We will present our findings to NHS England and keep you informed of developments and future plans. We anticipate that there will be further opportunities to contribute your views and experiences in the coming months. We will let you know how to get involved by updating you on our social media and by contacting local Sickle Cell Support Groups. In the meantime, if you have any questions about this work please do get in touch: firstname.lastname@example.org
What are the planned changes?
Below is the document NHS England has produced to explain why they propose the changes, what the changes may look like, and the possible effect on patients. Click on the image to view the document (or click here).