L-R: Chris Graham (Choice Senior Building Surveyor), Lisa, John and John Luke Faulkner (Choice Tenants) and Michael McDonnell (Choice Group Chief Executive).

Choice tenant Lisa Faulkner and her son John Luke and their family have recently moved into their new home in Crawfordsburn Road, Bangor. 

Their home has been fully modified by the housing association to meet the needs of John Luke who suffers from a rare condition named Angelman Syndrome (AS). 

Angelman Syndrome (AS) only occurs in 1:20,000 children and is a genetic disorder that primarily affects the nervous system. Symptoms include severe delayed development, intellectual disability, severe speech impairment and problems with movement and balance. 

Following consultation with Lisa and her family, a programme of extensive renovation and adaptions were designed and delivered by Choice’s Building Surveying team ensuring the property met John Luke’s specialised needs.  This included installing a downstairs wet room, wheelchair access and the provision of a hoist and Low Surface Temperature radiators.

John Luke suffers from a sleep disorder which can manifest by only sleeping for 20–30-minute naps on some nights or going without sleep for a whole night. He is not mobile and unable to talk.

The newly renovated property will allow John Luke to gain full use of his hospital bed, tailored for his needs which he previously had not been able to use  due to the lack of space in their former property.

John Luke, who up until this point has never had his own bedroom, will now also have a soft play sensory area  aimed at helping with a range of visual and auditory processing, as well as fine and gross motor skills. 

Talking about the process of moving into their new home, Lisa said: “My son John Luke, who is now six, was diagnosed in October 2018 after a very long battle over an 18-month period.  The condition is often put down to delayed development and/or autism and diagnosis is not fully achieved unless a genetic blood test is done to detect abnormality in Chromosome 15.  The Choice team along with their partner Fusion Heating listened to our needs and understood the importance that every detail of our new home would have on John Luke’s life. Dimmer switches, low pressure shower and low surface temperature radiators were all put in place to protect John Luke and keep him safe. 

“Moving into our new home hasn’t just ensured that John Luke can live a normal life like any other six-year-old, but it secures our long-term future as a family. Before this, we were never sure if at some stage fulltime residential care would have to be an option if we weren’t able to accommodate his needs at home”. 

Significant consultation was undertaken between Choice Housing and their partner Fusion Heating Ltd to ensure the property met the needs of John Luke now and for his long-term future. Working alongside John Luke’s’ Occupational Therapist Sara McCrea, the team developed plans that would be fit for purpose throughout John Luke’s childhood, accommodating a condition with wide ranging symptoms. 

The property which was acquired by Choice as part of their transfer agreement with Victoria Housing Estates (VHE) was included in a £25m renovation and refurbishment programme to bring the properties up to a high standard of living. The four-bed bungalow was identified by the Choice  Assets team as a possible fit to meet the specialised needs of John Luke.

Michael McDonnell, Group Chief Executive at Choice added: “When we acquired the VHE properties back in 2020, we were aware that there was a requirement for significant refurbishment to the properties.

“In the process of assessing these properties, the four-bedroom bungalow was clearly a viable option for Lisa and her family, and the refit ensured it met the needs of a family who could now look at their new home as their long-term home”.

Since John Luke’s diagnosis, Lisa has become a health advocate, raising awareness of Angelman Syndrome (AS), working with health professionals to highlight the day to day needs and challenges of this rare condition on patients and their families.

Lisa also speaks at and participates in parent forums aimed at gaining as much information about the condition as possible.  

For more information on Angelman Syndrome, you can visit 

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