The SCS Helpline Service provides confidential information, guidance, and emotional support to individuals and families affected by sickle cell living within the UK.
What can we advise on?
We understand that sickle cell disorders uniquely affect people, and can manifest into a range of further conditions. We also understand that a sickle cell disorder affects the wider social support network. That’s why we support any individual affected by sickle cell, including family members, friends, employers, teachers and healthcare professionals. The topics we cover include:
What can’t we advise on?
Although we can provide information and guidance on managing a sickle cell disorder, we are not medically qualified and are therefore unable to comment on individual health issues. We can, however, explore your options and signpost you to your nearest sickle cell and thalassaemia service.
We cannot provide professional legal advice or legal representation, however we can signpost you to organisations that may be able to help.
You can contact our helpline service on 020 8963 7794 between: 10am and 5pm Monday – Friday
These times do not include bank holidays. Sometimes we will be unable to answer calls immediately. If you are unable to get through to the helpline service, you will have the option of leaving us a message with your name and contact number. We aim to return all calls within 3 working days.
You can also use our confidential email service: email@example.com. We will respond to all emails within 5 working days.
If you need to talk to someone face-to-face, you can contact us on 020 8963 7794 to make an appointment.
We also have a wide range of information about sickle cell disorders under the resources section of our website.
Alternatively, please write to us: Helpline Services Team, Sickle Cell Society, 54 Station Road, London NW10 4UA.
All information shared via telephone and email is confidential. However there are limits to our confidentiality. Read our confidentiality policy.
Have your say
We aim to ensure the best possible helpline experience. In order to achieve this, we rely on your feedback. If you have recently spoken to a helpline officer via the phone or email and would like to comment on how we dealt with your enquiry, please do fill in our short survey. This survey is anonymous, and is made up of a few questions about why you called, how you would rate the support or information received, and whether we helped to make a difference.
Fill in the SCS Helpline survey.
Thank you for your help!
Read our complaints and feedback process.
The helpline service is not a substitute to medical care. Please contact your GP, haematologist, or sickle cell clinical nurse specialist if you have any concerns about your condition or treatments.