Caring for the whole person


Dr. Sarah Lidstone
University Health Network

The Movement Disorders Clinic at Toronto’s
University Health Network is among the top clinics in the world for treating
Parkinson’s disease. During her fellowship there, Dr. Sarah Lidstone will study
ways to improve treatment for people living with Parkinson’s, including studying
innovative models of care in Europe and the UK. Funded by Pedaling for
Parkinson’s in honour of Dr. Peter George Morse, her hope is to build a patient-centered
network of allied health professionals focused on Parkinson’s disease that
treat the whole patient. 

The Movement Disorders Clinic at Toronto Western Hospital is a global leader in treating Parkinson’s disease. That’s why Dr. Sarah Lidstone is eager to learn from the colleagues who will mentor her there.  

Lidstone, a neurologist, has been studying Parkinson’s disease for
18 years, including as a researcher before she earned her medical degree.

The most important thing she’s learned is that Parkinson’s “… is not just a movement disorder,” she says. “People’s whole lives are affected.”

Although people often think Parkinson’s affects seniors, people
with early onset Parkinson’s disease are in their 30s or 40s when diagnosed.
The disease affects their careers as well as the lives of their caregivers, and
alters family dynamics.

During her fellowship, Lidstone plans to learn from her supervisor,
Dr. Anthony Lang, about how to build a successful clinic. She hopes to add
innovative technological tools to care for people with Parkinson’s in all
aspects of their lives. Her research is made possible through a Clinical
Fellowship for $50,000 over 1 year from Parkinson Canada Research Program funded
by Pedaling for Parkinson’s in honour of Dr. Peter George Morse.

“The technology exists to monitor people’s tremors, for example.
Why are we not using it clinically?” she asks.

Although the Toronto Western Hospital clinic is cutting-edge, it’s
not always accessible to people outside the city. After her fellowship,
Lidstone plans to create a network of healthcare professionals, including
social workers, nurses, physiotherapists and speech-language pathologists. They
would be trained at the clinic, but specialize in treating Parkinson’s in their
home communities.

She plans to travel to The Netherlands, to Scotland and to the
United States to study the multidisciplinary networks there.  

Ultimately, Lidstone hopes a multidisciplinary approach will
ensure people with Parkinson’s get the care they need for all aspects of the

“My vision is to become a world leader in truly innovative ways of
treating patients with Parkinson’s disease. This includes actively involving a
physiotherapist early in the disease course, involving a social worker, and
placing a huge emphasis on teaching patients about their disease. This can
empower patients,” she says.

Lidstone has been interested in Parkinson’s disease since her
undergraduate days, when she became fascinated by how changes in the brain
correspond to people’s symptoms.

She forms close relationships with her patients.

“Having an opportunity to ask people questions about all these
different parts of their lives and do something to help them in all of these
areas is very rewarding,” Lidstone says.

“It’s these long-term patient relationships that I love and make
me want to come to work every day.”

Lidstone also hopes to study existing care versus multidisciplinary care to see which provides better outcomes.

Read about other researchers recently funded by the Parkinson Canada Research Program by visiting the research section of

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