Saturday, March 26, 2011

The graphic and gory...not for the squeamish

As I have mentioned in a previous post I was going to show photos of my scar so here they are in all of the graphic glory.

I feel it is important for me to keep a record of it all so that I can see how the healing and the scars developed.

The first couple show the radiation "sunburn" and my operation site. As my lump was relatively small it is hard to actually see it in a photo.

One photo in the radiation shots has the surgeon's scribble showing where he planned to cut. The last two show my scar as it is today. It is no longer my "shark bite".

It truly is a wonder how our bodies heal so well and rapidly. I am extremely grateful to have had the wonderful surgeons and after care team I have had. I truly believe it is their combined efforts (as well as my own body's hard work of healing itself) that allowed me to be where I am today.

I am grateful to the following people, who at some stage have been or continue to be, part of my treatment team:

Professor Peter Choong my cancer surgeon
Mr David McCombe my plastic surgeon
The Radiation Oncology staff at Peter MacCallum Cancer Centre
Ms Kate Rogers my physiotherapist
Ms Sue Hodson my GP
Ms Meg Schibli my hand therapist
Mr Ash Tainton my gym instructor

And as always my family and friends whose love and support strengthen me :-)





Saturday, January 29, 2011

What a difference a year makes...

It is now well over one year since I first thought about using this blog and then didn't. The reasons are many and I guess my primary focus became simply living with and managing my disease.

So I have finally decided that I want to keep this record, for my own use as well as for any use that it may be to others in similar circumstances. To that end I'll go back and continue my story from D-Day and beyond over the next few sessions.

Firstly, the here and now. Where I'm at. I am pleased to be able to say that for one year post surgery to the day 29 January, I am what I learned is termed NED (no evidence of disease). I'm not sure if what people call this is also remission, I doubt it. My post surgery journey has still got seven years to go. That is how long I've got to have check ups and visits to my cancer surgeon. More on that later.

What happened and how I got here is all a story in itself. I have many wonderful people to thank for their help and support along this journey. And because I think they deserve it I will be praising them along the way. Any opinions are my own based on my experiences of medical processes, procedures, etc.

Lastly, I will be posting pictures as well. I kept a bit of a photo diary of my scars in the early days and it is amazing to see the difference. So if you're squeamish at all, please don't complain if you choose to view them.

This post is dedicated to my mother, Marina Barrientos. My constant companion and carer when I needed her most. Thanks mum!

Wednesday, October 28, 2009

The story so far...up to D-Day

D-Day (Diagnosis Day) 1st October 2009. This is the day I received "the news". It was a work day like any other...until 11am. I remember the time precisely because I checked my watch oddly enough.

To backtrack a little...almost 3 months ago I found a lump in the lower bicep area of my right arm. At first I wasn't too concerned. Maybe I'd bumped it (even though I couldn't remember that)..maybe I'd strained it at the gym (even though I knew I couldn't have)...these are some of the "maybes" that we delude ourselves with when we're in avoidance. Thankfully I don't avoid too long and I pay attention to my body. I followed up with an appointment with my GP.

The GP said she also thought it wasn't anything but to be sure and given that we have resources available to us, she sent me for an ultrasound (U/S). The U/S came back inconclusive a few days later with a recommendation for further investigation using an MRI scan.

Usually an MRI can only be requested by a specialist otherwise it's deemed non-essential incurring high cost. As it happens, I work in an area that brings me into contact with many specialist surgeons. I asked one of them for a referral MRI. Again, the scan came back inconclusive and my GP then said it was biopsy time.

Dr Anthony Penington took a look at my lump and agreed that it would be good to get a biopsy for a better look at the lump. He referred me for a biopsy using a CT scan with one of the "best people for that job" and even arranged it for me. At this stage we were just expecting a confirmation of a tumour of some description though nothing beyond that.

Having a biopsy taken by using a CT scan to pin point the entry of the needle gadget is interesting. They scan the area so they can line up the entry point, then the actual sensation of the triggered needle is like feeling a strong hole punch. They did it twice and I ended up with a small incision. I was impressed that the entry was so precise there was only the one cut.

So a few days passed and I kept meaning to ring Dr Penington's office to make an appointment to get my results or else go see my GP. I couldn't remember which of them would do it and as the saying goes "no news is good news", I figured if I hadn't heard anything all was good.

1st October, I'm in the middle of the last part of a job and get a phone call from the office. Dr Penington had been looking for me for our appointment. "What appointment?" I said to my colleague..."Oh, he says he needs to see you...where are you?" At this point, my mind started to make connections and the next few minutes are a bit blurry. I knew, as soon as I saw Tony and the serious look on his face I knew.

Myxoid Liposarcoma. My diagnosis. My lump finally had an identity. Sarcomas are a rare group of cancers. Liposarcomas are soft tissue cancers.

There was shock, there were tears. Dr Penington was able to let me know that he had already spoken to Professor Peter Choong, a leading sarcoma specialist and that I had an appointment at 1.10pm.

Welcome...

Hi and welcome...this blog will be my way of communicating what's happening in my world health wise. It will let me keep a record of events, treatments, thoughts and give friends and family an insight into what it's all about.

In Spanish:
Hola y bienvenidos...este blog sera mi modo de communicar lo que esta pasando en mi mundo y con mi salud. Sera una manera de recuerdo para citas, tratamientos, pensamientos en general y les dara a mis amigos y familia la oportunidad de leer y saber de que se trata todo esto.
Cuando es posible, escribire en espanol tanto como en ingles, me perdonan si no lo hago siempre.

Irene