I have been very disturbed since the last CT-Scan results. We were progressing in such amazing ways that the sudden stop has been very unsettling. We knew it was coming. Everybody stop reacting to their Chemo cocktail at some point. 17 Chemo sessions is a lot to put the body through and expect stellar results. At some point the body just gives up and stops reacting. I am there.

The repercussions of this are not known. We live day by day not expecting much. This is not a negative feeling. You just have to learn to appreciate all things at all times.

I was lying in bed last night when the visual of walking along a precipice presented itself. I imagine a whole bunch of us walking along this precipice not daring to look down. Some stones crumble off the edge as we take our walks and fall silently into the unseen depths below us. A bit of our life chipping away? Fewer days ahead?

The edge of the precipice is crowded. Some are closer to the edge, others further up the small hill that abuts the precipice. We are all milling about, recognising some faces, talking, making new friends, contemplating, sitting in silence. We lose someone occasionally as the ground beneath them crumbles taking them in the void below. Some people congregate taking solace in the crowd, others stray farther afield treasuring their solitude. Yet others remain close to the entrance hoping against hope for a way out. The nature of the crowd changes continuously.

People move towards the precipice, as life is coming to a close, then back off as they are given a reprieve of sorts, more time. Time for whatever you think deserves it.

In the distance you see a wall behind which there are suitcases and backpacks and purses and containers. Everyone comes here with their baggage, real or imagined. They topple to their fate leaving it all behind. It accumulates gathering dust, rotting into the ether, a reminder of sorts. I will let your imagination sort that one out. There are tags on everything identifying the owner, some still with us, others long gone. The dust of time hangs heavy in the air. No one ventures further in.

Should you dare look down into the precipice, you will see nothing. Deep, cavernous, never ending, the sides shrouded in mist. People toppling over in silence. No screams or shouts of surprise at the fall. If you listen carefully, you might hear a heavy grateful sigh. A soul leaving the body perhaps, a sigh of gratification maybe.

There is a sense if resignation amongst the crowd. No one has given up. There is no sadness. The inevitable fall is staring us in the face. Yet, we mingle, compare notes, talk, laugh and make the best of it. No longer a question of why but rather one of when?

The first did not have an answer, and the second is no better.

I found myself being really short tempered for a couple of weeks. It seemed to pass once the Neulasta kicked in. Maybe there was a connection?

The effects of life on the brain and emotions is staggering. I am not sure if those are the right expressions, but it seems you sometimes have little control for what goes on in your head and how it manifests itself. Everyone around you is really careful not to say anything that might upset me. Yet, there it is, the short temper coming out when the phone rings and people say stupid things to you.

One of my pet peeves is the security questions that people like Hydro ask you. What is your name? And now for security reason, we have to verify some information. Your address, postal code and phone number. All three pieces of information are public. Open the phone book. All there. Hardly security questions. I found myself getting more upset than usual at these inane questions. Also at sales people calling from Florida trying to sell me new doors and windows. Insane.

The honeymoon is over. This is a bit like a marriage. At some point you wake in the morning and realise a new normal has set in. Like it or not, this is your new life. Adjust. Get on with it.

I am not in any way, shape, or form, minimizing my plight and the chronic condition I am in. The past two weeks have really brought home the fact that it this is the future. We have to get on with our lives. This means that Janet has to get out more often. People have to be a bit less careful around me. I have to get accustomed to going for naps in the afternoon. I went for a drive this morning to buy bread and stuff for the house. Drove Leslie to her dinner party in the evening. I can do these things, and come home in one piece.

I am not being rushed to hospital for anything. I am as healthy as a cancer patient can be. My immune system appears to be very strong in spite of the cancer. No, it is not easy, but this is the new life. A combination of hospital visits to see Doctors, or get treatments. Then a week of good strong health.

The mother of one of Leslie’s friends died the other day. The mother of one of Janet’s cousins died the other day as well. Somehow, these episodes appeared more dire to me than what I am going through. Seems strange to say this, but all of a sudden, I thought, how terrible. My life went into the background. Theirs seemed so much more important.

I am making plans. Thinking of the future. It’s all good. Not that much energy to carry things out, and a bit scared about that. How can you start a project and do it only every two weeks? But there are options, and most of them can be done online.

Option 1. Become a WordPress expert of some sort. Create themes and plugins that I can sell to others. Maybe set up blog s for people. Others are doing it, and I can to. Certainly fits in nicely with my background. I just need to gain some expertise in WordPress. There are lots of books out there. Also need to become better at markting the blogs. But all that comes with practive and a lot of reading.

Options 2. Become a therapist of sorts to help others with chronic conditions. Take some online courses.

Option 3. A lot of people are pushing me into the art world. Daryl just bought me a wonderful water colour paint set, including paints, brushes, and paper. Included in the package is a free course from her sister who is a painter of some repute. I could become a painter, and incorporate my pictures, and maybe even some calligraphy. The possibilities are endless.

Al I need now is the courage of my convictions to do something. I cannot carry on like this for very much longer. The healthier I get, the more urgent is the need to do something, anything. Word Searches can only help so far.

One more thing, I have not shaved my head yet. It is thinning out, but there is still so much of it, that most people cannot tell I am losing it. For now, the hair stays.

© 2010 I Have Cancer Suffusion theme by Sayontan Sinha