Co-Survivor Award: My Mom and My MAN

Way back when I was first diagnosed and wrote a profile for myself for Bumpyboobs and FacingCancer.ca, I identified myself as a survivor. Forget dictionary definitions, I defined a survivor as someone getting up every day, facing what needed to be done, learning how to thrive through uncertain realities, and living life on their terms.

My life, my definition.

So when FacingCancer.ca recently announced their Co-Survivor Award, it made me really happy to see their definition of survivorship:

We believe survivorship begins at the time of diagnosis.

And it made me even happier to see that they’ve decided to honour those who have supported us, honouring the support they’ve given.

And surrounding every cancer survivor, there are people who care: we call them Co-Survivors. Whether it’s a friend, a family member, a medical professional or an online supporter, use the form below to tell us who has made your cancer experience a little better with their selfless support.

There have been many people in my life who have helped. From friends in England, family in Canada, letters & emails from my friends during treatments, support during my crowdfunding, and the awesomeness and insight of those who get it online. But for the Co-Survivor award, if I could nominate someone (and I can’t because I work for FacingCancer.ca), it would be two someones: My husband and my mother.

Zsolt is Zsolt. You know him via this blog. He is softness and love and unconditional support. We’ve been through so much together and still we dance in the middle of the day. There’s so much to say, I really cannot begin to capture it all.

My mom, well, she’s my guide, point of reference and my friend. When I hear one thing regarding healthcare, I’ll take it to her for her opinion. And I’ll never forget how she left Canada and my dad for over a month (to sleep in our small one bedroom apartment on an air mattress in England) to help me recovering from the mastectomy – and then to help Zsolt and I weather that first terrible round of chemotherapy.

So here is the question: Who is your co-survivor, or co-thrivor, or co-awesomnesser?

award

If you live in Canada and can think of someone you’d nominate as co-survivor – then I invite you to pitch in your story over at FacingCancer.ca. Ten from the many will be chosen, and then we’ll agonize over them to land upon the first Co-Survivor recipient (but the ten will also receive goodies, too). Can you think of someone? Nominate here.

If you don’t live in Canada, and I know many don’t, but still want to share who has supported you , that’s what the comments are for ; ) People do read the comments, and they do pull inspiration from them – even folks supporting others, and needing to hear the positive impact their actions may have. Or even better – write about it on your own blog, and then link it back here. 😉

And you know what? Even if you haven’t had cancer (I hope), you may still have a co-survivor in your life, or co-supporter. I love stories about love, and about generosity, so I welcome you to leave your own reflections.

Now, that is all I have to say about that.

Except this P.S.!

P.S. I wasn’t asked or prompted to write this post for the award. I just like the idea. Everyone who does something kind for another person deserves to know their impact. This is just one really great way of saying thanks.

 

 

A Petition for #FairCancerCare

This is just one of the many reasons, and many stories lived and/or heard, that make me want to support #FairCancerCare:

When I was told it was definitely breast cancer in my lungs, I was also told it was slightly estrogen receptive. That means it kinda likes to eat estrogen. (A change from the first time, when it really liked to eat estrogen.) My options in this case involved hormone therapy.

Except I’d already been on Tamoxifen, the only breast cancer hormone therapy I know of for women before menopause, and it had stopped working.

That meant I needed to but put into menopause.

I would be put (back) on Zoladex, I was told, which is a drug that puts your ovaries to sleep. Zoladex is not covered by OHIP. The oncologist wasn’t sure if it would help, but he figured we should try that first and foremost before doing anything else. Except. . . except that monthly shot costs about 500 bucks a pop. Or I could pay 1500 a go and get the three month shot.

But insurance would pay for it.

Right?

Oh wait, you don’t have insurance? Well then, you need to have your ovaries removed via surgery.

!!

That is seriously what I was told. And if this post seems a bit fragmented in pace, it’s because to this day I’m stupefied by the solution to my struggling to afford medication – cut out perfectly healthy pieces of my body, despite there being an effective pill that could do the same thing minus the traumatic surgery.

Ultimately I was able to get onto Trillium because we’re a lower income family. Though even that has had its challenges – and of course I am grateful to have that. But for many others they end up paying loads out of pocket (not on the table here, but also worth mentioning is the cost of alternative treatments. Wouldn’t it be lovely if the cost of complimentary health care was built into our treatment plans?)

facingcancercare

Anyhow, for many, many reasons, I want to direct you to #FairCancerCare, an online petition for Ontario healthcare that moves for more treatment coverage. They want to gather signatures before the provincial election to bring urgency to these needs.

“As Canadians, many of us are understandably proud of our health care system. In Ontario, most of us believe that, should we ever be unfortunate enough to get cancer, OHIP will cover us. Unfortunately, in far too many cases this doesn’t happen.

Sometimes, the very best treatment that your doctor prescribes for your cancer is not covered by provincial insurance. Patients have to choose between a fully-covered treatment plan that may be less effective, or following the recommendation of their doctor and paying the high cost for chemotherapy out of pocket.

This is two-tiered health care. Wealthy patients and those with good private insurance have access to the best care. Those who are not so lucky either go deeply in debt or take their chances with what OHIP will cover.

In 2014, no Ontario cancer patient should be accumulating thousands of dollars of debt. And yet it’s happening more often than most of us would think.”

If  agree with their mission, then do sign the petition and please share their campaign.

 

Finally some good news

Every few months I get an x-ray of my lungs. This is done to check on the spots. You see, last summer when the spots were discovered by the CT, I’d also had an x-ray which didn’t show any cancer. The spots were too small to appear on that less precise form of x-ray imagining.

Therefore, I’ve had an x-ray since then with the idea being, if no spots show up than the cancer is stable. Truth be told, I am having a hard time handling these little hurdles in the metastatic way of life, and so I didn’t blog about their coming or their going. There was nothing to say, I was stable – i.e. nothing showed up.

Last week I went for a CT scan. My oncologist, Dr. Canada , has had hopes of adding me to the latest promising phase three study, where I may have (it is randomized) been given that drug in testing Palbociclib, which seems very promising for ‘extending life’ – which is very good and yet not good enough, if you ask me. If there was any change in the scan, I would be eligible.

I didn’t write about this scan last week. I couldn’t. It felt like my world was about to crash. Mixed between normality were cracks of panic. And what is very hard in all of this, is that these scans and checks are now a way of life. One scan or x-ray will always be followed be another in a few/several months. Metastatic breast cancer, unlike stage three and below, has no end of treatment. It’s living scan to scan, and I wonder if anyone can become hardened against this.

But I don’t really want to talk about that today. So I will stop there. Today I’d rather look at the encouraging things.

I had my results yesterday. They were good. We went out in the evening to celebrate with my parents, because even if I do need to go through this every few months – good news is GOOD. It means something is being done right. The cancer tumors were not just stable, but had somewhat shrunk across the board. Shrinking is a good thing.

Lord, I’m doing so much right now. There’s the vitamin C, the Zoladex, the supplements, the emotional work. So it is hard to say what is working. Maybe it’s my body’s immune system? Maybe it was publishing my novel? Maybe it is just everything all combined? All I know is this is good news, and I need to keep on with the routine. News like yesterday’s is my motivation.

So there is the update. I’ve had so much support from everyone visiting Bumpyboobs and beyond with the diagnosis, the book, living well . . . so when there is good news like this, we need to celebrate. Never mind what comes next.

🙂

Happy faces for everyone. Even if mine is still a bit tentative!

By the by, one of my friends is a doctor at the hospital where I had my results. While waiting for Dr Canada to arrive (after the nurse ushered us into a small treatment room), my friend knocked on the door and came in to chat. This was a very good thing. Everyone should have surprise visits from their friends while waiting for potentially life-altering news. It takes the edge off. So a very big THANK YOU for doing that. And I loved your outfit too, by the way. Polka dots are awesome.

P.S. I might be going to something called Sex-a-palooza via some free tickets. So, there could be a post in that!

P.P.S. This song is sooo good! You are invited to dance in your chair while listening to it.