Phelan-McDermid Syndrome Awareness Day: Spinnaker Tower dazzles night sky in green to highlight cause close to Worthing family's hearts

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Dazzling green light shone from Portsmouth’s Spinnaker Tower yesterday for a special cause close to a Worthing family’s hearts.

Vivid colours radiated from the monument – as well as landmarks worldwide – for Phelan-McDermid Syndrome (PMS) Awareness Day.

Sophie Farrell and Daniel Taylor’s daughter Willow, two, was diagnosed with PMS on October 21 last year – with the rest of the family being informed on awareness day.

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There are more than 300 families who are diagnosed with PMS in the UK and Ireland, and almost 3,000 registered cases worldwide.

Willow Taylor, dad Daniel Taylor, Sienna Taylor and Mum Sophie Farrell, from Worthing, in Portsmouth. Picture: Mike CooterWillow Taylor, dad Daniel Taylor, Sienna Taylor and Mum Sophie Farrell, from Worthing, in Portsmouth. Picture: Mike Cooter
Willow Taylor, dad Daniel Taylor, Sienna Taylor and Mum Sophie Farrell, from Worthing, in Portsmouth. Picture: Mike Cooter

Sophie described the diagnosis as ‘traumatic’, with her partner adding Willow’s condition means she has the mental age of seven months and is non-verbal.

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Portsmouth’s Spinnaker Tower to be lit up for Worthing toddler with Phelan-McDer...

Sophie said: “When you hear about the diagnosis, it hits you in the weeks and months to come. Each little attribute she has grows on you. It became real to us when she had a seizure a month afterwards, it lasted an hour and a half.”

The family thoroughly enjoyed seeing the Spinnaker Tower, which daughter Sienna, five, is fascinated by, and meeting other PMS families for the first time.

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The Spinnaker Tower lights turn green for International Phelan-McDermid Syndrome Awareness Day. Picture: Mike Cooter (221022)The Spinnaker Tower lights turn green for International Phelan-McDermid Syndrome Awareness Day. Picture: Mike Cooter (221022)
The Spinnaker Tower lights turn green for International Phelan-McDermid Syndrome Awareness Day. Picture: Mike Cooter (221022)

Sophie is hoping more awareness will increase funding for PMS research, with the disease impacting roughly 300 people in the UK and 3,000 worldwide. She added the support they received on social media was ‘heart-warming’.

“Just seeing the other families and different age progressions helps us relate,” she said. “Willow is sprinkled with a bit of magic dust – lighting up the faces of anyone she meets.”

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