Raising awareness of Rare Disease Day and Timothy Syndrome. Featuring the voice talent of Keith Allen and his daughter Teddie. The main objective of Rare Disease Day is to raise awareness amongst the general public and decision-makers about rare diseases and their impact on patients’ lives.
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Facial Palsy UK is still a very young charity (set up in 2012), the first charity to offer specific support to people affected by facial palsy due to any cause.
Facial palsy, sometimes known as facial paralysis, is a condition resulting from damage or absence or impairment of the facial nerve that supplies the muscles of facial function and expression, and affects blinking, closing the eye for sleep, eating and drinking, speech, smiling and frowning.
Facial palsy can be the result of multiple causes: disease, injury, stroke, birth trauma, cancer, or neurological condition – to name but a few. Whatever the cause, the physical, emotional and psychological consequences of living with facial palsy are usually the same, although to varying degrees, and they can be equally devastating for the people affected and their families.
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