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Author Topic: The Snakes Son  (Read 4833 times)
Shades_Elfen
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« on: August 26, 2006, 06:13:00 PM »
Seems as though I've been introduced already.... *Cough*

I'm Pythons son, Ian (or Known as Shades to my net mates)    8)

I'd like to say Hi to everyone and a big thanks to everyone who sent encouragement while I was in hospital.

I'm still recovering from the Op, aches and pains, you know? and the Itchyness of the new lines are driving my a little bit barmy  :D

odd as it sounds, I'm missing my PD at the moment... you'd think a break from it would be welcome.... but i think I am a bit  attached to it! (no pun intended!  :D )

hope to hear from you all soon!

- Shades
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Time been on Dialysis : 5 years and counting
"It Doesn't matter, now what happens, I will never give up the fight, as long as the voice inside tells me to stand and fight" - Myself
goofynina
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He is the love of my life......
« Reply #1 on: August 26, 2006, 08:49:24 PM »
Well hello Shades, nice to finally meet you.  Just wanted to say Welcome and i hope all is going well with you.  Take care and remember, we are here for ya... Hope to hear more from you...:)
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....and i think to myself, what a wonderful world....

www.kidneyoogle.com
Black
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« Reply #2 on: August 26, 2006, 10:51:39 PM »
Quote from: Shades_Elfen on August 26, 2006, 06:13:00 PM
Seems as though I've been introduced already.... *Cough*  ...


LOL, yeah, parents will do that sort of thing, but glad you're here and hope recovery is rapid!
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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
Bajanne
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Goofynina and Epoman - Gone But Not Forgotten

WWW
« Reply #3 on: August 26, 2006, 11:30:28 PM »
Welcome! It is great to meet Python's son finally.  Well, we are here for you.  Ask your questions, share your ups and downs.  You have a lot of posts to read.  You will find many of them extremely helpful, as I did.  Looking forward to hearing more from you.
We have an arcade, where some people need teaching a lesson.  Have a go!
« Last Edit: August 26, 2006, 11:34:52 PM by bajanne2000 » Logged
"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;
Rerun
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Going through life tied to a chair!
« Reply #4 on: August 26, 2006, 11:34:14 PM »
Welcome shades.  I'm glad you are home.  I hope you enjoy the site.
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Joe Paul
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« Reply #5 on: August 27, 2006, 01:46:54 AM »
Welcome aboard Shades, hope your recovery is quick.
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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
MattyBoy100
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What's dialysis?
« Reply #6 on: August 27, 2006, 01:54:36 AM »
Hi Shades,

Yes, your mum did a pretty good job of introducing you to us already!!!  I`ve also got Alports so know what its like!  Hope you`re doing ok.

Matty.
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SCOTLAND NO.1
Shades_Elfen
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« Reply #7 on: August 27, 2006, 02:49:30 AM »
Its Nice to hear from you all, and Mattyboy, we are a rare breed aren't we?  :D   

however, I've been hearing of more and more people who have Alports and its nice to know We (me and Python) aren't the only ones.

well, as stated before, I'm still recovering (from what seems to be another blunder in a line of em by a hospital  >:( )

....

I'm not going to say much more at the moment, I've just gotten outta bed 10 minutes ago, and i need to have at least half a cup of tea before my brain kicks in proper....
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Time been on Dialysis : 5 years and counting
"It Doesn't matter, now what happens, I will never give up the fight, as long as the voice inside tells me to stand and fight" - Myself
Python
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Bobby the Python
« Reply #8 on: August 27, 2006, 04:49:49 AM »
Welcome my little snakelet ;D
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Alports Syndrome - A Rare Breed Indeed!!!
Shades_Elfen
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« Reply #9 on: August 27, 2006, 04:54:21 AM »
*hisses*

Yessss, It's good to be here, informative, interesting and friendly people to ask questions/give help... and to talk about our experiences on dialysis (or just rant about it, doctors and hospitals in general  >:D )
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Time been on Dialysis : 5 years and counting
"It Doesn't matter, now what happens, I will never give up the fight, as long as the voice inside tells me to stand and fight" - Myself
Sluff
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« Reply #10 on: August 27, 2006, 07:31:10 AM »
 Welcome to the site.
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angieskidney
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« Reply #11 on: August 27, 2006, 07:01:07 PM »
Heard a lot about you! Glad you finally signed up! :)
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FREE Donor List for all Kidney Patients!

diagnosed ESRD 1982
PD 2/90 - 4/90, 5/02 - 6/05
Transplant 4/11/90
Hemo 7/05-present (Inclinic Fres. 2008k 3x/wk MWF)
Zach
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"Still crazy after all these years."
« Reply #12 on: August 27, 2006, 09:02:29 PM »
Welcome to the site!
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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."
Mom3
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« Reply #13 on: August 28, 2006, 03:02:57 PM »
Welcome. Wish my son would do the same...or at least something to educate himself...

Mom 3
 
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Sickness is a hindrance to the body, but not to the will, unless the will consent.
Epictetus
rimbo74
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My older brother and me (I'm on the right)
« Reply #14 on: January 09, 2007, 02:13:15 PM »
Shades,

I have Alports as well, I thought I was the only one who had it.  I still might be the only one who has it in Texas!
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1986 - Diagnosed with Alport's Syndrome
10/29/06 - Told Kidneys failed
02/07-07/07 - PD Dialysis
07/31/07 - Kidney Transplant (donor was my older brother)
nextnoel
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« Reply #15 on: January 10, 2007, 05:41:15 AM »
Welcome, Shades!  :welcomesign; It's good to have you with us!
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I can't reach the hill like I used to, but I'm not at a standstill yet!
KidneyMommy
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« Reply #16 on: January 10, 2007, 05:45:22 AM »
Welcome Shades!  Our household knows all about PD!  Our son was on it for 11 months.
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Jessica--Proud Mommy to Gavin
"What lies behind us and what lies before us are tiny matters compared to what lies with in us." --Ralph Waldo Emerson
angela515
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i am awesome.
« Reply #17 on: January 10, 2007, 05:54:47 AM »
 :welcomesign;
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Live Donor Transplant From My Mom 12/14/1999
Perfect Match (6 of 6) Cadaver Transplant On 1/14/2007
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