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Author Topic: Facts on kidney Diseases  (Read 5869 times)
kitkatz
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« on: June 21, 2008, 04:26:21 PM »

I am working on a speech on kidney disease and why people should get checked. I need some interesting facts about kidney diseases. I want to make it important to get checked out by a doctor.
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lifenotonthelist.com

Ivanova: "Old Egyptian blessing: May God stand between you and harm in all the empty places you must walk." Babylon 5

Remember your present situation is not your final destination.

Take it one day, one hour, one minute, one second at a time.

"If we don't find a way out of this soon, I'm gonna lose it. Lose it... It means go crazy, nuts, insane, bonzo, no longer in possession of ones faculties, three fries short of a Happy Meal, wacko!" Jack O'Neill - SG-1
pelagia
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« Reply #1 on: June 21, 2008, 05:06:32 PM »

From the PKD Foundation site: http://www.pkdcure.org/AboutPKD/ADPKD/tabid/218/Default.aspx

"ADPKD: Autosomal Dominant Polycystic Kidney Disease
 
Autosomal dominant polycystic kidney disease (ADPKD) is one of the most common, life-threatening genetic diseases, affecting 600,000 Americans and 12.5 million people, worldwide. ADPKD affects more people than Down syndrome, cystic fibrosis, muscular dystrophy and sickle cell anemia combined.
 
ADPKD causes fluid-filled cysts to grow on the kidneys. Over time, these cysts multiply and grow, causing kidney failure in 50 percent of cases. Dialysis and transplantation are the only treatments for kidney failure. There is no treatment or cure for PKD.
 
ADPKD affects 1 in 500 newborns, children and adults regardless of sex, age, race or ethnic origin. It does not skip a generation. Parents with ADPKD have a 50 percent chance of passing the disease on to each of their children.
 
Common symptoms of ADPKD include high blood pressure, pain in the back, side or stomach, blood in the urine, kidney stones, frequent urinary tract infections, a family history of kidney problems, heart problems or strokes. Anyone experiencing one or more of these symptoms should see a doctor."
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As for me, I'll borrow this thought: "Having never experienced kidney disease, I had no idea how crucial kidney function is to the rest of the body." - KD
Meinuk
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« Reply #2 on: June 21, 2008, 05:31:03 PM »

Kitkatz,

I'd go with the numbers  I found some outdated numbers on a FDA website

Approximately 217,000 Americans who receive ongoing dialysis, at an annual cost of $11.1 billion nationwide.

But there are also some studies that are saying that this population is growing by 7% annually

(Please correct me if my numbers are off, I jut did a quick search)

More important, lifestyle modifications can lessen impact on the kidneys if they are caught early.  Low Protein Diet, Controlling Blood Pressure, Controlling Diabetes etc.  Proper medical care can identify your risk, and maybe slow deterioration.  Once you have lost your kidney function well...  we all know what happens.

In these days of fast food, preservatives, sedentary lifestyles, well, our kidneys can become casualties to our lifestyles.  We need to treat them with care.  (even with genetic diseases like mine, I could have done better and bought a bit more time...)
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Research Dialysis Units:  http://projects.propublica.org/dialysis/

52 with PKD
deceased donor transplant 11/2/08
nxstage 10/07 - 11/08;  30LS/S; 20LT/W/R  @450
temp. permcath:  inserted 5/07 - removed 7/19/07
in-center hemo:  m/w/f 1/12/07
list: 6/05
a/v fistula: 5/05
NxStage training diary post (10/07):  http://ihatedialysis.com/forum/index.php?topic=5229.0
Newspaper article: Me dialyzing alone:  http://ihatedialysis.com/forum/index.php?topic=7332.0
Transplant post 11/08):  http://ihatedialysis.com/forum/index.php?topic=10893.msg187492#msg187492
Fistula removal post (7/10): http://ihatedialysis.com/forum/index.php?topic=18735.msg324217#msg324217
Post Transplant Skin Cancer (2/14): http://ihatedialysis.com/forum/index.php?topic=30659.msg476547#msg476547

“To doubt everything or to believe everything are two equally convenient solutions; both dispense with the necessity of thought.” - Henri Poincare
Bill Peckham
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« Reply #3 on: June 21, 2008, 05:49:02 PM »

Kitkatz,

I'd go with the numbers  I found some outdated numbers on a FDA website

Approximately 217,000 Americans who receive ongoing dialysis, at an annual cost of $11.1 billion nationwide.

But there are also some studies that are saying that this population is growing by 7% annually

(Please correct me if my numbers are off, I jut did a quick search)

More important, lifestyle modifications can lessen impact on the kidneys if they are caught early.  Low Protein Diet, Controlling Blood Pressure, Controlling Diabetes etc.  Proper medical care can identify your risk, and maybe slow deterioration.  Once you have lost your kidney function well...  we all know what happens.

In these days of fast food, preservatives, sedentary lifestyles, well, our kidneys can become casualties to our lifestyles.  We need to treat them with care.  (even with genetic diseases like mine, I could have done better and bought a bit more time...)
That's some old data Anna. We're up to about 390,000 on dialysis about 170,000 living with a transplant. You have to adjust the latest figures from the USRDS to come up with today's numbers - the latest data from the USRDS is 2006.

Here is a good link for your talk http://www.webmd.com/news/20071106/13percent-of-americans-have-kidney-disease
You can use the 1 in 8 Americans have CKD and most don't even know it.
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kitkatz
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« Reply #4 on: June 22, 2008, 10:41:29 AM »

Thank you all for the info.  Does anyone else have any other startling statistics they want to share?
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lifenotonthelist.com

Ivanova: "Old Egyptian blessing: May God stand between you and harm in all the empty places you must walk." Babylon 5

Remember your present situation is not your final destination.

Take it one day, one hour, one minute, one second at a time.

"If we don't find a way out of this soon, I'm gonna lose it. Lose it... It means go crazy, nuts, insane, bonzo, no longer in possession of ones faculties, three fries short of a Happy Meal, wacko!" Jack O'Neill - SG-1
Zach
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« Reply #5 on: June 22, 2008, 12:10:27 PM »


In these days of fast food, preservatives, sedentary lifestyles, well, our kidneys can become casualties to our lifestyles.  We need to treat them with care.  (even with genetic diseases like mine, I could have done better and bought a bit more time...)


One of the most important points to be made.
 8)
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Uninterrupted in-center (self-care) hemodialysis since 1982 -- 34 YEARS on March 3, 2016 !!
~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
No transplant.  Not yet, anyway.  Only decided to be listed on 11/9/06. Inactive at the moment.  ;)
I make films.

Just the facts: 70.0 kgs. (about 154 lbs.)
Treatment: Tue-Thur-Sat   5.5 hours, 2x/wk, 6 hours, 1x/wk
Dialysate flow (Qd)=600;  Blood pump speed(Qb)=315
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"Living a life, not an apology."
twirl
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« Reply #6 on: June 22, 2008, 12:16:00 PM »

kitkatz           most people do not know they have PKD
                    some evil people like me spread it to their children and grandchildren
                    so the evil never stops
                   
               
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monrein
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« Reply #7 on: June 22, 2008, 01:02:32 PM »

TWIRL, am I gonna have to come down to Texas in the heat I can't stand just to beat you up myself so you will stop doing it to yourself????  AARRGGHH girl, what am I gonna do with you.
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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
Meinuk
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« Reply #8 on: June 22, 2008, 01:07:13 PM »

Twirl,

You are not evil.  Don't beat yourself up.  I am second generation PKD.  My mother knew it was genetic, and was told not to have another child.  She was on the pill and in denial when she found herself pregnant with me.  Even though I've had to make some rather difficult life choices, I wouldn't have my life any other way.  It all works out in the end.

So, give yourself a break, love and educate your children and enjoy being alive.  Life is too short for regrets.
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Research Dialysis Units:  http://projects.propublica.org/dialysis/

52 with PKD
deceased donor transplant 11/2/08
nxstage 10/07 - 11/08;  30LS/S; 20LT/W/R  @450
temp. permcath:  inserted 5/07 - removed 7/19/07
in-center hemo:  m/w/f 1/12/07
list: 6/05
a/v fistula: 5/05
NxStage training diary post (10/07):  http://ihatedialysis.com/forum/index.php?topic=5229.0
Newspaper article: Me dialyzing alone:  http://ihatedialysis.com/forum/index.php?topic=7332.0
Transplant post 11/08):  http://ihatedialysis.com/forum/index.php?topic=10893.msg187492#msg187492
Fistula removal post (7/10): http://ihatedialysis.com/forum/index.php?topic=18735.msg324217#msg324217
Post Transplant Skin Cancer (2/14): http://ihatedialysis.com/forum/index.php?topic=30659.msg476547#msg476547

“To doubt everything or to believe everything are two equally convenient solutions; both dispense with the necessity of thought.” - Henri Poincare
monrein
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Might as well smile

« Reply #9 on: June 22, 2008, 01:09:18 PM »

Anna got it right.  Anna for president, Twirl for VP. :cuddle; :cuddle;
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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
Romona
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« Reply #10 on: June 22, 2008, 02:51:24 PM »

Not all Primary Care Physicians know the markers of kidney disease. The National Kidney Foundation is trying to make PCP's more aware of what numbers to look for. One of my doctors a retired Air Force doc, told me fatigue was the most common complaint. He had many guys have to go on dialysis the same day he diagnosed them. Just something I thought I'd share but not really startling for your speech.
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RuthWells
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« Reply #11 on: June 22, 2008, 05:09:40 PM »

kitkatz most people do not know they have PKD
 some evil people like me spread it to their children and grandchildren
 so the evil never stops

Twirl, I've seen a couple of threads now where you call yourself evil for having had children when you knew you had this disease.  I see other members are doing a very good job of telling you that that's baloney, but I want to add my perspective.  I have two beautiful children, one of whom has been diagnosed with PKD.  Yes, I knew I had PKD when I made the choice to have children.

Every time you call yourself evil for choosing to have had children, you are also condemning every other member of this board with PKD who chose to have children, and THAT offends me.  So please knock it off!

I am heartsick that my son has been diagnosed with PKD, but rather than beat myself up about it, I choose to FIGHT.  Last year I raised $9,000 for the PKD Foundation, and plan to break that number this year.  By the time my son is grown, there will be a CURE to PKD, or I will die trying.
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