Showing posts with label Kidney. Show all posts
Showing posts with label Kidney. Show all posts

Monday, 16 April 2012

Polycystic Kidney Disease And Peritoneal Dialysis

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I have PKD, Polycystic Kidney Disease, and in September of 2008 I started on peritoneal dialysis. In 2006 I was referred to Dr. Samuel Schorr, a Nephrologist here in Calgary where I currently live. I started with Haemodialysis in May 2008, I found the treatment to be effective, but time consuming, and felt I could do more for my own treatment. I decided to try peritoneal dialysis, it is a much gentler treatment, and can be done by myself at home. I had a catheter surgically inserted into my peritoneal cavity in the summer of 2008 at Foothills Hospital, and took training at the Col. Belcher Hospital (one of the last through there, there was moving schedules on all the notice boards, they tore the building down shortly after, it's dated from WW1, they had built the Sheldon Chumir Medical Centre to replace it, that is where I go now) at the end of August for peritoneal dialysis, followed by training for nocturnal peritoneal dialysis, the cycler.

I would start each day by draining the solution that had been in while I slept. I would then empty a 2 litre bag of Dianeal (1.5% or 2.5% sodium and water) solution into my peritoneal cavity, my stomach. That is good for 4 to 6 hours. I would take a 2 litre bag to work and do an exchange sitting at my desk during lunch, an exchange took about 40 minutes, and I could sit at my desk and work while doing this. I would do another exchange when I got home from work, clean my house, then do my last exchange before bed. This time I would use an Extraneal solution, 7.5%, that would last for 12 to 16 hours, while I slept. In the morning, repeat, no days off on Peritoneal Dialysis.

I only followed this routine for a couple of weeks, then I started on nocturnal peritoneal dialysis, the cycler! You must be very careful to maintain a sterile environment while on both types of treatment, I am normally a slob, but my apartment was very clean while doing this. I would scrub for at least one minute before doing an exchange, and I would wear a mask. When you swap bags you are exposing your stomach to the outside air, full of nasty things your tummy is never supposed to see, so you must be clean, and quick!

My name is Will Lake, I kive in Calgary, Alberta. I am divorced with three grown sons, and I inherited a chronic condition from my father, Polycystic Kidney Disease. I had a kidney transplant in 2009, the donor was my mother. I have been working with Internet Income University on developing my Internet Marketing skills, Internet Income University prides itself in offering an Honest, Ethical, and Legitimate online education experience. Please check my website: http://wclake.com/

Saturday, 14 April 2012

Polycystic Kidney Disease and Haemodialysis

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AppId is over the quota

I have PKD, Polycystic Kidney Disease, and in May of 2008 I started on Haemodialysis. In 2006 I was referred to Dr. Samuel Schorr, a Nephrologist here in Calgary where I currently live. Early in 2008 Dr. Schorr had ordered a shunt to be surgically created in my left forearm, the surgeon was Dr Yilmaz; he was my transplant surgeon as well. An artery was grafted to a vein and an access was created to accommodate the needles for haemodialysis, the increased blood flow made the vein expand in diameter.

I went to the Foothills Hospital Unit 27, the haemodialysis unit, on Tuesday and Thursday evenings, and Saturday afternoon, for a 4 hour 'run' each time. I was working full time, this schedule allowed me to keep working and go for treatment. I would be connected to the machine with 2 needles in my access, over the 4 hours my blood would go through the artificial kidney (filter) about 10 times. I could not move my left arm and do nothing but watch TV or listen to music during treatment. The treatment was a bit of a shock to the body; there is a lot of fluid transfer, but the elimination of the build up of toxins in the body felt great, more vim and vigour! A big downside was that I could do nothing to help; I had trained professionals trying very hard not to hurt me while they inserted these huge needles into my access. The diet and fluids were rather restricted, you must maintain a close watch on your drug interaction, treatment is cyclic in nature, and you didn't feel that good when you went back in for treatment due to the build up of toxins, time to scrub the blood and feel good again.

I was able to travel and get treatment while on vacation. My youngest step-son was graduating from Diamond Jenness High School in Hay River, NWT, and I had a 'run' in the new dialysis unit at H.H. Williams Hospital, operated by my old friend Roger. We had a good visit while I had my blood cleaned, enjoyed the graduation, almost got kicked out of my campsite! I then drove to Penticton, BC, to visit my mother, and went for two 'runs' while there. I did have to fax ahead and reserve space, and was lucky to get into Penticton on rather short notice, 6 weeks!

I was on this treatment for about 4 months, I was then on Peritoneal Dialysis for about 10 months, I then had a successful Kidney Transplant, the donor was my mother.

My name is Will Lake, I kive in Calgary, Alberta. I am divorced with three grown sons, and I inherited a chronic condition from my father, Polycystic Kidney Disease. I had a kidney transplant in 2009, the donor was my mother.
I have been working with Internet Income University on developing my Internet Marketing skills, Internet Income University prides itself in offering an Honest, Ethical, and Legitimate online education experience. Please check my website: http://wclake.com/