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Author Topic: Kidney with Bone Marrow Transplant  (Read 55751 times)
lainiepop
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« Reply #125 on: June 06, 2014, 12:40:06 AM »

How many biopsies do u have to have? Do they have to do them because of the trial ? As i thought thy are normally reluctant unless they think kidney is rejecting xx
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1982 - born with one imperfect kidney and no bladder, parents told i would not survive
1984 - urostomy op
1990 - bladder built out of colon
2007 - birth of son, gfr fall from 3O to 26
July2011 - birth of prem daughter, gfr 17%
August2011 - gfr drop to 10%
29th May2012 - RECEIVED KIDNEY 4/6 match from my wonderful dad !
Ninanna
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« Reply #126 on: June 06, 2014, 06:09:26 AM »

The paper work I have has three biopsies, but doesn't say when. I already had one biopsy, but that was a for cause biopsy (creatinine was 3.9). They will give me new paperwork with the schedule before they start the with drawl.
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Spring 2006 - Diagnosed with IgA nephropathy
June 2013 - Listed on transplant list
Feb 4th 2014 - Kidney and bone marrow tx (both from my mother) as part of a clinical trial at Hopkins
Ninanna
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« Reply #127 on: June 06, 2014, 01:34:39 PM »

After 4 1/2 months, my hair is starting to grow back!
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Spring 2006 - Diagnosed with IgA nephropathy
June 2013 - Listed on transplant list
Feb 4th 2014 - Kidney and bone marrow tx (both from my mother) as part of a clinical trial at Hopkins
cassandra
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When all else fails run in circles, shout loudly

« Reply #128 on: June 07, 2014, 07:05:33 AM »

Great news hon

        :cheer:


Lots of live, Cas
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I started out with nothing and I still have most of it left

1983 high proteinloss in urine, chemo, stroke,coma, dialysis
1984 double nephrectomy
1985 transplant from dad
1998 lost dads kidney, start PD
2003 peritineum burst, back to hemo
2012 start Nxstage home hemo
2020 start Gambro AK96

       still on waitinglist, still ok I think
SooMK
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« Reply #129 on: June 07, 2014, 02:19:26 PM »

Excellent!
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SooMK
Diagnosed with Uromodulin Kidney Disease (ADTKD/UMOD) 2009
Transplant from my wonderful friend, April 2014
Volunteering with Rare Kidney Disease Foundation 2022. rarekidney.org
Focused on treatment and cure for ADTKD/UMOD and MUC1 mutations.
Ninanna
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« Reply #130 on: June 09, 2014, 12:15:17 PM »

What an absolute shitty day!  Not a single lab result was good today :(  All cell counts were down, creatinine was up, my hemoglobin was 7.8.

Some good did come out of it though...they are lowering my Sirolimus target.  They were talking about lowering my MFF again as well (I take 500mg twice a day) but I'm not holding my breath for that one. 
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Spring 2006 - Diagnosed with IgA nephropathy
June 2013 - Listed on transplant list
Feb 4th 2014 - Kidney and bone marrow tx (both from my mother) as part of a clinical trial at Hopkins
jeannea
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« Reply #131 on: June 09, 2014, 01:33:23 PM »

Sorry. Transplant is a roller coaster. Hydrate well. Do something that is calming for you. Hopefully the next set will be better.
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SooMK
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« Reply #132 on: June 09, 2014, 03:28:58 PM »

Oh no. So sorry to hear this. Hoping for better next time.
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SooMK
Diagnosed with Uromodulin Kidney Disease (ADTKD/UMOD) 2009
Transplant from my wonderful friend, April 2014
Volunteering with Rare Kidney Disease Foundation 2022. rarekidney.org
Focused on treatment and cure for ADTKD/UMOD and MUC1 mutations.
lainiepop
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« Reply #133 on: June 10, 2014, 12:10:46 AM »

sorry to hear this, hope next lab draw is better, how r u feeling in yourself now? xx
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1982 - born with one imperfect kidney and no bladder, parents told i would not survive
1984 - urostomy op
1990 - bladder built out of colon
2007 - birth of son, gfr fall from 3O to 26
July2011 - birth of prem daughter, gfr 17%
August2011 - gfr drop to 10%
29th May2012 - RECEIVED KIDNEY 4/6 match from my wonderful dad !
cariad
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What's past is prologue

« Reply #134 on: June 10, 2014, 01:30:11 AM »

Sorry to read this. Jeannea is right, transplant is notorious for throwing curve balls, and there's a good chance this is just a blip that will come right in the end. You're in my thoughts. Keep drinking that water!
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Be kind, for everyone you meet is fighting a great battle. - Philo of Alexandria

People have hope in me. - John Bul Dau, Sudanese Lost Boy
Ninanna
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« Reply #135 on: June 10, 2014, 09:16:50 AM »

Thanks guys for the kind words.  Yesterday was just an accumulation of all my frustrations.  The rise in creatinine was minuscule really, but combined with everything else, It was the straw that broke the camel's back so to speak.  I just wanted to really punch something.  So glad I could come to this site and just let it all out.

The most frustrating part about this experience I think is how long it's taking to normalize things.  I knew it would be a much longer recovery time, but it still sucks.  After 4 1/2 months, my counts should be better, but they aren't because of that damned CMV.  At times I feel more tired and more out of breath than I was before transplant.

Thank god I am going back to work next week.  I need something to take my mind off all this and get me out of the house.
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Spring 2006 - Diagnosed with IgA nephropathy
June 2013 - Listed on transplant list
Feb 4th 2014 - Kidney and bone marrow tx (both from my mother) as part of a clinical trial at Hopkins
Deanne
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« Reply #136 on: June 12, 2014, 10:32:07 AM »

I've been watching and am amazed at the strength you've shown. When I first heard you were having this done, I was jealous. I wanted to go down this route, but I couldn't. Now that I'm seeing how difficult it has been for you and I'm amazed that you're still sane! I understand the need to go back to work as a distraction. I went back earlier than I had to for the distraction, too and my experience has been a breeze compared to yours.
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Deanne

1972: Diagnosed with "chronic kidney disease" (no specific diagnosis)
1994: Diagnosed with FSGS
September 2011: On transplant list with 15 - 20% function
September 2013: ~7% function. Started PD dialysis
February 11, 2014: Transplant from deceased donor. Creatinine 0.57 on 2/13/2014
Ninanna
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« Reply #137 on: June 12, 2014, 03:41:29 PM »

I've been watching and am amazed at the strength you've shown. When I first heard you were having this done, I was jealous. I wanted to go down this route, but I couldn't. Now that I'm seeing how difficult it has been for you and I'm amazed that you're still sane! I understand the need to go back to work as a distraction. I went back earlier than I had to for the distraction, too and my experience has been a breeze compared to yours.

Thank you so much for your kind words Deanne.  You've been through a whole heck of a lot too, so I wouldn't discount your experiences.  This disease is a bitch for everyone hehe.

I think part of the reason I felt so down Monday and Tuesday was because I needed blood.  I got 2 units yesterday and I feel soo much better.  I also got to units of platelets so I could get my chest cath out yesterday as well.  My shoulder is a little sore, but tomorrow I am looking forward to a normal shower!

Already they are thinking of altering the pre-conditioning a little to make it less strenuous. I had 3 days of ATG infusions, followed by 5 days of chemo and dialysis, then total body irradiation, and finally the transplant date.  There was also 2 days of high dose chemo post transplant to limit GvHD.  Now they are thinking of having a 2 day break between the IgG and chemo, and only have 3 days of chemo.  If the person hasn't done hemo before, they also want them to do some extra sessions to get used to it before hand.  I did tell them if I had to do extra days of dialysis I would have been pretty upset.  I threw up everytime (which actually was a relief because it temporarily distracted from my pounding migraine) and I had one tech that was a complete jerk, and at the end of the sessions I clotted the machine, so he pumped it back manually...it was scary as shit and it hurt my heart.  I did complain, and I got the sense he got in a lot of trouble and the lady said he would never treat me again, lol.
« Last Edit: June 13, 2014, 12:41:53 AM by Ninanna » Logged

Spring 2006 - Diagnosed with IgA nephropathy
June 2013 - Listed on transplant list
Feb 4th 2014 - Kidney and bone marrow tx (both from my mother) as part of a clinical trial at Hopkins
Ninanna
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« Reply #138 on: June 19, 2014, 04:56:40 PM »

So I'm back at work part-time and omg it's the best thing ever!  I am sooo happy to be back. The only problem now is I'm too amped up at night and excited for work the next day that I just can't sleep!

On another note, the last week in July is my kidney biopsy. Then if that looks good they start the taper of the prednisone and MMF. The taper has to be completed by the end of September. My birthday is the 26th of September, so that will make a nice birthday present if all goes as planned. Then I have to do another biopsy before they can taper the rapamune. It didn't sound like I would have any biopsies after that unless there was a problem.
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Spring 2006 - Diagnosed with IgA nephropathy
June 2013 - Listed on transplant list
Feb 4th 2014 - Kidney and bone marrow tx (both from my mother) as part of a clinical trial at Hopkins
SooMK
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« Reply #139 on: June 19, 2014, 10:07:41 PM »

How wonderful that you're able to start back to work and are excited to be there. I'm sure you'll settle down soon and be able to get some sleep (one of the most elusive activities sometimes). Congrats on this milestone.
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SooMK
Diagnosed with Uromodulin Kidney Disease (ADTKD/UMOD) 2009
Transplant from my wonderful friend, April 2014
Volunteering with Rare Kidney Disease Foundation 2022. rarekidney.org
Focused on treatment and cure for ADTKD/UMOD and MUC1 mutations.
Ninanna
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« Reply #140 on: July 10, 2014, 04:10:33 PM »

Platlets, white counts, and even my red blood cells are officially on the rise!  I have 33k platelets which is a record breaker for the past several months. I soo hope last week was my last blood transfusion. My Kidney biopsy is scheduled for the 30th of July which is three weeks away. If I am super lucky I might not need a platelet transfusion before hand!  Hair is continuing to grow and right now I couldn't be happier!
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Spring 2006 - Diagnosed with IgA nephropathy
June 2013 - Listed on transplant list
Feb 4th 2014 - Kidney and bone marrow tx (both from my mother) as part of a clinical trial at Hopkins
talker
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Talkers oil painting

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« Reply #141 on: July 10, 2014, 05:45:33 PM »

Platlets, white counts, and even my red blood cells are officially on the rise!  I have 33k platelets which is a record breaker for the past several months. I soo hope last week was my last blood transfusion. My Kidney biopsy is scheduled for the 30th of July which is three weeks away. If I am super lucky I might not need a platelet transfusion before hand!  Hair is continuing to grow and right now I couldn't be happier!

                                              :flower;         And may your bouquet of ' happier' flowers, fill all the places in your life.      :flower;
                                                                                                                   
                                                                                                             :cheer:    :grouphug;       :cheer:
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Be Well

"Wabi-sabi nurtures the authentic by acknowledging three simple realities: nothing lasts, nothing is finished, and nothing is perfect."

Don't ever give up hope, expect a miracle, pray as if you were going to die the next moment in time, but live life as if you were going to live forever."

A wise man once said, "Yesterday's the past, tomorrow's the future, but today is a gift. That's why it's called the present."
PrimeTimer
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« Reply #142 on: July 10, 2014, 07:07:40 PM »

That's SUPER, Ninanna! Congratulations on the good word! I have so admired you for sharing your journey with us here. Beautiful picture, too! You have more hair than my husband! (honey, if you read this, sorry in advance).
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Husband had ESRD with Type I Diabetes -Insulin Dependent.
I was his care-partner for home hemodialysis using Nxstage December 2013-July 2016.
He went back to doing in-center July 2016.
After more than 150 days of being hospitalized with complications from Diabetes, my beloved husband's heart stopped and he passed away 06-08-21. He was only 63.
Ninanna
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« Reply #143 on: July 11, 2014, 12:37:41 PM »

Thanks Prime Timer and Talker, it really means a lot!
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Spring 2006 - Diagnosed with IgA nephropathy
June 2013 - Listed on transplant list
Feb 4th 2014 - Kidney and bone marrow tx (both from my mother) as part of a clinical trial at Hopkins
PrimeTimer
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« Reply #144 on: July 12, 2014, 12:31:28 AM »

Thanks Prime Timer and Talker, it really means a lot!
No, thank YOU for being such an inspiration and a load of strength! I know, your poor body is hard at work but you are also performing a sort of "silent" duty to your fellow site members here, you just didn't know it! Thanks!  :bump;
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Husband had ESRD with Type I Diabetes -Insulin Dependent.
I was his care-partner for home hemodialysis using Nxstage December 2013-July 2016.
He went back to doing in-center July 2016.
After more than 150 days of being hospitalized with complications from Diabetes, my beloved husband's heart stopped and he passed away 06-08-21. He was only 63.
Ninanna
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« Reply #145 on: July 21, 2014, 06:35:38 AM »

Unfortunately I am in the hospital. I had a fever (has to be over 100.5 for them to be concerned) Sat along with the chills and some immense sinus pressure. I called the hospital at 3 am and they wanted me to come in as a precaution because I am their big expensive baby.  They started antibiotics but I still had a fever and symptoms last night, so if I'm lucky they will let me go tomorrow :(
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Spring 2006 - Diagnosed with IgA nephropathy
June 2013 - Listed on transplant list
Feb 4th 2014 - Kidney and bone marrow tx (both from my mother) as part of a clinical trial at Hopkins
lainiepop
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« Reply #146 on: July 21, 2014, 08:07:48 AM »

Oh im so sorry to hear this i hope u get better soon. How r u feeling? My tx centre is the same has to be over 38 celsius (100.5) for a concern. With utis they dont give me antiobiotics straight away unless i have temp of over 37.5. In fact im wondering if i have one at the mo, its hard to tell with my bladder as it produces mucus which when breaks up can make wee look bitty and cloudy. Doesnt smell and temp is 36.7 but i might get gp to send it to lab tomorrrow anyway just in case one is brewing.

Do they know what is causing the fever? I hope it comes down quickly. When i was in hospital 8 weeks ago for my bowel op my temp was regularly 38 or over 37.5 anyway, it baffled the docs as they sent off blood and urine cultures, scanned me, creatinine stable and i wasnt ill or had any symptoms of a fever except one! They let me go home and it came down in a day, i put it down to stress and anxiety, some docs say this can happen if u get yourself in a state like i did, however its not medically accepted but it must've been the case for me!!

Get well soon xxx
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1982 - born with one imperfect kidney and no bladder, parents told i would not survive
1984 - urostomy op
1990 - bladder built out of colon
2007 - birth of son, gfr fall from 3O to 26
July2011 - birth of prem daughter, gfr 17%
August2011 - gfr drop to 10%
29th May2012 - RECEIVED KIDNEY 4/6 match from my wonderful dad !
jeannea
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« Reply #147 on: July 21, 2014, 10:03:46 AM »

They're going to be fast with the hospital trigger for a while yet. They need to have you close to keep an eye on things. I hope you feel better soon and they're not torturing you too badly.

(I keep a hospital bag in my trunk at all times. You never know when you have to go.)
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MooseMom
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« Reply #148 on: July 21, 2014, 10:38:44 AM »

Well Ninanna, that's what you get for being their big expensive baby!   :P

Do you think you have a sinus infection, hence the "immense" sinus pressure?  I sure hope you feel better soon.
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"Eggs are so inadequate, don't you think?  I mean, they ought to be able to become anything, but instead you always get a chicken.  Or a duck.  Or whatever they're programmed to be.  You never get anything interesting, like regret, or the middle of last week."
Ninanna
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« Reply #149 on: July 21, 2014, 04:36:39 PM »

Thanks guys for the well wishes. Last night was pretty miserable but today I feel much better. I also got 2 units of blood because my hematocrit was low (again). They did a CT of my sinuses and said they looked like they did back in April when I was having trouble with them. They also said sme counts were a little elevated so they are ruling out other things (man do I hate getting flocked).

On a good note I can pretty much trouble shoot my own pump now when it starts beeping. I also walked all over the hospital today and got some real food!  >:D

It's funny MM when I called about my fever, the oncologist on call was about to just send over an antibiotic prescription and call it a day, but the more she looked at my chart the more she was like, "oh, you have a unique complicated history, I need to consult with another doctor on how aggressive they want to be, I'll call you back"

I also got a laugh at some poor fellow today when they did rounds, there were seven people in my room, and by the time he got his mask and plastic gown on the doc was done and leaving, so he missed the whole shebang lol.
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Spring 2006 - Diagnosed with IgA nephropathy
June 2013 - Listed on transplant list
Feb 4th 2014 - Kidney and bone marrow tx (both from my mother) as part of a clinical trial at Hopkins
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