An array of services available to patients with red cell disorders
Community Red Cell Service
This new specialist nursing care will support red cell patients in their own homes with close links to primary, specialist, social and community care to join up services and create a seamless experience for patients.
This service is a source of support, clinical care, advice, and advocacy for people with red cell disorders and their families. Our community service focuses on the individual and what they need at that point in time. It also recognises that these needs can change and be unpredictable. We will address the physical, emotional, and social needs of patients and families affected by red cell disorders.
This service does not replace the role of your hospital team, but works closely alongside them to provide broader, more joined-up support.
Patients can refer themselves to this service by calling 020 3316 8853 or by emailing ncl.
Service hours are Monday to Friday 9:00am - 5:00pm
Hyperacute Service
Based on feedback from patients, we have created a new expert ‘hyperacute’ unit to provide specialist treatment when people need it most, allowing them to bypass A&E in a crisis.
Located at North Middlesex University Hospital, closest to where the majority of people with sickle cell disorder in North Central London live, the service builds on the Trust’s existing specialist red cell service as well as specialist services at the Whittington Hospital and University College London and the haematology team at the Royal Free Hospital.
Contact details:
-
emergencies only: 07773735842 (this is a 24-hour hotline from 19 June 2024)
Sickle Cell Children and Young Persons Peer Mentoring Programme
The Sickle Cell Peer Mentoring Programme has been successful in terms of its engagement with children young people and parents, clinicians, commissioners, including the demand and uptake from most boroughs across London.
Referrals are now open and can be done by using this form.
If you have any queries, please do not hesitate to contact the Sickle Cell Society on info