A few weeks ago a story was published by The New York Times
called ‘Lost in Transition After Cancer’, the author Suleika Jaouad who at age
22 was diagnosed with Leukaemia. The story was published during Young Adult
Cancer Awareness Week. Suleika wrote about her life since cancer, as well as
highlighting the need for ongoing support for those, especially young adults,
who are transitioning from life with cancer to life after cancer.
Take the time to read the story here.
Suleika and my story are different in many ways. Suleika had
leukaemia, which meant different treatment to what I am on (treatment much more
physically demanding and taxing on her body) and a different prognosis –
Suleika’s treatment was always meant to get her to remission. Whereas, with
Stage 4 Melanoma, remission has never been the destination at the end of my
treatment journey – my doctor and I hope for time.
Suleika Jaouad (photo from The New York Times) |
However, beyond these differences, we have a connection. We
are both young women in our early 20s whose life has been forever altered,
physically and emotionally, by cancer. We share the same heartbreak of what we
have missed out on and for what cancer will continue to take from us in the
future. Underlying all of this is fear – fear of the unknown.
I want to write today about the fear of what consider a
hypothetical world, the world of remission, and how I totally grasp every
sentence written by Suleika.
There is always the expectation that when there is the
smallest bit of positive news, or in Suleika’s case the biggest news of remission,
that we should celebrate and be over the moon with excitement. From my
experience, this is often not the case and it is awfully tiring trying to fake
excitement for the sake of your family and friends, as well as bringing them
back to reality.
As Suleika said, ‘I sometimes feel a deep sense of guilt for
not
doing a better job of making lemonade out of metaphorical lemons’. I hear
you, girl, ditch the lemonade and pass the tequila and salt!
This feeling comes around all too often, precisely on the
days that I receive scan results. As many people like to tell me, no change is
great, stable is great. Deep down I obviously feel a great sense of relief, as
well as happiness, that I can breathe easy and enjoy more time with my friends
and family. But, on the other hand, there is the disappointment that there has
been no change for over six months now and that it does not look like these
little suckers are going to disappear. Your little slither of hope for
remission slowly slips away and instead of anticipating reduction at your next
scan (which I hoped for in the first six months of treatment), you anticipate
the doctor telling you that treatment no longer works.
Suleika did not feel the urge to celebrate her remission
like she thought she would, or ‘dance a jig’ in her hospital gown, instead she
thinks about the ‘countless invisible imprints’, both physically and
emotionally, cancer has left on her body.
I know that if I was to go into remission that the dreams that
I had prior to cancer will still remain altered and shaped by cancer. These
dreams are dreams not only put on hold during treatment, but dreams that will
need to be replaced by new dreams should I go into remission.
Going to dress ups as a pregnant lady was the norm for me. Odd, I know! |
I am not sure if you are aware, but I was put on this earth
to have babies – lots of babies. Although I have always had ambitions for my
career, first and foremost, I was going to be a mum.
Today, I manage to cope with the fact that Serge and I
cannot have children, but the idea that, if I was to beat this cancer, Serge
and I would still not be able to have children of our own. And if we some how
managed to find a way to have children (i.e. convince my sister to be
surrogate), that we would have to sit down and discuss the fact that my cancer
would more than likely return and that Serge will be a single father and our
children would not have a mother.
I can and will, if given the opportunity, create new dreams
for a future. However, life would be engulfed with fear – fear that the cancer
will return. Every little illness will take me to the doctors questioning
whether the cancer is back.
How can you look forward to life without cancer when your
life’s dream cannot be a reality and when life is lived in fear and the unknown?
I thank Suleika for writing such an important piece of
writing. The strength that it would have taken to talk about the struggles of
life after cancer is imaginable. Thank you for not falling into the pressures
of writing about what a wonderful gift remission is and what joy you feel. I
know that you are grateful and happy that you have the opportunity to
experience life after cancer, but you also have every right to feel the way you
are.
I hope that your story will bring awareness to the need for
continual support for those that find themselves in the unknown world of
remission.
Powerful, intense, thought provoking and truly honest writing Emma, Thank you x
ReplyDeleteWell written post. Best of luck for the future! Hoping that the cancer won't come back and that you can make your babies dream somehow come true. Would IVF be an option at all? With donor eggs?
ReplyDeleteThis is such an important topic, Emma! My best friend is struggling with this still, even though he has been in remission for nearly 10 years! He has faced many depressions and struggles to keep his fears under control. He also has a lot of medical issues related to the cancer treatment such as troubles with maintaining his weight, low bloodsugar and a poor immune system.
ReplyDeleteHe says none of his friends can fully understand him and that he feels alone in the world for that reason. It really helps knowing this, because he sometimes acts in ways that we would not understand unless we knew.
You're great <3
Hi Emma,
ReplyDeleteThank you for sharing your amazing story. My name is Evan. I was truly moved by your words and would love to speak more with you about your journey. I currently work for a startup called First Derm and we are aiming on lowering the barriers of access to cancer screenings and dermatologists around the world. Please let me know if there is any way I can help. My email is evan@idoc24, feel free to contact me at anytime!
Kind Regards,
Evan
Hi Emma,
ReplyDeleteThank you for sharing your amazing story. My name is Evan. I was truly moved by your words and would love to speak more with you about your journey. I currently work for a startup called First Derm and we are aiming on lowering the barriers of access to cancer screenings and dermatologists around the world. Please let me know if there is any way I can help. My email is evan@idoc24, feel free to contact me at anytime!
Kind Regards,
Evan
Hi Emma,
ReplyDeleteI pop into your blog to see how things are going. I am old enough to be your grandmama (63!!), last year I was given the dreaded news of Stage Four Melanoma, and yesterday after CAT scan then an MRI to confirm there are small spots on the brain (which I dreaded), so in some small way I know how you are feeling. I say in a small way, because of the great age that separates us and the dreams. Such as your dreams of children. I love the dress-up photo, keep up your having some fun and having a laugh. You look to me a great young woman with lots of strength of character, thank you for sharing your experience.
Sincerely
Delphine
Remain steadfast in the face of temptation. Remember, cancer is the one form of human trials. If we can deal with it means we are winning.
ReplyDelete