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Author Topic: Oh well the "List" isn't so bad  (Read 6722 times)
kimcanada
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« on: January 14, 2008, 01:34:42 PM »

Well I received news this weekend that my friend won't be able to donate a kidney afterall, there seems to be a new test that checks the antigens and something in my blood didn't jive with something in her blood...

I am out of live donor options now, and I am officially on the "list"  to say that I wasn't devastated would be an understatement,  I have lived my life over the last two years thinking that I would "soon" be getting my transplant.

I asked my coordinator what the approximate wait time would be , and she told me 2.5-3 years....

I hope ya all like me enough , seems I am here for awhile!

Kim :'(
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okarol
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« Reply #1 on: January 14, 2008, 01:38:54 PM »

 :grouphug; Sorry, but you never know what will happen. Try to hang in there.
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Admin for IHateDialysis 2008 - 2014, retired.
Jenna is our daughter, bad bladder damaged her kidneys.
Was on in-center hemodialysis 2003-2007.
7 yr transplant lost due to rejection.
She did PD Sept. 2013 - July 2017
Found a swap living donor using social media, friends, family.
New kidney in a paired donation swap July 26, 2017.
Her story ---> https://www.facebook.com/WantedKidneyDonor
Please watch her video: http://youtu.be/D9ZuVJ_s80Y
Living Donors Rock! http://www.livingdonorsonline.org -
News video: http://www.youtube.com/watch?v=J-7KvgQDWpU
willieandwinnie
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« Reply #2 on: January 14, 2008, 02:40:54 PM »

kimcanada, keep thinking positive, we were told the wait was 5-6 years and Len got the call in 11 months, so you never know. I pray for quick.  :cuddle;
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"I know there's nothing to it, but I want to know what it is there's nothing to"
paris
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« Reply #3 on: January 14, 2008, 03:24:49 PM »

Kim, you story is similar to mine.  Five people tested and here I am still waiting. Two years on the List.  They make it all sound so easy when you start the testing.  I guess they don't want to tell you all the horror stories until you are farther into the process.     I am sorry  and I understand how crushed you feel. That is why we are here--lean on us for awhile.  I am hoping you are one of the ones you get a kidney fast.   Big hugs  :cuddle;
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It's not what you gather, but what you scatter that tells what kind of life you have lived.
Romona
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« Reply #4 on: January 14, 2008, 03:40:46 PM »

Kim and Paris,
Please don't get discouraged. The right (or left) kidney isn't ready for you yet. I know you are thinking easy for me to say, I wasn't on the list long. I was dragging my feet when it came to testing. I was very much in denial. I admire you girls. You are very gutsy. You have accepted what is happening and are coping with it. I wasn't like that until about a month before my transplant. When I was told dialysis was to be starting soon. You both are in my thoughts and prayers.
Romona :grouphug;
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boxman55
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« Reply #5 on: January 14, 2008, 03:52:02 PM »

Tough news Kim, please know we are all rooting for you...Boxman
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"Be the change you wished to be"
Started Hemodialysis 8/14/06
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« Reply #6 on: January 14, 2008, 04:05:34 PM »

Nine people tested for Jenna. No match. That's when I began to consider the internet as a resource to find a living donor.
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Admin for IHateDialysis 2008 - 2014, retired.
Jenna is our daughter, bad bladder damaged her kidneys.
Was on in-center hemodialysis 2003-2007.
7 yr transplant lost due to rejection.
She did PD Sept. 2013 - July 2017
Found a swap living donor using social media, friends, family.
New kidney in a paired donation swap July 26, 2017.
Her story ---> https://www.facebook.com/WantedKidneyDonor
Please watch her video: http://youtu.be/D9ZuVJ_s80Y
Living Donors Rock! http://www.livingdonorsonline.org -
News video: http://www.youtube.com/watch?v=J-7KvgQDWpU
KT0930
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« Reply #7 on: January 14, 2008, 04:31:57 PM »

I had seven people tested, and I was convinced that my brother would be a match, due to both my parents being matches previously. No such luck, and I went through the same thing you're going through now. I took a day off work to feel sorry for myself, jumped every time the phone rang for about the first three months, then decided that I had to get on with living. I know, it's very easy to say, but trust me, I've been there. Take the time you need to deal with this blow, then get back to living.
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I received a 6 out of 6 antigen match transplant on January 9, 2008. Third transplant, first time on The List.
paris
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« Reply #8 on: January 14, 2008, 04:42:12 PM »

I am at the point that I don't even think about the transplant center except when it is time to update tests. If it happens, great-but I can't think about it anymore. I cringe when people ask how soon I will get a kidney. I have to be ok if the answer is never. So, now I  just don't stress about it and am working on being the best I can be right now.  I will still look for solutions, but need to put it on the back burner for awhile. 

Right now I am just rejoicing for Katie!!  I can't believe how much you are posting. Are you resting?  Take care, we love you.

Kim, you are in my thoughts--fingers crossed your wait time is short.  2008 could be your year too :bandance; :clap; :cuddle;
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jbeany
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« Reply #9 on: January 14, 2008, 04:45:45 PM »

It can seem like such a looooong time, but years go by faster than it seems possible.  I try to stay focused on the possibility that I might get a match sooner than the 4 to 5 year wait time they told me was the average here in Michigan.  Most of the time, I try not to think about it at all - it would just drive me crazy!  I've got to focus on making the best of life on dialysis in the meantime - I refuse to put myself "on hold" completely, even if a lot of the things I want to do with my life are going to have to wait for the transplant.

Hang in there, and remember that it's okay to be disappointed over the loss of your living donor - just try to hold on to what hope the list can give you.
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"Asbestos Gelos"  (As-bes-tos yay-lohs) Greek. Literally, "fireproof laughter".  A term used by Homer for invincible laughter in the face of death and mortality.

stauffenberg
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« Reply #10 on: January 15, 2008, 10:21:00 AM »

Does the name 'Kimcanada' imply that you live in Canada?  There has recently been a scandal in Canada because of the highly variable waiting times for a kidney depending on the province of the patient's residence.  British Columbia has the lowest waiting times of around 2 to 3 years, but in Ontario a decade ago the average wait was already 8 years, and waiting times have been increasing everywhere since then due to the stagnant number of new kidneys becoming available, in contrast to the rising demand for kidney transplants.  So you are fortunate in your misfortune not to have to face a wait of 8 years plus, as I did.
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Psim
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« Reply #11 on: January 15, 2008, 10:54:40 AM »

I'm so sorry to hear your live donor didn't work out. There are so many factors that have to match, eh? I can only imagine how hard it is to wrap your head around the news. But with this disease we get a lot of practice dealing with hard stuff and then going on to live our lives with as much joy as we can muster. Hope your wait is the shortest possible and that when you do get it, your new kidney lasts for decades.  :cuddle;
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kimcanada
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« Reply #12 on: January 15, 2008, 03:55:34 PM »

Thanks for the words of encouragement everyone, I think that the biggest change is going to have to be in my thinking... I mean for the last 2 years my thinking has been.... "Just wait till I get that transplant" well now that might never come, or might be a far way away, I am 41 and have to stop waiting till "that day" and start living life again.

I have decided that my answer to "when is your transplant?" is going to be "maybe never" 

My hubbie and I have been brainstorming over the last few days about any changes we should think about making, the first one might be to move closer to my treatments, I am now about 45 mins away, but in Nova Scotia in the winter it just adds alot of stress, so we will see about moving to the same town...

stauffenberg, I am Canadian, I live in N.S.  I am not aware of the past scandals , I am sorry that you had to wait 8 years

P.S.
I watched a show in TV last night about a new program in the UK that they might in force that states what if you don't sing yourself as a donor... you are assumed to WANT do donate instead of what is in now, that if you don't sign your donor card it is assumed that you DON'T want to donate...

What a concept



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stauffenberg
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« Reply #13 on: January 15, 2008, 05:31:18 PM »

The legislation that has been proposed in the UK is already the law in many countries, such as Austria, Belgium, and Spain, which all have extremely brief waiting times for a kidney transplant.  Anyone up for a change of citizenship?  Sprechen Sie Deutsch?  Habla espagniol?  Parlez-vous francais?
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kimcanada
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« Reply #14 on: January 15, 2008, 05:36:45 PM »

I am staying put.

But I was amazed with the concept, and then when they were saying how low the waiting time is in the countries that you mentioned, it was mind boggling.  I wonder what the people in those countries first thought when that was passed into law.  Do you know?
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KT0930
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« Reply #15 on: January 15, 2008, 05:44:35 PM »

Kim, one of my biggest challenges when I lost the possibility of a live donor was I had been looking at dialysis as a very temporary thing, and only paying fractional attention to the diet restrictions. Boy, was that a wake up call I could have done without! Best of luck with everything. Keep coming here to vent. We love ya!  :grouphug;
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I received a 6 out of 6 antigen match transplant on January 9, 2008. Third transplant, first time on The List.
charee
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« Reply #16 on: January 15, 2008, 06:11:43 PM »

The new legislation in the UK is exactly whats needed here :ausflag; but in the paper today an article stated " That Australia would not be taking such drastic measures as the UK " What the ....  we have one of the lowest donation rates in the world 140 people donated their organs last year in the whole of Australia, Something needs to be done ???
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Home Hemo  18 months
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from my beautiful sister
Royal Prince Alfred Sydney Australia

Live donors rock
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« Reply #17 on: January 15, 2008, 07:22:03 PM »

Kim,
My hubby has been on "THE LIST" twice.  He waited 5 and a half years the first time, and then didn't get a kidney from "THE LIST" (I finally -- in a miracle experiment -- got the chance to give him one of mine).  My kidney lasted a little over three years in Marvin's body (of course, once I gave it, I started calling it "his" instead of "mine" -- he said it was "ours").  When the transplanted kidney contracted the same disease that destroyed his original kidneys (IGA Nephropathy), he went back on dialysis and back on "THE LIST" -- that was four years and three months ago (and, no, the time he spent waiting the first time didn't carry over because they said he did get a transplant, even though it wasn't from "THE LIST").

Over the years, we had about a dozen people tested to be a live donor for him.  For various reasons, none of them worked out.  My sister got to the very last test (over about three months of intensive testing -- and we thought she was the one) before she, too, was ruled out.  When he went back on dialysis the second time (October 2003), Marvin took out a classified ad in 40 newspapers in our state (NC) looking for a live donor.  We had 125 people -- all strangers -- call and offer to be tested.  His transplant hospital wouldn't test any of them because they were strangers; the hospital said they didn't have the finances or resources to test all of these people and wondered if they had ulterior motives.  They said, "What would motivate a stranger to give you a kidney?"  We said, "It's a money thing?  Just exactly how much do you think Marvin's life is worth?" -- and then I threw in a couple of other words that are not fit to print here.  Bottom line -- his transplant center won't accept altruistic donors.  Geeze, I wish they had told us that up front.  By the way, our local newspaper is still running that "I need a kidney ad" after four years -- at no charge.  Marvin said he gave up thinking this would work, but, he reasoned, maybe keeping it in there reminds people that more organ donors are needed.  It can't help him now, but it can't hurt either.  At least people who read our local paper are still talking about organ donation; maybe one person who reads that ad will be an organ donor.  Marvin said if it's not a donor for him, it will be a donor for someone else like him and it will take one more person off the list and, thus, increase his chances.

Marvin has been pushing for "presumed consent" legislation here in the US for years.  He likes the "opt out" instead of "opt in" aspect.  He's contacted lots and lots of legislators.  Sen. Bill Frist (from Tennessee and a heart transplant surgeon) seemed the most interested in it, but he let it "fall by the wayside."  I think it's a controversial thing because people who oppose it say "presumed consent" is really not consent.  Obviously, those who oppose it don't have a loved one on the list.

I agree with the other statements made here.  You cannot let being on "THE LIST" consume you or your life.  Go on living the best you can.  The first time around on the list, we jumped every time the phone rang.  We knew each call certainly was "THE" call.  Marvin has had seven calls over the years -- he was told, "Don't eat.  Don't drink.  Stay by the phone, and we'll call you back."  We knew each one was the real thing.  Each time, the transplant coordinator called back to say the kidney either went to someone else or was damaged in the harvesting.  If you let it, being on "THE LIST" will break your heart.  Don't let it.  Being on the list will also give you hope -- hold on to that.

For those poor ignorant people who don't know how waiting for a kidney works and who ask Marvin, "So, when are you going to get your kidney?" his answer is, "Well, they called last night, but I said I had to watch the NC State - Carolina game on tv.  I told them I'd call them back Friday and see if it's still there."   There are just some things you can't explain to ignorant people, and it's not worth the trouble of trying.

I'd advise that you get on "THE LIST," but remember that it's exactly that -- a list.  Your name may get called sooner, later, or never.  For you, Kim, and for my Marvin, and for everyone else at IHD waiting, I hope it's soon -- very, very soon.
 
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boxman55
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« Reply #18 on: January 15, 2008, 07:52:19 PM »

well said petey, except if it was thier first time asking " when are you going to get your kidney" I would have gone with the Packer Panther game...Boxman
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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
kimcanada
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« Reply #19 on: January 16, 2008, 11:00:28 AM »

Petey.. Thank you, everyone that wrote can't imagine how much you helped me in a very hard time, I find that my partner is the most loving man ever, but there is some things that even he can't understand, I hope that during our time together I help someone else like you all helped me.
 :thx;

Kim
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« Reply #20 on: January 16, 2008, 12:13:47 PM »

Kim, when I re-read my message (after I'd posted it), it occurred to me that it sounded like I was saying the list sucks.  It doesn't.  Being on the list is great.  Being on the list and not getting a call as soon as you'd like...now, that sucks.  I'd rather Marvin be on the list than not on the list.

Boxman --- Marvin loved your response about the Packer - Panther game.  He wants to know if you'd mind if he copied it the next time the question comes up to him.
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paris
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« Reply #21 on: January 17, 2008, 03:06:35 PM »

Kim, I keep thinking about you. Time will help. I had been buying sleep pants and special things for the hospital but after a year, I got them all out and am wearing cute sleep pants all the time!  I have down days when I think it will never happen, but most of the time I just don't think about it.  Keep us up on how you are doing. :cuddle;
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KT0930
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« Reply #22 on: January 17, 2008, 05:11:49 PM »

Kim, you mentioned changes that you may be making in order to make the wait more bearable. Just be sure to take it one thing at a time and make sure you're completely comfortable with each step before taking on another. This is a stressful time (I know you know that). Take care.
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"Dialysis ain't for sissies" ~My wonderful husband
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I received a 6 out of 6 antigen match transplant on January 9, 2008. Third transplant, first time on The List.
kimcanada
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« Reply #23 on: June 06, 2008, 07:42:43 AM »

Well, here we go again

I had someone, a woman that is married to my cousin, come forward about 3 months ago to donate to me...  I just heard yesterday that there was antigins (sp) I didn't mention it because I figured that I would get my hopes up again... oh well it didn't work, I still got my hopes up and now I am in the hopeless fall...

If I am ever offered another kidney, I am tempted to tell the person, thanks but no... this feeling is devastating... I hate it  :'(
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xtrememoosetrax
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« Reply #24 on: June 06, 2008, 07:50:20 AM »

Oh Kim, I'm so sorry. :grouphug;
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