Awaiting results VEP + EEP
About 4 weeks ago I had a VEP + EEP done same day. Visual potentials made me super dizzy, EEP didn't hurt but my spine was killer about thirty minutes after.
I was told I would get results from this, that confirm if my CIS has 'converted' to MS like everyone keeps telling me it's obvious that it has, in 2-3 weeks. It has now been 4 weeks. Should I be contacting someone to chase this up? Or do I just have to wait for the results through the post?
My current neuro is Dr. O'leary.
For context: this has been a 3 year investigation into MS, with between two- four 'unclear' lesions observed on my C spine. Symptoms progressed from leg numbness/pain to daily crutch user minor dystonia/dysarthia, and for the past two years severe vertigo, dystonia, dysarthia, muscle tension pain, spasms, minor dysphagia and bladder hesitancy and now I am a manual wheelchair user. 25 y/o M.
@wheelrunconflux , give your Neuro's Secretary a call and make a polite enquiry. No harm in that.
It seems you're in Limboland, very awkward place to be and we empathise. A lot of us have been there for differing lengths of time but some people had a shock and were diagnosed straightaway, some even had unexpected news thrust upon them and were quite shocked so we cover all bases. Waiting is hell but at least you're part way there. I do hope you get news of one sort or another quite soon, at least you will be able to plan though I think that you have already planned to some extent as you are already in a wheelchair. Keep your chin up and keep us posted😍