I have m.e which is also known as cfs. With a tag on of flomid . Neawly diagnosed andstruggling with the diagnosis. Its a invisible illness and as such people are unaware of the pain I have daily. Mentally I am looking forward to university to do my criminology degree to further develop my appropriate adult career, but physically I will struggle to maintain my ability to pace myself and having the wheelchair will mean my muscles and joints will not be tested so much. Its on recommendation from my Gp and I have some NHS funding but not enough 😯