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A Fighter


“It doesn’t matter how much time you have left, it’s about what you do with your time that matters.”
If cancer taught me anything, it was to give back and pass on a positive chain effect of hope to others. Memories of my cancer treatment sprung into mind like it was just yesterday, I vividly remembered the pain, the fear, the hopelessness as well as the hefty cost of treatment, all of which I could not bring myself to go through again. I decided to make plans for the worst case scenario. I made a bucket list, and started living my dreams, ticking each item off my list, one by one. I did not think about the days I had left, for I was already living a fulfilled life, by my own standards. I embarked on more volunteer work, keeping the words of my husband close to heart – “Do things for others to the best you can with whatever time you have left.
I did not want to give up, but to fight on required so much effort, and so much determination, and I didn’t know how much fight I had left in me. I felt emotionally drained, but yet I knew there was no time for rest. I braved myself to endure the treatment process. There is always a part of me that fears the cancer will find a way back again. But I know I am not alone in this journey as my family has always stick by me.
“Cancer shouldn’t define me. It’s an illness that needs to be cured, but it isn’t what you are. You’re still you and hopefully through the experience you’ll emerge as a better person. Try to cope by taking a break and re-charging yourself by doing things you like to do and are comfortable doing. I’ve always wanted to holiday but this experience has taught me not to put myself first, but rather, use myself for the good of others.
Also, support from family and friends is very important. Don’t think I could have gotten through without my family and friends sticking by my side throughout the entire period. Not many people have my fortune to “survive” cancer, so I represent hope and I hope that others can feel encouraged by my story.”
My husband, Rus also added that the most difficult part of the caregiving process was seeing me in pain and trying to comfort me.
However, far too often, many of us struggle to reconcile with our gift and as a result, find it difficult to find meaning and purpose in life’s existence.
In the flesh, you would never think of me to be suffering from any illness, much less cancer. Fresh-faced and constantly breaking into a smile.
“It’s okay to be scared, but try to seek support and solace in support groups to tide you through the journey. Everybody comes laden with their own burden, however, you need to accept the disease and move on, knowing that there is a plan for all of us. Sometimes, things don’t happen the way we want, but everything happens for a reason, and maybe it is a chance to reconnect with yourself. As long as you surmount the strength to fight it, half the battle is already won. Most importantly, know that time is still on your side, so treasure every minute of it while you can.”

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I am Blessed...



Trust God! He truly is the healer! Get involved with other people. Give because it gets you out of yourself and keeps you focused on others.
I have also learned the value of rest. If your body is tired, rest. But do not give up! Remember that “baby steps are still steps!” Set goals. Live life. Get rid of negative influences. Be that living testimony! I like to let people know that I kicked cancer’s butt! Not now, but soon!
At home, my husband, Rusmanni keep me laughing too. Rus decided to make the hard choice between his work and caring for the love of his life. He devoted all his waking hours to care for me, accompanying me to the hospital, assisting me with daily tasks. When I was diagnosed, we had been married for 13 years and we probably laughed more after my diagnosis than in all our years together. I believed that every positive attitude makes me feel better and put all the people around me at peace.
But It wasn’t all rainbows and sunshine. And while my oncologist team brings peace to those closest to me, the people I see at the medical centre bring that same feeling to her. I feel like I have the best team working on me. They do it with a lot of empathy and a lot of care. They said “You’ve been through the most difficult time part of treatment and sailed through with flying colours. You have high hopes with a true fighting spirit, and I admire that. I am rooting for you!”
However, Rus provided me with a ray of sunlight in my period of darkness. Never once did Rus break down or show his vulnerability in front of me since I was diagnosed but rather, made it a point to remain upbeat and positive every single day so as to lift spirits. I gleefully recounted how during my stays in the hospital, Rus would greet me with a cheerful smile his face, rain or shine. I am married, so my sexuality is confined to my husband. That is still very unfolding. It is interesting with your partner, because they go through this all with you. They are not the primary person it is happening to. I get all the sympathy. Most of the table between us. We talk about it a lot. But it is also hard to progress constantly on every front and be responsible for his evolution as well as my own. At some point, he is responsible for his evolution. He hands in there the best he can. It is just something that is unfolding for me. There are no answers yet. It is different. Such unwavering dedication is testament to Rus love for me. During my stays in the hospital, Rus is there beside me, my ray of joy within the hospital walls.
I have my children. I was busy trying to protect them initially, which was a mistake. There are just 5 of us, so we have a very close family. They knew this was all going on. My trying to keep the emotional intensity from them were a mistake, because they we going through their own emotional intensity about it and their own fear of losing me. Because everyone was so worried about getting me through it, I think they put their own feelings on hold for a while. About a year-and-a-half into it, I had my collapse. All my children and my husband had steadfastness and certainty that I was going to survive, make it. In moments of great doubt on my part, their steadfastness has been tremendous. It has helped me. Sometimes you hang onto whatever you have there to hand on, to believe that you are going to make it through this thing, and it is going to consume you. It is not going be a sad story or the end of your story. You are going to make it through. I think my husband learned a lot about that through this experience, so that is a gift to him.
Apart from the support of her family and loved ones, I also found support in places I never expected to find. I found comfort and hope after reading about other’s cancer journey and how they overcame the disease. I also found support in fellow patients hospitalised in the same ward and I shared of how I would lighten up at the atmosphere by befriending those around me to rally a positive state of mind. The nurses and my oncologist nicknamed me the “leader of the ward” as I cheered those around me. What I found most comforting are friends who have battled cancer themselves sharing their own journey with cancer with me.
I believe you can get the best of health care in the world here, but you must pay for it. I had a good health plan, but now we pay a lot of money for this health plan. I paid a phenomenal amount of money every month for my monthly medicines and therapies. I also think it is sinful how much it costs. If I did not have the background and the resources that I have, I might not have had this kind of care, and I might not be here. I am an advocate for the whole country sitting down at a table and trying to figure out this whole health care issue: how to access if for most people, and how to make it so it is not unreasonable how much it costs.
Live strong means it takes a lot of strength to live. It is a way of feeling like a victim. It is empowering because it means that your body is your friend. Your body is able and capable, and emotionally, you are capable. You can live strong. You can be strong in your life.
I personally live strong by taking care of my body, making it as strong as it can be, considering its age, and what I have done to it and what has been done to it. Emotionally, I try to maintain a very clear light forward. Life is not an easy thing. You must have a lot of strength to live, to survive. I also acknowledge that the sickness made me irrational and cranky, and she found herself losing my temper and having emotional breakdowns more than I should.
I thank God every day, and I tell everyone I love them so they will always know how I feel. I do not think about when or if the cancer will come back. I think about tomorrow and spending it with my children, my husband, family and friends.
Having cancer makes one very brave. I do not give up hope and to continue to have hope, just as my doctor, husband, family and friends encouraged me.
My name is Rosalisa Aris, and I am stage 3B Endometrial (Uterine) cancer soon-to-be survivor.
To others battling cancer, I have this to say:
“Go through each day positively. It may not be an easy or fun process but not everybody is lucky enough to get a second shot at life. Every day is a blessing and you never know you’’ learn the value of life. Stay strong, especially if you have kids. And if you have loved ones, just know that they are praying for your recovery so you must do your part by staying strong and thinking positive. Support is very important especially for younger cancer patients. Just know that time will pass quickly and with each day you will emerge stronger. Every person diagnosed with cancer will change, one way or another, and for myself, it has changed me for the better, and I have become more appreciative, selfless and patient.
Just lead your life per normal. Don’t worry because there is always help out there. You need to be strong and learn to tolerate any mood swings or tempers that come your way. Just remember that you cannot let it get to you as you need to be the rational pillar of support to lift up your loved one. Also, it is important to properly plan your schedule so that you’re overwhelmed by stress during this period.”

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