Snap! I’m the same. No significant results on brain MRI so was referred to a neuro-octologist for vestibular function tests which I’m having the end of the month. They seem to be going down the migraine variant balance disorder road full steam as my medication is being increased to the maximum dose and I’ve been put on a very restrictive diet which means no chocolate, dairy, citrus fruits, fresh yeast or high yeast products, no red wine, no caffeine , nothing with MSG in so no Chinese food and no eggs! Plus i have to have regular meal and bed times, no exertion or exercise and avoid stress. They are ignoring all my other symptoms. Although I’m yet to get results on a spinal MRI and some blood work to detect muscle wasting type complaints. Should be an interesting month. Perhaps the diet will help me loose all the weight I’m putting on being on gabapentin and being so immobile. Best of luck x
How would you get the neuro responses you dis though and still have a normal mri? Baffled A
Moysek, have you had evoked potentials tests?
I’m very baffled too Arwin. Even the ophthalmologist yesterday says they all sound nurological. By the way it was him who told me my results yesterday he didnt realise I hadn’t had them. They arrived in post this morning. Going to contact my spinal consultant as ihave an open appt and it was him who suspected MS and originally referred me to nuro. And I’m ready for another coccyx injection. How’s you arwin?