come to the right place for information and reassurance and a laugh here and there too.  You'll get through this--we're here to help you.  Best of luck on your journey...
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MissRene12
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« Reply #5 on: January 17, 2012, 02:55:13 PM »

Hello from another Texan! We're still new to this process too. I've only been on this board for a couple of weeks, but I've learned a lot so far from this group, and I'm much more at ease than I was before.  Don't be afraid to ask questions, everyone is very helpful.
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Fiancée of my hon, who has been living with CKD for more than 10 years.  Our story:

   - 2000: Hon hospitalized with renal failure.  Stabilized and sent home.  

<3 2003: Introduced through mutual friends following a comedy show. 
<3 2003 - 2005: Became awesome friends. 
<3 2005: FINALLY started dating - total goofy, silly love.  
<3 March 2011: Engaged!

   - 2 days later: Hon notified of dropping function, kidney or treatment needed in near future.  
   - Jan. 3,  2012: Hon's PD catheter placed. 
   - Jan. 17, 2012: Starting home PD training.  

<3 Wedding plans in full force, driving towards our June 2012 date. I know this is dripping with cheese, but we do manage to have fun through this craziness.
texasstyle
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« Reply #6 on: January 17, 2012, 04:50:32 PM »

Hi Becka! I know my name says texas style but I'm from PA. (long story lol)  My husband has been on dialysis for 4 years now. I've been coming to this site for a couple. One thing I have learned is that the renal diet is VERY important. Try to learn what you can about that. Too much fluid also can cause problems. But.... learning what you can, having a good ATTITUDE, and really wanting to do the right thing can make your life on dialysis eaiser. There is still a lot of living you can do! Things may just be altered, have to be adjusted to do so, but you can. Everyone is great!
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caregiver to husband using in-center dialysis 4 years
lmunchkin
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"There Is No Place Like Home!"

« Reply #7 on: January 18, 2012, 03:36:59 PM »

Hi & Welcome Becka!  Yes, this Kidney Crap is very scary for everyone.  You need to know that we all have and are going through this and we are so glad you found others you can relate to.  First, just try to calm yourself down, it is what it is, so make the best you can of your situation. Learn all you can about kidney failure.  Look at all your options, and definately get listed (transplant).  It may be awhile before one comes up, but the sooner you get on a list, the better.

Follow doctors orders. And definately follow a renal diet.  You might can delay dialysis for a little bit by doing a strict diet.  But I do think that they are preparing you for the inevitable!

I know it is hard to hear all this bad news, but the good news is you found this site!  Wonderful, helpful people here.  I know that I was thankful to find them! Just know that we will walk you through this.  You are definately not alone!

Again Welcome & God Bless,
lmunchkin
 :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
Lindia
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« Reply #8 on: January 18, 2012, 08:59:19 PM »

Welcome -   my daughter lives in Austin.    My hubby has been on dialysis for 9 months -  we have learned a lot on IHD.
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Subeat
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« Reply #9 on: January 19, 2012, 10:44:40 AM »

Hi Becka!  I'm also in Texas.  Been doing this dialysis thing for about 6 months now.  You've come to the right place to learn.  In fact, I've taught the pros at my center a couple of things that I read about here!
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looneytunes
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Wishin' I was Fishin'

« Reply #10 on: January 19, 2012, 05:31:44 PM »

Hi Beckah and glad to have you here.  There are plenty of wonderful folks on this forum who will help you in every way they can.   :welcomesign;
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"The key to being patient is having something to do in the meantime" AU
Lowilson
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« Reply #11 on: January 21, 2012, 01:14:44 PM »

I am 47 judged started dialysis. It is a bit overwhelming. I am on short term disability while I get started in in center hemo dialysis. I thinking once I get the hang of it perhaps I can try the in home dialysis. But right now I feel a little to green. I think will let the professionals get me going. In my center the doctor seems to be avound quite a bit so I feel safe. Like you this is all so new and foreign. I am trying to stay positive and not get depressed but admittly difficult. I am not yet on the LIST. Hopefully, approved so I can start moving up towards the top. Perhaps this forum will help as we both move through this journey good luck. Misery loves company!!  And appears there a lot of us living the dialysis dream ha ha!!

Lori
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drgirlfriend
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« Reply #12 on: January 21, 2012, 03:13:22 PM »

Welcome, Beckah!

 :welcomesign;

I've been coming here for several months and the exchange of information is fantastic! Don't be afraid to ask anything and everything - both here and at your doctor's office.  My boyfriend and I were just in Houston and hope to move there soon.
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Boyfriend diagnosed with renal failure Feb. 2011. Cause unknown.
PD Catheter "installed" June 30, 2011.
Began CAPD August 11, 2011.
On transplant list 11/23/11.
Started Liberty Cycler 12/1/11.
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