91 - 100 of 879 results for "Rare Genetic Conditions and Supportive Patient Care."
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Accessing health services for someone else (family and carer access)
GP surgeries can give someone secure access to another patient's GP services, so they can help them manage their health and care.
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Care services, equipment and care homes - Social care and support guide
Includes home adaptations, help at home from a paid carer, staying safe and housing.
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Find your local integrated care board (ICB)
Integrated care boards (ICBs) replaced clinical commissioning groups (CCGs) in the NHS in England from 1 July 2022.
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How and when to take methotrexate
NHS medicines information on dosage for methotrexate, how to take it and what to do if you miss a dose or take too much.
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Carer's assessments - Social care and support guide
See if you can get support from your council, such as extra money or a break from caring.
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Our policies
Policies relating to the NHS website, including terms and conditions of use.
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Rett syndrome
Read about Rett syndrome, a rare genetic disorder that affects brain development and causes severe physical and mental disability from early childhood.
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Gilbert's syndrome
Find out about Gilbert's syndrome, a genetic condition where a substance called bilirubin builds up in the blood and causes jaundice.
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Charcot-Marie-Tooth disease
Charcot-Marie-Tooth disease (CMT) is a group of inherited conditions that cause nerve damage, leading to muscle weakness and numbness
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Progressive supranuclear palsy - Diagnosis
It can be difficult to diagnose progressive supranuclear palsy (PSP), as there’s no single test for it, and it can have similar symptoms to other conditions.