Over the last 12 months my personal Facebook has gone off. I
feel like I am the new cool kid on the block. I have had an influx of friend
requests from people that I have not seen for 20 years (take note that I am
only 23!). Friend requests from friends of friends. Friend requests from my
sister’s friend’s sister. And friend requests from complete strangers. I
apologise now for deleting 90% of these requests.
As you can guess, I haven’t been short of people offering
love and support to me over the last 12 months. I have the most amazing family
and friends who have been with me every moment of the journey. But
unfortunately, I have lost some friends along the way and shed many tears over
what some people consider being supportive.
My wonderful best friends! |
Everyone wants to be helpful and supportive. Most of the
conversations I have are very encouraging, but on the other hand, some are less
then helpful.
Over the last little while, I have started to document some
of the silly things that people say to me. I am now at the point in my cancer
journey that I can laugh about the crazy things people say and do, but it has
taken me a long time to get to this point.
I want to highlight now that I understand completely that it
is difficult for people to know what to say to someone experiencing great hurt
in their life. What may be offensive to one person may not be offensive to the
next. This post is not about shaming, but it is a post that I hope people can
relate to. I also hope that this may help guide you in how you support someone
through this difficult time.
Most of the points below are mine, but I have also included
suggestions from my Facebook post last night (https://www.facebook.com/dearmelanoma1).
Stay positive/Keep on
fighting – This one is a shocker! I am not going to lie, this is one that I
don’t ‘grin and bare’. As I was leaving an appointment one day I was told, by
someone who should know better, that I should stay positive and that they know
people in my situation who have lived for 10 years (this is just after I had
been told I had 3 months to live). I promptly turned around and said in my
usual delicate way; ‘I think I am pretty bloody positive for a 22 year old that
has just been told they are dying!’
Many people ask me what has been the most difficult part of
my diagnosis. My response is always the same - I struggle when people tell me
to ‘stay positive’ or ‘keep fighting’. Even though people mean well by saying
these words, every time I hear them I feel that I am not trying hard enough or
doing everything I can do to survive this disease. You don’t want to live the
little time that you have feeling this way.
‘When am I seeing
you?’ – I remember in the first few months after my diagnosis that there
was a lot of pressure from people to catch up. I felt, and was even told
directly by someone, that people wanted to catch up with me straightaway
because I was dying and would not have much time. There should never be
pressure put on someone to catch up. No matter where you are in your cancer
journey, you are going to have up and down days and won’t feel like catching up
with people… definitely when it means that you will have to recount the same
old cancer story every time. And if the person doesn’t have much time, it is
their choice how they spend their last however long. You should not take
offense, but concentrate on the time that you have had with this person. They
will contact you if/when they are ready.
Do not just send a
Facebook friend request – Remember that just because the person has cancer,
it doesn’t mean that they have lost their privacy and dignity. I suggest you
think before you send a request. Are you sending the request for a genuine
reason? Or do you just want to see what happens in the life of someone with
cancer? My suggestion is that you send a message to them and leave it up to
them to add you. No one wants to feel like a performing animal in a circus!
Did your parents not
use sunscreen when you were young? –This is just horrendous! Never blame the
person, or their family, for having caused their cancer! This one can come down
to ignorance and lack of knowledge of melanoma – Melanoma is not only a result
of sun damage, but can be due to a genetic pre-disposition. But you can use a
bit of tact. Asking this question in a different way would be a lot less
troublesome.
You don’t look sick/You
look so healthy - I hear this one all the time, and in some ways it makes
me feel really good about myself. Who doesn’t like being told they are looking
great?! However, when this statement comes with the person doubting whether you
are actually sick, it completely changes meaning. No one wants to feel that
people doubt the seriousness of their illness. I feel very lucky that I am on a
treatment that has limited side effects and that my metastasis are only causing
pain and are not hindering the function of any of my organs. But, it is really
difficult to feel the need to justify what is happening in your body, and that
you indeed have stage 4 melanoma. No
lies here!
You are so brave, how do you do it? – It is quite simple… we don’t
have a choice! Instead of making it a patronising question, you could send a
text and tell the person that they are doing really well and that they are so
brave. You don’t have to add the rhetorical question to the end.
Your doctors are
liars – I received a letter a few months ago where somebody (with no
qualifications relevant to cancer) had spent a whole page explaining why my
doctors are liars. This upset me because I believe that the most important
person in your cancer journey, apart from yourself, is your doctor, opposed to
Dr Google or an untrained self-labelled ‘expert’. You want to have complete
trust in your doctor or you will spend your days questioning your treatment. It
is your job as a support person not to question this trust.
I know how to cure
your cancer! – I may not know the person yet, but I promise you that I can
tell you who it will be… it will be an oncologist and I will be among the first
to be told! I have so many people offer their advice on how I can cure my
cancer – Go to Mexico! Drink green smoothies! Ingest liquid cannabis! Go and
see this woman who cured her own cancer!
People mean well by sharing their knowledge and what they
have heard along the grapevine, but this kind of advice should only be given
when welcomed.
Steer clear of using
‘at least’ or ‘only’ – Using these words never seem to end well. Here are
some examples:
'You are lucky that it is only melanoma.'
'At least it
is only breast cancer; wait until you get bowel cancer.'
Need I say more? I think you get the picture.
You are so young! –
A regular response that I get when people hear that I have cancer is, ‘you are
sooooooo young!’ followed by, ‘that is so unfair’. Yes, I am aware that I am
young. And yes, I am aware that life is unfair. It is quite patronising and I
also do not need to be reminded on how shit it is that (a) I have cancer, and
(b) I have cancer at 23.
The Ring Theory (from Mamamia article) |
Don’t put your own
needs before the needs of the person directly affected by cancer – This
is a really difficult one for family and friends because everyone is affected
by a cancer diagnosis. However, it is important to recognise that your feelings
should come second… or even third or fourth, depending on how close you are to
the person. Mamamia published a fantastic article earlier in the year
explaining this (http://www.mamamia.com.au/social/saying-the-right-thing-to-someone-with-cancer/)
It is in God’s
will/God will heal you – For many, religion provides comfort through
difficult times, like a cancer diagnosis, but be aware that this is not the
case for everyone. Instead of telling someone with cancer that ‘it is in God’s
will’ or that ‘God will heal you’, simply let someone know that you are praying
for them and that they are in your thoughts. For me, these statements make me
question if there is indeed a God, why would he have given me cancer? Be aware
that people may have similar feelings.
We are only given
what we are strong enough to handle – If that is the case, I wish I was a
hell of a lot weaker than I am!
One positive scan –
so you are cured now? – I love this one. I have scans six weekly and every
time I have a positive result, some of the more elderly people in my family
like to think that I am now going to be miraculously cured. I have a giggle
about this, but deep down it is difficult. You don’t want to have to explain to
someone every six months that melanoma is still going to get me in the end.
Don’t compare their
experience with cancer to anyone else’s –Do not whip out a story about your
sister’s friend’s best friend who died from cancer. Hearing a story about how
cancer has killed their friend or relative is not what you want to hear when
battling cancer. On the hand, sharing a survival story can also be difficult.
Everyone’s cancer story is different and should never be compared.
As I said at the beginning of this post, I have some pretty
amazing friends and family. Based on my
experience, here are some suggestions on how to navigate this difficult time.
My dear friend who asked me what I needed from her. |
Ask the person
directly what they want from you – I remember early on in the year I was
having a difficult time with some friends putting a lot of pressure on me to
see them and update them on everything that was happening in my life (CANCER,
CANCER, and more CANCER). One dear friend called me and asked me directly what
I wanted from her in terms of support. I told her to call when she can, text
when she wanted to, but to not expect that I will reply every time. Knowing
that she was there and thinking of me meant so much.
Send a text, letter,
leave a voicemail, but don’t expect a reply – It means the world!
Know your friends and
family, and know who is best suited for each situation – This was so
important to learn early on in my cancer journey. Some of my best friends I do
not go to for emotional support, because I know that it is too hard for them.
But these people are the best people to go to when I want to forget about
cancer. On the other hand, I have friends that I know I can talk to about every
single detail of what is happening in my body, and I know that they can handle it.
Be strategic.
Dealing with a cancer diagnosis is not easy for anyone
involved. It is normally our support people that hold us together in this
difficult time. It is often these people that go unrecognised and them who
sacrifice their feelings in order to be the best support to the person in need.
Unfortunately sometimes what one person can think is supportive, may not
translate to the person receiving the support. It is also extremely difficult
to know what to say to someone with cancer. I hope this post helps those
providing support to a loved family member or friend fighting cancer.
Jo Hilder has written an ENTIRE book dedicated to discussing the dos and don’ts on this topic. Her book is ‘Things Not To Say To Someone Who Has Cancer’. Take a look!
Great post - thanks for your advice, we`ll try and put it into action, love Cat Will & Jemima x
ReplyDeleteHi Emma, I was diagnosed with Stage 4 Melanoma at 33 and can relate to so many of these :-) The one most people struggled to understand was the "Stay Positive". It drove me nuts! I felt positive, I acted positive. I also had fears, I had responsibilities and I needed a contingency plan in case things didn't pan out the way I hoped. I videotaped myself reading bedtime stories to my small kids and wrote letters and stories for them. I discussed alternate futures with my husband. This was me being the best mum I knew how to be under the circumstances, but friends thought it meant I wasn't "being positive". Like you, I learnt to laugh or dismiss, but I swear if one more person told me to think positive thoughts......grrr. Love and light to you. Kerry x
ReplyDeleteIcould really relate to this topic. Since my diagnosis I have spent time raising awareness of melanome, fundraising and helping others cope with diagnoses and cancer treatment. I have been labelled by some of my closest friends as being morbid and I need to put it behind me and move forward. Difficult when you have 3 monthly pet /CT scans, skin checks and live with lymphodeama in the leg everyday. This is who I am now, accept it and support me or move on, don't blame me for breakdown of a long term relationship.
ReplyDelete