Gene therapy for sickle cell and beta thalassaemia
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Clear guidance on the gene therapy journey for sickle cell disease and beta thalassaemia, from the first conversation to long-term follow-up, alongside the people who have already been through it.
This site is completely non-profit.
The journey
What actually happens, step by step, from the first conversation to long-term follow-up.
Who are you here for?
Written for parents, partners, siblings, friends, and the professionals around them.
What is gene therapy?
How it works, who it is for, and what it can and cannot do. In plain language.
The whole path, in order
Most people arrive somewhere in the middle. Wherever you are, you can see what is behind you and what comes next.
Written from published sources
This page is written from published guidance and research by regulators, the NHS and peer-reviewed journals. Every source is listed at the bottom of the page so you can check it yourself.
Lived experience
Written by a person describing their own life. It is not clinical guidance and has not been reviewed as such.
Talking to a person
Asking for support, and sharing what you have been through, are two different things. Choose the one that fits.
Would you like to speak to someone who has been through it?
A page can only go so far. If you would rather talk to a person, you can ask. You will be contacted first. Nothing is published.
Share your experience
If you have been through it, you can say how it was, and choose a nickname or your real name to sit with those words. If you are willing to talk to someone who is still deciding, there is a question about whether your contact details may be kept. Nothing is published.
This platform is in development. Guidance is being written and reviewed, and no page is published until a named clinician has approved it.