Colin Farrell has set up a foundation for people with Angelman Syndrome
This week, Irish actor Colin Farrell announced he was setting up a foundation for people with Angelman Syndrome.
The actor was inspired to set up the initiative by his son James, who was diagnosed with the neurological disorder when he was a young boy.
Farrell said he wants to ensure people with Angelman Syndrome are given the appropriate care.
The Colin Farrell Foundation will offer support for adult children with intellectual disabilities. The foundation will offer this support through advocacy, education, as well as innovative programmes.
Speaking to People, Farrell said he’s setting up this foundation in honour of his son James.
Farrell shares his son James with ex-girlfriend Kim Bordenave.
The actor explained that James and others with this condition have “earned the right to have a greater degree of individuality and autonomy in life and a greater degree of community.”
But what is Angelman Syndrome?
Angelman Syndrome is a neurological disorder caused by a change in a gene.
The main symptoms of Angelman Syndrome include delayed development, problems with speech, balance issues, seizures, and mental disability.
Those with the condition will also struggle with sleep and may suffer from strabismus and scoliosis.
Other signs include smiling and laughing often, seeming happy, as well as being easy to excite.
There is sadly no cure for Angelman Syndrome, but there are treatments available for patients.
People with this neurological disorder will live close to a normal life span.
Farrell said his son would be happy with his decision to launch the foundation.
The Banshees of Inisherin star shared: “This is all because of James – it’s all in his honour.”
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