Meningioma UK brain tumour survival
Being told you have a meningioma brain tumour is devastating, whatever type of tumour it is. Patients (I'm one myself so I know what it's like) need support and information. Several years back my friend and I started a self-help group for patients and carers in the UK. FYI Meningiomas are rare tumours of the brain or spinal cord, and funding is hard to find so we run our patient support on a shoe-string. Our website is homemade and it looks it!
Help! Is there anyone out there who could create a great logo for us and give our website a face-lift ? Related Link