Proudly this year we supported
the “WHITE SHIRT CAMPAIGN 2022”
ran by “OCRF Australia”.
Image: Dr Thomas Havas supporting this event
“The OCRF is on a mission to make early detection a reality. The annual White Shirt Campaign plays a significant role in helping raise the funds needed to support essential ovarian cancer research projects.”
"Now in its 14th year, the Witchery White Shirt Campaign has contributed more than $14.3 million to research that is tackling early detection and improving treatments - research that will save lives. Now more than ever, the campaign is relying on your continued support.
The Witchery white shirt symbolises the lab coat worn by the researchers dedicating their lives to researching new and better treatments to improve outcomes for those diagnosed now, as well as developing an early detection test for future generations."
Our Clinic has been supporting the fight against Ovarian Cancer for decades and would love you to join! More information about this amazing foundation HERE
Stabyl: The App that makes technology accessible for people living with tremors
Havas New York and Havas Germany have teamed up in their joint mission to help people with tremors use tablets.
Parkinson’s Disease, which impacts an estimated 10 million people worldwide, is a primary cause of tremors. These involuntary, rhythmic muscle contractions make using technology very difficult.
The Stabyl is a free app that uses an iPad’s internal accelerometer data to create visual countermovements when the tablet is shaken in order to keep the display steady on the screen.
Tested with people living with Parkinson’s in the US and Germany, the app provides standard browser features such as bookmarks, history, and tabs with compensation settings that can be adjusted based on the strength of a tremor. Staybl arranges buttons vertically and increases readability through larger typography and other visual elements. While it is currently only available on iPads, the goal is to add it to other devices in the future.
“Parkinson’s is a disease that confronts those affected with everyday challenges that are not top of mind in society,” German Parkinson Association managing director Friedrich-Wilhelm Mehrhoff said in the press release. “We are grateful for Havas’ commitment to inclusivity and looking beyond traditional medicine therapies to make a difference. We appreciate the collaboration with Havas and believe that the Staybl app can improve the lives of those suffering from Parkinson’s.”
Learn more about Stabyl here.
New podcast series explores the impact of vaping on Australians
Independent publisher The QUO has produced a ground-breaking five-part podcast series on the social and public health impact of vaping in contemporary Australia called Chasing Clouds.
Chasing Clouds is an evidence-based exploration drawing upon the expertise of young people. doctors, educators, vapers, academics, and frontline community organisations to bring to light what we need to do moving forward.
What does the research say about how harmful nicotine and non-nicotine vapes are?
How serious a problem is vaping among teenagers and young people in Australia?
Should e-cigarettes be considered a legitimate form of harm reduction for smokers who just can't quit?
How can vaping rates be most effectively reduced among Australian young people?
These are some of the questions answered in the series.
The QUO in collaboration with the Prince of Wales Hospital Foundation and Head and Neck Cancer Foundation will be creating an interactive, online learning module to be rolled out to Australian school-aged students across the country. This will not be fearmongering but rather it will invite young people to think critically about the issues with all the available health data and research. In turn, this will empower them to take the lead through peer-based education where young people themselves share their stories of experiences with vaping with their peers and what they have learned as a result.
To listen to the series on Apple Podcasts, please click here.
To listen to the series on YouTube, please click here.
World Sinus Health Awareness Day
September 29 marks the inaugural World Sinus Health Awareness Day, a public health campaign aimed at educating patients around the world about the causes of their nasal and sinus symptoms as well as how they can improve these and when they should seek additional specialised care
One of the key drivers of World Sinus Health Awareness Day is to delineate chronic rhinosinusitis and rhinitis from COVID-19-related symptoms. If you have sinus symptoms and have had a negative COVID- 19 test, book an appointment with Professor Havas to talk next steps.
Successful laser resection preserves
our patient's voice box
The team in action this morning performing a laser resection of early laryngeal cancer this morning. The patient was home by early afternoon without the need for radiation and with his voice box fully preserved.
Professor Havas' service is truly 10 out of 10
Omer Hastor is a 60-year-old man who was diagnosed with laryngeal cancer a few months ago and is currently in the process of recovering from a curative operation.
“My personal experience with HAVAS ENT Clinics was great. Initially, I found out about the clinic from my GP who recommended that I see a specialist. To tell you honestly, once I met Professor Havas, everything was alright even though what I went through was a scary experience,” he says.
“Professor Havas gave me clear information, he even drew a picture to explain to me what was happening in my voice box,” Mr Hastor adds.
Like many patients, when it came to his diagnosis Mr Hastor initially found it difficult to accept what was happening to him. However, as a lifetime smoker, he understood that he had significant risk factors for cancers of the head and neck.
His operation, called a Vertical Hemilaryngectomy, was particularly daunting. Fortuitously, Mr Hastor was able to have his operation at the public hospital by a world-class surgeon despite having private health insurance. This meant that he didn’t have to pay for what was usually a $70,000 to $100,000 operation with a substantial gap and still received top-quality care.
“At the hospital, everyone was explaining to me what the next step was and was trying to make me feel at ease. To tell you honestly, after this experience, I told my wife Kim, thank god we are in Australia. That’s how I was happy with the service,” he explains.
“I come from Bosnia and I am still in contact with my family and friends there. I know the situation so that’s why I said thank god we are here because this whole process took less than two months from the beginning to end without the need to wait. The next step was already for me prepared and waiting,” he says.
Usually, laryngeal cancer requires an operation as well as chemotherapy or radiotherapy. However, Mr Hastor was effectively cured by his operation alone, which means that he can now focus on his recovery and does not need to additionally manage side effects including nausea, dry mouth, and loss of appetite.
“It was great news for me but at the same time, I have fought all of his life. So in the hospital when they showed me exercises to get back my voice, I really pushed myself and now I am recovering better than was expected,” he says.
“I also appreciate that without the right attention, the right advice, and the right support, I wouldn’t be here. Professor Havas’ service was truly 10 out of 10.”
Australia's most experienced microlaryngeal and laser surgeon
Professor Havas is Australia’s most experienced laryngeal micro and laser surgeon.
For over 25 years, he has been pioneering techniques of minimally invasive endoscopic laryngeal surgery for benign and early malignant conditions of the larynx in both adults and children. Remember that if you have any symptoms related to voice, difficulty swallowing or a lump in the neck, early presentation is critical. We encourage you to get an opinion from our team to understand what the possibilities are. Early presentation leads to minimal intervention, a better outcome, and longer and better quality of life.
From thyroid cancer at 25 to motherhood
From the outside, 34-year-old Katrina Mae is an accomplished young woman who has managed to strike a perfect balance between work and family. She is a Special Counsel at a top commercial Australian law firm and has a healthy 6-month-old daughter, Amelia. Katrina is also a survivor of papillary thyroid carcinoma, the most common form of thyroid cancer and one that primarily affects younger people. We interviewed Katrina about her head and neck cancer survival journey and how it is has changed her.
Can you tell me about the circumstances surrounding your initial diagnosis?
I received my diagnosis in 2012 when I was 25. I had just gotten engaged, was planning my wedding and my fiancé was away overseas so you can imagine that it was rather dramatic timing. My symptoms began as a sore throat with a little lump. I told my mum and sister who said it’s probably nothing serious but that I should still get it checked out. So I went to the local doctor who said it’s probably just a nodule on the thyroid. They did a biopsy which came as a surprise to me; I thought it would be a swab or something less invasive, but they were sticking needles into my neck while I was awake. If it came back benign, I would have just needed some thyroid medication. My father had had some thyroid issues previously so I assumed it just ran in the family. My doctor then told to see the specialist ENT surgeon Professor Jonathon Clark. When I arrived, he told me that I had papillary thyroid carcinoma (thyroid cancer) and that it may be in my lymph nodes and neck as well. He said he would need to do more biopsies to work out the scope but that I would definitely need surgery.
As a young woman, any type of cancer is not something that one necessarily has on their radar. How did this diagnosis impact you on a personal level?
It was a terrible shock. I went to my appointment with Professor Clark thinking that I’d only be getting some medication. My parents had actually offered to come with me to the appointment because my fiancé was away, and I had said there was no need and that I could go by myself. When I got out, I was overwhelmed and distraught. I immediately rang my parents and told them what had happened. I had actually planned to go out for dinner with some friends afterward as I was so confident I would be fine. I went to that dinner and told my friends that while I have cancer and I’m worried about whether I’m going to live, everything is fine. It was a bit of a denial for a while. It wasn’t until I actually spoke to my fiancé later that night when he rang me from East Timor that it hit home. His reaction prompted my reaction, and I finally recognised that it was very serious and poor timing with my other half out of the country. I’m lucky that I have a good family around who looked after me. I think the medical team that subsequently took me through my surgery and treatment was also phenomenal so I can’t complain.
What did your treatment involve?
I had a radical neck dissection where they removed my thyroid and 159 of my lymph nodes, and I was then treated with radioactive iodine. They also had to remove a small part of my thyroarytenoid muscles which is the muscle that sits next to the voice box, as the cancer was growing into that. I had all my surgery out of St George Private Hospital but then about 8 weeks after I’d had the surgery, I went into St George Public Hospital to their oncology unit for the radioactive iodine which involved swallowing a pill that kills cancerous cells while leaving other body cells relatively unharmed. Part of the thyroid's job in the body is to absorb iodine so it essentially tricks any cancerous thyroid tissue that is left in the body after surgery into sucking up the radiation. They had already removed most of the cancer but if there was anything else floating around my body, they were then able to kill that off with the radioactive iodine treatment. At the end of the treatment, they scanned me to check how much radiation I was emitting which was still only a low frequency. The fact that there was nothing or not much showing up was indicative of the fact that there hadn’t been much left behind by the surgery which gave me quite a bit of reassurance.
Did your treatment affect your voice production?
I saw a speech therapist at St George Public Hospital for a handful of sessions. With the nature of my work as a lawyer, I do a lot of speaking and my voice was getting tired very quickly which affected my projection. I actually didn’t realise it would be a possible side effect before the surgery. The doctors came in while I was in ICU afterwards, asked if I could talk, and then inspected my voice box and throat. I was very lucky that it didn’t affect me severely. After a couple of speech pathology sessions, all I needed to do was put into action the things that they taught me in those sessions.
Did you have access to any peer support services during your recovery?
I haven’t connected with anyone else who’s had head and neck cancer at all. On a few occasions, I’ve been interested to meet either colleagues, clients, and friends down the track who had other types of cancer when they were quite young. We bonded over those experiences to a degree. I actually haven’t even met anybody else who’s had head and neck cancer at all, let alone in my age group. I feel like it’s something that is rarely talked about.
Did you want more patient support during your treatment and subsequent recovery?
I had the support I needed but I was very lucky in that my surgery and treatment were effective the first time around. It was a fairly rough three months, but it was only a three to four-month period that I was having surgery, recovering, and undergoing treatment. This is a relatively short period as compared to people who might have another form of head and neck cancer and need multiple surgeries or multiple rounds of treatment. That said, I can imagine it would be very helpful to speak to other people who have already recovered. That way, you can gauge what are you in for and see a light at the end of the tunnel. I always think that makes you feel better knowing that people feel better with time
Did having thyroid cancer mean certain milestones were delayed for you?
I had to wait at least 12 months to become pregnant after the initial treatment. About three years in, when I went back for some more radioactive iodine for scanning purposes, I again had to wait a further year to conceive. So all up I had to wait four years after the surgery. The other factor is that iodine is quite important for the development of a baby so they have to monitor your medication quite closely before you decide to have a baby, once you’ve had your thyroid removed. Given that I’ve now got my healthy little baby Amelia with me, it all seems worth it.
How do you feel changed by your experience of thyroid cancer?
I grew up being a very gentle, timid kind of person and I was always terrified by medical procedures. I really had to toughen up. It does build resilience. As my mum said to me subsequently, I think about the things that I have gotten through in life and if I can get through that, I can get through anything. The silver lining was that it showed me that I was made of a bit more than I thought in terms of my personal strength.
I am now nine years since my initial diagnosis and remain cancer-free. It was such a scary time, so I would love to do anything to help others facing the prospect of a head and neck cancer diagnosis. Beyond this, I want to support research to find targeted ways to remove all types of cancers that don’t injure the host as much as traditional chemo or radiotherapy.
A game-changer for pain relief
Dr Anders Sederis (our 2019 grant recipient) recently completed his masters thesis in a biodegradable novel mesh impregnated with nanoparticles to prevent pain and optimise healing after tonsillectomy.
This project is part of a group of research projects directed by Professor Havas in the development of novel technologies to treat and improve the quality of life not only of patients with head and neck cancers but also patients undergoing necessary common operations.
The Prince of Wales Hospital Foundation has very generously provided seeding capital for this project to go to second-stage animal studies. We are optimistic of being in a position to commence clinical trials mid to late-2022.
Professor Havas uses special safety precautions while performing laser surgery
In the Covid era, special precautions need to be taken when performing laryngeal laser micro surgery.
Professor Havas has been a leader in this field for over 30 years.
He has not only performed over 1000 Microlaryngeal laser surgeries for a variety of conditions, ranging from benign polyps to aggressive laryngeal cancers, but he has also been seminal in the design of appropriate surgical instrumentation.
If you have a problem with your voice or larynx, he is certainly the man to see.
The Head and Neck Foundation's Fordham School of Translational Medicine
Our multi-disciplinary, problem solving-focused vision: A school of translational medicine in Otolaryngology, Head and Neck Surgery
The traditional definition of translation medicine focuses on translating medical advances from the laboratory to the bedside. However, at the Head and Neck Cancer Foundation, we have a different vision that begins by identifying a clinical need.
“We’re all about looking after patients, treating clinical conditions, getting some insight into where we’re providing good treatment, and understanding where we’re not, so we can work backward to fill a need,” says Professor Thomas Havas.
Although Otolaryngology, Head and Neck Surgery is far from the glamour areas of science research, approximately every third visit to a General Practitioner is for an ENT-related issue. There is huge prevalence with massive community cost and treatments are often more profit-focused than problem-focused.
Professor Havas explains a practical application of this.
“About ten years ago, it started to become popular to wash your nose out with salt water spray. There’s no good evidence that it achieves anything and yet last year in America, Americans spent over $2000 million buying saltwater to wash their nose out with. It’s not science-based but profit-based and it’s usually the manufacturers of the saltwater spray who hire a couple of prominent Otolaryngologists with a significant financial incentive to spruik a product with little evidence backing it up,” he says.
The future School of Translational Medicine in Otolaryngology, Head and Neck Surgery will focus on science-driven solutions to clinical needs as opposed to the current framework that is too often fear and economically driven. We will create an independent school with academic credibility, staffed by senior Otolaryngologists and researchers who appreciate that the hackneyed commercially-driven approach is no longer appropriate.
“The school will provide a grassroots approach ranging from common problems to innovative treatments for Head and Neck Cancer. It will be holistic and ecumenical, focused primarily on improving patient outcomes,” explains Professor Havas.
Another unique aspect of our school will be controlling the commercialisation process. While profit from medical advances is important, it needs to be reframed to become more eco-friendly. This means that a significant amount of profit will not only go to the individuals who own the intellectual property but will be used to support universities and to a lesser extent, hospitals.
“You don’t have to make obscene profits to make medical advances profitable.”
The Head and Neck Cancer Foundation Research Group is already engaging in a multi-disciplinary approach to research. We have been collaborating with biomedical engineers and other scientists for the last three years as evidenced by our research reports.
“What strikes me is that hitherto and in many other areas, how little interaction there is between biomedical engineers and clinicians generally. We bought half a dozen of these students into the operating room and they have never been in an operating room. They are intelligent, they have enormous skill bases that we as clinicians don’t have, but there has been no integrated vision or foresight in terms of bringing the two together,” says Professor Havas.
The School of Translational Medicine will be unique worldwide in its multidisciplinary, inter-disciplinary, problem-focused, and product development-focused approach. As a clinician-led school, it will also include basic scientists, biomedical engineers, and lawyers to teach students about both intellectual property and the commercialisation process.
“The quicker we can bring to market, the quicker it is at the bedside, and the quicker patients benefit,” says Professor Havas.