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About us
Your Later Life
Oncology
Life sciences
Men's Healthcare
Clinical Trials
Healthcare
Rare Diseases
Rare Diseases Q1 2024
New national strategy will address challenges faced by people living with rare diseases
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Choosing compassion: what it takes to support children with disabilities and rare diseases
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Hereditary ATTR amyloidosis: a rare disease with a unique Irish connection
Rare Diseases Q1 2024
Rare disease initiative: recognising and supporting PLWRD globally
Rare Diseases Q1 2024
Elevating specialised rare disease care across Europe
Rare Diseases Q1 2024
Living with a rare disease: why the community voice matters
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Gene editing innovations targeting multiple variants for rare diseases
A Cork-based research team is developing groundbreaking gene editing strategies that target multiple variants to tackle rare diseases. At the genetic level, we each have many, small variants in our DNA that make each of us unique. Occasionally, one of these variants disrupts the instructions for making an essential protein in our body. This is … Continued
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A supportive community for people living with tuberous sclerosis complex (TSC)
Rare Diseases Q1 2024
Why we should start seeing the 1 in 17 affected by a rare disease in Ireland
Rare Diseases Q1 2023
How much of an impact do female hormones have on our bodies?
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New rare disease plan needed to improve Ireland’s rare disease pathways
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Hereditary ATTR amyloidosis — a rare disease with a unique Irish connection
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Recognising hereditary ATTR amyloidosis early can improve your quality of life
Genetic testing and screening are available for this serious, debilitating and sometimes fatal hereditary disease, hATTR amyloidosis. Rosaline Callaghan, a retired Barrister living in Derry, learnt that she carried the gene mutation that causes hereditary ATTR amyloidosis, in 2007. At that time, she was told that finding a treatment for this fatal disease was unlikely. … Continued
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An evolving story: improving care for hereditary ATTR amyloidosis
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Empowering rare disease communities and pioneers to strengthen research
Rare Diseases Q1 2023
Don’t live with the pain and discomfort: how to manage ATTR amyloidosis
Rare Diseases Q1 2023
Gene-silencing drugs are among the innovative treatments for stiff heart
Rare Diseases Q1 2023
Increasing recognition of ATTR cardiac amyloidosis can improve outcomes