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Author Topic: If i were a horse ..  (Read 2674 times)
KICKSTART
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« on: August 28, 2008, 09:36:55 AM »

you would have shot me by now ! Well apart from a permanent cough , a mystery virus that has hung over me for nearly 5 weeks now and a hemoglobin of 7.2 everything is just rosy !

One or two of you mentioned having a low hemoglobin and possible blood transfusions. What i wanted to ask was , how long did it take for the hospital to treat you ? I have been told i need to build my iron stores up firstly , then reduce my b.p. then start on epo. The thing is, i have had only one lot of iron since.I even rang to ask if i was coming in this week for more , but no one knew (and i havent been called in) I am just finding it difficult at the moment living on my own , the tiredness is worse , but ive noticed my breathing is hard work and i cant walk the same distances i could a few weeks ago , without having to stop and rest. They have already told me it will take time to build my iron levels back up etc , but its never going to happen if they dont give me any or make me wait weeks between times. What was your treatment like ? when did you notice a difference ?
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OH NO!!! I have Furniture Disease as well ! My chest has dropped into my drawers !
paris
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« Reply #1 on: August 28, 2008, 12:17:53 PM »

Hi Kickstart, I have had iron infusions to help build the iron stores.  The infusion itself took about 4 hours.  It then took awhile to start noticing a difference.  I started getting the epo shots before the iron infusions.  My numbers kept going up and down for over a year.  Now we seem to have found a good routine and my numbers have stabilized.   I hope they can figure out a good solution for you.  It does take awhile and patience is NOT my virtue!  Hope you start feeling better soon. :cuddle;
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It's not what you gather, but what you scatter that tells what kind of life you have lived.
Deanne
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« Reply #2 on: August 28, 2008, 12:21:04 PM »

I can't answer your question, but I'm glad you aren't a horse!
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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
twirl
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« Reply #3 on: August 28, 2008, 01:06:05 PM »

If I were a horse....... I would want to belong to Tim McGraw
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monrein
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Might as well smile

« Reply #4 on: August 28, 2008, 01:50:31 PM »

I had a series of 10 iron baggie drips in a row(into my lines during D) and I get an Aranesp shot every two weeks.  My BP used to be really high and I was on 5 different meds, pretty high doses foe each.  Since starting dialysis my BP is low (post dialysis standing pressure today was 108/59) and I now take only one half tablet of a beta-blocker med and that may go too after my next clinic appt.  I do want to ask again if I ought to be taking an active form of vitamin D but last time I was told there was no need. 

Your hemoglobin seems really low, no wonder you feel super fatigued etc.  I think I would try again to get a hold of someone with a clue or two (not easy I know) to discuss the scheduling, the exact outline of how this situation with you is going to be treated and handled.  You want dates, a timeline of what is going to happen when with the iron infusions because it sounds a bit like you're slipping between the cracks some where along the line.  I was given the iron infusions starting two days after it was determined that I might benefit from some iron.  I've personally never heard of all the things you have to wait on first before they'll start the Epo but others on this board might have a better understanding of the reasons for that than I do.

I wish for you to get this straightened out soon and to start feeling better.  It is especially hard doing it all on your own and attending to meals etc while feeling weak, tired, virusy and worried.
Any chance of a new doctor under your medical system there???
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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
boxman55
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« Reply #5 on: August 28, 2008, 01:57:26 PM »

if I where a horse I would look like my avatar...Boxman

I got iron shots prior to starting dialysis I think it was once a week (not sure, maybe every 2 weeks) can't remember if they did any good I suppose they did but, I was on the downward slid to dialysis fairly quick so my breathing, walking, fatique, etc never really rebounded
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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
twirl
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« Reply #6 on: August 28, 2008, 03:08:34 PM »

and Boxman you would be a beauty of a horse
my answer about iron shots would match Boxman's
but those shots hurt and I got them every other week
I just got worse and then got on D
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frankenarm
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« Reply #7 on: August 28, 2008, 11:45:08 PM »

I have had a problem with anemia and my iron stores since I was a pre-teen, they tried to get me to take oral iron for years and I just couldnt due to the... tummy side affects. Currently I get iron and epo at my center (epo every run and iron once a week.) Usually when they said you need your iron stores up before they can give you blood its because well, you just dont have iron in your system to support the new blood. However, if its getting as bad as you say (and im not doubting! Ive totally been there, it sucks!) then they really need to boost you anyway. Its not safe to leave it.
Try again! Start yelling at people to pay attention... though that does take a lot of energy so make sure your sitting down! lol
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"Laughter is higher than all pain..."

Chronic renal failure since birth (1986)
Grade 5 reflux for 17 years
Hemodialysis for 9 months in 2001-2002
Living-related kidney transplant 2002
Rejection of said transplant Sept. 2007
Restart Hemodialysis Feb. 2008
Current: In-Center Hemodialysis with upper left arm fistula, on some crappy machine that alarms to loud.
KICKSTART
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« Reply #8 on: August 29, 2008, 03:44:38 AM »

Thanks everyone ..my treatment does seem a bit hit and miss , a week of IV iron here and a week there. I did ask when my next one was due bout no one knew , im going to try again to see whats going on.
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OH NO!!! I have Furniture Disease as well ! My chest has dropped into my drawers !
twirl
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« Reply #9 on: August 29, 2008, 05:08:11 PM »

I changed my mind, I'd rather be Clint Black's horse and live on his ranch in Willis, Texas----- right down  the road
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carson
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« Reply #10 on: September 17, 2008, 09:11:11 PM »

...I have a horse...his name is Carson....He is my therapist and holder of all secrets!
My name is actually Lisa
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2009 infection treated with Vancomycin and had permacath replaced
2009 septic infection that wouldn't go away
2007 began Nocturnal Home Hemo with Permacath
1997 began Peritoneal Dialysis
1982 had cadaver transplant
1981 diagnosed with GN2 and began Peritoneal Dialysis
Sugarlump
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10 years on and off dialysis

« Reply #11 on: September 17, 2008, 11:43:18 PM »

if you were a horse you'd probably eat me !!!
Prior to starting dialysis i had four iron fusions lasting about an hour each one a week to
boost my iron levels then epo injections twice weekly which did help.
Now that my kidney transplant is failing i have the same problem my hb is now 8 and
i feel exhausted all the time so you have my sympathies. I yawn all the time (lack of
oxygen) and my brain feels sluggish too.
I'm starting epo injections this week again which will hopefully improve my levels or i'll
have to go back on dialysis soon...
Don't try and do too much while your hb is so low, apparently it puts a real strain on
the heart to try and get oxygen round your body.
Best wishes
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10 years of half a life
3 years HD 1st transplant Feb 08 failed after 3 months
Back to HD 2nd transplant Dec 10 failed after 11 months
Difficult times with a femoral line and catching MSSA (Thank you Plymouth Hospital)
Back on HD (not easy to do that third time around)
Fighting hard (two years on) to do home HD ... watch this space!
Oh and I am am getting married 1/08/15 to my wonderful partner Drew!!!
The power of optimism over common sense :)
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