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Author Topic: Hi, I am alchemist New member  (Read 3352 times)
alchemist
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« on: January 05, 2012, 11:42:16 PM »

Hi I am alchemist New member.

I have a GFR of 10.11%
Serum Creatine = 4.9 mg/dL
Potassium 3.5 mg/dl 
CKD 5

I need a stem cell transplant it cost 12,500 dollars US.
I need a KIDNEY.
 
I am not sure how long Iam gonna live. If I had not replied then it probably means I am already.
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Riki
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« Reply #1 on: January 05, 2012, 11:54:38 PM »

Welcome.

I will say you have a bit of a pessimistic view on things.  I doubt I have any function left at all.  Dialysis keeps me alive pretty good, and has for not quite 8 years.

Are you on dialysis?  Or just looking for a kidney?  I know nothing about stem cells.  I didn't know they were doing anything with them in humans as of yet.  Can you give us some info on that?
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Dialysis - Feb 1991-Oct 1992
transplant - Oct 1, 1992- Apr 2001
dialysis - April 2001-May 2001
transplant - May 22, 2001- May 2004
dialysis - May 2004-present
PD - May 2004-Dec 2008
HD - Dec 2008-present
RichardMEL
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« Reply #2 on: January 06, 2012, 12:29:41 AM »

I agree with Riki.

Welcome though, alchemist - I do hope your stay is a LONG one.

Since you already posted about the stem cell trial in another thread, which has got a fair bit of debate going, and it seems clear you are very much focused on this as a potential treatment. Have you actualllty been involved in this trial or something similar? Do you not have any love donors for a potential "old style" transplant?

Dialysis does not mean the end at all. Many of us have spent years on D and live perfectly productive lives. Yes, some have troubles from time to time and it's not perfect for everyone, but neither is transplantation in its current form.

I hope you don't pin all your hopes on stem cell research. This is still very very new and unproven technology. I am sure down the track this will become something we, or future generations(more likely) can consider wonderful medical science, but until then we should be wary of something that is both hard to obtain and not conclusively proven in large scale trials and accepted worldwide. To that matter because the science is developing all the time even the treatments, techniques etc are changing all the time as we learn more and more. There is real hope.

Anyway welcome to our community. I hope by being here that you can see that stage 5 is not the end and find ways to live with your situation, dialysis etc and perhaps work towards a transplant and as for stem cells.. who knows!

RichardMEL, Moderator
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3/1993: Diagnosed with Kidney Failure (FSGS)
25/7/2006: Started hemo 3x/week 5 hour sessions :(
27/11/2010: Cadaveric kidney transplant from my wonderful donor!!! "Danny" currently settling in and working better every day!!! :)

BE POSITIVE * BE INFORMED * BE PROACTIVE * BE IN CONTROL * LIVE LIFE!
willowtreewren
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« Reply #3 on: January 06, 2012, 08:12:21 AM »

Welcome, Al!

From living with an eternal optimist, I've found that a positive outlook really improves quality of life.

But, I, like others, hope you are here for a long time.

 :welcomesign;

Aleta
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Wife to Carl, who has PKD.
Mother to Meagan, who has PKD.
Partner for NxStage HD August 2008 - February 2011.
Carl transplanted with cadaveric kidney, February 3, 2011. :)
Riverwhispering
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« Reply #4 on: January 06, 2012, 10:49:53 AM »

Hi Alchemist and welcome to IHD,

What did your nephrologist say?  Is he the one that told you you need a cell stem transplant?  Did he tell you if you don't have one and a new kidney you will die?   

Are you actually under the care of a nephrologist?   

Just cause you have a kidney disease doesn't mean it's a death sentence.   Please tell us more
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It's only one step from the Jungle to the Zoo
Traveller1947
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« Reply #5 on: January 07, 2012, 01:11:42 PM »

Welcome, alchemist!  None of us knows how long we're going to live.  Most of us focus on what will keep us going in the present.  For a kidney patient at stage 5, that means dialysis, getting yourself on the transplant list and staying as healthy as possible.  Hold on to the hope for a stem cell transplant, but in the meantime...all the best to you in your journey.
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lmunchkin
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« Reply #6 on: January 07, 2012, 07:22:39 PM »

What ever you decide to do, we will be here for you!

God Bless,
lmunchkin
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11/2004 Hubby diag. ESRD, Diabeties, Vascular Disease & High BP
12/2004 to 6/2009 Home PD
6/2009 Peritonitis , PD Cath removed
7/2009 Hemo Dialysis In-Center
2/2010 BKA rt leg & lt foot (all toes) amputated
6/2010 to present.  NxStage at home
Ang
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« Reply #7 on: January 15, 2012, 05:06:43 PM »

 :welcomesign;
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live  life  to  the  full  and you won't  die  wondering
alchemist
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« Reply #8 on: February 24, 2012, 11:39:12 PM »

Yes, dialysis means the death to those who do not have money!

I live in a shitty 3rd world asian country the philippines.

I do not have money for dialysis nor does the government have any free health services. It is all false promises.

I am dead before I even have the chance to live. It is so unfair.

anyway, If can not reply to this thread then it means I may have died already.

Damn these irregular heart beats, constant back and side pain. Sometimes, I can not breathe because my lungs get filled with water or what they call as edema and sometimes sudden heart squeezing pain.

I am under a nephrologist Dr.Arnold Tan of Cebu Doctos/Chung Hua Hospital Philippines.

I do not have any available kidney donors and even if I do, I do not have money for it nor is it a guarantee that it will help you get cured or have a longer life.

Most people on kidney only live 3 - 5 years.

The buying and selling of kidney has been outlawed and is now illegal so it is getting harder and harder to live.

Blood pressure is at 145/90.
Creatine is now at 4.9 mg/dl
Poatssium 3.5 mg/dl
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Bajanne
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« Reply #9 on: February 29, 2012, 12:16:22 PM »

A belated welcome to our community, Alchemist!   Please keep reading and keep posting.  This is a wonderful place for information, support and encouragement.




Bajanne, Moderator
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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;
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