I cannot sleep in this hour so to make myself sleepy. I need to fill this portion of my Blog.
Today I will tell you what..
As I always says, being a dialysis patient is never easy because you need to deal with different kinds of preventative measures. From your water intake, food input and of course your health condition.
I never like the idea of this treatment maybe because no one educate me on how this treatment will work and of what I heard about it, and when the Doctor told me that this is the last resort I have. I have no choice but to take it and envelope my life to this threatening ordeal.
Anyway, let me take you back.
This is me when I was still enjoying life and what it could offer. So I say, when I was still healthy.
And this is me in my first month of taking the treatment. The one that you see in my neck is my AVF where tubes are inserted for my blood to clean.
And this is my Fistula in my right arm. They need to transfer the outgoing and incoming of the blood for me to prevent infections. It hurts pretty bad, I know. :)
See that? That is how it needs to be done. That's the tube and my blood.
This is what I get if one of the nurse didn't do their job well. I will get a swolen arm and I need to wait for another week to use it again.
This is me during my treatment, as you can see in my right side is the machine that helps me clean my blood from toxic and it helps to take away my excess water in my blood.
The lobby where we have to wait for our turn for our treatment, bloody cold in here.
The inside of the Center.
Taken last night with my new eye glass. :)
Today I will tell you what..
As I always says, being a dialysis patient is never easy because you need to deal with different kinds of preventative measures. From your water intake, food input and of course your health condition.
I never like the idea of this treatment maybe because no one educate me on how this treatment will work and of what I heard about it, and when the Doctor told me that this is the last resort I have. I have no choice but to take it and envelope my life to this threatening ordeal.
Anyway, let me take you back.
The place where I need to be treated. (Mindanao Dialysis Center) They are equipped with the latest machine.
The center is my second home. I have my session every Monday and Thursday from 6 Pm to 10 Pm. A four hours treatment that sometimes will bore me to death. Thanks for the Tv and for the pocket wifi, it helps me a lot not to think about the long process.
To end this post, here's my selfie.
To God be the glory.
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