Dr. David Grimes

Like father, like son, the saying goes. But Dr. David Grimes was dead set on making his own way in the world of medicine.

Son of the much-admired neurologist, Dr. J. David Grimes, he never thought he’d wind up in the same field, let alone studying the same exact disease, as his father — but life had other plans.

Now a Neurologist and Associate Scientist at The Ottawa Hospital, and Director of the clinic that his father founded — the Parkinson’s Disease and Movement Disorders Clinic — Dr. Grimes is leading a new generation of researchers as they take on Parkinson’s and treating some of the very same patients his father did.

Find out how Dr. Grimes got pulled into the field of neurology and what advice he has for people diagnosed with Parkinson’s.

Q: What were your early years like?

A: I was born in Cleveland, Ohio, but I grew up in Ottawa’s west end.  

I went to Sir Robert Borden High School, where I struggled at English but the sciences were up my alley. My wife always teases me that I almost failed Grade 13 English then went on to write two books and over 100 research publications. But back then, I was a science guy and a gym rat. I played every sport available through grade school and got into football in high school. 

Family was very important growing up. I was one of six siblings, and every Sunday was family day; you had to be around. My father would arrange various nonsense games or tennis tournaments, and there were enough kids that we’d have our own teams. I’m the second born, and my older sister was my boss. It’s a family joke that she got into hospital administration when I got into medicine. 

Q: How did you decide to study medicine?

A: I knew I wanted to be a doctor quite early on. My grandfather was a dermatologist, and my father was Dr. J. David Grimes, founder of the Ottawa Parkinson’s Disease Research Laboratory at what was then the Ottawa Civic Hospital. I admired them both.

I also started working at the Civic as a porter when I was 16 and stayed until second year medical school. Back then, many sections of the hospital weren’t air conditioned, and we’d have big buckets of ice with fans blowing on them all summer.

While I knew I wanted to be a doctor, there was this cliché of following in your father’s footsteps, and I didn’t want to do that. I wanted to branch out on my own, so I started in internal medicine and studied at the University of Ottawa.

Q: How did you wind up in neurology and specializing in Parkinson’s?

A: The problem is, my father and I tended to have pretty similar personalities. I was helping him with his research and early books while I was doing internal medicine, and after a couple of years, I realized I did like neurology. But I said I wouldn’t pursue movement disorders specifically like he did. Lo and behold, I did like movement disorders. I liked caring for patients with Parkinson’s, and it was the patient population that gave me the most joy to work with.

Dr. David Grimes and his father, Dr. J. David Grimes

What drew me to neurology was our lack of understanding of the brain. There was a classic knock against neurologists when I started that they can diagnose things but can’t treat anything. It was apparent to me that there were a lot of things we could treat, and there seemed to be a very bright future. This was back in the ’90s, and we had started to see people who had potentially devastating strokes, and now they were surviving. There were more and more opportunities to look after people and make a difference in their lives.

Q: How has the treatment for Parkinson’s changed since you started?

A: Levodopa has been the gold standard for treating Parkinson’s since the 1960s, and it does make a remarkable difference, but we understand the drug a lot better than we used to. We’re more careful about dosing and spacing and we can add on other medications.

Did you know? Levodopa was made famous partially by the 1990 movie Awakenings, in which Robin Williams plays a neurologist using the drug to treat catatonic patients.

Just this year, Health Canada approved a way to give levodopa under the skin, and we were one of the first centres in Canada to use this drug. We also offer DUODOPA, which is levodopa infused right into the stomach. Because we’re a subspecialized clinic, we can offer things like this really early.

We also have more advanced therapy options, like deep-brain stimulation. We’re one of the few places in Canada that offers it. The idea is that by putting electrodes in the brain, you can change the abnormal loops that are associated with Parkinson’s and help people move better again.

Q: What’s something surprising about your field?

A: It’s very complicated and expensive to get new drugs to market. We’re about to embark on a new clinical study for which we got a very large donation, but it’s amazing how quickly you go through the money. I don’t know if everyone understands how complex the process is.

We’ve been very fortunate to have our Parkinson Research Consortium. Through it, we’ve been able to raise many millions through local donations, and we’ve been able to recruit new people, fund six basic science students, and support clinical programs with that money. Local donations are absolutely crucial to start a new project and get things going.

Q: In your role as a scientist, what research are you currently working on?

A: We are currently working on a 40-person trial trying drug repurposing. We’re using a rheumatoid arthritis drug called Plaquenil, which can affect certain inflammatory pathways that we think play a role in people with Parkinson’s.

I’m also looking at the role of MRI scans in diagnosing Parkinson’s. We helped develop a software that uses an AI algorithm to look at standard MRI scans and can, with good accuracy and sensitivity, tell you whether you have regular Parkinson’s or something else.

We also have studies looking at genetic subtypes of Parkinson’s, and we are part of the Parkinson Study Group, which is the most prominent Parkinson’s clinical trial group in the world.

We have a very large and active clinical trial program here at The Ottawa Hospital. When we approach someone and say, “We’ve got something new we want to try,” they say, “Yeah, sign me up.” Even when we recently had one trial come back negative, the compound we tried wasn’t working, most people said, “OK, what do you have next for me?” This level of enthusiasm isn’t necessarily common in all patient populations.

From a patient engagement standpoint, our Parkinson’s patients are extremely engaged.

Dr. David Grimes

Q: Chantal Theriault came to us with early-onset Parkinson’s, what makes cases like hers unique?

A: The earlier somebody’s onset is, the more likely their Parkinson’s is to have a genetic basis. In general, people with a genetic cause tend to progress more slowly, but they also tend to have more trouble with motor function fluctuations. We think up to 10% of people with Parkinson’s have a genetic mutation causing it. We can test for these genetic mutations now, and with that knowledge, we are hoping to develop treatment to block the progression. Unfortunately, there’s not a lot now in the clinical realm, but in the research realm, it’s a very active area. It speaks to the idea of precision medicine and coming up with very specific treatments for people with very specific genetic forms of Parkinson’s.

Q: What advice would you give someone who has just been diagnosed with Parkinson’s?

A: In general, I tell people that although it does progress, and although we don’t have a cure, it does typically progress slowly. I encourage them to be active and enjoy life. We know exercise is a key part of treating Parkinson’s — it helps people feel better and function better.

It’s important to tie in significant others as well. Pulling support from a lot of different places is critical for patients to do the best they can and have the best overall quality of life.

I make sure they know there’s a lot of research going on, and we are going to be able to come up with treatments that affect the progression.

People have this vision that they’ll be in a wheelchair within a year of diagnosis and that’s just not true. We really do keep most people feeling and functioning quite well with Parkinson’s for many years and for some decades. I try to instil a feeling of hope.

Q: How will a new, state-of-the-art health and research centre to replace the aging Civic Campus mean for your patients?

A: A fluid back-and-forth between clinical research and patient care is being built into the new campus development. If we’re going to be a leading-edge hospital, we need to do that. When we see research patients and clinical patients in the same place, that’s where we’ll make our most rapid advancements.

From infrastructure for new technologies to connecting patients to new research, the new campus will make everything that much more accessible and advance the field that much faster.

Q: Where would we find you when you’re not at work?

A: Most people who know me think of me as being on my bicycle. I bike all year round, and the residents make fun of me when I show up for work on a snowy day in my biking gear.

My wife and I also have three children, and we enjoy spending time with them. I play on their volleyball team, where I’m the old guy trying to keep up.

Otherwise, you’ll find me at my cottage where I have all the classic cottage projects on the go: building bunkies, docks, and various other things. It’s just 90 kilometres from my house, so I can bike to my cottage or commute from there in the summer.

Dr. Tien Le

At the start of his career in the mid ’90s, Dr. Tien Le was the only gynecologic oncologist for the entire province of Saskatchewan. Today, he’s one of about 40 gynecologic oncologists in Ontario reshaping gynecologic cancer care. Dividing his time between delivering care to patients and conducting practice-changing research, this academic Gynecologic Oncologist and Scientist at The Ottawa Hospital brought his skills home to Ottawa in 2002 to join a dynamic, multidisciplinary oncology team committed to delivering the best cutting-edge longitudinal cancer care for women with gynecologic cancers. 

Find out how the field of gynecologic-oncology has drastically changed since Dr. Le’s early days on the Prairies and what he’s most excited about today. 

Q: What were your early years like? 

A: I grew up in Ottawa, but I originally emigrated from Vietnam as one of the “boat people” when I was five. I went to Glebe Collegiate, where science was my favourite subject. I was always drawn to physiology and an understanding of how things work.

Outside of school, my hobbies were mostly writing code for computer games and learning about computers. Back then, we still had dial-up internet access. Coding helps you think about problems in a defined stepwise manner and solve problems logically. Learning to apply that method to my work today has been very productive and rewarding. I do a lot of my own data analysis and statistics as I pursued a degree in epidemiology and biostatistics after my fellowship.

Q: How did you decide to pursue medicine? 

A: Back in Vietnam, my father was an ophthalmologist, but when we moved here, he worked as a family practitioner, so I got some exposure to medicine in my early years. 

When I applied to university, I knew I wanted to do something healthcare-related, but medicine wasn’t particularly high on the list yet because the competition was very fierce. I did my undergrad in biochemistry and physiology at uOttawa, and at the time, I was considering a career in research or dentistry. During my first year of university, though, I became more and more interested in physiology and anatomy and how the different organ systems work together in health and disease. Eventually, I felt more drawn to apply this knowledge to disease management. I realized medicine would be the perfect fit and was accepted to the University of Toronto medical school after only two years of undergraduate study. 

Q: What drew you to gynecologic-oncology specifically? 

A: Back when I was in medical school, women’s health was a relatively underdeveloped specialty. I saw a lot of opportunities for research and personal growth. During my obstetrics and gynecology residency at the University of Manitoba, the program was strong in gynecologic-oncology. The program director, Dr. Garry Krepart, was one of the founders of the subspecialty in Canada. The field continued to grow on me as I progressed through my residency because it was the perfect marriage between surgical oncology and medical oncology, which is unique to this subspecialty. 

Dr. Tien Le is a doctor specializing in gynecologic oncology at The Ottawa Hospital.

Q: How has the field of gynecologic-oncology changed since you started out? 

“Patients continue to live longer with a better quality of life.”

— Dr. Tien Le

A: The field is advancing very rapidly, and there have been huge advancements in the field of gynecologic-oncology since I was in medical school. For example, when I was a medical student, the median survival for a patient with advanced ovarian cancer was not even 12 months. When I was a resident, it had increased to two years. Now, it is five years, and patients continue to live longer with a better quality of life. All this can be attributed to better therapeutic strategies, including surgery, chemo, and the use of maintenance therapy. For example, for ovarian cancers, the use of PARP inhibitors (an oral tablet called Olaparib/Niraparib) that can keep the cancer in remission is now commonly recommended. 

With ovarian cancer, while oncologists have been very successful at pushing the cancer to remission after primary treatment, most patients with an advanced stage of disease will have their cancer recur. More and more, we’re looking at ovarian cancers as a chronic disease, like diabetes or asthma, where we have effective therapies to manage these chronic conditions.  

Q: What is the most exciting research currently happening in your field? 

A: Running clinical trials is an essential component of all oncological practices because it’s how we identify the most effective therapies and offer the most cutting-edge treatments for specific cancers. At The Ottawa Hospital, we’re currently running a number of trials on ovarian, uterine, and cervical cancers.  

Specifically for ovarian cancers, we’re studying a new class of medication called antibody drug conjugate, or ADC. ADC is made up of an antibody that links to an active drug that’s toxic to cancer cells. It’s like a magic bullet or Trojan horse: the drug only gets taken up by the cancer cells, leaving normal cells unaffected.  

The other therapy that’s been causing a lot of excitement in the gynecologic-oncology community is immunotherapy for the treatment of uterine and cervical cancer. It works very differently from traditional chemotherapy in that immunotherapy stimulates a patient’s immune system to seek out and destroy cancer cells. It’s been very effective, and we routinely use it for metastatic, advanced uterine and cervical cancers. 

Finally, another therapy we’re using here at The Ottawa Hospital is hyperthermic intraperitoneal chemotherapy (HIPEC). During the treatment, we administer heated chemotherapy into the abdominal cavity during surgery. It’s been shown to prolong survival in patients with ovarian cancer. The Ottawa Hospital is only the second hospital in Ontario to provide this treatment. 

Q: What made Jennifer Hollington’s cancer journey unique?

A: Jennifer is the perfect example of our longitudinal, multidisciplinary model of care. She was initially diagnosed with a large pelvic mass, and her gynecologist referred her to our gynecologic-oncology team at the General Campus. I ended up being the surgeon who performed the surgery. She was subsequently treated with chemo, receiving support from our extended team of nurses, pharmacists, residents, fellows, and allied healthcare professionals during her cancer journey.  

After genetic tests on the tumour revealed that Jennifer had the BRCA2 gene mutation, which increases the risk of both ovarian and breast cancers, she decided to get a preventative mastectomy. This knowledge also helped shape her ovarian cancer treatment. Olaparib is especially effective in those with this BRCA2 gene mutation, so we started her on this maintenance strategy personalized to her tumour profile. 

Jennifer also had melanoma, which was an unlucky coincidence, and our care team supported her through that as well. 

Something to keep in mind about ovarian cancer is that it’s a relatively rare cancer compared to breast, colorectal, or lung cancers — the three most common cancers in women. Women with ovarian cancer often have very nonspecific symptoms that don’t always clue them into the cancer diagnosis right away. The nickname for ovarian cancer is “the disease that whispers” — it’s a silent killer that is typically asymptomatic in the early stage of the disease. By the time symptoms occur, the cancer has often already metastasized. At this stage, it is much harder to cure and treat. It is important to emphasize that if a patient is facing unexplained, persistent symptoms — such as pelvic pain, abdominal pain, increased abdominal size, bloating, difficulty in eating and a feeling of fullness, or urinary urgency and frequency — they should seek medical attention right away and not ignore these symptoms. 

Q: How does community support for research help patients?

“Together with community support, we can work together to advance and improve care for our patients in Ottawa region.”

— Dr. Tien Le

A: The development of new therapies and the incorporation of new technologies takes money. Ongoing community support for The Ottawa Hospital’s mission has been wonderful. Speaking for my department, through donations we were able to bring robotic surgery to gynecologic-oncology patients undergoing uterine cancer surgeries. This technology allows the surgeons to see better and patients recover faster and with fewer complications after surgery. It results in huge savings for The Ottawa Hospital as well, with shorter inpatient hospital stays and fewer post-op complications to manage, which allows us to use the money for other things to improve patient care. For the robotics program, unless we had donations, we would never be able to bring this technology to our patients. It’s a costly machine. Together with community support, we can work together to advance and improve care for our patients in Ottawa region.

Q: Why did you choose to work at The Ottawa Hospital?

A: I love our model of care: it’s patient-centred, longitudinal, and multidisciplinary. A personal reason why I have been here since 2002 is the camaraderie among all team members. We have a very good team in gynecologic-oncology in Ottawa dedicated and committed to care for our patients. We work in a collaborative, friendly environment — physicians, nurses, pharmacists, and allied healthcare professionals all doing what we enjoy doing and helping patients under our care.

Fighting the good fight on the lab bench or at the patient bedside: Dr. Michael Ong is an oncologist and associate professor at The Ottawa Hospital who has spent his career discovering new therapies against cancer by enrolling patients in clinical trials.

His research and practice have focussed on prostate cancer, bladder cancer, and melanoma, and over the last decade he has been the lead investigator in Ottawa for countless clinical trials. He currently leads several national and international clinical trials that are poised to change how we treat cancer, including how we use cancer immunotherapy, where a patient’s own immune system is harnessed to attack cancer. Dr. Ong’s research is changing the way we deliver care at The Ottawa Hospital, and far beyond.

Read on to learn what piqued Dr. Ong’s early interest in science and why immunotherapy works a little differently with prostate cancer than with some other cancers.

Q: Can you tell us a bit about your early years?

A: I was born and raised in London, Ontario, which was a great place to grow up — my dad was a local dentist, and my mom managed his office. I spent a good deal of my younger years playing and competing in classical piano festivals. I was also on the tennis and badminton teams at school, and I liked being a part of student council.

I had a subscription to Scientific American, and it was cool because you were exploring the world and universe. My dad was into science fiction, and it was a family tradition to watch Star Trek every week with him and my brother — it was our boys time.

In high school, while everyone was finding their way, I knew I would end up in science — but the field is just huge. Back then, we didn’t have the internet, and it was hard to know what career paths were even available.

Q: When did you realize you wanted to become a doctor, and specifically an oncologist?

A: Medicine opens up many doors, and I think that was the initial attraction to the field. I had to decide if I wanted to stay in London and assume my father’s dental practice, however, I knew the journey through medicine would open my mind through varied experiences and adventures — and it has absolutely lived up to this promise.

“The breadth of people and patients I have encountered during my career — in situations both stressful and miraculous — has exceeded the drama and delivery of any TV show.”

— Dr. Michael Ong

My training in medicine has taken me to nearly every province in Canada and across Europe. The breadth of people and patients I have encountered during my career — in situations both stressful and miraculous — has exceeded the drama and delivery of any TV show.

In my undergrad, I studied biochemistry at Western University, which probably laid the foundation for what I currently do in medical oncology. But, it wasn’t until I was in an internal medicine residency searching for my raison d’être when I had an unexpected selective rotation in oncology. I found my calling. There were so many things that excited me about the field — the compassionate, highly specialized team; the multidisciplinarity; the scientific, evidence-based approach; the incredible focus on research and improving outcomes; the “best of the best” science that has resulted from billions of dollars of research.

Now, 15 years after that decision to join the field, I have seen complete revolutions in how we treat cancer.

Q: What drew you to the research side of oncology?

A: I had a great mentor, Dr. Eric Winquist, who had seen something in me, and he encouraged me to apply to a training program in writing and conducting cancer clinical trials in Flims, Switzerland, put out by the American Academy of Cancer Research. As part of this program, you had to come with a clinical trial proposal, refine your concepts, make it feasible, and write an entire 100-page clinical trial protocol that you bring back to your institution to run the study. My application for the trial was accepted, and whoosh, I was off to Switzerland that summer!

There, leading my training group in the middle of the Swiss Alps, was Professor Johann de Bono, arguably one of the most influential, cutting-edge prostate-cancer oncologists in the world. At the end of the course, he said, “Mike, what are your plans? I would like you to come work for me at The Royal Marsden Hospital in London, U.K.”

I spent two years in London at their Institute of Cancer Research developing new cancer treatments. It was mind blowing to see what was happening at these top institutions, to see how you could bring science from the bench straight to the bedside. I learned how to design clinical trials that — once published and presented — could change clinical practice in the whole world.

Q: Can you describe the research you’re currently working on?

A: I am a cancer clinical trialist. While it is a huge effort on the part of patients, staff, and researchers to enrol and participate in clinical trials, it is ultimately one of the best ways that we end up meaningfully changing patient care. I focus on providing access to clinical trials that test new immune and targeted therapies for patients with prostate cancer, bladder cancer, and melanoma.

For prostate cancer, I have been trying to develop personalized treatments that are not simply taking the “one-size fits all” approach. I am leading an international study across the USA and Canada to show that the best way to add chemotherapy on top of hormone therapies is to look at a certain antigen to look for early evidence of resistance to treatment. Our goal in this clinical trial is to prove that when we customize the choice of chemotherapy, we improve how long and well patients live with cancer.

Dr. Ong with his UK counterparts

I am also the co-chair of a national study that we have completed in Canada where we have tried to personalize the treatment of men with prostate cancer using a blood test called “circulating tumour DNA.” We tested various new cancer treatments based on the results of this blood test and have found that we can effectively choose which patients might benefit from specific treatments, such as cancer immunotherapy.

Q: Why does immunotherapy work better for some types of cancer?

A: The reason immunotherapies work is that some cancers look very ugly to a person’s immune system, and the immune system will naturally see them as foreign and try to attack the cancer. Cancers will then cloak themselves in something called PD-L1, which is like an invisibility cloak to the immune system — it’s a survival instinct for the cancers. Immunotherapies remove that PD-L1 cloak with an IV infusion given to patients, which reveals the cancer again to the immune system, and the results can be incredible.

We’ve struggled to make immunotherapy work in prostate cancer because incidences of this cancer looking ugly to the immune system happen in a low number of cases — probably fewer than 5%. We’ve done a lot of trials, but the majority of patients do not benefit from immunotherapy. But that does not mean we should give up on this approach! What it means is that we should take a personalized approach for patients and do testing to identify that 3–5% of patients who may benefit from immunotherapy. One recent study showed that immunotherapy benefitted 86% of prostate cancer patients who tested positive for something called “mismatch repair deficiency,” which I test for in my practice — but it’s not standard across Canada to test for this yet.

Q: You worked on Larry Trickey’s prostate cancer case. What made his situation unique?

A: Larry’s case is the perfect example of how important it is to find these cases of mismatch repair deficiency. Larry had participated in that clinical trial where we took a blood sample and tested his cancer DNA for evidence of mismatch repair deficiency. His blood test report showed that he was possibly sensitive to immunotherapy. He enrolled in the clinical trial, which uses two cancer immunotherapies. Almost the moment he started treatment, his cancer was attacked by his immune system, and he has achieved a complete remission from his cancer so far.

It’s important not to treat prostate cancer as one big basket. Hormone therapy is very important, chemotherapy is important for some, and there’s also radiation, immunotherapies, and targeted therapies such as PARP inhibitors that only benefit those with specific altered genes such as BRCA2. We’re making huge attempts to personalize treatment for patients.

Q: Why did you choose to work at The Ottawa Hospital?

A: My wife (also a physician) and I both chose to come back to Ottawa, and at the time our first son was one year old. We wanted to be at a centre providing top-tier care, and for me that meant a centre that had the capability to do cancer drug development and phase I-III cancer clinical trial research.

We also wanted to balance our life in a city that could provide everything to help our growing family to thrive. Our second child was born about two years into practice in Ottawa.

I would also say that I have the privilege with working with some of the most incredible colleagues in the Division of Medical Oncology. You would be hard pressed to find a group of more talented, dedicated and compassionate individuals.

Q: Where would we find you when you’re not at work?

A: I’ve been trying to develop as a jazz piano artist. I’m a classically trained pianist, but branching out into jazz is one of the hardest things I’ve ever done. I liken it to learning a completely different language.

I also play tennis and squash regularly. I’m out a lot with my two boys; both are in competitive soccer and tennis. My wife is a big skier, so we’re out on the slopes every weekend in the winter.

I love travelling — this summer I was in Ireland, Quebec, New York, Barcelona, Majorca, Victoria, and Whistler — and I’m a big photographer, so I document my travels!

Fun fact, in my early years, I also spent some effort learning how to salsa dance, and my friends and I would travel around to conferences to do this. The first time I met my wife (we’re talking around 1998!) my friends and I took her out to a salsa club, which I think won me a few extra points.

When a trauma case bursts through the doors at The Ottawa Hospital, it’s Dr. Jacinthe Lampron’s team taking it on. As the Trauma Medical Director and a Clinical Investigator, Dr. Lampron is constantly working on improving our trauma care — whether directly with patients or through her quality improvement research.

When every second counts, Dr. Lampron is the one counting them out as she delivers lifesaving care every day.

Keep reading to find out what drew Dr. Lampron to trauma, what she learned in Afghanistan, and what she might have been had she not pursued medicine.

Q: What were your early years like?

A: I was born in the area of Trois-Rivières in Quebec, and I was raised in Nicolet on a dairy farm. It was a lot of work, but I tried my best to help my parents. It was a bit challenging for a child or teenager because I was far from the city and extracurricular activities — I was into swimming, hiking, and rock climbing. But I also had so much space to run around and experience other things, like driving a tractor.  

In school, I enjoyed everything around science. In CEGEP, I studied biochemistry, math, physics, and biology. I loved to learn and to try and understand things or solve the equations. 

Q: What did you want to be when you grew up? 

A: When I was four, I wanted to be a florist. At the farm, we had a big vegetable garden and a big flower garden. My grandmother lived next door, and I spent a lot of time with her. We would look at flowers, and my first name — Jacinthe — is a type of flower. I suppose I became interested in flowers then.  

Q: How did you wind up pursuing medicine, and becoming a general surgeon in trauma? 

A: In terms of medicine, it was a progression. Things were going well at school and at CEGEP, and some of my friends said, “Well, why don’t we try medicine?” I didn’t know that much about it yet, but it sounded interesting, challenging, and it would help others, so I applied.

Then, as a medical student, I enjoyed all the topics. I remember thinking, “Oh man, I don’t know what I’m going to pick as a speciality!” We started clinical rotations, and my first was in general surgery. It was very exciting to really see what it was to be at the hospital, seeing patients, and looking after them. I didn’t know anything else yet, because it was my first rotation. But none of the others hit the spot. At the end of the year, general surgery was the rotation I had the most fun in.

I remember I was working with this brilliant team of aspiring, motivating residents. I’m still very fond of them all, and when I interact with them professionally, I’m still in awe.

Q: Can you tell us about your two tours in Afghanistan as a civilian physician and how it affected your approach to medicine? 

A: It felt very different. The OR was not as technologically advanced as ours here, but there was everything I needed to do surgery and help injured people. The hospital was made out of sea containers and plywood, with big cement blocks to prevent rocket attacks!

The military base was quite large, close to 10,000 people all living there, and multinational. It was so interesting to see so many different countries in the same place at once. Military personal on the base had to wear a weapon, but everyone had to wear a frag vest, a type of body armour. Every once in a while, there would be a rocket attack — an alarm would sound, you’d go to the bunker, and you’d wait for the “all clear.”

Obviously it was very tragic and dramatic, and I can’t say I was feeling joy in the middle of the war, but I was pleased by the work I was able to do. I learned that we could do surgery with not that much.

Trauma care evolves with war, so the Afghanistan conflict brought new concepts that were then translated to civilian care. For example, it changed the way we do resuscitation: we moved towards using more blood products instead of crystalloid solutions. And while the use of tourniquets has waxed and waned over the years, Afghanistan showed us it’s quite advantageous to save lives, so we’re using them more often now.

Q: What’s something interesting about trauma care? 

A: Our team lives at the pulse of the city and society. When it’s Canada Day, we’re on standby because we know a lot is happening. When it’s autumn, and everyone is putting their Christmas lights up, unfortunately, we know many people will fall. When it’s May, and motorcycles are just getting out on the road, we know we’re getting crashes. We live through the seasons and what’s happening.

Q: You worked on Brandon Peacock’s case, where he was an innocent victim of a drive-by shooting. What made that case unique?

A: It was a very intense episode of care. His injury was a penetrating trauma, and those are high-intensity, especially if there’s a blood vessel injured. When that happens, the person can bleed out within minutes. Caring for an injury like his requires a lot of resources: having blood available for transfusions, having the operating room ready, having a team available and ready to perform all the tasks needed for resuscitation. Everyone moves fast, everyone needs to know what they’re doing, and that’s how we save people. We have a system in place and a team ready to go; that’s why trauma patients do better at trauma centres.

Q: In your role as a clinical investigator at the Ottawa Hospital Research Institute, what are you currently working on?

A: I work on the quality improvement angle of trauma. We look at our performance indicators, and if we’re not performing at the level of our peers, we dissect the data and look at what we can do to try and make it better. Then we’ll do a quality improvement project and see if it improves. I also work on improving the trauma system, which means facilitating the flow of patients and processes.

Research like this means patients will receive better quality care.

Q: How does having the most technologically advanced facility make a difference to your work?

A: Trauma mostly needs a well-trained team that’s going to do all the work together. The new campus is going to allow this by providing state-of-the-art ORs, access to the best technology, and space for video-recording and simulation to train the team members. The other big thing is the new heliport: instead of crossing the street, as we currently do, they can land on the roof. This is critical, because in trauma, every second counts.

Q: What would we find you doing when you aren’t at the hospital?

A: On my bicycle, running, baking, or spending time with my nine-year-old daughter.

Dr. Vimoj Nair is a radiation oncologist at The Ottawa Hospital Cancer Centre.

Surgery without surgery — it sounds like a riddle, but it’s what Dr. Vimoj Nair does every day at The Ottawa Hospital. As a radiation oncologist, Dr. Nair specializes in radiosurgery, an extremely precise form of radiation that doesn’t involve a single incision. By using exciting new technology like the CyberKnife and conducting practice-changing research, Dr. Nair is reshaping how certain cancers are treated, and ultimately creating better outcomes for patients at The Ottawa Hospital and beyond. 

Keep reading to find out why Dr. Nair chose to pursue medicine and how the field has changed since he first started out. 

Q: Can you tell us a bit about your early years?  

A: I was born in Kerala, which is a beautiful state in southern India. My dad was an accountant with an American firm, so I started travelling as a baby, and I think all that travelling made me a bit of a global citizen. 

I did all my schooling in Kerala, though, and my favourite subjects were math and science. STEM subjects came easily to me — I’m a bit of a geek. At around 15, I got into computers and early coding, and I did a diploma in computer applications. Back in the early ’90s, having a computer was a luxury, and there was no high-speed internet yet, so there was very little information I could get, but it’s part of what made it so fun. Later, I think this early experience with computers brought me to an identity where the intersections of pure medicine and technology could change lives. 

Q: When did you decide to pursue medicine and become a doctor? 

A: Because of my broad interest in everything STEM, I didn’t know what direction to take. I took math and biology, and I got into software engineering and med school for university, but with everything I had seen growing up, I realized that the best way I could help my fellow human beings in any part of the world was by being a physician.  

“I think I went into radiation oncology because it’s the perfect combination of math, physics, and medicine — it mixes everything at the precise right dose.”

— Dr. Nair

Q: How did you wind up at The Ottawa Hospital? 

A: I always thought I’d wind up working in the US. After my residency in radiation oncology from Northern India, I completed my neuro-oncology fellowship from the Tata Memorial Hospital in Mumbai — the largest cancer centre in Asia. While I was there, I was selected for the American Brachytherapy Society Fellowship in Texas. The awards ceremony was in Toronto, after which I did my one-month fellowship in Texas. That stop in Canada made me realize I wanted to live here, that this is where I wanted my kids to grow up. I applied for immigration while finishing my residency in India, and I moved here to be the first CyberKnife fellow at The Ottawa Hospital.  

Q: How has the field of radiation oncology changed since you started?

A: The same way cell phones today are different from the cell phones of the 1990s, the field of radiation oncology has changed immensely. It’s a field where we’ve had the simultaneous adoption of both hardware and software, so we’ve had huge changes in technology that mean the precision with which we target cancer has gone from centimetres to millimetres and now less than a millimetre. The dosing and accuracy have improved incredibly. 

We’ve seen the introduction of radiosurgery, artificial intelligence, and virtual reality. The Ottawa Hospital has been a fast adopter of technology, and we were one of the first centres in the world to develop our own virtual reality–based system for improving the target delineation — or outlining the target — for treatment during cancer radiation therapy.  

Q: You worked on Erin Brown’s case; what made her situation so unique? 

A: With Erin, we had this brilliant young lady who had an aggressive, rare tumour that was mostly removed surgically before coming to me for radiation. We knew if we did something too focused, it was going to come back at the surgical site. But we also didn’t want to go too wide and cause unnecessary damage to the surrounding normal brain tissue. Picture it like a tree in a lawn: the surgeon plucked out the tree — or removed the tumour — and I had to go after the roots left in the lawn — the lawn being her brain. The art of the science was knowing what to spare. We wanted to protect her memory centres, so she could have a full and happy professional and personal life.  

Many years later she did have a recurrence in a different part of her brain, far away from the original site, suggesting cells migrated through the fluid in the brain. As the tumour came back after two rounds of surgeries in this entirely new site, we had to give more radiation to this area to prevent it from growing back.

Giving a second round of radiation to a young brain does create more technical challenges. But with the technology we have in the Radiation Medicine Program at The Ottawa Hospital, and the world-class team with decades of experience, we are able to successfully repeat irradiation to the brain with excellent results sparing her uninvolved memory centres.  

I’ve been so happy to see her finish her education, and she became a nurse right here at The Ottawa Hospital. 

Q: In your role as a clinician investigator at the Ottawa Hospital Research Institute, what are you currently working on? 

A: I’m a broad-spectrum radiation oncologist, so I dabble in many things. Right now, I’m working on a world-first clinical trial for studying the role of the gut microbiome on brain cancer with my collaborator Dr. Terry Ng. Another innovative study was with collaborators Dr. Jean-Philippe Thivierge from the University of Ottawa School of Psychology and Dr. Janos Szanto in radiation physics (now retired) to see what radiation does to brain cells and how we can use it as a painless scalpel in non-cancerous cases. We are also studying various medications that could potentially reduce side effects and improve effectiveness of radiation. All this research is funded by donors or by winning competitive grants.  

Dr. Nair presenting at the society of neuro oncology 2023 conference

Q: How important is support from the community in advancing your research at The Ottawa Hospital? 

A: We are blessed to live in a city where people believe in giving back to the community. When I started as a fellow here, in 2011, I was able to support fundraising for research work using the Cyberknife. Fast forward to today, and the novel research I’m doing on the gut microbiome, or radiation’s effect on the brain, was only possible due to the generosity of our local donors. 

Q: Where would we find you when you’re not at work? 

A: Spending time with my wife and my two kids. I enjoy learning everything and anything out of my comfort zone. Technology, economics, space tech, med tech, the list goes on. As a family, we all spend a lot of time reading and chatting about these topics. At the same time, we make it a family policy to unplug ourselves from technology and travel to see more of this beautiful blue planet of ours. We love travel, whether it’s within in Canada or roaming all parts of the globe — from hiking the Montserrat mountain in Barcelona to the gruelling climb up the Grouse Mountain in Vancouver, or what people call mother nature’s Stairmaster. 

Dr. Nair and his family in Vancouver
Dr. Nair and his family hiking in Japan
Dr. Nair and his family in Montserrat
Dr. Kwadwo Kyeremanteng is the head of the Critical Care Department at The Ottawa Hospital.

Dr. Kwadwo Kyeremanteng describes himself as “on a mission to keep you out of the ICU.” It’s not that he doesn’t want to see you; it’s more that he doesn’t want to have to treat you. A researcher, clinician, and advocate for The Ottawa Hospital’s ICU and palliative care, Dr. Kyeremanteng’s focus is on preventing health issues from bringing people into the ICU in the first place on one hand, and on how to reduce costs and provide the most efficient and compassionate care on the other.

When Dr. Kyeremanteng’s not busy at work, you might find him talking about his book “Unapologetic Leadership”; running his podcast, “Solving Healthcare with Kwadwo Kyeremanteng”; or sharing healthcare delivery insights (and so much more) to his vast following on LinkedIn, TikTok, Instagram, or Twitter.

Want to know the childhood experience that made Dr. Kyeremanteng want to study medicine and what keeps the Edmonton born-and-bred physician here at The Ottawa Hospital? Keep reading to see.

Q: What were your younger years like growing up?

A: I was one of four, and as a kid, I was pretty big on sports. Hockey, soccer, baseball, volleyball, basketball — if we could do it, I’d play it. I was also the class clown. I did a little improv and was a big comedy fan. I’ve always loved to smile and loved to giggle, and I try and bring that to my household and work environment every day. 

Q: How did you decide to pursue medicine, and specifically work in the ICU and palliative care? 

A: I had pretty bad asthma as a kid, and I spent a lot of time in hospital. 

My pediatrician— Dr. Conradi — was my hero because of how he’d make us feel. For a kid that’s walking into a hospital and can’t breathe, the mom’s a bit panicked, his calm presence was super healing. Because of his impact on me, I was driven to be a pediatrician, to fill the gaps. 

I took a two-year gap between degrees and bartended and travelled and met my wife. In hindsight it was one of the greatest times of my life. Once I got into medical school, I realized being a pediatrician just wasn’t a good fit. I did a rotation in the Foothills Hospital in Calgary in the ICU in 2004, and I was like, “This is my home; this is perfect.” 

Later, I met Dr. John Seely when I was doing rotations. He was a palliative care doc, and I saw his impact on patients — the reassurance, the compassion. I wanted to be able to bring that to my practice. 

Q: What do you work on in the ICU? 

A: When people land in ICU, they often don’t leave as the same person. Either they don’t survive or they leave with significant disfunction. And my research interest has always been how to be more efficient with healthcare dollars — on how we reduce our spending but maintain or improve care. 

For me, the “aha” moment was during the pandemic, when you saw a lot of people with comorbidities that could be modified. I realized we had to focus on prevention. So, from an advocacy perspective, any time I have a public forum, any time I go to social media, I’m covering a lot of the ways for folks to stay healthy and avoid seeing me. Now, we’re dipping into that from a research perspective as well. 

For example, one thing we’re working on is how to help racialized community members in Ottawa reverse their prediabetes and diabetes through diet, exercise, stress management, and community building. It’s probably one of the projects I’m most excited about.  

Q: What’s the biggest challenge facing ICUs and critical care right now? 

A: Right now, it’s probably burnout. With supply and demand, we have an aging population that’s going to be leaning on the ICU resources more than ever, and we have issues with staff being burned out — many have left the critical care environment. 

It’s getting better, but it’s still going to be a challenge moving together. It brings it back to keeping people healthy and out of the ICU. And then there’s the wellness side for our physicians; we’re doing research on wellness and ways to work more efficiently. We’re working on leveraging AI to do some of the work so we can focus on patient care. 

Q: What’s some of the most exciting research in your field right now? 

A: It’s going to be on personalized care. On what’s the best approach for you, because it’s not necessarily the same approach for me. It’s the ability to cater personalized treatment based on demographics, genetics, etc. And that’s going to be the future of research, not just in the ICU, but in all of medicine. And I think it’s the right path, too. Because it’s clear that one treatment is not always optimal for everyone.

Q: Why do you choose to work at The Ottawa Hospital?

A: I did my undergrad and medical school in Edmonton, and a Master of Health Administration at Dalhousie in Halifax. I did an elective in infectious disease in Ottawa in 2004, and my wife and I fell in love with the city.

“The research side here is bar none, elite. It’s straight up elite.”

— Dr. Kyeremanteng

What keeps me is the people. I’m surrounded by the most amazing staff, who are exceptional clinically and academically. The research side here is bar none, elite. It’s straight up elite. Whether hematology, the emergency group, or our own group in critical care, this is an elite level of research, and it’s great to be a part of that. I learn every day. It feels like it’s my family outside my family.

Q: Why is diversity important for a successful healthcare system?

A: I think diversity is essential if we want to stick with our mission of compassionate care. For us to provide that care and fulfil our mission, we need to have multiple perspectives. Looking at the example of AI, a lot of studies are based on white males, so we can’t apply that data to our general population. We need that diverse representation in our research. But we also need diverse leaders at the level decisions are being made to be role models for those who are underrepresented. It’s not just on the floors and doing the groundwork, but at a leadership level too — diversity is key.

Q: Where would we find you when you’re not at work?

A: Playing street hockey with my boys, throwing around a football, or playing some ice hockey myself. I’m very active, so I hit the gym and walk the dog — Coco the Aussie doodle — a lot. I’m always working on podcast stuff, doing social media production, or speaking engagements. Or I might be having a dinner date with momma bear.

Dr. Sarah Brandigampola

Becoming a psychiatrist wasn’t always the obvious choice for Dr. Sarah Brandigampola. Interested in the arts from an early age, her passion for psychiatry emerged after a chance rotation during medical school. Today, she’s a psychiatrist in The Ottawa Hospital’s offsite On Track program for people experiencing early symptoms of psychosis, and she’s part of an essential team helping people get back to the life they want to live.

Scroll down to read more about how Dr. Brandigampola is helping people with psychosis rewrite their stories — and the surprising career she would have chosen if she didn’t pursue medicine.

Q: Can you tell us a little about growing up and your early years?

I grew up in Listowel, in the middle of Mennonite farming country. It’s a small town, with two stop lights. Growing up I was interested in a lot of different things, but I wanted to be a neurosurgeon or a star on Broadway. I did a lot of theatre, dance, and music. Our music program was a vocal program, and I was fortunate to travel a lot with our choir; we even performed at the Notre Dame cathedral in Paris.  

Q: When did you decide to pursue medicine, and specifically psychiatry?

I was finishing high school, and I had to make a difficult decision. I wanted to pursue both the sciences and the arts. In the end, I always wanted to help people. I had a strong sense of social justice and wanting to contribute in a meaningful way to helping people. So, I chose medicine because I thought it would be more fulfilling for me.

I studied cellular biology at Western University in London, Ontario, and then came to Ottawa for medical school. In third year medical school, you rotate through different areas, and I was not interested in psychiatry; I wanted to be an oncologist. But, when I went into the psychiatry rotation, I found it so meaningful looking at people from a global perspective — not just at their medical illness, but at their living situation, their relationships, their childhood, their income, at what makes them a person — and how can we help them with their illness. I also loved the teamwork aspect — it felt side-by-side with nursing, social work, occupational therapy, recreational therapy, everything; everyone was really working as a cohesive team with this vision of how we could help this person as a person.

“When you’re looking at the story of people’s lives, it’s a lot like reading a book; you pull out themes and look for critical moments.”

— Dr. Sarah Brandigampola

Now that I think about it, I think a lot of my skills were aligned with psychiatry. Psychiatry wound up being a meeting point between neurology and the arts. When you’re looking at the story of people’s lives, it’s a lot like reading a book; you pull out the themes and look for critical moments for communication. With psychiatry, we can help people tell their stories in a way that has meaning to them.

Q: How has the field of psychiatry changed since you started?

I definitely think there’s a lot less stigma about mental health now than when I started. People are talking about it a lot more. There’s a long way to go, specifically around severe and persistent mental illnesses. In terms of the future, there’s so much research that needs to be done. We still don’t truly understand what causes schizophrenia or most mental illnesses.

Q: You worked on Sean Heron’s case. What made that case challenging or unique?

“He really jumped into the program. Everything we suggested, he said, “Yes.” We have a walking group, a social group, a sports group, occupational therapy, recreational therapy, medication. He did it all, and we just saw him come to life.”

— Dr. Sarah Brandigampola

Sean is one of our star patients. It’s the kind of story you want to hear. When we met him, he was very unwell, and he’d been unwell and untreated for about a year and a half. That was worrisome because the longer the duration of untreated psychosis, this does have an impact on people’s prognosis. The goal of our clinic is to intervene earlier in the illness.

In spite of that, he just did so well. He really jumped into the program. Everything we suggested, he said, “Yes.” We have a walking group, a social group, a sports group, occupational therapy, recreational therapy, medication. He did it all, and we just saw him come to life.

The number one predictor in the program is whether they have a supportive and involved family member, and once he was in it, he started going out for walks every day with his mom again.

Q: What advice would you give to someone experiencing first-episode psychosis?

What I hope people can learn about schizophrenia is that there’s so much hope for this illness. Most people with schizophrenia do very well if they get into treatment.

We take self-referrals, so if people have a loved one, or if they’re wondering if something is happening to themselves, they can call us, and we’ll see them and help them figure it out.

It’s also important for people to know a symptom of schizophrenia is a neurological one called anosognosia — the inability to know something is wrong. The part of your brain that tells you something is wrong turns off. It can be really frustrating for family members, because they’re trying to reason with the person. It’s best to focus on things like not going to school, not seeing friends, or other changes, and start the conversation there.

Q: What is The Ottawa Hospital doing in psychiatry and mental health that is exciting or groundbreaking? 

Our On Track program is the model of care that I would hope everyone with mental illness could be a part of. I think it is very exciting what we do as a clinic — we have such amazing success stories. When you talk to people about a diagnosis of schizophrenia, you just see their face change and their parents are often shocked. But we have such great outcomes at this clinic. This illness does not have to dramatically change your life, and I would say it’s because of the model of care we provide.

Our leadership is also really great. Dr. Jess Fiedorowicz, Head and Chief of the Department of Mental Health, is amazing. He’s an endlessly optimistic person who sees what we could be doing and pushes us to be doing more. I think he’s striving for mental health to be even more comprehensive.

Q: As a psychiatrist, why did you choose to work at The Ottawa Hospital?

Dr. Sarah Brandigampola and the On Track team at a music festival

I did six months in the On Track program for my residency, and I wanted to keep working here with this team. They are amazing. This is not work you can do on your own, and it’s wonderful to have such a great clinical team, but also this community of people where there’s a genuine camaraderie. I never have any doubt people are going above and beyond. I know I can trust people’s judgment. It can be difficult sometimes, but there’s a lot of humour and friendship and genuine caring for each other.

I’m also so grateful for my patients and to be trusted with their stories and their care. They teach me everything.

Q: What would we find you doing when you aren’t at the hospital?

I have my family, and we like to get outside. I also love reading and travelling. If I can, I enjoy seeing live music and things that keep me engaged with the arts.

Dr. Sarah Brandigampola hiking in Gatineau

It was only a glimpse she caught, standing on the side of the Trans-Canada Highway as it curved along Lake Superior, but since then, Terry Fox has remained a source of inspiration for Dr. Rebecca Auer. His vision and determination helped motivate her to where she is today — an award-winning cancer clinician-scientist.

Dr. Auer combines revolutionary cancer research with hands-on patient care every day in her role as Executive Vice-President of Research and Innovation at The Ottawa Hospital and CEO and Scientific Director at The Ottawa Hospital Research Institute. 

As a surgeon, Dr. Auer sees with clarity that, while surgery may be the best chance for a cure in most cancers, patients are particularly vulnerable to both infections and cancer recurrence in its aftermath, in large part because the immune system is suppressed in the postoperative period. Dr. Auer’s research program is focused on understanding the mechanisms behind this effect and reversing them with innovative therapies.

In recognition of her practice-changing research, Dr. Auer has been named the 2023 recipient of the Chrétien Researcher of the Year Award. 

Keep reading to learn about her childhood stint at CHEO and an alarming late night in the lab.  

Q: What were your early years like? 

A: Ottawa has always been my home; I grew up here, went to high school here, and went away for my undergrad in Toronto and medical school in Kingston before coming back to Ottawa for my surgical residency. 

I wasn’t fantastically good at school when I was younger. I had a learning disability related to writing, called dysgraphia, but I was good at math. My mother, a psychologist by training, would say, “If you’re good at math, do math, and you’ll figure out the writing stuff later.” 

We were super early adopters of computers, so I had an Apple computer by the time I was six, which was unusual. Being able to work on the computer took away a lot of the challenges of dysgraphia. 

Q: What made you decide to pursue a career in medicine? 

A: In high school, I really enjoyed sciences, especially biology. When I was 15, I was hospitalized for about three months with a bone infection in my knee called osteomyelitis. Even though I was stuck in my room on bed rest, I loved CHEO. I met a lot of interesting kids my age, most of whom had way more significant problems than me, but that didn’t seem to matter. We played practical jokes on the nurses, snuck ice cream from the kitchen, and laughed together after lights out. At a time when the only thing that mattered in high school was being cool, I found a place where people cared only about the things in life that really matter. I wanted to work in that kind of environment. 

Q: How did you wind up in oncology, specifically? 

A: When I first got into to medical school, I wanted to be a neurologist because I was fascinated with the way the brain works … but in practice, it wasn’t what I thought. Then, I considered obstetrics and gynecology because I enjoyed the operating theatre. In the end, I did a rotation in general surgery and it was love at first sight. It wasn’t rational, but I knew. Maybe it was the adrenaline of looking after sick patients, the diversity of different types of diseases, or the incredible feeling you get when you save someone’s life by fixing a hole in the intestine or stopping life-threatening bleeding. Every day would start at 5:30 a.m. and end after 6:00 p.m., and I never once looked at my watch. It was just a really intense experience. 

When I got into surgical residency, I had no idea what I wanted to specialize in. I thought maybe trauma or even rural surgery, but I found I was more interested in molecular biology than the other things I was supposed to be studying, like hernia repair techniques or the technical approach to the inflamed gallbladder. I decided to do a masters of science (MSc) in molecular genetics during my residency, but no one really wants to take a surgical resident for a one-year MSc if they’ve never done any work in the lab. One day, my mentor, Dr. Hartley Stern, who was the head of the Ottawa Regional Cancer Centre, overheard me complaining and called senior cancer researcher, Dr. John Bell. Suddenly I was doing a year in his renowned translational cancer therapeutics lab.  

I had so little experience working in a lab that I got teased a lot. Once I threw away a DNA gel because I thought I had cut the piece of DNA in half. I remember Dr. Bell joking that even a surgeon as skilled as me could not cut a piece of DNA with a scalpel! DNA is so small you have to use enzymes to cut it. I also used to keep the hours of a surgical resident in the lab, and one late night, I recorded a massive radiation reading with the Geiger counter. I was sure there had been a major radioactive spill. I called the postdoctoral fellow, who asked if I was pointing it at the fridge with the big radioactivity symbol on it … where we kept all our radioactive substances. When I admitted that was true, he said “Yes, yes, the fridge is full of radioactivity. Now please put the Geiger counter down and go home to bed!” 

“I realized what a privilege it is to look after cancer patients.”

— Dr. Rebecca Auer

Being in the lab was an amazing experience, and in the end, I decided to go into cancer surgery so I could have a research program in cancer biology. It was only later, during my senior residency and fellowship at the Memorial Sloan-Kettering Cancer Centre (MSKCC) in New York, that I realized what a privilege it is to look after cancer patients. It is their courage, resilience, and ability to show gratitude, even during some of the most trying times, that I find so remarkable. 

Q: What is the focus of your research? 

A: My research program is focused on understanding how surgery impacts the immune system. We know the immune system is highly effective at destroying cancer cells, but in the aftermath of surgery, the immune cells are almost completely dysfunctional for at least a week and up to a month or more. The research from our lab suggests that this postoperative immune suppression is responsible for cancer recurrence after surgery.  

As a surgeon, I take cancers out, but I don’t change the biology of disease. If the cancer is completely contained and there are no cancer cells floating in the blood stream or implanted in distant organs, the patient can be cured. Unfortunately, for many patients that is not the case, and months to years later, those cancer cells — the ones that were present at the time of surgery floating around undetected — grow into new tumours. The Auer Lab has hypothesized that if you reverse or prevent this immune suppression and have a strong and functional immune system after surgery, it could clear these left-over cancer cells and prevent the patient from getting a recurrence. We have demonstrated this is true in mouse models, and now we need to show it can be achieved in cancer surgery patients. We do wet-lab research to understand why the immune cells are dysfunctional and then experiment with different “perioperative” immunotherapies, given around the time of surgery, to see which work the best and then try them in clinical trials.  

Q: You are being recognized for an important clinical trial published in one of the world’s top medical journals. Can you tell us a little bit about this trial?  

A: PERIOP-01 was my very first clinical trial, and like most things in my life, I reached a bit too high. It was a national, multicentre randomized controlled trial, designed to change practice. Since then, we have done PERIOP-02 to PERIOP-06, all of which have been smaller scale. 

The trial was looking at whether perioperative administration of a blood-thinning drug, called tinzaparin, could help the immune system kill cancer cells following surgery for colon cancer and reduce cancer recurrence. Interestingly, the trial was negative, in that cancer recurrence was not lower in the group that got the tinzaparin, but what it did show was that you don’t need to give patients extended treatment with blood thinner after surgery to prevent blood clots. The trial was practice-changing, even if it wasn’t what we were hoping to see. 

On a personal note, translating a preclinical finding, discovered in my lab, into a human clinical trial conducted in collaboration with my surgical colleagues across Canada, was a major accomplishment. 

Q: How do you feel about receiving this award? 

A: This award is a huge honour, especially when I look at the people who have won the award in the past. It’s hard to believe I’m in that category. I’m also very proud of getting this study published and finished — it was the monkey on my back for many years. Like all research, it was a team effort and I cannot thank the co-investigators, collaborators, and research staff enough for all their support. This is especially true of my co-principal investigator and senior author, Dr. Marc Carrier. He is an incredibly accomplished researcher and former recipient of the Chrétien Award. Working with Marc and his team was a highlight of this project. 

Q: Why is research so important for the healthcare being delivered today at The Ottawa Hospital? 

“Never has it been more obvious than in cancer today, but research is care.”

— Dr. Rebecca Auer

A: In many cases, research is the best option for care, or the only option. The line between research and clinical care is increasingly difficult to draw clearly in the sand, and it is time to recognize we are creating more problems by trying to keep them separated.

Dr. Rebecca Auer speaks with a patient at The Ottawa Hospital Cancer Centre.

When it comes to rapidly advancing technologies, like molecular testing or personalized therapies, they are moving so quickly from bench to clinical studies that if we don’t embrace research as part of care, we are doing our patients a disservice. Every patient deserves an opportunity to participate in research, and as an academic hospital, it is our responsibility to provide those opportunities to patients. Research can fuel hope for patients by providing a new or alternative treatment for them or the potential to help others in a similar situation in the future. 

Q: What’s something people might not know about you? 

A: I think most people know Terry Fox is a hero to me. There are so many facets to his story. He had a bold and audacious vision to run across Canada on one leg to raise money for cancer research — a vision which he articulated the night before his amputation for cancer. He was steadfast in his determination, having run halfway across Canada in training miles before he ever dipped his toe in the Atlantic Ocean. He inspired others to join his cause and be part of something bigger than themselves. As the mother of three boys, I want them to know Terry’s story and understand the value of working hard for something you believe in. Every September, for the past decade, we have participated in the Terry Fox Run as a family, raising over $120,000 for cancer research.  

Auer Family Terry Fox Run 2014 – 2020

My one claim to fame is that I got to meet Bruce Springsteen at a fundraiser when I was the Chief Fellow at MSKCC in New York City. At the time, his long-time friend and E Street Band member, Danny Federici, was being treated for metastatic melanoma. I told Bruce about Terry Fox, his legacy in Canada, and how much research had changed cancer care since his death in 1981. Although Bruce probably didn’t remember any of it, I like to think that maybe Terry’s story gave him hope. 

Auer Family Terry Fox Run 2021
Auer Family Terry Fox Run 2022
Auer Family Terry Fox Run 2023

Dr. Shawn Aaron never intended to go into research. Early in his career, the respirologist — a doctor who specializes in lung disease — saw his future as working directly with patients. But after falling in love with research at The Ottawa Hospital, Dr. Aaron became a senior scientist working at the intersection of research and clinical care.

Dr. Aaron is also Principal Investigator and Director of The Canadian Respiratory Research Network, whose goal is to bring together researchers across disciplines to work together to improve the understanding of the origins and progression of chronic airway diseases in Canada.

In recognition of his practice-changing research, he has been named the 2023 recipient of the Dr. J. David Grimes Career Achievement Award.

Read on to learn why Dr. Aaron chooses to work at The Ottawa Hospital, what he’s excited about for the future, and why research isn’t like tennis.

Q: Can you tell us a little bit about your path into medicine?

A: I was born in Montreal, back in the dark ages of 1964. I’m the last of the Baby Boomers. I grew up in Montreal, went to public school there, went to McGill for my undergraduate degree, and then continued into medical school at McGill. When I finished, I went to Toronto and trained to be an internist and a respirologist — that is a doctor who specializes in lung disease. After that, I trained in intensive care medicine. When I finished, I just couldn’t get enough of training. So, I came to Ottawa, and I did a master of science in epidemiology. I finished my masters in 1999, and by then, at the age of ’99 minus ’64, I thought I was finished.

And then I started my research career.

Q: What drew you to research?

A: I thought I was simply going to be a physician in the community doing respiratory medicine. But when I was looking for a job in that field, my wife — who is an obstetrician gynecologist and grew up here — wanted to come to Ottawa. I reached out to The Ottawa Hospital, and they said, “We’d love to have you, but we want you to train to be a researcher.” I said, “Great. Sure. I’ll try it.” In the end, I fell in love with the idea of doing research for a living.

“Research is not a single-person sport.”

Dr. Shawn Aaron

Research is not a single-person sport. It’s not tennis; research is football or baseball. I work with statisticians, research program managers, and research coordinators. There’s a whole team that supports research. And without that team, there’s no way that I could ever have been successful. I am perhaps the coach of a football team.

Q: You specialize in cystic fibrosis and COPD, two chronic lung diseases. Can you tell us a little bit more about them?

A: They’re both debilitating lung diseases. Cystic fibrosis is genetic, so it affects young people, in their infancy. In the old days, when I first started practicing, our patients were routinely dying in their 20s and 30s. It was devastating. You can imagine how awful that is for the patients and their families and even for their healthcare providers. The good news is that in the last five or six years, we have dramatically improved treatments for cystic fibrosis. Our patients are living almost normal lives. And we expect their life expectancy, when we have more data, will probably be at least in the 60s or 70s. It’s a fantastic achievement, and clinically, it’s brought me incredible joy in my career.

COPD (chronic obstructive pulmonary disease), is the exact opposite of cystic fibrosis. It’s a disease of older people. It’s debilitating because it causes people to become very short of breath. Many of them require oxygen, you might see them on the street, walking with oxygen tubing in their nose. The most frustrating part of COPD is that we haven’t yet developed those magic cures like we have for cystic fibrosis. Unfortunately, in my 30 years of practice, my patients with COPD are still quite disabled, and still, unfortunately, dying of their disease.

Q: How is the research you do changing the care patients receive?

A: I turned my master’s thesis into a New England Journal of Medicine article, so you could say I peaked early. It was a study where we took patients presenting with acute crises in their COPD. We showed that when we gave them prednisone, a strong anti-inflammatory steroid drug, they had fewer relapses. We proved prednisone works for this. The proof wasn’t there before, and now prednisone is the standard of care.

Later on, I worked on a study on using a combination of inhalers to treat COPD. We wanted to see if we could prevent crises by treating them with a combination of inhalers. We hypothesized — I mean, it’s not rocket science — that if you combine inhalers, you might get better bang for your buck. We did the first clinical trial to use triple therapy for COPD, and we showed it was better for many outcomes.

In terms of research I’m doing now, we have a large study that will finish in January 2024. The research is trying to address that fact that we as health care professionals are currently doing a poor job of picking up and treating COPD. The basic problem with COPD care in 2023 is that by the time the patient comes to see a doctor complaining of shortness of breath, it’s too late. They’ve already lost their lungs; their lungs have been dissolved out. Unfortunately, this means doctors are closing the barn door after the horses have bolted; we’re trying to treat a disease that already has progressed dramatically. What I’m addressing with my research is whether we can catch the disease at a much earlier stage than with conventional diagnosis — and get treatment started much earlier to prevent disease progression, disability, and death.

In this study, we’ve recruited over 3,000 randomly selected Canadians who are complaining of respiratory symptoms but have never been diagnosed with any lung disease. We’re using spirometry, a simple test in which the patients blow into a tube and we measure how quickly they blow. The test is safe and simple and takes 15 minutes. Based on those tests, we’re diagnosing people with either COPD or asthma that has never been diagnosed before. In other words, these are people who are walking around in the community who are short of breath or coughing or wheezing and don’t know they have a disease. Once we find the disease, we’re doing a clinical trial where we randomize them into intensive treatment or usual care. Our goal is to see if by finding the disease early, and treating it early with intensive treatment and education, we can improve patient outcomes. I think it’s very exciting because we’re actually doing something that’s never been done before to try and catch and treat people early to see if we can improve the course of their disease.

Q: Why have you chosen to work at The Ottawa Hospital for so long?

A: The Ottawa Hospital gave me my big break. I was sort of like a rookie being drafted, and they thought I was promising enough to take me on, so I guess I’ve always felt an affinity to them. There are other reasons, though. The Ottawa Hospital and the University of Ottawa really nurture young researchers, and they allow us to develop at our own pace. They provide us with the support we need.

“The Ottawa Hospital is an amazing place to do research and clinical work, not just in Canada, but within the world.”

Dr. Shawn Aaron

The Ottawa Hospital is an amazing place to do research and clinical work, not just in Canada, but within the world. We have an incredible group of researchers who are world class. It’s things like cell-based therapeutics, clinical epidemiology, muscle physiology, molecular biology, and neuroscience. If you come here, you’re going to obtain great mentorship, you’re going to have great opportunities for collaboration, and you’re going to come into a very supportive environment, which is going to nurture you towards success.

Q: What excites you about the future of respirology?

A: I think the exciting part about the future is figuring out new modalities to treat COPD and asthma better. As I said earlier, one of those is going to be identifying patients early and trying to treat them early. I think in the next five years, we’re going to look at the clinical benefits of identifying patients early, but also the economic benefits. We’re also going to try and figure out how to use machine learning techniques, or AI, to do this early identification even better. Right now, we’re doing it with good old-fashioned questionnaires and phone interviews to figure out who might be sick and who should come in for testing.

Q: How does it feel to receive the Dr. J. David Grimes Career Achievement Award recognizing the work you’ve done?

A: I felt a few ways. One was incredibly humbled; I really didn’t feel I was deserving of the award because I know amazing scientists at The Ottawa Hospital, and I know many of them are much smarter and better than I am. I was surprised I actually got the award. But I was very pleased, obviously. My second reaction was to have a little bit of chagrin, because the Grimes award is for career achievement, so it’s usually given to people who are either on the verge of retiring, or who have retired. This was a sign that I am getting near the end of my career, but I think I still have five years left before I fade into oblivion. I am determined to make the best of what I have left and to continue to do important research.

Q: Where would we find you when you’re not in the lab or clinic?

A: That’s easy. I’m going to be at the cottage, in the Outaouais, kayaking in the summer, snowshoeing in the winter. It’s my happy place. I’m hoping I can retire with my health and enjoy those activities.

Dr. Shawn Aaron snowshoeing
Dr. Alvin Tieu

Dr. Alvin Tieu has been driven to make a difference for patients since the start of his academic career. From an early interest in the scientific method to a realization that research has a tangible impact on patients, Dr. Tieu’s journey has been shaped by how he can help others. 

After an undergraduate and master’s degree at Western, Dr. Tieu came to uOttawa to pursue his MD/PhD and become a clinician scientist. Working under the supervision of Drs. Duncan Stewart and Manoj Lalu, his bench-to-bedside research could change the care of tomorrow. 

In recognition of Dr. Tieu’s research, which takes laboratory discoveries one step closer to helping patients, he is the 2023 recipient of the Worton Researcher in Training Award.

Read on to learn what ignited Dr. Tieu’s interest in science and what exciting discoveries he’s working on today. 

Q: Can you tell us a little bit about your early years? 

A: I was born and raised in the Greater Toronto Area, in Scarborough. Both my parents were immigrants from Vietnam and worked multiple jobs to support our family growing up. Although they did not have a background in science or research, I can say for certain that my work ethic is a direct reflection of their daily commitment to ensuring I had the educational opportunities they never had.  

I’ll be the first to admit that I wasn’t a great student when I was young. I was really into athletics, as I think a lot of kids are, and back then, if I’d really had to choose, I probably envisioned myself being an athlete. Luckily, my involvement in sports taught me how to work in teams and dedicate endless hours to activities I was passionate about. To this day, athletics still play a big role in my life.

Q: What made you choose to pursue a career in research and science? 

A: I can still remember the exact time when I developed a love for science and research. Early on, I wasn’t interested in academics at all, but in Grade 7, I finally had a dedicated science teacher and course. Our first assignment was to write an essay on any topic we wanted, and for some reason, I chose the Big Bang Theory, about how the universe was formed. It was a big scope for a Grade 7 kid, but reading about it really sparked my interest. Learning that someone was able to conceive this complex theory with their own mind, math, and research was astonishing. That’s when I knew I wanted to incorporate science into my future career. 

Q: How did you decide to study medicine specifically?  

A: My bachelor’s and master’s were both in pharmacology. That’s when I began learning about the interesting physiology of the human body and disease. With pharmacology, you really have to know how drugs work to influence different body systems.  

At that time, my affinity for research really grew. I was part of different labs and led a clinical trial during my master’s that investigated how to optimize the management of antihypertensive medications in patients on hemodialysis. These experiences inspired me to continue pursuing a career in scientific discovery with the goal of positively impacting the treatment of patients moving forward.  

After this, I decided on the MD/PhD program at uOttawa — a seven-year program. When I was accepted, I remember my mom asking me, “Why are you in school for another seven years?” Although I had an appetite for research, I also developed an equal passion for medicine during my undergraduate studies. I had the opportunity to be a member of global health teams and saw how physicians can impact patients’ lives through active listening and patient-centred care. It inspired me to pursue a clinician-scientist career where I can both treat patients individually, face-to-face, but also conduct impactful research that can hopefully improve lives globally. 

Q: What drew you to Ottawa for this phase of your career? 

A: I heard great things about the medical school program in Ottawa, including their dedication to student wellbeing and clinical skills development. In terms of research, The Ottawa Hospital has one of the best research institutes in Canada. You have endless opportunities to be supervised under, or even collaborate with, scientists that are world leaders and experts in diverse disciplines. 

Q: Can you describe your research? 

A: I study extracellular vesicles, which are tiny particles naturally released by every single cell type in your body. Research in the past five to 10 years has shown that different cells communicate with each other through these little particles, thereby maintaining normal function in your body. However, they’re also involved in disease progression. For example, cancer cells can excrete these little particles as well, which may play a role in the development of disease locally and in other organ tissues.  

Dr. Alvin Tieu in the lab

I’m interested in isolating these extracellular vesicles from stem cells as an approach to treat lung diseases. Stem cells have been studied for decades now, and they show clear therapeutic potential in the lab. However, we have yet to translate that potential to patients. By isolating these little particles in high concentration, we can potentially harness the benefits of stem cells in a more practical way to treat devastating lung illnesses. 

Q: How do you feel about winning the Worton Researcher in Training Award? 

A: When I first heard that I was selected for the award, I was super excited because I know a lot of the previous recipients. Some of them were students, like me, and a lot of them I knew based off work they’ve done that really pushed the frontiers of scientific research. Being named alongside them is a great honour. Over half of my PhD was completed during the COVID-19 pandemic, which introduced a significant number of obstacles. All non-COVID research was halted for several weeks, and I had to completely alter my research objectives to include COVID-19 research. In the end, I was able to create what I think was an innovative, interdisciplinary thesis. I was thrilled to be this year’s award recipient and be recognized for my ability to adapt during these difficult times.    

Q: Where would we find you when you’re not in the clinic or the lab? 

A: Going to the gym is a way I relieve stress. As someone who played sports competitively growing up, playing volleyball or basketball with friends remains my main method of resetting my mind and maintaining wellness.  

Other than that, I love to travel. Next year, I will be visiting Europe four times for vacations and weddings. Being able to be immersed in diverse cultures, tasting local delicacies, and summiting mountains in different parts of the world are experiences that can’t be beat!