Understanding fatigue in young people with Charcot-Marie-Tooth disease

Developing a tool to improve understanding, research and care.

Understanding fatigue in young people with Charcot-Marie-Tooth disease

July 1, 2026
Developing a tool to improve understanding, research and care.
Read Transcript

The challenge 

Charcot-Marie-Tooth disease (CMT) is the common inherited peripheral neuropathy. It affects peripheral nerves, which carry signals between the central nervous system and muscles. As the disease progresses, it can cause muscle weakness and sensory loss which significantly affect mobility and independence.

Fatigue is a common symptom experienced by children and adolescents living with CMT. Around 80% of parents report that their child tires more quickly than their peers during physical activity, yet the impact of fatigue remains poorly understood and difficult to assess. Without a reliable way to measure fatigue, clinicians and researchers have limited ability to understand its impact or evaluate whether future treatments improve this important aspect of quality of life.

Monica Marzouk and her team are addressing this critical gap by investigating how fatigue presents in young people living with CMT and developing the CMT Fatigue Scale (CMT-FaS), a tool designed to provide a more consistent way to assess fatigue in clinical and research settings.

The role of philanthropy

Hearts & Minds funding, as nominated by Magellan Investment Partners, has enabled Muscular Dystrophy NSW to award a full-time postgraduate scholarship to Monica Marzouk, providing her with dedicated time to focus on this research and accelerate progress towards a better understanding of fatigue in children and adolescents with CMT.

This philanthropic support has also helped leverage additional funding through the Nigel Clark Memorial Travel Grant, enabling Monica to present her research at the Hereditary Neuropathy Foundation’s 2026 Summit. This opportunity increased the visibility of the project, strengthened connections with the global CMT research community, and created opportunities for future collaboration.

What this could unlock

The development of the CMT-FaS has the potential to strengthen how fatigue is understood and assessed in children and adolescents living with CMT. By providing researchers and clinicians with a clearer picture of this often-overlooked symptom, this work could help inform future studies and the evaluation of treatments aimed at improving outcomes for people living with CMT.

This project is supported by Hearts and Minds Investments, as nominated by Core Fund Manager,  Magellan Investment Partners. For further information and updates, visit Muscular Dystrophy NSW.

The challenge 

Charcot-Marie-Tooth disease (CMT) is the common inherited peripheral neuropathy. It affects peripheral nerves, which carry signals between the central nervous system and muscles. As the disease progresses, it can cause muscle weakness and sensory loss which significantly affect mobility and independence.

Fatigue is a common symptom experienced by children and adolescents living with CMT. Around 80% of parents report that their child tires more quickly than their peers during physical activity, yet the impact of fatigue remains poorly understood and difficult to assess. Without a reliable way to measure fatigue, clinicians and researchers have limited ability to understand its impact or evaluate whether future treatments improve this important aspect of quality of life.

Monica Marzouk and her team are addressing this critical gap by investigating how fatigue presents in young people living with CMT and developing the CMT Fatigue Scale (CMT-FaS), a tool designed to provide a more consistent way to assess fatigue in clinical and research settings.

The role of philanthropy

Hearts & Minds funding, as nominated by Magellan Investment Partners, has enabled Muscular Dystrophy NSW to award a full-time postgraduate scholarship to Monica Marzouk, providing her with dedicated time to focus on this research and accelerate progress towards a better understanding of fatigue in children and adolescents with CMT.

This philanthropic support has also helped leverage additional funding through the Nigel Clark Memorial Travel Grant, enabling Monica to present her research at the Hereditary Neuropathy Foundation’s 2026 Summit. This opportunity increased the visibility of the project, strengthened connections with the global CMT research community, and created opportunities for future collaboration.

What this could unlock

The development of the CMT-FaS has the potential to strengthen how fatigue is understood and assessed in children and adolescents living with CMT. By providing researchers and clinicians with a clearer picture of this often-overlooked symptom, this work could help inform future studies and the evaluation of treatments aimed at improving outcomes for people living with CMT.

This project is supported by Hearts and Minds Investments, as nominated by Core Fund Manager,  Magellan Investment Partners. For further information and updates, visit Muscular Dystrophy NSW.

Disclaimer: This material has been prepared by Hearts & Minds, published on July 1, 2026. HM1 is not responsible for the content of linked websites or content prepared by third party. The inclusion of these links and third-party content does not in any way imply any form of endorsement by HM1 of the products or services provided by persons or organisations who are responsible for the linked websites and third-party content. This information is for general information only and does not consider the objectives, financial situation or needs of any person. Before making an investment decision, you should read the relevant disclosure document (if appropriate) and seek professional advice to determine whether the investment and information is suitable for you.

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