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A Dialysis Journey


 Do You Know Why You Are Ill?
 


I don’t know what you believe; each to their own.
I believe in God, I’m on a spiritual path instead of a religious one.
A friend sent me this
and it fits here.

I asked God to take away my habit.
God said, No.
It’s not for me to take away, but for you to give it up.

I asked God to make my handicapped child whole.
God said, No.
His spirit is whole; his body is only temporary.

I asked God to grant me patience.
God said, No.
Patience is a byproduct of tribulations; it isn’t granted, it is learned.

I asked God to give me happiness.
God said, No.
I give you blessings; Happiness is up to you.

I asked God to spare me pain.
God said, No.
Suffering draws you apart from worldly cares and brings you closer to Me.

I asked God to make my spirit grow.
God said, No.
You must grow your own! But, I will prune you to make you fruitful.

I asked God for all things that I might enjoy life.
God said, No.
I will give you life, so that you may enjoy all things.

I asked God to help me love others, as much as He loves me.
God said, Ahhhh, finally, you have the idea.

“Suffering draws you apart from worldly cares and brings you closer to Me.”
This line is the reason I put this post here.
This IS what suffering does.
This IS why I am ill.
I had to learn.
And, I am still in the process,
because I am still here!

Read it again . . .

thank you
Mandala

Any questions?


Posted by Mandala at 1:14 PM - 2 Comments   Add a Comment  
 

 My Drugs . . .
 

One of the things that ill people do have to deal with is drugs. They can get changed often; but, the more time you spend in your illness the more stable the drugs become. I thought I’d list mine here just to give you an idea:

Epoetin is given via the machine, it has to do with my physical strength and how I feel as is
Iron
Coumadin is to keep my blood thinner so that graphs don’t clot
Aspirin is given to “all“ patients; same reason everyone should take a Bayer a day, helps regulate the heart/blood
Lexapro is the new Prozac, same reason
Lipitor to lower cholesterol
Renagel with most all food, balances the phosophorus and calcium
Reglan, I take this sometime because I have a “diabetic” stomach
Nephrovite is a vitamin designed for all dialysis patients
Zinc . . . ? don’t know what that is for
Kaexelate is a brown, grainey liquid that is taken to reduce the amount of potassium in the body
Valium on hand “if”
and two pain medications

As much as I hate being broke
being broke allows me to get my drugs for little
The medication world is far beyond me
The money .?.?.?.?
Thank God for things that HELP
I haven’t yet experienced the change that Medicare part D will be
that comes in the next week or so
we’ll see . . . .

I have taken many drugs through this process.
When I had the kidney transplant (TX) there were MANY drugs that I came home with: expensive and hard on the body. With the TX drugs my eyes immediately grew cataracts (doctor removed), my gums grew up over my teeth (my dentist took off the grown gums with laser), and I had bouts with deafness plus other things that I’m not remembering at the moment.

Any questions?



Posted by Mandala at 8:49 PM - 2 Comments   Add a Comment  
 

 Death, In One Way or Another, Is Often On My Mind
 

Not the way one would think about dying ... It sorta sneaks it’s way into the mind when something else entirely is hanging around. ... I can’t ever get settled with the subject. I think that it is strange to think about how you are going to die. By now, it should be an easy subject. That’s what old age does, or those of us who are chronically ill. I’ll think it all through plenty, then, I’ll let it go and whatever happens happens (can’t change it anyway).

I’ve been through it once (doctor telling me I had minutes to live) and at that time it was just a matter of course. But, now, there is more time between now and then.

I don’t want Leonard to be there before I’m gone (that would be waayyy tooo many tears); nor do I want “friends” that have done little more than leave me alone (I don’t want my last hours to be pissed off ones!!).

I still can not believe it: I have my leg taken off and Sally (who lives here), who had been around with me for the last several years, whom I’ve known for many, many years, and I have barely seen her since I came home from the hospital; I haven’t seen Leonard (from WV) at all; Jeff came before the surgery, came several times while I was in the hospital and then, again, at Thanksgiving; and Linda Kaye, we did dance together as children, hadn’t seen her much through the years while she was having four great girls, and she comes a long and takes me out and about ... which is great/necessary, but, doesn’t feel like a real friendship either ... you know, the kind that you just have loads of whatevers to talk about. And Billy lives in Florida, we can almost always talk all night long.

I miss people dropping in ... like it was in my twenties (please, don’t tell me the difference; I DO get it, I just don’t like it much ... I don’t mind being this age ... I just don’t like not having interesting folks around). AND, I know full well, that if I did drugs (of the recreational type) and alcohol I would STILL be having people drop in and out. I miss that sociability so much, I have OFTEN thought about going back to those recreational habits.

What do people think I’m made of? They think I can do it all ... whatever I need for myself because I always have. Only now, I’m a gazillion times slower, if I get it done at all, it puts EVERYTHING on hold.

The doctor at Duke told me friends most likely wouldn’t be around (81-82). They tend to think that illness will rub off on them. .......DUH ......... They did; and it didn’t!!!

I don’t know why I should expect these years to be so very different ... I’ve always pretty much been on my own ... everybody else is married, parents, grandparents and I didn’t go that route ... never dawned on me that I would still be here in this town where they don’t grow interesting people. Not for me, they haven’t.

Bottom line: I’m an only child, not married, no children of my own, I thought I’d be teaching in college by this age (But, nooooo!!), just on and on a life that I have been on my own. Leonard’s been in my heart for 30 years; but, nobody’s come breaking my door down, either.

I’m way too independent ... but, if that is what I am .....

Where friends are concerned, there are several, good, upclose and personal ones that I have lost ... they have just left me, no comments, no complaints, no discussion, just no longer in my life. Several; like a pattern. It’s another thing that I don’t get. That’s two BIG things that I don’t get about my life and who I am!!!



A nurse friend one time told me I didn’t need to be so strong. Especially as long as I’m on my own, I don’t have any idea how to be anything else. When I am with the right man, then I don’t have to be so strong. But, by my self, I(I) have to get it done. It’s not like I have someone to lean on either litterally or emotionally.

PLEASE ••• STOP ME NOW ••• BEFORE I KEEP ON AND ON ••• GOOD NIGHT
Posted by Mandala at 3:27 AM - 2 Comments   Add a Comment  
 

 I Do Love What I Know How To Do
 


Everything I tried to do was a battle/struggle/didn’t work out. I never have understood that about me in this life ..?
 
Maybe it was the fact that I gave up the battle. I didn’t like the battle or the struggle (professionally). Who does? Unless you are at the top and providing hassle for others, you are lower on the totem pole and are receiving battle and struggle from those ahead of you. ..........DUH

ALL I ever wanted to do was to do my work and learn how to do it better. I function very well as the second to the top. That person is hardly ever worthy of being at the top and would rather go out and about doing something of lesser value to the business he is running. ................DUH I have known of very few who have been in top positions, were truly good at it, really liked what they were doing and who they were doing it for. Some have instinctively known how to play the game and went home at the end of the day and had a good time leaving work at work.

I was serious (there’s that word again —> way too serious for my own good). Responsible ... I would stay at the office for HOURS beyond necessary because I was into working out the design of things. My partner would do it now, while I wanted another five minutes to do it better. It was that way at the TV station, too. The director didn’t care if it needed more work, he wanted it now.

I had studied, had gotten degrees, and everything I tried to do was a battle/struggle/didn’t work out. I kept on dealing with what I could do with my career, the next job, when jobs have been so very thin-pickin’s. When you hear about how to go about getting a job, one of the statements is to treat your job search as if you were working at it eight hours a day. Well, in this town, at that rate, the job search is over within a week (seriously) ... maybe, two weeks if you go and visit all those you already know within your area of search.

Like, if I wanted to work in graphics/design, I already knew the majority of designers. Maybe there would be some new positions in the new companies ..? I was, however, looking for marketing/communications that could easily include my knowledge of graphics/photography/writing and then I’m talking about maybe five to ten positions in this town. There wasn’t anything that I REALLY wanted to do. I was interested in a position or two at Centra Health (our umbrella for the majority of health business in this town).

My doctor was on the board and he said that they asked if I had enough energy ... YES! (and then some) ... BUT, nobody wanted to hire me ... didn’t want me on their insurance ... some people that worked for CH also had had transplants, etc., but they had already been working for the company before the surgery became something they had to face.

All of those examples, and a few more, left me out to dry ... (so to speak) ... and very sad that the things I know how to do well had no place in this town to show themselves. I know very well someone should have hired me. Even ill I do better than the majority.

Nothing came my way to do free lance, either. I did the SCENE Magazine for six years. I got almost nothing wage-wise. I thought I was doing myself a huge justice by doing the magazine while being on dialysis and having had a transplant. The magazine was very professional and we are both still very proud of our work. But, it lead to nothing more for either of us.

I’m thinking about the battle, .... the struggle and that I might have very well not done much of anything to move forward inspite of being an ill person. And I subsequently gave it “up for lent.”

I’m always too tired to really do a good job. I couldn’t work if anyone wanted me to cause when I’m too tired now, I have to go do something else, go lay down, and I also can’t think as well cause my brain is like mush.



Posted by Mandala at 9:14 PM - 1 Comment   Add a Comment  
 

 EARTH DAY ........ 4/22nd every year
 


E .. enjoy
A .. and
R .. respect
T .. this
H .. home

Get out and enjoy the Earth

Posted by Mandala at 8:33 PM - No Comments   Add a Comment  
 
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  About Me
Author: Mandala
From Central Virginia, USA
 
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This is to help others on dialysis or maybe chronically ill ...
 
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