Being a patient with Ehlers Danlos Syndrome often means living with little to no public healthcare. This is due to a lack of awareness and poor understanding of the condition and related issues. We are fundraising on here to help to obtain treatment for Diana, in order to address connective tissue disorder, including the neurological symptoms occurring due to cervical spine instability and its other comorbidities. This includes spinal neurosurgery and the cost of the pre-operative processes that the NHS could not provide.