At the end of March, I went back to see my surgeon for the first time since my craniotomy in January. Let me take you back to that day. The morning started out with a CT scan. When you frequent the diagnostic imaging department at the hospital this becomes routine...you know the run-down before you show up, so you can basically skip Step One: the instructional lecture from the nurse; "remove any jewellery or metal from the area being scanned, if you have buttons, zippers, or an underwire in your bra please remove your clothing and slip into one of our ultra fashionable hospital gowns (if Kim Kardashian can make it work, you can too...right?)".
Kim K is happy to be in that gown. |
When I was done at diagnostic imaging for the day, I was off to the surgeon's office where the images from my CT scan were already waiting...and yes, believe it, it is actually possible for hospitals to be efficient and prompt under the right circumstances.
My surgeon made the ever-so-slightly obvious observation that I had gotten a haircut and tried to crack a few jokes in hindsight of having a brain tumour, but it's a good thing he's intelligent, because for some reason I imagine that "funny" and "good sense of humour" would not be first on his list of personality traits.
If you've been following my journey from the beginning, you know that I was initially diagnosed with a non-malignant tumour called a Meningioma. Although the doctors seemed pretty confident in their diagnosis, they also inform you that there is no way for them to be 100% sure until you're knocked out and they're rummaging around inside your skull. Once again, very reassuring; so...my only option was to take it all with a grain of salt. Now, I like to maintain a certain degree of excitement in my life...so, naturally, the pathology results of my tumour did not lack shock value. Just as I was getting comfortable with the pronunciation of Meningioma,
I was forced to learn a bigger, scarier word: my new diagnosis. Hemangiopericytoma (say that 10 times, fast!).
This new diagnosis, luckily, is still classified as non-malignant, but makes up for less than 1% of all Central Nervous System tumours...I knew I was special!! However, having a "special" diagnosis only really means that the research on this type of tumour has been minimal and there was very little information that even the surgeon could give me about it; so I'll let you in on all I know...
I thought I was rid of this thing for once and for all when the surgeon announced that he was able to remove all of it, but here comes that shock value again...there's somewhere around a 90% chance that my archenemy and I will meet again somewhere down the road, and a possible chance of it metastasizing (a.k.a. spreading or growing {it's okay, I googled the definition too}).
I'll be back at the hospital for regular MRIs to monitor any unwanted growth. I'm in good hands and will continue to keep my head up. I've conquered this thing once, I'm determined to do it again if need be.
Now, here comes my shameless plug for a charity that has become so important to me in the last 8 months.
On May 3rd, 2014, my family and I are participating in the Spring Sprint for the Brain Tumour Foundation of Canada. Any and all donations make a difference. To sponsor us and the BTFC, you can click here.
If you've been following my journey from the beginning, you know that I was initially diagnosed with a non-malignant tumour called a Meningioma. Although the doctors seemed pretty confident in their diagnosis, they also inform you that there is no way for them to be 100% sure until you're knocked out and they're rummaging around inside your skull. Once again, very reassuring; so...my only option was to take it all with a grain of salt. Now, I like to maintain a certain degree of excitement in my life...so, naturally, the pathology results of my tumour did not lack shock value. Just as I was getting comfortable with the pronunciation of Meningioma,
I thought I was rid of this thing for once and for all when the surgeon announced that he was able to remove all of it, but here comes that shock value again...there's somewhere around a 90% chance that my archenemy and I will meet again somewhere down the road, and a possible chance of it metastasizing (a.k.a. spreading or growing {it's okay, I googled the definition too}).
I'll be back at the hospital for regular MRIs to monitor any unwanted growth. I'm in good hands and will continue to keep my head up. I've conquered this thing once, I'm determined to do it again if need be.
Now, here comes my shameless plug for a charity that has become so important to me in the last 8 months.
On May 3rd, 2014, my family and I are participating in the Spring Sprint for the Brain Tumour Foundation of Canada. Any and all donations make a difference. To sponsor us and the BTFC, you can click here.
(We'll be participating at the Kitchener-Waterloo event)
I know what it's like to be one of the 27 Canadians that gets diagnosed with a brain tumour daily. Donate in memory or honour of those who have had stories similar to mine.
No comments:
Post a Comment