I have decided to share with you what would have been my
first ever blog post on Dear Melanoma… but I chickened out! Here it is a year
and one day on!
Tomorrow we celebrate Mother’s Day, a day that has always
been low-key in my family home, but still a day that never goes without some
kind of token to celebrate or treat my mum. I want to write about some of my
own feelings that have been with me for some months now. Feelings that I have
not openly shared.
I have always thought that I was born to be a mum. When I
was at school, especially in high school, I was asked what I wanted to be when
I grow up; I never really had an answer. Most of my peers would list endless
careers, but I couldn’t. I just knew I wanted to be a mum. My career would simply
have to fit around me being a mum.
My lovely mum! |
Almost six months ago this all changed for me. I was
sitting, recently engaged, in a small room with my fiancé, mum and dad, and my
oncologist. This was my first meeting with my oncologist after being told my
Melanoma was no longer operable. The appointment was largely a blur. I was told
in this appointment about the reality of Stage 4 Melanoma. A reality that
wasn’t fantastic. A reality that was far from fantastic. I was to start
treatment that on average would give someone a prognosis of 18 months. I knew
that this meant that there were people at opposite ends of this average, and
the positive side of me asked what would happen if I survived this. The
oncologist once again highlighted the reality of my prognosis. But, I continued
to ask questions. Questions about having children – Should I freeze my eggs?
Will I ever be able to carry the pregnancy on my own? If not, could we use a
surrogate? All these questions were answered, but once again, it was highlighted
that it would be unlikely that I would survive, let alone be able to explore
these avenues.
At this point, I would like to make it clear that everything
my oncologist said was not with the intent to be pessimistic or not to hope. In
my cancer journey, I have learnt that, for me, being realistic is the right way
to handle the disease. I know there will be people that read this who would
like to criticise how this was handled or tell me that there is hope and I
could be cured. Yes, I could be one of those very lucky people that respond to
treatment. But, only myself, my husband, Serge, my family and my doctors know
the extent of my disease. So, I ask you please not criticise or suggest how I
should be feeling about motherhood.
My ratbags! |
With Mother’s Day tomorrow, I feel that I can share what
have been my moments of sorrow and the many tears I have shed behind closed
doors or at night as I go to bed next to my husband. Tomorrow is a day that
celebrates everything that I wanted to be and will be a reminder of what I
won’t be.
I keep the sorrow I feel to myself because both my sister’s
are living out the dream I wanted for myself. Ashlee has three children under
four and Sarah has a baby boy due in June. I am not envious of my sisters and
do not wish that they weren’t experiencing the joy of the motherhood. But to be
honest, sometimes it is so hard to not be sad and it sucks big time!
I wish that I could be waddling around with a big fat beach
ball of belly in front of me. I wish I could get away with wearing super tight
clothes to not show off my not so flat tummy, but instead show off my beach
ball of a belly. I wish I could go and buy all the cute clothes ready for
bubbas arrival. I wish I could watch Serge’s face when he hold’s his baby for
the first time. I wish I could watch them take their first steps. I wish I
could take them to their first day of school. The list is endless.
Love watching little Harry grow up. |
I am lucky that I get to watch Ashlee’s children grow up and
be part of their life. I know that when I am not here, they will be told about
me and will always have part of their Emmy in their heart. For Sarah’s baby who
I am so excited to be able to meet – something that three months ago I thought
I might not able to do – Harry may not remember me, but I know that I will be
spoken of. So, as hard as it is to know that I won’t be a mum, being Aunty to
these children is definitely a close runner up!
I spend a lot of time thinking about this little baby that I
hoped would be Serge and mine. One of the hardest things about knowing that I
have terminal cancer is imagining life after I am not here. Serge and I have
spoken about my wish for him to move on, marry and hopefully be a dad. Many
tears have been lost to this, because even though I wish this for him, it is
sad to think that we are not able to have this together. In the lead up to
Mother’s Day, and as we talk about celebrating our mum’s and spoiling them, I
know, and deep down hope, that one day Serge will be doing this for someone
that is not me. A thought that is bittersweet.
Tomorrow I will be thinking about my Mum and sisters who are
the best mums (or soon to be mums) in the world. Tomorrow is going to be
bittersweet, but I will celebrate them and thank them for all they have done
for me.
A great article Emma and it feels as thought I could have written it myself. I wanted to be a Mother from my earliest memories as a child and even in primary school, when I was 10 years old I used to look after and 'mother' the younger children in the school. I had chosen my babies names by the time I was 16 and had decided which hospital I was going to have those babies in. Then as the years went by, and I struggled through countless numbers of IVF cycles (I stopped counting at 12), as well starting the process of overseas adoption, all the while having to put up with well meaning family members telling me "you're meant to be a Mother", I realised at the age of 50 I am never going to be a Mother. Although I don't have melanoma (my brother is stage 3B), in some small way I can understand how you are feeling.
ReplyDeleteOh Em...I doubt that anything I write here will make much sense - the tears in my eyes are making it hard to see, let alone make sense! Everything you say here is just so honest and heartfelt, it's hard not to let this wet-stuff well up. I hope and pray that your Mother's Day (as mum of Ralph!) and daughter to your own mum, was as special as it could be. Knowing you, it would have been pretty amazing. Sushi soon. And wine. Please xxx
ReplyDeleteThis is a beautiful post Emma. I always wanted to be a mum as well and have a career that would fit around my kids. I am truly blessed to have my daughter. I could not imagine how you must feel. It is so unfair. From reading your posts you can tell that you would have been one of those inspirational mums admired by everyone around you.
ReplyDeleteYour nieces and nephews are very lucky to have someone like you in thier life. Thanks for sharing this post.
Hi Emma, Sorry I am posting on your post however, I have great news and a massive congratulations is in order. Your blog has been nominated into the Voices of 2015 program. Can you please contact Cassandra at Kidspot on cassandra.jones@news.com.au for more information. Thanks, Cassandra
ReplyDeleteHi Emma.
ReplyDeleteI don't know what to say. Part of me identifies with your poignant words.
I've had 2 different malignant cancers in 18 months - now 3yrs today since first Dx.
I wish you peace and gentle days . Congratulations on your nomination too.
Dear Emma, can you please contact me - maxine.fisher@slq.qld.gov.au - at the State Library of Queensland regarding archiving your blog in PANDORA, Australia's web archive http://pandora.nla.gov.au/. I just need to email you the necessary permission form. With thanks...
ReplyDelete