Three days shy of my 36th birthday I was informed I had cancer. Some weeks and many painful and invasive tests later, my doctor informed me that I had advanced and aggressive non-Hodgkins lymphoma. Without treatment, I would die within a couple of months. With treatment, he was not willing to predict my chances.
I’d known for about a year that something wasn’t quite right but back pain was a long familiar companion and being a little more tired and a little more run down than usual was, I thought, to be expected given I was a working single parent of two small children.
In shock, I began chemotherapy and started making arrangements for my children’s future if I died. They were two and five.
My first thoughts were for my kids. For their sake, I had no choice but to live. And I was determined that my illness and treatment should change things as little as possible. I resolved to continue working so that I could pay the bills and keep our home, and, as much as I was able, to remain their primary carer.
I am by nature a happy optimist. But as chemo wore me down, the kids-work-cancer juggle became increasingly difficult. I shed weight, permanent exhaustion and bone-deep aches set in alongside steroid-induced mood swings and all manner of other uncomfortable and unpleasant side-effects. Towards the end of treatment, just one activity a day would wipe me out. Getting the kids up, dressed and fed and dropped off at school and day care shattered me for the rest of the day. Showing up to work and producing something meaningful for my tolerant and understanding employer was almost impossible.
I was extremely fortunate to enjoy the help and support of a large and loving network of family and friends, without whom my children and I would not have made it through that year in such good shape. They cooked, shopped, helped with the kids, gave me a great cleaner, gardened, sent me music and movies and other happy distractions, took me out when I was up to it and in many other small ways carried me through the most difficult year of my life. I’d always worn my independence as a badge of honour; that year I learned to accept all manner of help with grace and gratitude.
One of my most important supporters was and is The Warwick Foundation, which showed me that I was not alone. Despite the unexpected and glorious outpouring of love and community spirit, until I found The Warwick Foundation I felt acutely different. I knew of nobody else my age fighting cancer. I certainly knew of no other parents of small children who were in my situation. Every three weeks I spent a day in the chemo ward for treatment, surrounded by people in their 60s and 70s. Later, the daily visits to radiation oncology proved little different.
It was a great relief when The Warwick Foundation put me in touch with other young adults living with cancer. Established by Samantha Lehmann after her brother Warwick died of cancer in 2005 at the age of 35, it is Australia’s first organisation set up specifically to support young adults with cancer.
Discovering that others my age had gone through the same struggles helped. Being sent – with my Mum and sister – on a delightful long weekend was another terrific boost when I felt that it was all too hard. Just knowing there was a caring support network of dedicated people made a difference for me.
The Warwick Foundation’s mission is to bring hope, inspiration and support to 20-40 year old Australians living with cancer. It has a mentorship program, treats, getaways, and other programs addressing their psychological, social and emotional needs. It also provides crucial information and referrals.
I’ve now been in complete remission for just over a year, and the lovely folk at The Warwick Foundation are still there for me as I negotiate this new, post-cancer world. I am honoured to call myself a Community Ambassador for The Warwick Foundation, and to help other young adults with cancer get the kinds of support that I found so valuable.
Kylie Walker is a 30-something single mum who fought and won against advanced non-Hodgkins lymphoma.
Through her battle she learned to truly appreciate the value of love and community. Along with family, friends and colleagues, she was supported throughout by The Warwick Foundation, a charity for 20-40 year olds living with cancer.
Now in complete remission, she is a 2012 Community Ambassador for The Warwick Foundation.
To become a member of or support The Warwick Foundation please go here.








Comments
30 Comments so far
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My mum was diagnosed with a rare & aggressive non Hodgkins lymphoma last July & spent the rest of the year in hospital. She’s going back in for a stem cell transplant soon. Having never even spoken to anyone who’s been through this, I gotta say I’m pretty scared for her.
Kylie – looking after mum’s needs, as well as my toddler & baby was hard enough (& I wasn’t even the sick one!). You sound like one amazing, brave mum! A trying time like you’ve been through really shows the importance of family & friends. Thank you for sharing your story & best wishes to you & your family.
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You are doing an amazing job supporting your mum through a difficult time for both of you. Stay strong and please accept help when it’s offered. I hope you have somebody to look after you through this tough time.
Strength and health to you and your mum.
Kylie x
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Kylie,
Thank you for your honesty and eloquence in describing what is a pretty shitty process (apologies moderator!).
I’m writing this as I sit in a unit provided by the wonderful people at the Leukemia Foundation at Westmead.
I’m mid way through the chemo conditioning process leading up to having a bone marrow transplant.
Getting to watch the cricket on telly uninterrupted is little consolation for having to spend six weeks away from my kids.
Skype is no substitute for a snuggle, but hopefully the end result will be worth it.
In many ways, your story parallels my own.
I have benefited from the same loving and considerate support and I hope I end up with the same positive and affirming outcome as you have.
I was also diagnosed with advanced and nasty Non-Hodgkins Lymphoma (stage IV) in my mid-thirties just as I was contemplating a long life of fun with my kids aged six and two.
I work at the ABC in Canberra and did a couple of TV stories about living with cancer and what it’s like becoming an instant baldy.
http://www.abc.net.au/news/2011-07-08/topic-of-cancer/2787914
Since then I have also benefited from the understanding and generosity of the Warwick Foundation.
They provided information and contacts with other people who have lived with cancer as well as a treasured weekend retreat at the beautiful Kudos Villas in Victoria’s Spa country.
It is a wonderful organisation with a profile that is deservedly growing.
The Warwick Foundation and the lovely people at the Leukemia Foundation provide genuine, practical help to people during the worst time of their lives.
I’m ashamed I did not know more about them prior to getting sick.
Kylie, congratulations on becoming a Warwick ambassador and thank you for sharing.
Many good vibes
Chris
(temporarily???, of Westmead)
Ps – hello to Kristy at the top of these comments! Good luck being a school mum!
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Hi Chris,
I heard about you from Ross S. I will drop you an email at work.
Best luck with your treatment and with juggling treatment, work and parenting.
Kylie x
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Well done Kylie on a hard fought battle, I am so happy to hear of your wonderful outcome.
My husband was diagnosed with acute non Hodgkin lymphoma in late 2007 when our daughter was just 9 months old. We waged a massive fight including chemo, stem cell transplants, time in ICU and after such bravery he lost his battle 6 months later.
Life would never be the same.
My little girl and I have fought hard with our grief and trying to accept life without him.
This week she started primary school…she is the spitting image of him. He would be So proud.
We miss him so much but he is with us every step.
To everyone fighting the battle, we send you love
Xx
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Thanks Kristy. I’m so sorry for your loss.
Kylie
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Kylie, thank you, thank you, thank you. I have been searching for this sort of support over the past few months.
My husband was diagnosed with a brain tumour in October last year, at 38 years of age. We have three children aged 3, 6 and 9 years. The past four months have been like living in a nightmare. It has been long and hard, as you would know. One of the hardest parts is sitting at the radiology clinic every single day, watching other patients come and go. And you’re right, most of them are over 50, usually with prostate or breast cancer. Very few patients were close to our age. There were a few times when I had no choice but to take our three children to the hospital while my husband had his radiation treatment. I tried desperately to keep the kids quiet but that’s really hard when there’s three of them and we’ve been at the hospital for hours. We are lucky to have a great group of family and friends around us who will cook meals or take the kids (yes, all three of them together please) overnight at short notice. Unfortunately, the Christmas school holidays coincided with the last three weeks of my husband’s radiation treatment so that just added an extra element to the daily juggle of doctors and pathology.
But now, we are seeing light at the end of the tunnel. The tumour has been removed, they say they got it all but regular MRIs will monitor that. My husband has returned to work part time, the radiation is over. He has six more months of chemo but he can do that and still work. Life is good.
My eldest has stopped asking if daddy is going to die. That was a question I was never prepared for. There were times when I felt like I couldn’t continue to be the wife, mother AND carer for our family. I was worn out holding everyone else together. It would have been good to have someone who really understood to share all this with when it got tough. I don’t feel like we need any support at the moment, because life is good. But I have bookmarked the Warwick Foundation in case we ever need it.
Thank you again Kylie
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Hello,
great news that your husband is through the worst of it and things are looking up!
It was tough keeping this piece to 700 or so words – I could have written 10,000 or more (and maybe one day I will). One of the things I would have liked to have explored was the question of how I handled my illness in conversation with my kids. We were lucky to have the Camp Quality puppets come for a performance at my son’s school which helped enormously to normalise our experiences for him but it also raised a lot of questions for him that I hadn’t expected to have to handle, including that of death. I always tried to respect my children’s right to know the truth but to hear it in a gentle and age-appropriate way. When they asked if I was going to die, my reply was always “I hope not”, followed by reassurance that I and the doctors were doing everything possible to make sure I got well again. When they raised the issue I also talked to them about death generally and they understand that everybody dies eventually.
It sounds like you’ve been doing an amazing job juggling all of your roles. I wish you all good health and strength.
Kylie
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Thank you for writing this Kylie…you are amazing, courageous, and many other things that I cannot even put into words x
My friend lost her battle against cancer on Christmas Day 2009, leaving behind her ten week old, four year old, and fifteen year old sons. She found out she had a rare form of melanoma when she was six months pregnant, and she too mistook symptoms for something else, something normal. Now that I am a mother too, it breaks my heart to think of how it would feel to be given a matter of months to say goodbye to your children. She fought a good fight, and showed true spirit, and will foever be inspirational to me.
Good luck for the future x
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I am very sorry for the loss of your friend. And thank you for your kind words.
Kylie
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Thank you for sharing your heartfelt story – you are an inspiration and so, so brave. I’m really happy to read that you are in remission and you will make an amazing ambassador for the Warwick Foundation that helped you.
Your fight and determination is truly remarkable and hopefully will inspire others to be in the moment and live each day to their fullest! Thanks again for sharing your story.
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This was almost too hard to read. My bestie died 4 months ago of aggressive non Hodgkins Lymphoma. Aged 37 and with a 2 year old and 4 year old. The parallel gives me chills. Having said this, I am so so happy that you are in remission Kylie and I wish you a long life.
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Blossom, I’m so sorry to hear of your friend. It’s very tough to lose a loved one. Go gently with yourself.
Kylie
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Kylie, what a terrible ordeal you’ve had to go through, so sorry and so happy for you to hear you are in remission. good luck with everything & your little ones x
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Amazing story. True inspiration Kylie all the best for the future.
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This is a great piece…thank you so much and blessings to you and your familiy and supports.
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Great story. I was 30 newly married with 7 and 8 year olds, when I was diagnosed with brain cancer. Earth shattering but like you tried to continue on with life. Learning to accept help was a huge lesson for me but was an absolute necessity as I couldn’t drive for twelve months.
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Kylie, thank you for sharing your story. My husband was diagnosed with Hogkins Lymphoma two days before Christmas. These past few months have been very hard for us and our three kids aged 8, 6, and 3. Its so much to get our heads around, chemo, scans, blood tests, his lethergy and mood swings.
I have never heard of the Warwick Foundation but will definitely be looking them up. I wish you continued good health and happiness. We also hope to be in remission in six months time. Xoxo
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Sorry to hear of your husband’s diagnosis. I’m glad that you’ll check out the Warwick Foundation – you won’t regret it. Go well with the tough road ahead.
Kylie x
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Thanks so much for sharing. I’m also a young mother who suffered a debilitating illness I knew I could physically overcome it, but mentally recovering and rejoining the world. Each day gets better.
I know what you mean about being exhausted by doing one thing and then having to recover for the rest of the day.
Wishing you and your family all the best for the future. Thanks for the contribution you are making for others too
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Both my parents are cancer survivors. Mum had breast cancer and Dad had prostate cancer. I’m so proud of their strength. I wish you all the best. You’ve shown great courage.
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And we are so very grateful, Kylie, that you beat “Colin” – the unwelcome guest. The world would be a poorer place without your beautiful spirit. So wonderful that you are working for the foundation – you’ll be a great ambassador!
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I am so relieved for you that you are in remission. It is great to hear happy endings.
I understand how you feel about feeling alone. I was diagnosed with a brain tumour at the end of last year when my son was 7 months and my daughter was nearly 3. Yesterday I had radiosurgery. Sitting in the oncologist’s waiting room is sobering as there are so many people sicker than me. But then I realise that I am the youngest there by several decades and it just doesn’t seem fair. I have tried to tell Miss C a few times what is happening without scaring her but it sticks in my throat. I hope that we can get through the next few weeks without too much disruption to their lives.
It frustrates me that there isn’t that much support – I’ve had to look around for support groups etc. Thankfully, thanks to Mamamia, I found @Faybian who is also going through this and she has been a great support to me.
I wish you all the best in your future recovery.
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Hi, I am so sorry to hear about what you’re going through. If you’re in the age group, please consider contacting the Warwick Foundation. They can help.
However you choose to deal with this disease, I wish you the best of heart and health.
Kylie
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Hey, we’ve got each other.
I’m in my early forties, so just outside the age bracket, but my kids were 22,19, 9 and 6 when I got diagnosed. Due to the ages of my kids I had inbuilt help, but the fallout is immense and everyone felt it. My last surgery 2 months ago today, got the rest of the tumour. I think the Warwick foundation is a great idea. Having grown kids, I don’t feel that young anymore, but when I go to the surgeon’s office, radiology or see others with a disabled parking permit (mines only a year long one). I do realise that I am pretty young for this rubbish.
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I’m so happy to read that you are in remission Kylie. What a terrifying thing to have to go through!
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Congratulations on your remission! I wish I had known about this foundation last year! My husband passed away in January (bowel cancer) – he was 34 and we have a 4 year old daughter. We had the same experience of sticking out in the Chemo ward where everyone else was 60+ We found it things were either oriented to older people or kids. Good luck with it & I hope lots of people show their support!
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Thanks for your lovely comments. I am so sorry for your loss.
Kylie x
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A beautiful and brave story, offering hope and help to others. Thanks so much for sharing this, Kylie. You’re graceful, gutsy and inspirational – the perfect ambassador for the Warwick Foundation. xo
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Kylie I am so glad you’re in remission, I’m wishing you the best of luck in the future! Looking at the foundation page now