Anne Hogden is a neurologist based in Sydney, NSW 2052. She works with people who are dealing with nerve and muscle conditions that can be hard to live with day to day. Neurology isn’t just about scans and tests. It’s also about planning for what comes next, keeping symptoms as steady as possible, and helping families feel more supported.
In her clinical work, Anne looks after patients with motor neuron diseases, including amyotrophic lateral sclerosis (ALS, also known as Lou Gehrig’s disease). She also supports people with primary lateral sclerosis. These conditions can affect movement, strength, and day to day function over time, and that’s why follow-up and clear communication matter so much.
At times, care may also include support around feeding and swallow-related needs. Her work includes gastrostomy care, which can be a big step for many families. When this kind of treatment is needed, it helps to have a steady plan, simple explanations, and practical guidance. The goal is to reduce stress and make sure the person is looked after in a way that fits their life.
Neurological symptoms can change without much warning, so patients often need more than one appointment. Anne focuses on understanding what is happening now, what tends to happen next in similar cases, and what can be done to improve comfort and safety. She pays attention to the small things too—like fatigue, difficulty with eating or swallowing, and changes in mobility—because these can have a big impact on quality of life.
Her medical training includes completing doctor education and specialist neurology training. Over time, she has built her practice around caring for people with long-term neurological conditions, where ongoing support and a team approach are often the key.
There are also times when decisions about treatment options need careful discussion. Anne aims to keep those conversations calm and clear. You can expect information to be explained in plain language, with room for questions and time to think things through. It’s not about rushing. It’s about making sure patients and families know what to expect and feel supported along the way.
