Hi All,
After being in Limbo Land for just short of a year, i finally got diagnosed. This was after being fobbed off by a general Neurologist, and me asking to be referred to a MS Specialist.
Anyway, the consultation went as well as can be expected, with me getting upset when she diagnosed(which apparently is normal), upto that point i suppose i kept thinking it wasn’t MS, but hey ho, i will not let this stupid Disease beat me!!!
Basically, as the consultation was coming to an end, she told me to think about which DMD, i would like to try, read up about the various ones, then to let her know through the MS Nurse, and she would then apply for funding…is this the normal way/ as unfortunatly i know very little.
Also i would love to hear other peoples experiences with their choice of DMD, as i am fully aware that one does not suit all.
Thanks Guys xx