Finished!

I finished my official cancer treatments on October 6th, the day after I did the Run for the Cure. I am still taking hormone treatment for the next 10 years (yes, 10 years!!) but the official, go to the hospital, major side effects treatments are done! It was a weird mix of emotions, happy, excited, yet nervous and unsure what to do next. My life for the past 10 months was focussed on doctors appointments and waiting for the next treatment or appointment, others telling me where I had to be and when and everything else revolved around that, but now I have to figure out how to get back to my “regular life”. Other women who have had cancer and finished their treatments told me they had the same feelings, some just a general unsettled feeling, others became very depressed. So far I’m still just feeling unsettled, many days I feel like I’m forgetting something like I should still be going to the Tom Baker and am missing something. Hopefully that will go away but after going there every single day for a month I guess it is a natural feeling.

Fortunately the wonderful resources at the Tom Baker (and I’m assuming other cancer centres across the country) do extend to helping with the transition back to regular life. Throughout this blog I will mention the amazing resources and assistance available in Canada for those dealing with cancer. So far I have only attended the transition post-treatment session but there are also other education sessions both at Tom Baker and other organizations like Wellspring, books at the library at the hospital and access to therapists if needed.

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The side effects from cancer treatments can also last for a long time after treatment is done. I still have a number of them, some still from chemotherapy which I finished in May, some from surgery and radiation. I won’t get into them on this post, but I mention it here as it is not just the emotional effects that occur at the end of treatment but the physical ones are still lingering.

Anyways, I guess time will tell how I will feel about everything going forward. As one friend told me, it is just now that I have the time to really deal with and understand what I’ve gone through because I have been focussed on making it through treatment, and that I need to cut myself some slack and take the time to absorb what has happened. Most people call it a journey, which it is, and it is one I’m not done with yet, even though I am technically done with treatments. So the journey continues, wonder where it will lead?

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About Laurie

I was diagnosed with breast cancer in November 2013. I was 39 years old and I couldn't believe it. Fortunately my doctor is amazing and I started treatment within 3 weeks of receiving my diagnosis. All of a sudden I was off work and my life became a whirlwind of doctor's appointments, blood tests and treatment. I immediately went into survival mode, I did what the doctors told me, went to my treatments and otherwise basically tried to ignore what was going on. I tried not to spend too much time thinking about what the diagnosis meant, although that was nearly impossible to do most days. As part of that, other than what the doctors told me, I didn't do any research and didn't want to talk about it. I spent most of the first two months doing nothing but watching TV and going to appointments. After the shock started to wear off I realized I wanted to know more about what was happening but there wasn't enough information available on the little things, those crazy side effects no one tells you about, or for younger people with cancer (young in the world of cancer means under 50). I also decided I needed to start doing more things to help make me happy other than just watching Harry Potter movies and Downton Abbey. One way I made it through was to still try and do the thing I love which is travel. Everyone needs to find something or someone they can turn to during their cancer journey, their happy place that makes them smile and feel like themselves. I had two things, traveling and spending time with my nieces. As a result, in my posts where I don't have a specific photo related to the post, I will be posting pictures from the trips I have taken since my diagnosis because they make me smile and hopefully they will make readers smile too. I'm writing this blog to share those experiences with others, to provide information on those annoying side effects you don't know about until you are in the whirlwind, and to share how I made it through which will hopefully help others, particularly younger people, who are diagnosed with cancer.
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