2.07.2013

To Be, Or Not

Yesterday, my seatmate at dialysis talked to his doctor about planning on NOT coming back to dialysis because the site in his arm is so pitiful and they spend about an hour trying to get it to work and the blood flow to be adequate enough to dialyze.  I instantly went back to when my Dad had the same conversation.  On the 10th of December, 1993, the docs told him they had fixed all they could fix and this was the last spot on his body that could be stuck with the two needles required in dialysis.  That was a Friday and it was my older Army son's 21st birthday, stationed in South Korea.

Dad announced to us on that Friday that he wasn't going back to dialysis.  Nine days later, he died, after spending a little over a week indulging in everything the center said he should avoid.  Coffee.  Nuts.  Strawberries.  Orange juice.  All the liquid he wanted to consume.  He was happy and actually the healthiest I had ever seen him.  Whenever Hospice came in to do his vitals, I wondered if he was making the right decision - but in the end, yes.  I think it was the right decision.  He had little quality left to his life.  Sleeping most of the day.  Being confused when he was awake - thinking that whatever was on television was happening in reality.  Using a walker.  Wetting himself.  Not being able to eat much of anything and then throwing up when he did.

So - I related to my neighbor but was sad about it too.  This one decision (to not come back because our sites quit working) is one we all face eventually.  So far for me - I'm doing great.  It's been three years (thirteen for my neighbor).  Transplant is the only saving grace and for my friend that is not an option.  He is too ill, veins too wrecked, to handle a transplant.

Then today I got a letter from the transplant center stating that I was **back** on hold because my finances will not be able to handle one of the non-covered anti-rejection drugs I am required to take.  With my insurance, that one particular drug is still $550 out-of-my-pocket a month.

It's daunting to think that maybe I'll have to make this same decision some day.  To not go back to dialysis.

2.04.2013

Writing About Nothing

Sheesh - I've written nothing in the new year.  Bet you think I fell off the earth or something.

I cannot believe how time flies when I have nothing but mundane things to do with my day - all boiling down to dialysis.  I really, really try not to make it a priority in my life but on the other hand, it is a necessary evil to make it my number one focus.  There's all that food to NOT eat.  There's the blood pressure.  The heart rate.  Will the sites work TODAY.  And then, after having my kidneys removed, there's all that water to NOT drink.  The rule of thumb for my little food diary is, "if you like it, you can't have it."  Foods with potassium (think any citrus fruit, chocolate, dairy).  Foods with phosphorous (meat, eggs, dairy, actually anything you can think of).  I am limited to 20 oz of fluid a day (including soup, jello, ice cream, ice, alcohol).

I am my own bobblehead.

I plan out my food and liquid.  So - if I have dinner with the girls on Wednesday - I won't eat all day but I'll enjoy a steak and salad with my friends AND a coveted cocktail.  Lemon Drops are only 4 oz.  Woo Hoo.

In the meantime, I'm not writing.  Why is that?  Things have shifted so much in my life and the creativity gene just isn't functioning.

Just know that I am plugging along and actually feeling darned healthy!  If I could just have a second brain to worry about all that icky potassium and phosphorous and sodium stuff.