181 - 190 of 1900 results for "Rare Genetic Syndromes Support Information."
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Subarachnoid haemorrhage
A subarachnoid haemorrhage is a rare but life-threatening type of stroke that needs emergency treatment.
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Being a young carer: your rights - Social care and support guide
If you are 18 or under and you care for someone you are entitled to help and support.
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Sharing data from your health records – Information in different languages and formats
Get information about choosing to share your health record data for planning and research in different formats and languages.
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Epidermolysis bullosa
Epidermolysis bullosa (EB) is a general term used to describe a group of rare, inherited skin disorders that cause the skin to become very fragile.
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Money, work, benefits and social care - Social care and support guide
How to pay for care and support, and where you can get help with costs.
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Myalgic encephalomyelitis or chronic fatigue syndrome (ME/CFS) - Diagnosis
Find out how myalgic encephalomyelitis (chronic fatigue syndrome or ME/CFS) is diagnosed.
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Granulomatosis with polyangiitis (GPA)
Find out about granulomatosis with polyangiitis (GPA), including what the symptoms are, how it's diagnosed and how it's treated.
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Oesophageal atresia and tracheo-oesophageal fistula
Oesophageal atresia is a rare birth defect that affects a baby's oesophagus (the tube through which food passes from the mouth to the stomach).
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Myositis (polymyositis and dermatomyositis)
Find out more about myositis, the name for a group of rare conditions that cause muscle weakness.
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Side effects and risks of the combined pill
Find out about common side effects of the combined pill and some of the rare health risks associated with taking it.