Rare disorders
In the UK, a rare disease is defined as a condition that affects fewer than one in 2,000 people.
Patients and families with rare disorders face challenges to navigate complex care pathways, cope with emotional stress, and seek specialised support.
Our clinical teams can help tailor specialist clinical care for a range of rare disorders.
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We know how to manage rare disorders
Understanding the specific needs of patients with rare conditions and providing personalised care is key to improving outcomes.
Our dedicated teams provide clinical services at home, ensuring that patients receive the necessary intravenous or subcutaneous infusions.
Tailored treatment for rare disorders
We understand how to provide specialist clinical therapies for a range of disorders.
hATTR Amyloidosis
A genetic disorder characterised by abnormal protein deposits (amyloid) in various tissues. Symptoms affect the nerves, heart, and other organs. Early diagnosis and management are crucial for improving outcomes.
AHUS (Atypical Haemolytic Uremic Syndrome)
A kidney disorder characterised by abnormal activation of the complement system. It can lead to kidney damage, anaemia, and other complications. Treatment may involve plasma exchange, immunosuppressive drugs, and supportive care.
Paget’s Disease
A chronic condition that disrupts normal bone remodelling. It leads to enlarged, misshapen bones, prone to fractures. Treatment aims to manage symptoms and prevent complications.
Hypophosphatasia
An inherited metabolic disorder affecting bone and teeth development. It results from low levels of an enzyme called alkaline phosphatase.
Learn more about our other nurse led treatments
Every day, our specialist clinical teams deliver a wide range of clinical therapies, for patients and their families.
