Showing posts with label cancer. Show all posts
Showing posts with label cancer. Show all posts

Monday, 11 December 2017

The Magic of Emperors Palace Garden of Lights

Emperors Palace kick-starts the festive season with the dazzling Garden of Lights
Christmas Lights! There's nothing that kick starts the festive season better than Christmas Lights! Emperor's Palace has switched on their magic Garden of Lights for the tenth time this year.

Best of all! You spread kindness by going! The proceeds from the R25 entrance fee will be donated to The Cancer Association of South Africa, and the Peermont Childrens and Education Trusts. Children under two go in for free, and a family of five only pays R100.

This is the first time we saw the Garden of Lights! It is well worth the drive to Emperors Palace if you are not staying nearby! The Garden of Lights was switched on on Thursday night, and the night was perfect at the Peermont D’oreale Grande Hotel gardens. The rain gave us a little break to have a wonderful unforgettable experience!
Emperors Palace sunset

Monday, 31 July 2017

Celebrate Women - Young cancer survivor Jenna Skews

Twinsaver Celebrate Women in August - Jenna Skews
Twinsaver honours special Women in August with a special edition pack supporting breast cancer survivors by donating a portion of the 9-pack to charity.

The story of  one of the young survivors, Jenna Skews, hits very close to home. Our Eldest also had to deal with finding a lump in her breast. It was a big shock, as we realized that 18 year olds can get breast cancer! The first diagnoses was that is was non-malignant, and that we should not even worry. Luckily we got a second opinion, and now we know that she cannot ignore it, and needs to check it regularly. So far the fibroadenoma has not increased in size, and the hope is that it will disappear after a few years. But we cannot ignore it! It needs to be checked!

Friday, 24 June 2016

SA Musician Garth Taylor to fight for children fighting cancer

Garth Taylor #YouPledgeIFight #cancer #children Little Fighters Cancer Trust
Garth Taylor #YouPledgeIFIGHT
Fridays are for caring! On this blog, at least!
There is so much wrong in this world, but fighting for a good cause and channeling your energy into giving or helping someone are what this world is all about! And what makes it worth the while!

That's why I get all excited when I see local musician Garth Taylor getting involved into a fundraising effort for the Little Fighters Cancer Trust. He was the South African Amateur Kickboxing Champion in 2014 in the Light Contact category. (I did not know that!!) The Childhood Cancer Charity, Little Fighters Cancer Trust, offers individualised and practical support to children fighting cancer, and their families, across South Africa. 

children, cancer, Little Fighters Cancer Trust,
Little Fighters Cancer Trust
Garth says, “After having my sister, Joanne, taken away from me by cancer, I have even more of a soft spot toward people who are fighting cancer. Having watched what she went through as an adult fighting this disease, I can only imagine how much worse it is for children who are suffering from cancer, to fight this battle. So, I figured, how bad can it be? Me, stepping into the ring and getting punched around for kids who are fighting for their lives every single day. I might as well see what I can do, if not through my singing, then by getting into the ring and doing something more exciting, so that people and companies pledge money and hopefully we can raise enough funds to help these little kids. I see cancer as a big bully hurting these children, and that is what I will be fighting for.”


Pledges and donations to get Garth into the ring will be administered via Garth Taylor You Pledge I Fight
Once the target amount of R100 000.00, has been raised and/or pledged, Garth’s boxing match, which will be part of “White Collar Boxing 14” will be confirmed and his opponent will be announced.


Read more: Garth Taylor You Pledge I Fight
 

Monday, 15 February 2016

International Childhood Cancer Day

CHOC

I can't think of anything worse than hearing that your child has cancer.
We luckily don't have any child in our nearby family that has cancer, but we had a little boy in the extended family who had cancer the previous year! We followed along on the journey on Facebook (they are living in another country), and we rejoiced with the parents when he was finally clean!

I know for a fact that all parents would happily exchange the suffering of their children with their own.

Today is International Childhood Cancer Day (ICCD). This day is part of a global collaborative campaign to raise awareness about childhood cancer and to express support for children with cancer, survivors and their families.To support ICCD, you are urged to wear blue on the 15th February, just as thousands of school-children will be doing throughout the country. Anything blue will do. It will all help in the effort to spread the message and create awareness.


The great news about cancer in children: 80% of children survive it and continue to live healthy lives!



To support CHOC and ICCD, join the CHOC Facebook page
Visit the website at CHOC
Call 086 111 3500.


Monday, 26 October 2015

Walking for a purpose - iThemba Walkathon


We took part in the yearly iThemba Walkathon yesterday. We first started when we became aware that nobody is exempt from breast cancer, not even an eighteen year old! It has been a yearly fun day for the family. Unfortunately The Student could not join us yesterday, although she was home (because of the lock-downs at universities), but she still has the rubber arm.


Little Miss did very well, and walked most of the way. She had to be bribed with an ice-cream, and "it's just around the corner", but she made it! (I think we struggled more, being as unfit as we are...) But we finished the 8 kilometres!


It took nearly twenty minutes to get past the starting line yesterday morning at eight. It's not strange if you know that there are 25 000 people taking part. But it was NOT fun stuck in that crowd not being able to move for quite a while!


Of course our beautiful city saved the day with it's skyline, it's purple streets and the friendly people!



That was the final walk for the MomAgain@40 clan!
I am glad that iThemba Walkathon gets so much participation, but it seems that the services and structures are struggling with the high numbers!

A photo posted by Karen Du Toit (@karentoittoit) on
Did we miss seeing you there?

Monday, 12 October 2015

It's not too late! You can still buy your bandana today! #BandanaDay


The slogan for this year's National Bandana Day! "We heart Bandana Day!"

By buying a bandana from Pick 'n Pay, you will be contributing towards paying for the expensive tissue typing (DNA) tests for new stem cell donors to join the South African Bone Marrow Registry (SABMR). You will be helping to save lifes!



For more information on Bandana Day or how to become a stem cell donor:

Toll free helpline: 0800 12 10 82
www.sunflowerfund.org.za

You can also take part in this fun pet competition!


Because it's a Monday, I forgot to put on my bandana, but there's still time...
Watch out doggies!!

Thursday, 11 April 2013

A Story of Cancer Survival: How I Made It as a New Mother



A guest post by Heather Von St. James, who is trying to raise awareness about a deadly little known cancer, which is totally preventable, and also about the dangers of asbestos!

As a mother and friend to many who have been through this challenge, I hope you are never diagnosed with cancer. I was 36 when I was informed that not only did I have cancer, but I had a case so specific that it was going to be a real challenge to overcome. The year that I was diagnosed, I went through extreme highs and lows. The happiest day of my life was when I gave birth to Lily on August 4th, 2005. She was my husband Cameron and I's first and only child. However, just a few months later, we would experience a devastating blow to our new life together. 

I had an incredibly smooth pregnancy. Everything leading up to my cancer diagnosis never could have prepared me for what was going to happen. When Lily was born, we brought her home and prepared to share every moment with her, raising her to be a successful and kind woman. I realized soon after we got home that things didn't feel right. I didn't have any energy and often felt as if I was exhausted with the basic tasks. On top of everything, I was losing weight. It grew to be too much, and when I couldn't work any more, I had to go in for tests. 

About three months passed before the tests results came in. It was just three days before Thanksgiving. We were in the full holiday swing of preparing for baby's first Christmas as well. Sitting in the doctor's office and listening to him say that I had malignant pleural mesothelioma, I immediately felt myself going into a breakdown. On top of that, I was only given 15 months to live if I didn't go in for treatment right away. I simply couldn't believe it. I stared at my husband, tears in my eyes, shaking, and he realized that I needed help. The doctor was giving us a variety of treatment options, but I couldn't even think straight. All I could see was Lily growing up without a mother and missing all of the memories that I had thought of as a new mother. It was devastating. Cameron, seeing me in my state, listened to each treatment option and knew which one was best right away. I had to see a specialist in Boston who had a history of successfully helping mesothelioma patients. 

My treatment was going to be a challenge from the very beginning. The cancer had infiltrated multiple parts of my chest. I had to lose one of my lungs, parts of my heart, chest and diaphragm with a surgery called an extrapleural pneumonectomy. It would take me over two weeks to recover from the surgery in the hospital. Then, I would face the next challenge. I had to go through two months of chemotherapy and radiation. Even then, it was unclear whether I was going to beat mesothelioma. I had the highest of hopes, however. I continuously thought of Lily and how no matter what, I had to be there for her for as long as I could possibly be. It was even more difficult because I wasn't able to see her for many days while I was in treatment. The dreams that I had as a new mother seemed so far away, but I never lost sight of them. 

Lily lived with her grandparents during part of my treatment in Boston. Cameron was working full time. Such a sweet man, he was my rock and caregiver during this time. He never wanted me to know what was happening, but he needed help, too. When I went to live with parents and Lily in North Dakota to recover from my treatment, he continued to work and support our family. He was only able to visit once during this time. It was then that help started to pour in from other family members, friends, co-workers, neighbours and even strangers. I met people who had been through similar experiences or knew what it was like to go through cancer treatment, and all of those experiences made me even more hopeful that I would get through cancer treatment and be the mother I needed to be for Lily. 

Finally, I started to get ahead of the cancer breaking down my body. With mesothelioma, 95 percent of those diagnosed don't make it. I was able to not only beat cancer, but seven years later, I'm still cancer-free. I can never thank the people who came through for my family enough. They did so much to ensure that we had everything we needed to get through this battle. 

Now we have a healthy, beautiful family and a growing seven-year-old girl who just loves to tell people how she saved my life. I can't argue. It was the thought of her that got me through so many tough moments.



More can be read about Heather's story on her blog: http://www.mesothelioma.com/blog/authors/heather/


Thursday, 27 October 2011

Breast cancer awareness

Ithemba Walkathon 2011
I saw this on Laura's blog at Harassed Mom, from where she was tagged by Celeste over at Reluctant Mom.

I would like to answer these questions as well, because breast cancer is something that you can do something about. Before it is too late!



The Questions:


When did you have your first mammogram?
I went for a test in my twenties when a van came to our workplace. Never again after that!

Does anyone in your family suffer from cancer?
Luckily, no! But my teen gave us a scare about two years back when she discovered a big lump in her breast. It is called a  fibroadenoma, but she now has to have it checked every six months!
See: 18-year olds can get breast cancer

Why have you not gone for a mammogram?
I should have done it earlier... Guilty!
But I went in support of my teen for a sonar in July (also because the doctor insisted), and as soon as I stop breastfeeding I will go for the mammogram!

What were your mammogram results?
The sonar was fine! (A mammogram does not show the correct results when still breastfeeding.)

How bad is “going for a mammogram” on a scale of 1 to 10?
I can't remember that it felt that bad. I would give it a 3

When is your next appointment?
Three months after I stop breastfeeding. Don't know when that is going to happen!

Do you know anyone who has had breast cancer?
Yes, I have a colleague who went through a harrowing experience having to remove both breasts but now are declared 100% healthy. She caught it even before it developed into breast cancer! It is through her that I got the referral for my teen. We now feel very safe knowing that Dr Benn (Specialist in her field) will give us the right advice!

What is my point?
Do not accept the advice of doctors when they tell you to not come back again, or that you should wait until the diagnosis is cancer. NOOOO!
We were told not to come back for a regular check-up by a gynecologist...
My colleague was told that she should have her breasts regularly checked until the cancer is finally confirmed... (Scary!)

If you feel uneasy about a decision or opinion, get a second opinion! 
It is your health and your life!







Sunday, 16 October 2011

iThemba Walkathon 2011

The slogan: "Early detection saves lives!"

It was the yearly iThemba Walkaton against breast cancer today. There were even more pink people (literally) walking today than last year. We had great fun.Walking and watching all the people dressed to the "pink" passing us on the road.

We got involved from last year when the Teen discovered a lump in her breast. It turned out to be a fibroadenoma, but she still has to have it check every 6 months. Lesson: do not let anyone tell you to let it be... It can turn serious!

I also have a colleague who were told to leave her pre-cancerous breasts until it becomes cancer! NO!
Luckily she did not accept that advice as well! She went to see an expert in breast cancer. Se had to go through the whole traumatic decision of having her breasts removed, but she did it. Last week she got a clean bill of health! She is cancer free, and she can continue with her life!

I registered us for the 8 km walk, although we said we would  turn at the 5 km turn when we feels it is too much! There never came a 5 km turn because they joined us at some stage, so we did the 8 km again! (Pat on back! We got in some serious exercise today!)

The Toddler enjoyed the walk as well! Luckily we could still push her for most of the way!
Getting sleepy

Sleeping
Riding backwards and standing
On Dad's neck
Walking
"Avon Justine iThemba Crusade of Hope raises funds for breast cancer education and awareness in South Africa.
A donation will be made to Bosom Buddies and Look Good...Feel Better.
"
Related posts:

18-year olds can get breast cancer
The merry ways of Retha Buys: "Happy birthday dear Silliboobs..."
iThemba Walk against breast cancer 






Tuesday, 26 July 2011

The merry ways of Retha Buys: "Happy birthday dear Silliboobs...."

Pink Ribbon
I have a colleague who decided to have her boobs chopped before they become the dreaded C!

She took charge of her life and health, and I am amazed every day to see how positive and inspiring she is about the life-changing decision she made!

She picked up a couple of lessons along the way, and shared it on her blog.


The merry ways of Retha Buys: "Happy birthday dear Silliboobs....": "Yes, they are one month old today, or rather, one month young! And what a month is has been.... I decided to dedicate this day to lessons ..."

Sunday, 17 October 2010

iThemba Walk against Breast Cancer

We walked a full 8 kilometers today for the iThemba Walk against Breast Cancer from the Marks Park Sports Complex in Greenside, Johannesburg. Everyone was pink, and we had a whole lot of fun!

We pushed the toddler, and for the most part she was happy to sit for the ride.

I had registered us for 5 km, but when we got our numbers back it was indicated we were up for the 8 km.  When we came to the split during the walk, we decided on the longer route. It was a good exercise as well. I am proud of us!

I am glad that we were able to contribute in a very small way in the crusade against breast cancer. It is a wake-up call every time I see people walking “in-loving-memory-of”!

The motto to remember” “Early detection saves lives!”

The teen and I had a bit of a scare last year when she did a breast examination and she found a lump. It turned out to be a fibroadenoma, and the gynaecologist confirmed this year that it is nothing to be worried about...
But we had a big scare! I can just imagine when you realize the lump is SOMETHING to worry about...


iThemba raises funds for breast cancer education and awareness in South Africa. A donation is also made to the Bosom Buddies breast cancer support group.

Wednesday, 14 October 2009

Standing still

One of our dear friends Juanita has just started with her first chemo treatment. She’s got Hodgkin’s disease, but it is the cancer with the best prognosis with regards to chemotherapy (says the doctor). She sent me a sms yesterday that it is affecting her very badly. She has sores in her mouth, her muscles hurt and it goes into spasms. When they went to see the doctor, he said that it is part of the symptoms, and its effects are different for each person. She asked me how it is going with us, and it felt strange to sms back about our ordinary lives where our biggest news is that Mieka is more interested in walking than in crawling. I feel guilty and grateful that our story is as boring as it is.
It is strange how we all go through different phases of living and dying in our lives. We have a new life in our lives. My mom on the other hand had an operation on Monday on a frozen shoulder, and she is also de-activated from normal living for a few weeks. The frozen shoulders had a huge impact on her quality of life before she went for the operation.
Life sometimes brings you to a standstill, and then you’re off speeding again. The secret is to enjoy the stops and the accelerations. (Before I start gagging on the clichéd expressions, let me stop!) The wisdom most probably rubbed of from one of my favourite authors, Neale Donald Walsh… (Smile). I have been reading two or three pages every night of “When everything changes, change everything” for the past three months. Having a baby in the house changes your reading habits dramatically (sigh). But I will get there again, reading until the early mornings…
Juanita, we hold thumbs that all goes well with getting healthy again! Mom, I hope you will be able to hold Mieka very soon again!

(It is Bandana Day in South Africa today, where funds are being generated for cancer patients).

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