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Author Topic: New Member! (and yes ihatedialysis is a bit negative come on ;) )  (Read 3889 times)
jontwindsor
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« on: September 09, 2011, 03:27:00 PM »

I've browsed these pages before and finally joined!

I'm Jon, 25, been on dialysis since summer 2010 and I'm a teacher (in the UK).

My physical health had been decreasing gradually so that I bearly noticed - until the symptoms accelerated - but even then I put it down to stress/getting old etc (in early 20s...).

Looking back the last 6 months before diagnosis were on the edge. I was on my PGCE - and anyone who's done 1 knows how tough they are. Every day on my drive into and from school I'd be falling asleep at the wheel. I didn't sleep at all at night for about 6 months. Couldn't walk to the shops without heart going mental. Had a really hard class on my placement and was wondering why I couldnt find the energy to eal with them - lack of sleep I thought - and lack of sleep from stress. Hmm. I could go on forever so I'll stop there on that front - but basically having seen 1 doctor in April and being told it was depression and I needed to exercise more - I was finally diagnosed with <5% kidney function in July 10.

Before all that I was very fit - and thanks to diagnosis I am not far away from how I was aged 16 - which is pretty amazing really. Obviously very hard to juggle haemo at the hospital with school - time is definitely an issue - but come on don't hate what's transforming your lives! Love Jon! 
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boswife
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us and fam easter 2013

« Reply #1 on: September 09, 2011, 03:43:45 PM »

Great intro and WOW!  what a road to the big D for sure.  Im sooooooooooooo glad you found out what was causing your downward trend, and are doing so well on dialysis  :yahoo;   We (ok, im the wife of a D man) dont hate dialysis either, but surely would be nice to just be plain healthy instead,,,but, so glad that D does the trick for us so we have a life together.  We came home with NxStage (home hemo)  about 7 months ago, and thats even better  ;D  good to hear from you and be sure to share some of your stories.  It's always good to see the goods and the bads of it all..   :welcomesign;
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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
Dannyboy
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« Reply #2 on: September 09, 2011, 03:55:11 PM »

Welcome Jon.   :welcomesign;

---Dan
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ESRD Summer 2011
Started using NxStage September, 2011
"Everything is funny as long as it is happening to Somebody Else"--Will Rogers

Alcoa and Reynolds are in a bidding war to buy my serum Aluminum.
monrein
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« Reply #3 on: September 09, 2011, 04:32:22 PM »

 :welcomesign; to IHD
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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
jbeany
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« Reply #4 on: September 09, 2011, 05:29:20 PM »

 :welcomesign;

Ahh, but that name grabbed your attention, now didn't it?  We aren't all negative - not by a long shot.  This is one of the biggest support groups for ESRD online - we've got over 6000 members.  Our founder started a sister website about all the things he loved about one of the new developments in HD - all about loving NxStage.  But he had days he hated ESRD and everything that came with it, so he chose that name for both the truth and the shock value of it.

So - when you get that crummy tech who can't find the right spot with that honkin' big needle, but CAN find every nerve ending in your arm...
or you really, really don't want to eat a "sensible, small amount" of some forbidden food that everyone at the table is raving over...
or you are craving a huge glass of cold ice water on a blistering hot day....
or you have to go to dialysis when all your friends are off to the event of the season...

Well, then it's hard not to hate those moments.

And if you come talk about those moments here, you have an audience who fully understand every bit of.  Knowing that is some times all that saves our members' sanity.

Stick around and you'll see it in action!

jbeany, Moderator
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gkcoley
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« Reply #5 on: September 09, 2011, 05:48:58 PM »

im 24 and been on dialysis 16 years, a few months is nothing, it gets worse over time, so, yeah...anyways, welcome! lol  :bandance;
« Last Edit: September 09, 2011, 07:28:41 PM by gkcoley » Logged

There's No Smile Of An Angel Without The Wrath Of God
edersham
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« Reply #6 on: September 09, 2011, 07:03:54 PM »

It's great you joined and more power to you that your doing well on dialysis. There are people here that have done well for a number of years and I hope you are one of them. But for most of us this site is perfectly named and it isn't about being negative, just brutally honest. We fight through the challenge and either find a mode of dialysis that works for us or seek a transplant and there is more to be learned on this site about those options and the benefits and risks than anywhere  else period. Good luck with whatever path you choose to fight this disease and I believe you will find more support and understanding here than anywhere. I know I have

Ed
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Rerun
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« Reply #7 on: September 10, 2011, 04:49:24 AM »

im 24 and been on dialysis 16 years, a few months is nothing, it gets worse over time, so, yeah...anyways, welcome! lol  :bandance;


            :rofl;  Amen Brother

Jon, work as long as you can.   :welcomesign;

Rerun, Moderator     :waving;
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looneytunes
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« Reply #8 on: September 10, 2011, 07:18:14 AM »

Hi Jon and welcome to our group!   :welcomesign; 
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"The key to being patient is having something to do in the meantime" AU
Bren-tam
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« Reply #9 on: September 10, 2011, 12:01:37 PM »

 :welcomesign; Nice to see another fellow UK member (not sure how many there are) I'm a newbie too and have found loads of great information and support and I've only been on for a few days. I must admit I find the website name hysterical - when I told my friends about it they were horrified but the sick humour in me loved it!!
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Diagnosed with Iga Nephropathy January 2008
Started Hospital HD 20 July 2011
Poppylicious
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« Reply #10 on: September 10, 2011, 12:48:57 PM »

 :welcomesign; Jon!

I was on my PGCE - and anyone who's done 1 knows how tough they are ... Had a really hard class on my placement ...
Oooh yes, very tough (I did mine in the fourth most deprived area of the UK).  Only one hard class?  Lucky bugger!  Thankfully I never had to juggle teaching and haemoD - my Blokey is the one on dialysis; I come here for support and the understanding of people who are going through the same thing.
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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.
jontwindsor
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« Reply #11 on: September 10, 2011, 02:20:41 PM »

I did have a look for other dialysis forums, and yes bren-tam i was wondering if there was a decent UK 1 - nope! This is by far the biggest, with the most useful information, and now I've managed to join seems amazingly supportive too. So I suppose hating dialysis together is more positive than loving it on my own   :flower;


jbeany the reason i joined is all the fantastically helpful stuff i've found on those late night google searches - although we don't get the hot weather problem  ::)


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Bajanne
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« Reply #12 on: September 10, 2011, 03:45:16 PM »

Welcome to our community, jontwindsor from one born under (Barbados) and living under (British Virgin Islands) the Union Jack! Glad that you have found the best place for information, support and encouragement, even if the title doesn't thrill you!   This website was a godsend to me when I was first diagnosed with ESRD and it continues to be one of my weapons in the fight against this renal challenge.  Inspite of the name there are loads of positive things here and we have become more than a website; we are a genuine family :grouphug; - caring and sharing.
Continue to read and to post, so we can know how you are doing.
Looking forward to hearing from you.




Bajanne, Moderator
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I LOVE  my IHD family! :grouphug;
CebuShan
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« Reply #13 on: September 11, 2011, 06:06:27 AM »

   :welcomesign;  jontwindsor!

When I first heard of this site, the name made me laugh! I'm always looking for the things that can make me laugh because I hate to cry!! It is so great to hear that you are doing so well.    :2thumbsup;
I do hate dialysis even thoiugh I know that it is keeping me alive. I hate being cooped up in the Summer and I hate having to get out during the Winter. But I have my IHD family that is always there for me. Unlike my other family and friends, everyone here understands completely what I'm going through.
Please, come back often and keep us updated how you are doing!
   :grouphug;
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Think GOD doesn't have a sense of humor?
HE created marriage and children.
Think about it! LOL!
Jean
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« Reply #14 on: September 12, 2011, 12:27:35 AM »

 :welcomesign; :welcomesign; to IHD. Yes, at first, the name is a tad negative, but you could find no better place for support than this one. You have practically the whole world at your fingertips and a family to boot. Whenever you have any kind of a problem, this is the place to come. You will  enjoy IHD for sure.
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One day at a time, thats all I can do.
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« Reply #15 on: September 12, 2011, 03:53:42 AM »

Hi Jon, first of all welcome to the site, so glad you joined us. We live in Nottingham, not to far from you. Have you asked your unit if you can do your hemo at home. They are promoting this in Notts. My husband is on an overnight cycler. Did they give you a choice of PD or did you just opt for hemo?  What age group do you teach, I should imagine teaching is very tiring with out being on dialysis. Look forward to your posts.    :welcomesign;
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« Reply #16 on: September 12, 2011, 08:32:03 AM »

 :shy; Welcome to the board Jon, from one newbie to another.

Iwannabean
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willowtreewren
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My two beautifull granddaughters

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« Reply #17 on: September 12, 2011, 04:12:51 PM »

 :welcomesign; :welcomesign; :welcomesign;

Hi, Jon!

What a story! Love your attitude!

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. :)
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« Reply #18 on: September 12, 2011, 07:25:09 PM »

thanks to diagnosis I am not far away from how I was aged 16 - which is pretty amazing really. Obviously very hard to juggle haemo at the hospital with school - time is definitely an issue - but come on don't hate what's transforming your lives! Love Jon!
My husband gregory says his first dialysis (at age 19) was one of the best feelings he's had in his life, the change from the way he'd felt before to having "clean" blood.  Mind you, now that he's a transplant-guy, when he contemplates dialysis things get pretty hectic.  Touch wood he'll have one of those transplants that chug along for 40 years.
Good to see that you are going "well" on dialysis, and keeping your plans on track.  That's what its all about really, being able to get on with life.
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Natalya – Sydney, Australia
wife of Gregory, who is the kidney patient: 
1986: kidney failure at 19 years old, cause unknown
PD for a year, in-centre haemo for 4 years
Transplant 1 lasted 21 years (Lucy: 1991 - 2012), failed due to Transplant glomerulopathy
5 weeks Haemo 2012
Transplant 2 (Maggie) installed Feb 13, 2013, returned to work June 17, 2013 average crea was 130, now is 140.
Infections in June / July, hospital 1-4 Aug for infections.

Over the years:  skin cancer; thyroidectomy, pneumonia; CMV; BK; 14 surgeries
Generally glossy and happy.

2009 - 2013 PhD research student : How people make sense of renal failure in online discussion boards
Submitted February 2013 :: Graduated Sep 2013.   http://godbold.name/experiencingdialysis/
Heartfelt thanks to IHD, KK and ADB for your generosity and support.
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"There Is No Place Like Home!"

« Reply #19 on: September 12, 2011, 07:41:30 PM »

Great Intro!!  Welcome

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
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"Still crazy after all these years."

« Reply #20 on: September 13, 2011, 11:27:24 AM »

Glad to have you here!
 :beer1;
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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."
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