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Author Topic: I thought this was pretty cool!  (Read 2298 times)
sammiejo23
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Quand la vie devient dure, deviens plus dure.

« on: March 01, 2011, 11:51:55 PM »

I started an event on Facebook to see if I could do something to raise awareness for Kidney Disease Month and World Kidney Day, and I only expected maybe a handful of my close friends and family to participate. At the moment, over 1000 invites have been sent out thanks to people spreading the word and 150 people have said yes to wearing green this month! :) 150 is only a small portion of 1000, but it's more than I expected. Haha. I feel accomplished.  :cheer:
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01/05/2011-Full Right Nephrectomy (Malignant Tumors)
01/24/2011-Permacath Placed; Dialysis Started
01/28/2011-Fistula Placed
Current: In-Center Hemodialysis/3x a week
YLGuy
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« Reply #1 on: March 01, 2011, 11:56:10 PM »

 :thumbup;  :2thumbsup;  :clap; Awesome!
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galvo
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« Reply #2 on: March 02, 2011, 03:08:19 AM »

Cool. I must join. How do I find you on FB?
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Galvo
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WWW
« Reply #3 on: March 02, 2011, 09:29:22 AM »

 :2thumbsup;
Cool. I must join. How do I find you on FB?
Seconded.   ;D
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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.
sammiejo23
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Quand la vie devient dure, deviens plus dure.

« Reply #4 on: March 02, 2011, 12:10:35 PM »

Haha, you guys can find me by searching Samantha Moncur. :) You'll know it's me by the picture. (It's a Kidney Chipmunk!) Hahaha.
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01/05/2011-Full Right Nephrectomy (Malignant Tumors)
01/24/2011-Permacath Placed; Dialysis Started
01/28/2011-Fistula Placed
Current: In-Center Hemodialysis/3x a week
lou
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« Reply #5 on: March 02, 2011, 12:19:12 PM »

brilliant!! :clap; will try and find you on fb   :2thumbsup;
« Last Edit: March 02, 2011, 12:23:06 PM by lou » Logged
sammiejo23
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Quand la vie devient dure, deviens plus dure.

« Reply #6 on: March 02, 2011, 12:34:23 PM »

Yes, please anyone feel free to add me! :) But, if you could, let me know who you are, haha. I know usernames and real names aren't necessarily the same.
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01/05/2011-Full Right Nephrectomy (Malignant Tumors)
01/24/2011-Permacath Placed; Dialysis Started
01/28/2011-Fistula Placed
Current: In-Center Hemodialysis/3x a week
Brightsky69
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« Reply #7 on: March 02, 2011, 02:26:25 PM »

Excellent!
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Transplant June 11, 1991 (1st time) my mom's kidney
Received my 2nd kidney transplant Oct. 19th 2010.
Bajanne
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« Reply #8 on: March 02, 2011, 03:13:18 PM »

Really cool idea! :thumbup;
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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;
Riki
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« Reply #9 on: March 12, 2011, 09:09:21 PM »

yeah.. that's better than what I had, which was a FB event for the seminar that the Kidney Foundation of New Brunswick and PEI was putting on Thursday night.  I was the only one who said I was going to attend, at least on FB.  So many showed up, who didn't rsvp, and they didn't have enough seats.  There were a lot of people standing on the sides of the room
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Dialysis - Feb 1991-Oct 1992
transplant - Oct 1, 1992- Apr 2001
dialysis - April 2001-May 2001
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texasstyle
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« Reply #10 on: March 13, 2011, 08:39:08 AM »

You sure are an inspiration girl! Great job. Your great attitute is going to do wonders for you in life.
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caregiver to husband using in-center dialysis 4 years
sammiejo23
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Quand la vie devient dure, deviens plus dure.

« Reply #11 on: March 13, 2011, 10:33:13 AM »

Thanks ts! :)
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01/05/2011-Full Right Nephrectomy (Malignant Tumors)
01/24/2011-Permacath Placed; Dialysis Started
01/28/2011-Fistula Placed
Current: In-Center Hemodialysis/3x a week
texasstyle
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« Reply #12 on: March 13, 2011, 06:48:03 PM »

Oh you're most welcome. I may have missed a few posts our yours but the ones I have seen are always encourging, determined, and hopeful. I don't think you realize that about yourself. If you do get "down days' which I'm sure you will, that's ok. Come here ESPECIALLY those days. The positivity you give to others will come back to you. Karma I guess you could say. I am a caregiver (but sometimes feellike a dialyis patient) and it gets to be hard sometimes. Not only can I talk with the other caregivers, but the people on dialysis too. Some people "think" they know what dialysis is, but unless you're living it you don't really know. All of us DO. Even just having kidney disease is stressful. Some here are not on dialysis now.Some have had transplants.Such a diverse group with one thing in common: Kidney disease. I'm sorry you have to be here Samiejo but I also GLAD you are!
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caregiver to husband using in-center dialysis 4 years
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