Showing posts with label CT scans. Show all posts
Showing posts with label CT scans. Show all posts

Thursday, 25 October 2012

news news news

1. Had the new CTs and all is well for now.
2. Had a terrible meeting with the oncologist that ended in a pool of tears and anger.
3. Had the avastin without the other chemo drugs. It is much better.
4. Had a nice party for the end of this year's chemo circle.

Wednesday, 8 August 2012

2nd of the 2nd of the 2nd!

Yesterday was the second chemotherapy, of the second circle of chemotherapies, of the second time I got cancer. Hihi. Fun times...
However, my scary scary doctor that enjoys telling me always the <<truth>>  ,(quoting: "well, if you have five more metastasis next time, evidently this chemo isn't working and (subtext) you're screwed...") said that the last CT's are good. Which means they are veery good. Weeee! Good for him also because I experience a terror inflicted nausea in his office and recently I was ready to puke on his doorstep. He just dodged a bullet there.
I don't know why he always has this deadly seriousness and he prefers to highlight the difficulties, the bad chances, the worst case scenarios. Yes dear, by now I have realised exactly where I stand. But, please , do not drain my hope, do not scare me more. Give me a reason to keep up, inspire me, help me, sympathise with my pain, be my real doctor. In my case, statistics are not good, so I need all my strength and courage. I need to fight and if you, my doctor, do not believe in me, you hurt my morale, you make me stumble, you demotivate me.
Just don't take my hope away...

Sunday, 5 August 2012

Something broken.

While I was waiting for the results of my CT scans, to see what happened with the metastasis in the liver, something changed in me. All this fear of hearing potential bad news rose to a point of no comparison. I feel like there was a string in my heart that got stretched way too far. And then, it broke.
From that moment, I cannot connect with my feelings as I did. I am constantly searching for distractions, whatever might keep my attention so I won't think about my condition.
Maybe a part of my soul switched off, trying to protect me from falling into pieces, from having a nervous breakdown. 
Even though the news were encouraging, I will never be the same. I cannot talk any more of my pain and my fear because simply, the horror is too much to put into words. Only those that faced the same situation can understand. These are things that normally, no one touches in conversation, taboos. And yet, now I have to deal with it every day.
Don't get me wrong, I am not as desperate or as gloomy as I sound. But this blog' s purpose is to merely mirror deep feelings that I can't usually entrust to my loved ones. How can I say to my sister that looks on me for a role model that I am battling with desperation, fear, loss of faith, loss of incentive to keep fighting. How can I tell her that sometimes, I just get so tired of fighting that I am afraid I will just give up and get lost in depression?
No, I have to keep a face, be strong, be brave, be true, be more than this mortal flesh, be someone that leaves the world a better place, someone that filled a lifetime with love and caresses.
I wish to be a person radiating warmth, safety, faith, inner beauty. My body might be cut and sewed back, my external beauty gone, but I can still offer so much to my loved ones.
This is my war, and I intend to fight with teeth and nails.