watercolor of couple on bench with words 15 acts of kindness that helped cancer patients through treatment

15 Unforgettable Acts of Kindness That Helped Cancer Patients Through Treatment


Throughout the challenges of a cancer diagnosis and treatment, it’s the kindness of others that often brings hope and positivity to your day. Whether it’s as simple as a phone call or as big as a donation towards your treatment, friends and even strangers can never underestimate the power of kindness on someone facing cancer. Their actions will likely never be forgotten.

We partnered with Fuck Cancer to ask our communities what acts of kindness they have witnessed throughout their cancer experiences. The heartfelt stories they shared reveal that to a person going through cancer, knowing someone is thinking of them and wants to help make their day brighter can help them face their diagnosis. If you know someone with cancer, let these stories serve as inspiration as you support your loved ones.

Here’s what the community shared with us:

1.When I had cancer, around 12 years old, I was horrified of losing my hair. Most of my male classmates and my best friend (a female) shaved their heads for me and broadcast it on a screen that was in my ICU room since I couldn’t be around anyone. I’ll never forget that day.”

2.We had a group of friends who dropped off many meals and snacks throughout the eight rounds of chemo. They had coolers put on our back deck. They dropped ice and pre-made meals into the coolers and texted us before and after drop off. They didn’t want to bother us if we were not up to answering but wanted us to know they cared. They even had a list on the preferences of our family. It was pure love that went into that cooler. And felt deeply in our hearts. Thankful for that crew of 10 families who supported the cooler project for six months. Dedication.”

3.My sister was my caregiver while I was sick and always went the extra mile to try to make my mental state hopeful and take my mind off worrying/feeling overwhelmed. She would take me to markets, out for drives, and to the beach to put my feet in the sand. At times I didn’t feel like doing anything or even leaving the house, but she was always there to encourage me and remind me of all the beauty left in the world to experience. She would also try to help me with meals when I was on a restrictive diet for treatment and even followed the diet with me during one round. I still believe her love and presence was a major part of my mental and physical recovery.”

4.On the day I went in for my last round of chemotherapy, I looked and felt like absolute garbage. As I sat in lab medicine waiting to have my port accessed a kind woman came up to me and said, ‘In all of my years sitting in the Dana-Farber waiting room I have yet to see someone look as beautiful as you.’ She told me how my smile (the one I thought I lost a long time before this day) radiated from across the room. This woman reminded me that if I got through this last round of poison I could sit in the DFCI lobby for years to come and make other struggling cancer patients smile just as she did for me.”

5. “There was is a little girl, about 9, who has leukemia, and she used to visit me when I first started chemo. Every time she saw me she’d come running over as fast as she could and tell about all the Pokémon that she had caught. She knew I was in pain, and all she wanted was to take my mind off of it… it kills me that a kind and sweet little girl has to go through so much.”

6. “It’s happening right now. We had a burst pipe so a restoration company was brought in. USAA has been wonderful to us. They and the contractors have done many extra things to help us in the house. Old friends are becoming fresh again. I’m treated surely better than I deserve by most. We are humbly grateful to all who have helped or just been kind to us.”

7. “I was diagnosed stage 3 positive breast cancer at 31 (last year) with no children of my own and no time to postpone treatment for six weeks. My oldest friend offered me her eggs to be able to have my own children. Unfortunately due to my cancer type I still cannot carry my own children. There is no bigger gesture.”

8. “I went to check out my town’s brand-new cancer ward. The receptionist asked if I had an appointment, I told her no, I just wanted to see what it was like, as I was looking at a ‘giving tree’ with hats on it. I stopped at one with a breast cancer symbol and I guess she noticed because she asked if I knew someone with it. I told her yes, my aunt did and it runs in my family. She told me to take the hat to give to my aunt and that she’d pray my aunt beat it. My aunt had been looking for hats she liked and that one became her favorite.”

9. “Five years ago my grandfather [died from several types of cancers]. Prior to him losing his life, he had to travel five hours to get chemo, and it was taking a massive toll on my grandmother. The community banded together and made up a driving roster and meals roster so my grandmother didn’t have to worry about the driving or food, it was all taken care of.”

10. “My children and my grandson were there with me each time I had my chemo. In fact, my grandson made me so proud when he went to the cafeteria to get a burger. He was young but when he returned with his burger, one of the other patients getting treatment asked him what he had. He offered to get a burger for the other patient and asked his mother to hold his, not once thinking it would get cold. He went all the way down to cafeteria to purchase a burger for that person. When he returned his own burger was cold but he never complained. At that moment I was so proud that I never felt the pain I was going through. I will never forget that for as long as I live.”

11. “I have tried every treatment option for this cancer and there were no clinical trials in the Midwest. So down to Texas I went to get a second opinion and they had a spot in an immunotherapy trial! But travel and medical expenses were an issue. So out of the blue my childhood friends set up a GoFundMe page that raised $10,000 and ex-coworkers set up this huge benefit for me and my family! All the love and support from friends, family and our community was amazing. I am so blessed to have these wonderful people in my life!”

12. “Friends from church minded my boy while I had chemo, fed my family for three months and cleaned my house. These women from my church were amazing. They made sure my little girl who was 3 did not feel left out, ringing her little gifts when they arrived. No words can express how much they did for us as a family. Their support allowed us to rest and be together rather than shopping and cleaning… In the middle of all this the bank rang. They had noticed we kept going into overdraft and wanted to introduce a new local manager. I explained what we were going through and they suggested an overdraft, $3,000, at no cost to us, for three months. This allowed us to pay the multitude of bills that were coming in and financially survive.”

13. “We just found out my mom was sick and I was supposed to go to a LuLaRoe (leggings) party. Since I had to cancel, the consultant sent leggings to us for free with a cute card. At the bottom she put this. Cancer sucks but we have so much love and support, it will never ruin our spirit!”

piece of green paper with words PS fuck cancer

14. “My daughter who will be 2 in February has leukemia, and she has been greeted with smiles and hugs each time we enter clinic appointments. Her nurses and doctors all have a special place for her in their hearts, and it shows in everything they do. Her social worker gave us a $500 gift card to help us out with medical bills. That woman is a blessing.”

15. “I’m a stage 4 non-Hodgkin Lymphoma survivor who has been healthy for two years. I had a lot of unexpected kindness from the relative who sent me a card every week when I was sick (at first I thought she was getting older and didn’t realize she had already sent me a card, but she was just genuinely lovely), to a friend across the U.S. who sent me random packages of small things to make me smile, to my hairdresser who didn’t charge me when I cut off my hair to donate when I started chemo and did a free makeover when I got better, to my best friends who gave up our annual girls weekend away and turned it into dinner two towns over from me just so we could be together.

You know who your friends are, but you don’t know the level of compassion people have until you go through a major illness.”

Have you experienced an act of kindness in your cancer journey? Share your story in the comments below.

The Mighty, in partnership with Fuck Cancer, is asking the following: Write a letter to yourself in regards to a cancer diagnosis. What would you say or wish someone had told you? Find out how to email us a story submission here.

15 Unforgettable Acts of Kindness That Helped Cancer Patients Through Treatment



, Listicle

How to Fully Embrace the Transformative Process of Illness


Most of us are familiar with the butterfly as a symbol of transformation. The tricky part is, it is the symbol of manifested transformation, rather than the path that brings us there. And while it’s nice to have the final goal in mind, it can be overwhelming to try and figure out how to transform ourselves, especially when our desires for transformation are often large in nature and involve changing beliefs, habits and so forth that are holding us back from full transformation.

In my mind, if you seek transformation, you might chose the caterpillar as your muse. Caterpillars are born knowing the one thing they need is nourishment to grow. Bit by bit they take small bites that grow their bodies and energy stores, trusting they will know what to do and what they need. The energy is slow, deliberate and purposeful. They are in tune with their process, they know when it is time to rest and time to do. When the urge comes to construct the chrysalis in which they will cocoon themselves for the final stage of transformation, they find a safe and protected place to settle. They stay inside their cocoon until they know they are ready to emerge. Even once the transformation is complete, they take the time they need to open up again, prior to lift off.

Many of us who are diagnosed with a life-threatening condition hope the experience will help us transform in some way. It is the silver lining of facing death. Yet, the experiences we have gone through to heal ourselves are often traumatic, and it takes time to process what our body, mind, spirit and self have been through.

Recently I was working with a cancer survivor who is about to end treatment, and with her permission I will share some of what we discovered. In the session, she was identifying how some old patterns of thinking and feeling have begun to re-emerge as treatment comes to an end. Patterns she had gotten a reprieve from while she was going through treatment. Her artwork reflected an empty circle in the middle (representative of identity confusion she has experienced throughout her life), with a chaotic dance around her of the parts of herself she values but feels unsure of how they can cohabitate. The added layer of this dilemma is wondering which of these parts were authentic expressions of who she is and which parts she developed to please others.

As we were exploring how this was impacting her through art, her own wisdom spoke to her to give her guidance about her needs. There was a visible relief, because she truly wants to benefit from the transformative power of facing cancer and was dismayed to feel old patters re-emerge.

Nietzsche once said, “When we are tired, we are attacked by ideas we conquered long ago.” As a psychotherapist, I have seen this be one of the driving forces that brings people into counseling. For nothing is more disheartening than to find ourselves slipping into mindsets or behaviors we thought we had mastered. Major life events can often trigger a resurgence of these old patterns, in part because when we are being challenged to confront a major life event, we are being simultaneously pushed to examine our unfinished business.

So find your inner caterpillar. Trust any sparks of inspiration that help you connect to that concept. Be gentle and patient with yourself, for you are in a tender and vulnerable point in your life. There is no need to rush. Finding small “bites” to tap into your experience and feeling them will allow you to grow and ultimately transform.

At the end of the session I described above, I asked my client if she wanted to draw an angel card at random to see if it would offer a bit of insight or inspiration for moving forward. She did, and we both got goosebumps when she discovered the word she drew was birth, or in this case, rebirth. I am with you in solidarity, whether it is through this blog or in person. I hope you can feel it.

We want to hear your story. Become a Mighty contributor here.

The Mighty, in partnership with Fuck Cancer, is asking the following: Write a letter to yourself in regards to a cancer diagnosis. What would you say or wish someone had told you? Find out how to email us a story submission here.

Image via Thinkstock.


I'm Giving My Family Permission to Celebrate the Holidays Despite My Illness


When I became very ill for the first time, many people around me started walking on eggshells – especially around the festive season.

silver reindeer decoration Though I personally do not mark Christmas very much, in the places where I live (UK) and where I was born and raised (Germany), Christmas and the New Year are widely celebrated. But during that festive season especially, my close family does not know what to do for me.

When I was diagnosed with breast cancer it was May. By December, the chemotherapy (not the cancer) had left me too ill to make a short flight to join family for Christmas in Germany, which is our tradition. I was too weak and frail to do very much at all. My parents were too old to come and visit me.

I did not mind. I was too unwell and tired to make a drama out of it. But for others, the situation had turned into an issue of personal conflict, loyalty and social etiquette.

When no one talked about it initially, I knew something was up.

Eventually, after some probing and encouragement, my parents and others opened up.

Was it OK to celebrate Christmas? Was it OK to visit others? Was it OK to put up the old Christmas tree in its usual place? They were worried what it might be like for me if they did.

My parents were…

  • worried I might think they did not care.
  • worried I might think their lives had not been affected.
  • struggling with how to cope and live with the knowledge that their child might die before them.
  • grieving that all their hopes and dreams about their life in old age had been shattered.

They needed my permission and blessing and support. I knew that and my heart went out to them.

And then there is the issue of social etiquette – conforming to social expectations. Depending on where you live, this can be felt strongly, or not. And I think that also played a part in the uncertainty and need for my blessing. “Karin said it would be OK….” I do not blame or feel offended. I understand.

Clearly, December, Christmas, New Year’s and life (both theirs and mine) would never be the same again.

The diagnosis, illness and treatment had been like a massive earthquake, destroying everything. How was I going to rebuild? Was there time to rebuild? My life has been shortened. While the diagnosis was not terminal, predictions vary. So much uncertainty.

With all that going on, and radiotherapy just starting, I felt overwhelmed by others struggling to do “the right thing” by me, by themselves and by others. I understood it, but I was also saddened and angered by it.

I did not want Christmas to be yet another thing that was affected and destroyed by my change in fortune.

Everything had been thrown into question, and to have some continuity of tradition was strangely reassuring. Even though I do not decorate my own home much at all, it did matter that my parents’ home would be as it has always been.

I did not want to have to emotionally rescue others when I was struggling to rescue myself. My energy was and remains limited.

I was angry to be put into this situation, because it felt like others were weak when really I needed them to be strong and take charge. This might be unkind, but that is what I felt then.

So, I did give permission and honest encouragement to “celebrate” as much or as little as they saw fit. It mattered to me that, unlike concentric circles, my illness did not push away everything.

For now, life continues with me. At some point, life will continue without me. I do not want or need drama.

I want and need normality that works for me, even and perhaps especially during the festive season.

This post originally appeared on Karin’s blog: Between Self and Doubt.

We want to hear your story. Become a Mighty contributor here.


The Emotional Impact of Cancer Does Not Disappear Post-Treatment


Not knowing how to cope with life after cancer treatment is common. Sometimes we have seen too much, gone through too much, fear too much to relax into “remission.” It can feel like our life has turned into one big uncertainty. What to do?

With fewer medical appointments, and the potential expectation of people around us that life will go back to what it was, we may find it hard and experience anxiety, depression and loneliness.

Treatment side effects may reduce or disappear altogether; physical energy can start to rebuild, and some people return to work. Cancer becomes a less frequent topic of conversation.

Sometimes people try to continue with their lives where they left off, in the hope those weeks and months of trauma, panic, chaos and fear turn into vague memories of a distant past.

However, it is not always as simple and straightforward as that.

Cancer is a life-changing disease, and this includes life post-treatment.

While every person with cancer will have a different experience and different way of coping with the emotional impact of treatment and having (had) the condition, there can be common post-treatment realities:

Delayed reaction to the trauma of diagnosis and treatment: often everything happens so fast that there isn’t time to digest the enormity of what is happening.

The ending of regular medical care and appointments: you may only have check-up appointments, which might make you feel vulnerable without regular medical attention.

Life around continues “as normal” in the world, at home, at work, with friends, while you have undergone one of the most life-changing experiences: You cannot be expected to go back to “normal” and pretend your cancer never happened.

Perhaps the most potent issue of all is that of uncertainty over whether the cancer is coming back, or not. Most people will have been told the symptoms of secondary cancer, which depend on the nature of the initial cancer. This might result in a heightened sensitivity and alertness to any sign of discomfort. At least that is my experience — some days are easier than others.

Some people will have experienced financial hardship during their cancer treatment due to their inability to work and pay bills, rent or a mortgage. Others are still not well enough to return to work, may never be able to return or proactively decide against returning to their previous work schedule.

Some people will have had less supportive relational experiences during their treatment from family and friends. It is not uncommon for some (for reasons of their own) to find it difficult to be around people with serious and terminal diseases.

Fear, uncertainty, anger, anxiety and depression can be associated with these experiences, which can lead to emotional exhaustion. This is why the emotional impact of cancer does not disappear post-treatment.

This can be a common occurrence, and it does not mean the person finding himself or herself in this position has done anything wrong or failed, or has not done other things well enough.

The key issue is what are you going to do about it. Some of this requires a mental shift, a slightly different way of looking at things.

1. What you are experiencing is normal, which does not make it less easy — but you are not alone in feeling this way.

2. You are entitled to your anger and outrage about having (had) cancer — the pain, loss and uncertainty you are facing.

3. You have options and choices of how to manage your life and relationships. Often a cancer diagnosis and treatment can change your perspective.

4. You might find yourself emotionally and physically more fragile than you may have been before. Looking after yourself and avoiding stressful situations is essential. This can range from small things like avoiding a packed bus or going shopping at less busy times, or reviewing your work and domestic arrangements.

5. Take regular (even small) breaks throughout the day, where you focus on yourself.

6. Self-care can include a healthy diet, regular (not necessarily energetic) exercise and fresh air to help reduce stress and assist your physical and emotional well-being.

7. Be aware of what triggers your anxiety and stress, such as an upcoming check-up or arguments at home.

8. Follow your intuition and start saying “no” when you want or need to.

9. Remind yourself how much you have endured and how well you have done so far.

10. Dealing with cancer is more complex than a “10-point to-do list” could ever attempt to tackle. Your cancer experience is as individual as you. Design your own “10-point list” and update it from time to time as you continue to change and move through your life as best as you can.

Counseling can also assist in digesting and working through the emotional impact of a cancer diagnosis, treatment, life with and beyond cancer. Talking to someone who is independent can help release difficult emotions, free up space for renewed thinking and making positive choices.

A version of this post originally appeared on Between Self and Doubt and was based on an article written by the author on Counselling Directory.

We want to hear your story. Become a Mighty contributor here.

The Mighty, in partnership with Fuck Cancer, is asking the following: Share a story about one moment or conversation related to a cancer diagnosis or experience that made an impact on you. Find out how to email us a story submission here.

Image via Thinkstock Images


What I Realized About My Cancer Journey After I Fell Off My Bike


There are few words more harmful to me right now than “we would like to give you as much time as we can.” Those words are being said to me often, though, and so I’m trying to adjust accordingly. I am in no way shape or form dying, but those words hit me right in the heart. How do I respond? I laugh. Not psychotically, but just because I need to. Let me explain.

When I was diagnosed, my baby brother, already dying, turned to me and said, “Welcome to the club, Kelsey!”

“Welcome to what club?” I responded, already smiling.

“To the cancer club, of course!” he said, a big grin on his face.

I laughed and laughed even further still when he started calling us the “terminal two.” I wasn’t terminal, but he surely was. And when he started going down to the point past possible return, he would still turn to me and say with a smile in his voice, “Kelsey, we’re the terminal two!”

I laughed. I always laughed. Because even though it wasn’t and is still not true for me, it was true for him, and laughing was the only way to get through it.

As my recurrences get more frequent and closer and closer together, I have my freak-outs and then I pause to laugh like a person who doesn’t have a care in the world. I would rather it that way.

Many people outside of my immediate family are still horrified at the ways in which we handle bad news. But they don’t understand that laughing is simply the best way to deal with the anvils that drop frequently and joking about bad stuff really does help in the wake of the destruction that those things actually leave.

I went on a relatively short and beautiful road bike ride through the trees this weekend. The fall colors were incredible. We kept biking through little pockets of cool air, and the trees looked like they were glowing and on fire. As we made our way down the trail, I realized two things: My muscles have atrophied because weeks of radiation following recovery from surgery is not conducive to a rocking bod, and that I was feeling lucky. It was during my euphoric realization of being happy that I crashed unceremoniously and slowly to the ground.

I fell twice on that ride — a road ride, an easy road ride — partly because I’m now too slow to unclip from my pedals fast enough to stop myself, and partly because my muscles get angry and tired and reluctant — really quickly.

During this current round of radiation, my body is really feeling it, and I feel as though sometimes my body just tries to give me the finger when I am pushing it.

As I brushed the scrapes and twigs and pebbles from my legs and arms and picked up my glasses from where they flew when I went down, I started to chuckle. I laughed at the ridiculousness of the fact that my body is actively fighting me, I laughed at the picture in my head of me slowly tipping over, I laughed with the beautiful day and the luck that I felt to be there. I laughed harder still when I got home and saw the bruises that seemed to bloom like weird flowers, the darkest of blues, absolutely covering my legs and arms.

“This is what my cancer looks like,” I thought. Bruises and pain and scars and not being able to ride my darn bike during treatment for fear that I will tip over. But I will do it anyway. And I will get better and stronger, and I will ski and jump and dance and act the fool that I am because if I do not do that, I am not giving my life the justice it deserves. At the end of the day, I would rather fall asleep with a trace of a smile on my face thinking about how absurd the world is than thinking about how scary it can be.

So when you see me in 80 years in my rocking chair with a cup of tea and a good book next to a fire and the person that I love, I will be the opposite of bitter, with a smile on my face and a laugh in the air.

We want to hear your story. Become a Mighty contributor here.

Lead photo source: Thinkstock Images

The Mighty, in partnership with Fuck Cancer, is asking the following: What was one thing you thought immediately after your diagnosis that you completely changed your mind about? Find out how to email us a story submission here.


What Working at a Children’s Cancer Organization Means to Me


Two months ago, I lost my father to lung cancer. Years ago he had survived prostate cancer and treatment, but he just couldn’t win the battle against his stage 4 diagnosis.

As I sat with him in his hospital room, seeing him helpless and breathing through a ventilator, I wished he had caught the cancer sooner. I wished for him to be cured and be the dad I saw just 10 days earlier laughing with his granddaughter. That’s what most people who have a loved one diagnosed with cancer wish for, but in most cases, the wish doesn’t come true.

I admit that my spirit was a bit broken after he passed away. It wasn’t easy to go back to my job as the content manager for CureSearch for Children’s Cancer, an organization dedicated to finding pediatric cancer cures.

In fact, it was emotionally draining to write stories about children being diagnosed with Ewing sarcoma at 3 months old and about parents who had to watch their only child lose their fight against brain cancer. Every story I read reminded me of my father, and it reiterated that cancer can strike anyone, young or old, at any time.

Despite the difficulty of easing back into my job, I immersed myself in it. It was what I needed to do to move on, and it was what I wanted to do to learn more about this deadly disease. Through my organization, I learned more about the 43 children diagnosed with cancer each day, the 60 percent of cancer survivors who cope with late-term effects like heart failure and secondary cancers and the more than 15,000 parents who will hear the words “your child has cancer” this year.

I learned that on a national level, pediatric cancer research receives only 4 percent of
funding, and that researchers who want to find cures for cancer are the most vulnerable to these federal funding shortages.

It’s always shocking to hear statistics and facts like this, especially when they refer to children. However, it is easy to feel detached when there isn’t a specific name or face associated with it. 

That’s how I initially felt until I started hearing firsthand from parents and cancer survivors. I talked to Board member Annie Gould, a mother who lost her daughter, Eloise, to rhabdomyosarcoma. She has made it her mission to keep the memory of her daughter alive and to raise awareness for the need for research. To date, she has raised over $250,000 in walk and hike events to go toward cancer cures.

I attended a local walk event in Virginia where the featured speaker was Beau Swallow, who was diagnosed with Ewing sarcoma when he was 12 years old. He is a survivor and now attends college, and he never takes for granted a single day of his life. After he spoke, as part of every CureSearch walk event, parents and loved ones released gold balloons into the air. They were in memory of the children lost to cancer. It was heartbreaking to see, but when I looked around at all the people standing here for a common cause, it made me feel that although I may have lost one member of my family, I just gained many more.

Then I learned that a father, Ralph Currey, is going to donate money from his CureSearch Legacy family foundation to help fund research for Ewing sarcoma. Ralph’s son, Nick, survived leukemia as a young boy, but he later developed Ewing sarcoma and passed away at the age of 19. Childhood cancer survivors are nine times more likely to develop a sarcoma or experience devastating side effects that result from toxic therapies, and that’s exactly what happened with Nick. Ralph is going to donate thousands of dollars toward the work of Dr. Mary Beckerle, whose goal is to find new and improved therapies for Ewing sarcoma that either represent a real cure or are less toxic than conventional chemotherapy.

These are the stories of real people who have been affected by cancer, just like me. These are the stories of people who continue to push for a cure so that people like me won’t have to deal with the devastating loss of a loved one. These stories inspire me to move beyond my grief and to do something that matters.

I’m honored to work for an organization that I’m personally connected to and whose mission is to put an end to cancer.

If you are someone affected by cancer, consider making a donation to CureSearch and give at least one of the 40,000 children undergoing cancer treatment in the U.S. some hope.

We want to hear your story. Become a Mighty contributor here.


Real People. Real Stories.

150 Million

We face disability, disease and mental illness together.