Saturday, August 18, 2012

Breakfast Burrito - Low Phosphorous - PD friendly!


I'm trying to vary what my husband takes to work for his lunch, so today I made him some Breakfast Burritos.


Breakfast Burritos - PD Friendly

1 pound ground pork
1/4 teaspoon cayenne pepper
1 teaspoon ground sage
2 tablespoons of water

Mix those 4 ingredients together and refrigerate for a few hours or overnight for the seasons to flavor the pork.

6 palm sized potatoes
1 tablespoon of margarine
12 eggs

Once the pork has had time in the refrigerator, brown in a large frying pan.  After browning, drain by putting the pork on paper towels that are on a plate.

Take the 6 potatoes and cut them into fourths.  Chop them in a good processor until they are the desired size.  In the same frying pan that you used for the pork, brown shredded potatoes in margarine.

Once the potatoes are brown, add in the pork.  Scramble the eggs using a fork and then add to the frying pan.  Cook until the eggs are completely cooked, mixing most of the time to really blend everything together.

Put a spoonful inside a burrito soft shell and roll, wrap, and freeze.  It's ok if you want to eat them now too :)  The night before you want to eat them, put them in the fridge and then reheat at meal time.

You can also add any fresh veggies... tomatoes, peppers, onions... whatever you like to make it tastier!  Just remember NO cheese, unless your dietitian has said it is ok.












Friday, August 10, 2012

Supplement shakes

Hubby has been struggling with eating.  He is so tired and beat when he gets home from work, that he doesn't work to eat.  I spoke with his renal dietitian today.  She said there is only one supplemental shake that is recommended for dialysis patients and that is Nepro.  Nepro is a high protein, low phosphorus and low potassium shake.  It is also expensive.  Only one store carries them locally and that is Rite Aid.  For a box of 4 8oz shakes it is $16.


I gave the company a call and through their very friendly customer service found that they would send us some coupons for the shakes.  I also found out that for dialysis patients they offer a special price on a case of 24.  They said that the dialysis unit would need to fill out a form for the better price, but I definitely think it is worth the extra work.  Just make sure you like the shakes before purchasing a case.

Thursday, August 9, 2012

What to do with the boxes?

With everything going on with dialysis, appointments, medicine changes, and life in general, what to do with all the dialysis boxes really is a small issue, but they do tend to pile up.  We have an empty box every single day.  That is 30 boxes a month and 365 a year!

The boxes are sturdy and I hate to just recycle them, so I tried giving some away.  A few found homes, but I still end up with tons of boxes piling up.  Tonight I spent some time searching the internet for some creative ideas for using all those boxes!  Some will still end up in the recycling bin, but maybe an idea or two will appeal to you and when life slows down a little you can work on a creative project.


Find 40+ projects pinned on my Pinterest page!

Saturday, August 4, 2012

2 weeks of work

Hubby started back at work 2 weeks ago.  The first week he worked 4 days, the 5th day he had an appointment.  This week he worked 3 days, he wasn't feeling well one day and the other he had an appointment.

He did well considering.  He did come home tired, but I'm so proud of him for going.  Speaking with a nephrologist on the phone (not his), he said the most successful kidney failure patients are those that go back to work.  This was great to hear and know.  I'm not sure it is possible for dialysis patients to ever function as well as they did before kidney failure, but it is possible for them to have a good productive life.

I can't say life is "normal", because there are still countless appointments, blood tests, pills, daily dialysis, and he does suffer from fatigue, but he is alive, he is trying, and today is a good day!

*Do you have a positive story about having a good life after starting dialysis?  Would you like to share your story?  Send me an email using the email button on the right column.  I would love to be able to share some positive stories.  The entire story doesn't have to be positive, because as we know dialysis comes with it's own set of challenges, disappointments, and failures.... but if the main theme or the ending of your story is positive... I want to share it!

Thursday, August 2, 2012

It isn't an energy star

Today I got our first electric bill after using a full month of dialysis.  It was high, much higher than it normally would be this time of year.  Using the machine for 10 hours a night, every night does end up using quite a bit of electricity, especially since this isn't an energy star appliance.

I still wouldn't have it any other way.  Peritoneal dialysis is what is best for Hubby, but it is going to require quite a bit of budget changes.  If you are on a fixed income and can't handle any increases, this is something to consider.

I did call the electric company to see if there is any help at all or special programs that we can apply for, but sadly I was told no.


Monday, July 30, 2012

Not the news we wanted

Today we got a call from the hospital where Hubby "applied" to be part of the transplant program.   Our current hospital was willing and ready to start the process of getting Hubby on the transplant list (he already met with the transplant doctor), but our insurance wouldn't cover a transplant there so we had to move on to hospital C.  Today hospital C told Hubby that they won't even start the process until he is at the weight he needs to be for transplant.  He has worked hard and lost a lot of weight, Hospital B saw the progress he was making and was pleased enough to start the process.  Sadly Hospital C won't do anything, except allow him to go to the informational class, until he loses the weight.

I'm devastated.  Losing weight is difficult for the average person, but add to that not feeling well, doing dialysis, and trying to work full time.  I know he can do it, but how long will it take?  How many years will he have to continue dialysis without even the hope of a transplant?  I am thankful he has dialysis to keep him alive, but transplant has always been the goal.

I guess it will be a while before I'm able to share the transplant process with you.  I do hope you will take something away from this though.... if you are over weight, lose the weight.  Trust me, I know how hard it is, I'm fat and I hate it.... but we never know when we will need life saving medical care and it is devastating to think that weight can stop our lives from being saved.

Friday, July 27, 2012

No one said this would be easy

I don't think I believed that everything would be ok, once Hubby started dialysis, but I guess I hoped.  Each month he goes back to the hospital to meet with his dialysis team consisting of a nutritionist, dialysis nurse, doctor, social worker, and blood taker.

The doctor wasn't pleased with how his exit site is healing, but the nurse felt it was looking pretty good.  Since I clean it and see it everyday, I have seen the improvement since the surgery.  I think Hubby is just a slow healer.  Hubby is also still experiencing some issues he had before dialysis and that dialysis should have helped with, the doctor is waiting for the blood work to decide what changes will be made.

This morning we got an email from the nurse about the blood work, it isn't good news.  I'm not sure why I thought it would be smooth sailing after starting dialysis.  It is an every day challenge.  Every day there seems to be a new "thing" to worry about, think about, consider.  Don't get me wrong, dialysis is still worth it.  I have my husband alive and that makes all the rest worth it!

I mailed the packet to the new hospital on Tuesday, they should have received it on Wednesday, so now we are just waiting to hear back.

Something that I have started doing to make set up easier, that I would like to share with you.... Hubby uses two different bags a night for his dialysis.  They are each a different strength, I have started opening the boxes and putting the two bags together that he will need that night and stacking them in our bedroom.  That way I just grab the one box and get to work.  It sounds simple, but it has actually made quite a difference in setting him up each night.  Over time the prescription of the strength will change, but for now this simple step has really helped.