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Issabella
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« on: July 14, 2009, 12:48:03 PM »

Hello everyone. I am 24 years old and have Kidney failure. In November, I was feeling very fatigued and had extreme bruising. I was not sure what was wrong and did not have health insurance, so was reluctant to go to the doctor or hospital. The final straw was when my entire body started to itch constantly and I started to swell in my ankles. I went to a doctor in my area and told her my symptoms. She seem liked she was reluctant to draw blood considering how young I was and she probably thought nothing was wrong. She told me she would speak to me in about a week about the results. Well, we got a call later that night and she told me I was very sick and needed to go to the ER. She really did not give me and insight on what it could be, so me and my fiance went to the ER and that was the beginning of everything.

I went to the ER and they took my blood and were shocked at the results. I obviously had renal failure and the doctors could not believe that I was actually able to function. I was going to work, school, and taking care of my 3 year old boy. They did a biopsy and found that my kidneys were basically completely destroyed. They had no clue on how it happened and still really do not know because it was so far gone. They figure that it had been a problem for a long time. I stayed almost two weeks in the hospital where they started me on dialysis. I was going to the center for it 3 times a week 4 hours a day until I got on PD.

PD totally fits my lifestyle where I am basically able to do anything I want. I am not sure what I would do without my fiance through this whole thing. He has been so supportive and I owe him so much. We have been together for 5 years and plan to get married as soon as possible. About a month ago my son was having some issues and we took him to the doctor. My fiance made them take a urine test and we found that he is spilling protein. His kidney function is completely perfect and we did an ultra sound on his kidneys and they look good as well. We have taken him to a nephrologist and they are gonna see if it goes away because it is common in little boys. If it does not though, we are gonna have to do a biopsy on his kidneys. My doctors are very interested if my son receives a bioposy because it will hopefully give some insight on my condition.  I am just thankful that we caught it in time so hopefully my son does not have to go through the same thing as i am.
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circleNthedrain
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« Reply #1 on: July 14, 2009, 01:07:44 PM »

Welcome Issabella!  Sorry you are going through this at such a young age, or ANY age, fot that matter.  I'm glad you have your fiancee to support you through this.  I too was diagnosed with ESRD at 24 with unknown cause, started hemo but switched to PD, which I did for 10 years.  Best of luck to you on this journey....glad you found this website!
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1979 Diagnosed with kidney failure
1979 Right arm fistula
1979 Start hemodialysis
1980 CAPD catheter
1980 Start CAPD
1989 Cadaveric kidney transplant
1995 2nd cadaveric  kidney transplant
2007 Start hemodialysis
2010 Still drawin' wind
dwcrawford
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Getting the heck out of town.

« Reply #2 on: July 14, 2009, 01:49:24 PM »

I am amazed what some people go through and have gone through at such a young age.  It is hard not to feel grateful for having this later in life (though feeling grateful about it at all is hard to do too.  lol)

I am amazed at  some of the people in here, including Circlethedrain, and how they have managed.  I'm sure they can be an inspiration to you too.
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Come to think of it, nothing is funny anymore.

Nothing that I post here is intended for fact but rather for exploration into my personal thought processes.  Any slight, use of words with multiple connotations or other percieved insults are totally unintended.  I reserve my insults for private.
Romona
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« Reply #3 on: July 14, 2009, 08:02:12 PM »

 :welcomesign;
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oswald
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« Reply #4 on: July 14, 2009, 09:30:42 PM »

 :welcomesign;
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ESRD 11/95
1st Transplant 7/1996 (failed; Nephrectomy 12/1996)
2nd Transplant 3/1999 (lasted 6 years)
3rd Transplant 5/2007 (lasted 4 years)
Maxridex
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« Reply #5 on: July 15, 2009, 04:54:46 AM »

Welcome Issabella.
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'' Never give up '' & '' You will never walk alone ! ''

* ARSENAL FC for life *
* AVRIL LAVIGNE FAN *

Feel free to contact me on my msn.
matthew_as123@hotmail.com
MandaMe1986
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« Reply #6 on: July 15, 2009, 10:24:25 AM »

Happy to have you Issabella.  I hope we can get to know each other. I am 23 have been sick for a few years now and not yet on Dialysis. But yeah sure we will see eachother around.  :welcomesign;
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Blessed are the poor in spirit, for theres is the kingdom of heaven.
Blessed are they who mourn, for they will be comforted.
Blessed are the meek, for they will inherit the land.
Blessed are they whohunger and thirst for righteousness, for theywill be satisfied.
Blessed are the merciful, for they will be shown mercy.
Blessed are the clean of heart, for they will see God.
Blessed are the peacemakers, for they will be called children of God.

Matthew 5:3-9
peleroja
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I have 16 hats, all the same style!

« Reply #7 on: July 15, 2009, 12:39:44 PM »

Welcome to the group, from another PDer.  Lots of good info here.  Come on back and post often.
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cariad
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What's past is prologue

« Reply #8 on: July 15, 2009, 01:15:50 PM »

I am so glad you went to your doctor before it was too late!

Best of luck to you and your little boy. Hooray for your fiance! What a star!

 :welcomesign;
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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
willieandwinnie
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« Reply #9 on: July 15, 2009, 02:45:20 PM »

 :welcomesign; Issabella. You have been through so much in your short life, hopefully a transplant will be in your future. We are so happy you found us, we have tons of information and even more support to offer here. Your fiance sounds like a gem, give him a big hug from me and please post often.  :cuddle;
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"I know there's nothing to it, but I want to know what it is there's nothing to"
Hanify
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Hadija, Athol, Me and Molly at Havelock North 09

« Reply #10 on: July 15, 2009, 04:33:20 PM »

Nice to meet you.  Stay in touch.  Good luck with your little one.
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Diagnosed Nov 2007 with Multiple Myeloma.
By Jan 2008 was in end stage renal failure and on haemodialysis.
Changed to CAPD in April 2008.  Now on PD with a cycler.  Working very part time - teaching music.  Love it.  Husband is Paul (we're both 46), daughter Molly is 13.
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