Have posted before. Will recap. Had ON mid Feb, followed by MRI which was abnormal and Opthalmologists letter to GP said it showed “probable MS”. Referred me to a neuro surgeon which wasted 3 weeks. Finally got an appt with a neurologist for 20th august!! Now although I don’t seem to be suffering very much, some altered sensation in my left arm and leg, and an irritable bladder I am finding it very difficult to live with the uncertainty.
I also know that an appt won’t answer my questions immediately, but I just feel that a conversation with someone who knows what they’re talking about will help me to get my head round it.
So, I have arranged to see the same neuro privately . Even since making the appointment I have started to feel less anxious.
I just think it’s awful that you have to wait so long for an appointment and wondered what sort of waits other people have had. I still have to wait til next Tues, but that’s a lot better than 3 months!!