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Newborn screening and early treatment for spinal muscular atrophy can save both lives and money


Newborn screening and early treatment for spinal muscular atrophy can save both lives and money
Gene therapy for spinal muscular atrophy might have a high up-front price tag. But by screening and treating infants early, the therapy can save both lives and money in the long term.
By the time an infant with SMA starts showing symptoms, they ve already lost 90 per cent of their nerves – which is why early detection and treatment is so important. Photo: Unsplash
Spinal muscular atrophy (SMA), a type of motor neurone disease, is one of the deadliest genetic illnesses an infant can be diagnosed with. Caused by a missing or faulty gene called ‘SMN1’, the disease causes muscles to shrink and become weaker, limiting a baby’s ability to sit, walk, crawl, or even hold their head up. ....

United States , New South Wales , Sophy Shih , Michelle Farrar , Emily Henderson , Innovation For Children Health , Health Economist , World Health Organization , Luminesce Alliance , Medicine Health , Big Data Research , Associate Professor Michelle Farrar , Sydney Children , ஒன்றுபட்டது மாநிலங்களில் , புதியது தெற்கு வேல்ஸ் , மைக்கேல் ஃபரார் , எமிலி ஹென்டர்சன் , ஆரோக்கியம் பொருளாதார நிபுணர் , உலகம் ஆரோக்கியம் ஆர்கநைஸேஶந் , ளுமினேஸ்செ கூட்டணி , மருந்து ஆரோக்கியம் , பெரியது தகவல்கள் ஆராய்ச்சி , இணை ப்ரொஃபெஸர் மைக்கேல் ஃபரார் , சிட்னி குழந்தைகள் ,

Funding supports Australians living with rare disease


Date Time
Funding supports Australians living with rare disease
UNSW Sydney researchers have been awarded $1.9 million for a project that will develop and deliver rare disease resources, education and training.
UNSW has been awarded $1.9 million in federal government funding for the Rare Awareness, Education, Support and Training (RArEST) project. The project will develop and deliver rare disease awareness resources, education, support, and training with a focus on mental health, and social and emotional wellbeing.
The funding is part of the $3.3 million announced by federal Minister for Health and Aged Care, Greg Hunt, to support the approximate two million Australians living with one of 7000 rare diseases. ....

Adam Jaff , Yvonne Zurynski , Michelle Farrar , Greg Hunt , Gareth Baynam , Elizabeth Emma Palmer , Macquarie University , School Of Women , Children Health , University Of Western Australia , Medicine Health , Rare Awareness , Aged Care , Professor Adam Jaff , Associate Professor Michelle Farrar , Rare Voices Australia , Professor Gareth Baynam , Western Australia , Associate Professor Yvonne Zurynski , National Strategic Action Plan , Rare Diseases , Action Plan , Torres Strait Islander , மைக்கேல் ஃபரார் , கிரெக் வேட்டை , மக்வரீ பல்கலைக்கழகம் ,