Living with an incurable cancer
With his diagnosis carrying a median survival rate of four years, Fareed Bruintjies, 47, accidentally bumped into a patient who'd survived the same cancer for twelve years, in the chemotherapy room.
That woman, 11 years his senior, had undergone multiple treatments for 10 years. He realised that there was strength in the support of fellow-survivors. Her very existence confirmed the hope he'd picked up on, in researching the disease, a beacon for optimism. Fareed was optimistic and he knew he would have access to the best treatment. Though Fareed's story encompasses just about everything that can go wrong in a cancer survivor's journey, he's emerged more determined than ever to do battle with his persistent illness. He shares his story in his own words.
Bodily aches hide a cancer diagnosis
When lower back pain I had felt in December 2014 persisted through January 2015, I finally went to see a GP. I informed the doctor that I had been zip-lining in December and probably hurt my back in the process. I got pain killers and anti-inflammatories for the suspected muscle injury. Then when I didn't get better, in April, she referred me to an orthopaedic surgeon who suspected a slipped disc and continued medication, but added a spinal cortisone injection. After that I went for a Thai massage - and ended up in the emergency room over a long weekend. Again, they suspected a slipped disc.
By late April, 2015 I was on crutches and in a lot of pain, with nerve pain down both legs. I was ordered to stay flat on my back for two weeks and to take a bunch of drugs, which seemed to help. I went to see a chiropractor in May and she got me back on my feet, but the localised back and nerve pain persisted. On June 18th, I picked up my daughter, then 2-years-old, and pulled something in my right arm. I had stocks of anti-inflammatories, but when the pain remained for three weeks, I returned to my GP. She suspected a rotator-cuff injury and sent me for X-rays.
X-rays open Fareed's eyes to his reality
I remember it all well. It was the 8th of July, 2015. I got to my car and opened the sealed X-Ray envelope. Where the right humerus was supposed to be it was all black instead of white. The report spoke of suspected carcinoma or Stage 4 cancer that had spread from somewhere. I was in utter shock and disbelief. I'd had regular prostate screenings and no family history of cancer. I recomposed myself, went home and said nothing.
I'm the go-to person in our extended family. Until my diagnosis, I was an independent financial consultant for small and medium enterprise companies. I felt this couldn't be happening to me when I have so many other people depending on me! The GP's secretary called me the next day. I was to come in immediately. The young locum standing in for the GP found it emotionally difficult to break the news. I still kept it from my family as I wanted it to simmer for a few days, to give me time to confront my own demons. When I saw an orthopaedic surgeon for my arm, he sat me down to help navigate a way forward with the cancer, adding, “Oh, by the way, your arm is fractured”.
Straddling state and private healthcare
So, it was off to Helen Joseph Hospital in Johannesburg for a process of elimination via various tests. At 7:30, I was number 128 in the queue. Four hours later, I was seen for about 10 minutes. More X-rays and off to the lab, with a long shopping list of tests. They said come back in a week. Then, another long wait, with my arm now in a sling and me using a walking stick to get around. Then I was booked for a scan at Rahima Moosa Hospital. From there I went for a nuclear scan at Baragwanath Hospital. It was now July 27th. I left with the scan reports. Reading them, I learnt of a pathological fracture of the right humerus, compression fracture of the spine, three lesions on the thoracic spine and two on my left ribs.
I began trickle-feeding the cancer news to my family, based on what I knew they could handle. All hell broke loose, even though I said doctors didn't know exactly what it was. When my arm had been pinned and the biopsy done, I did physiotherapy. My shoulder had collapsed from disuse. Then I was referred to Charlotte Maxeke Hospital's oncology department with another list of tests. I was losing weight and quite sick.
I began chemotherapy on October 12th, for five months. I started suffering from an irregular heartbeat and a narrowing of the arteries in my limb extremities, which damaged the peripheral nerves in my hands and feet. We sorted the meds out and my heart settled. Another bone marrow biopsy showed I was in remission.
As part of the indicated treatment, I received an autologous stem cell transplant, where they replace your bone marrow to grow healthy blood cells. It's like a computer reboot for your immune system, but you're extremely vulnerable to infection. I picked up a gastric infection which caused blisters from my lips to my stomach. But I recovered. The tests showed that I'd achieved the best possible remission, but still needed four more months of chemo to consolidate everything. The physical collateral damage of one of the meds was osteonecrosis – death of bone in the head of the thigh bone at the hip. I'll need hip replacements in the future.
Dealing with an incurable cancer
I think Discovery Health Medical Scheme has a brilliant people in their oncology section who really understand how to deal with people suffering from the disease. They made my life a lot easier. In August 2017 I find myself on an oral chemo maintenance regime for six months at a huge cost, luckily I am covered by Discovery Health Medical Scheme. I've not been able to work for two years and this has almost crippled us financially. We had to sell one of our two cars. At some stage, it'll be back and I'll start all over again. This cancer is not curable. At least I have age on my side. Meeting that woman in the chemo room was a turning point for me. She was 58 and seemed well. We're in this together. You can draw a lot of strength from other patients.
Advice for fellow cancer survivors
- Hold on to your medical file as if your life depends on it, because it may.
- Allow yourself to be cared for. Let people help you. Don't be too proud.
- When you're in a corner with your back against the wall, there's no way out, except to move forward. When you realise this, you find amazing strength.
- It was more difficult for my family to deal with this than it was for me. I've moved forward, but some of them are still battling (emotionally). For support of cancer survivors, I'd say draw your strength from other patients.
I've gained complete trust in the ways and will of my Creator. You completely submit yourself - this is how it was ordained. Just accept it. That's life-changing, to be honest. Now I chose who to spend my time with and do what I really want to. Our time here is finite - but we live as if it's infinite.
Brian Anderson, is a minor walking miracle. He's had 93 operations, including two kidney transplants and been on intermittent dialysis for 22 years. He's passionate about raising awareness around Chronic Kidney Disease and organ donation.
Kidney disease has largely indistinct symptoms, which means that most people have no idea they're headed for renal failure. Here's how to find out if you're at high risk, and what to do about it.
Driven by her high-pressure job, Amy Rabie, 24, believed long hours were the cause of her tiredness, headaches, constant thirst and blurry vision. Little did she expect she had life-threatening Type 1 diabetes.