I'd never heard of Angelman Syndrome until Colin Farrell opened up about his son having it last night on David Letterman. Farrell seems to be quite a private guy in recent years and him opening up and speaking so tenderly about his son's neurodevelopmental disorder made me admire him that much more.
I knew he was a dad to two sons. Henry (seen here with Colin) is almost 2 and his mother is Alicja Bachleda, Polish actress and singer. His son James with model Kim Bordenave is who has Angelman Syndrome.
James is 7, and started walking when he was 4. Originally it was believed he had cerebral palsy.
Farrell explained that the misdiagnosis is common. It is also often confused with autism because they share traits. Angelman's is very rare, affecting one in 30,000 children -- though CureAngelman.org notes one in 15,000 live births.
James is non-verbal but high-functioning and Colin said he is a "really happy boy." Children with Angelman's may have intellectual and development delays, seizures, jerky movements particularly with the hands, and often are laughing or smiling.
When I learn of something like this, it stops me. Makes me reflect. We do what we can for our kids with what money we have, but then you see a big star like Colin who surely makes a lot of money and yet that won't cure his son. There is no cure. We can only give them love. Teach them the best we can. Be our own child's biggest advocate. And that is exactly what Colin is doing. I so admire him for it. Especially because he seems like such a private man, a father who is protective over his sons.
Farrell used his celebrity for good and talked about how Angelman Syndrome could use more funding and those who want to help can make a donation at CureAngelman.org.
I hope for a cure, a breakthrough of some sort, to help families who are affected.
Have you heard of Angelman Syndrome?
Image via Splash News
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Comments (51)
Ive actually never heard of angelmans syndrome before. Im glad Colin was able to give the foundation a nice plug on tv. Perhaps there will be more people willing to donate money to its research.
Its so easy to take things for granted. I thank God that my children are all healthy. It seems Colin is pretty strong, and very supportive of his son. Good for him.
Yes I have
Angels have such happy disapositions: despite the grief of finding out your child has an incurable disability, I think Colin will be able to move past this and will come to really enjoy this experience in his life.
Yes,I have heard of Angelman Syndrome-but for the reason it is stated above-it is often confused with Autism (I am a mother of an autistic child)
I applaud Mr. Farrel-You are right,the biggest thing you can do is not focus on pity or sorrow,but advocate for your child,and enjoy the little things in life you might otherwise overlook.
I agree with Victoria Goins statement above.
I heard about angelman's syndrome a while ago, but still only because of Farrel's son ... he seem like a great dad . I have all the respect in the world for him .
i have never heard of it untul now. he seems like an awesome devoted father
I had not heard of it until now either but what a wonderful thing he is doing for his son.
I recently attended an early childhood conference (mainly for educators, but parents were welcome as well) and in the parents' session, one of the presenters was a parent of a child with Angelman syndrome. I think any devoted parent, regardless of their status, their income, etc. should be commended for doing everything they possibly can for their child. I have yet to meet a parent in the special needs community (I have two children on the autism spectrum) who don't do all they can in order to give their children the best life possible.