To visit our general transition homepage click  here.

You might have heard your team talk about transition and wondered what it is. These pages have been designed to help provide information and support as you become more independent and take more responsibility for managing your Sickle Cell.

We will start talking to you about this when you are about 13 years old but the time the move to the adult Sickle Cell team happens will usually be when you are around 16 years old. The team will work with you to help you feel ready for this and to think about when and how the move can be best planned. The move to the adult team can feel daunting but the adult services aim is the same as the childrens, to care and support you throughout your time in hospital. It is just in a different setting and works in slightly different way.

Who can help you with this?
You might already know a lot about your condition. At the start of the transition process your Sickle Cell team will ask you about what you know about your condition and how to manage it and give you further information and support to ensure you are ready.

Your parents may have been important in helping you manage your Sickle Cell. It is good to talk together about how you can manage your health and independence. You can help in this process by starting to ask more questions during your clinic appointments, keeping important numbers in your phone and contacting the team yourself outside of clinic appointments.

During transition your Sickle Cell team will help you prepare for adult services by:

• Ensuring you have the knowledge and skills to manage your condition
• Seeing you for part/all of your clinic appointment on your own
• Introducing you to the adult Sickle Cell team
• Making sure you know when to get help and who to contact in an emergency
• Helping you understand the impact of Sickle Cell on your life as you get older

Will the adult service be different?
Your Sickle Cell team will describe to you ways in which the adult clinic will differ from those you are used to and you will have an opportunity to meet members of the team before you transfer to adult services. The main difference is that you will be more independent in managing your Sickle Cell and making decisions for yourself. You will be given all of the information to help you make the right choice for you and you can be guided and supported by your parents and friends.

These pages contain information to help you manage your Sickle Cell and know about the care we can provide for you.