For the fourth edition of our newsletter, we are pleased to introduce Nicola Montesin, a Speech-Language Pathologist with a special focus on ageing, dementia and progressive neurological conditions.Nicola holds an MA in Ageing and Dementia Studies and has extensive clinical and educational experience supporting people living with dementia, particularly in the areas of communication, swallowing and person-centred care.
As a committee member of the Malta Dementia Society and founder of MDS Communic-Aid, Nicola is dedicated to promoting communication, connection and quality of life for people living with dementia and their families. She is actively involved in dementia education, awareness, research and advocacy at both national and international levels.
What inspires and guides the Malta Dementia Society’s work?
The Malta Dementia Society is driven by the belief that a diagnosis of dementia should never mean losing one’s identity, dignity or place within the community. As trained professionals, we support people living with dementia, their families and the general public through education, awareness, support groups, activities, advocacy and opportunities for social connection.
What would you most want families to know after a dementia diagnosis?
Firstly, you are not alone. A diagnosis can be frightening, but dementia does not take away the person’s identity or ability to experience meaningful moments. Seek information and support early, focus on what the person can still do, and value the person rather than the diagnosis.
What can a “good day” look like for someone living with dementia?
A good day is one where the person feels safe, valued, connected and involved. It might be listening to favourite music, looking through photographs, going for a walk or simply having a cup of coffee together. Families can create more good days by maintaining familiar routines and focusing on activities the person enjoys.
How important is it to support family members and carers?
It is essential. Dementia affects the whole family, and carers can experience significant emotional and physical strain. Supporting the carer is also supporting the person with dementia. Families need information, practical support, respite and somewhere to talk openly about their experiences.
How can professional caregiving support at home make a difference?
Good professional care can help maintain routines, independence and safety while also providing much-needed respite for family carers (who are at increased risk of caregiver burnout). Having someone trained in dementia care can give families reassurance and reduce some of the pressures of caring. Asking for help is not a failure– it is an important part of caring well.
What advice would you give families about maintaining communication and connection?
Remember that communication is more than words. Give the person time, use simple language and avoid correcting them. Talk about familiar and meaningful things, look at photographs, listen to music, reminisce and enjoy activities together. Focus on the connection rather than getting every detail right.
Why are awareness and education so important?
Dementia еducation helps reduce the stigma and misconceptions surrounding dementia. It helps people understand that someone with dementia is still a person who deserves dignity, respect and inclusion. The more society understands dementia, the more compassionate and supportive our communities can become.
What activities and services does the Malta Dementia Society offer?
The Society offers a range of support and activities, including support groups, social and recreational activities, group therapy focusing on communication and reminiscence-based therapy, creative activities, outings, educational talks and dementia awareness initiatives. These provide valuable opportunities for people living with dementia and their families to connect with others, learn, participate in meaningful activities and feel supported.
I invite you to follow the Malta Dementia Society’s website and social media channels to keep up to date with upcoming activities and opportunities to get involved.
For further information or support, you can contact us at info@maltadementiasociety.org.mt or visit our Facebook page.
Are there any upcoming initiatives or opportunities that you would like our readers to know about?
We will be organising our Annual Fundraising Dinner on the 11th September 2026 at 7.30pm at The Xara Lodge in Rabat. We welcome everyone to join us and support our work.
Our Annual Memory Walk for Dementia will take place on Saturday 26 September 2026 in Valletta, starting at 9.30am in front of Parliament Buildings. It is a wonderful opportunity for families, friends and the wider community to come together in support of people affected by dementia.
As a Society, we also participate in European initiatives, where we contribute to discussions on dementia care, policy and advocacy. We will also be attending the Alzheimer Europe Conference in October 2026, providing an opportunity to share Malta’s perspective, learn from developments across Europe and strengthen collaboration with organisations working in the field of dementia.
If you could share one message with everyone in Malta about dementia, what would it be?
Dementia does not define a person. The person is still there, with their own history, personality, relationships and emotions. Let us look beyond the diagnosis, treat people with dignity, remain connected and make sure that people living with dementia continue to feel that they belong.
