Kidzcan Children's Cancer Relief

KidzCan Vision: A compassionate world where children with cancer are given the chance to lead healthy and fulfilling lives. Kidzcan Mission: KidzCan is dedicated to increasing the survival rate of children with cancer in a loving and caring environment. Strategic Objectives: To provide a supportive and caring environment for children with cancer and their families. To improve early detection and effective treatment for children with cancer.
Mar 11, 2013

Kidzcan Volunteers

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Why do I volunteer with Kidzcan?

Kidzcan volunteers play with the children in the hospital playroom every weekday morning. Play is what a child does best, and we find this a valuable tool for distracting them from their illness, loneliness, and pain.  Kidzcan’s group of dedicated volunteers who visit the children to play with them, read to them or lead them in activities are the back-bone of the work that Kidzcan does.

Sally is Kidzcan’s volunteer coordinator. She not only spends time each week playing with children in the ward playroom, but also attends to the needs of our volunteers - liaising with and registering new volunteers, keeping the group in communication, and leading our monthly volunteer meetings. 

Here is her feedback when asked why she volunteers - 

I had spare time on my hands and knew that I would like to be involved with Kidzcan, so offered my services. This has opened up a new world to me. Initially I was concerned that being with such sick children would be difficult. At the same time, I also knew that if in any way I could make their lives just that little bit better then I had to give it a go.

Going into the playroom and being with the children for a couple of hours a week is an incredibly humbling and uplifting experience.  I know it is important that these children get some 'time out' from what is happening to them and are able to participate in activities (whether it be painting, playing card games, playing 'quiet' physical games, singing, etc.) to take their minds off their illnesses. When I see their joy when we play with them, it makes my efforts to facilitate this all worthwhile.

I have always felt that it is important to give something to others, especially to those less fortunate than I am. But I realized it would be a commitment, and unless I was prepared to fully commit myself then I felt I should not offer my services, whatever they may be.   I am also a person who generally feels more comfortable when given specific tasks to do rather than seeing what is needed to be done so in the past have been cautious about offering my services.   

Volunteering at Kidzcan has put me in touch with amazing folk who give so selflessly of their lives/time and for this I am also very grateful.



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Dec 11, 2012

A Visit with Karen & Christmas Trees Decorated!

A Visit with Karen

 “Love is what makes you smile when you’re tired.”  I think of this quote from the mouth of a 4 year old, while I sit talking with Karen and her family. How tired they must have been over the past year, and yet, they are all smiling and enjoying time together. 

 Karen is 12 years old. She was diagnosed with Leukemia last year. Her mother remembers the day vividly. It was November 18, 2011. Karen had been unwell and had a lump on her neck.  On the advice of her local doctor, Karen’s mother, Maidei, took Karen to Parirenyatwa Hospital. They travelled from Norton, 45 kilometres outside of Harare.  Karen was frail, so she was immediately admitted to the hospital.  Both Karen and her mom stayed at the hospital for over a week, waiting for the results, knowing there was a chance that Karen had cancer.

Meanwhile, Maidei’s sister, Daderai, was at home taking care of Karen’s younger brother and the other household members. Daderai and Maidei, work together selling vegetables and fish in Norton. They travel to Mbare, Harare’s largest market, to buy the vegetables and other items, and then to Darwindale, where they buy the fish. These sisters are very close, not only in business, but in their family lives. They were living together and raising their children together when Karen fell ill.  

Daderai not only helped at home, but also spent many days visiting Karen in the hospital, where Karen has spent many months over the past year. When Karen came down with an infection in February, she was readmitted and remained there for almost 3 months. She then came back for another 6 weeks when her health failed again in July. Both times, the doctors stopped chemotherapy until she was stable. It was during these times that both Madei and her sister worried that Karen would not make it. 

Karen’s aunt tells me about these times and the point at which Karen said, “Help me God, I need a rest. I now surrender.” Such poignant words from a young child. But Karen is a stoic pre-teen. Not many words from her, but what she does share is thoughtful. 

Karen leaves the room and comes back with this photo - it’s of her when she’s at one of her lowest points. She wants me to share it so that others can see that you can go from this to feeling well and strong again.

Karen is a typical tween who wants a cell phone so that she can join Facebook and What’s Up  - to chat with her uncle in South Africa, she tells me.

Karen is back in school, and seems to have not missed a beat. After missing 3 terms, she has managed to catch up and reenter at her grade level. Her mother transferred Karen to a school that has smaller class sizes after learning of the importance of keeping Karen away from possible sources of infection - crowds tend to be a major culprit. Not only that, but they have moved out of the house they were sharing with Daderai and her family, to further reduce Karen’s risk of infection. This must be a financial burden for Madei, but a sacrifice she is willing to make for her child.

Karen mentions her best friend, Panashe (who happens to be Daderai’s grand-daughter). I ask her what they like to do, and she tells me, “play with dolls, do puzzles and play Uno.” She tells me that she learned to play Uno at the hospital.  “Sally, Christine and Vimbai taught me how to play.” She says. “They used to play with me when I was stuck in hospital. And, I taught Panashe.”

Sally, Vimbai and Christine are Kidzcan Ward Volunteers. They visit the children on the wards each week and play games, do arts and crafts, or simply read to the more frail children.  Their gift of spending time with the children continues to give long after a child leaves the ward.

Karen seems strong and on the track to survival. She will continue chemotherapy for 2 more years, traveling back and forth from Norton for monthly treatments. 

Madei hopes to afford a bone marrow transplant for Karen, however the nearest facility for this is in South Africa. Once she raises enough funds, they will go down there, stay with Madei’s brother, find a donor match, and get Karen the bone marrow transplant. This is beyond the scope of services Kidzcan provides, but we continue to provide services here in ZImbabwe. We hope that Madei and Karen are successful in their efforts to secure funding for the transplant. When it happens, Kidzcan will be here waiting to help when they return to Zimbabwe for their follow up treatments.

 

Christmas Is Coming!

Kidzcan Volunteers have been busy making Christmas decorations with the children in the A4 Special Playroom. They set up the Christmas trees and decorated them with the children this week, and everyone is excited about the gift-giving on December 13th!  

We will send you photos of this next week!


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Sep 18, 2012

Kidzcan's Gold Medalist!

Mckeena Today, 9 years old
Mckeena Today, 9 years old

Her favorite singer is Rihanna; she’s an award-winning swimmer at her elementary school; and lasagna is her favorite meal. 

Sounds like the average 9 year old girl, right? 

But, Mckeena is not your average 9 year old girl. Five years ago, she was diagnosed with Wilm’s Tumor, which is a solid cancerous mass found in one or both kidneys, usually in children between the ages of 1 and 5. 

Some of you may remember Mckeena from the story we shared with you when she was 4 years old and had just completed her final round of chemotherapy.  

Mckeena went through 3 months of chemotherapy before her surgery to remove a massive lump on her right kidney, as well as several lumps on her left one. She then underwent a year of monthly chemotherapy treatments, which landed her in the hospital for several nights each month. Followed by the accompanying 2 weeks of feeling sick and uncomfortable. 

Now it’s 5 years on. 

Mckeena is a healthy 9 year old, and is looking forward to going back to school next week after the August school break. She had her last scan a week ago, at which the doctor told her and her mother, Jean, that she was “all clear”. They do not need to continue to return for their yearly scans - just for check-ups, or if Jean feels there is anything wrong with Mckeena. 

Mckeena talks about school and her cousins. I learn that she is such the star swimmer at her school, her classmates call her Kirsty after the Zimbabwean Olympic Gold Medalist.  “When you come out of the pool, you’re hungry!” she says.  (Coincidentally, Mckeena’s favorite stroke is the same one that Kirsty Coventry swims - the backstroke).

She talks about Sestah, the nurse matron on the cancer ward at Parirenyatwa Hospital.  Mckeena spent a lot of time with her over the years, and she misses her, she tells me.

Jean and I talk once again about the time when Mckeena was diagnosed and then undergoing treatment. When Jean speaks about Mckeena’s treatments of 5 years ago, she seems to remember it as if it were yesterday - she speaks about it with complete clarity.

We discuss how it is difficult for the parents, and how Jean continues to go in to visit the ward, and the nurses there. She spends time with Sestah. She reaches out to parents who look forlorn and confused and sad. Trying to give them comfort in the knowledge that their child too can survive - like hers. We also talk about how we have to remember that no matter how hard it is for the parents, it’s that much more so for the child who is the patient, and how sometimes we forget that. 

She relates that it wasn’t until she needed a canula (an implement primarily used for the administration of intravenous fluids, for obtaining blood samples and for administering medicines) inserted into her vein once when she was unwell last year, that she could finally understand the pain that Mckeena was feeling with all those sticky needles. “Yeah, it hurt!” intercepts Mckeena.

I ask Mckeena who her best friend is, she tells me about Amy.  I remind her about the time we met when she was four and I had asked her who her best friend was - she told me “Francis” (Francis is Kidzcan’s Medical Support Officer). McKeena smiles and laughs when I remind her of this.  Francis had spent a lot of time with Mckeena and Jean over the years, organizing scans, and medicine collection, visiting with them on the wards and in the playroom each time Mckeena was an inpatient for chemotherapy treatments.

Makeena and her mom promise to join us for the next outing to Greenwood Park for inpatient children, and we say goodbye.

  •  Kidzcan provided Mckeena with free Chemotherapy drugs, prescription medicines, x-rays, CT scans, play-therapy, and family psycho/social support. 
Mckeena 6 years old, with Francis
Mckeena 6 years old, with Francis
Mckeena 4 yrs, with Francis
Mckeena 4 yrs, with Francis

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