@TracyDeVinney. My first neurologist told me that but he also told me he could not say for sure if I had MS without a spinal tap and he would not prescribe any meds until I had had t flare ups. I was glad when he moved and I had to get a new neurologist. She is an MS specialist. My first visit she told me I didn't need a spinal tap because she could tell by my MRIs, she also prescribed a medicine. My primary care guy is actually a Nurse Practitioner. He's been more helpful than most of the specialists we see.

I've never had a seizure but it is one of the first things my first neurologist told me could happen

Hi Trace, I’ve had a history of seizures for years and was dx’d with rrms because of it (seizures).

It *may have a lot to do with where a lot of myelin damage has been located.

Example: prefrontal lobe area with extensive area/s of damaged, missing myelin sheath.

I do fall into that small 2-5% as listed above by MyMsTeam. I’m assuming those numerics are accurate? Idk 🤷‍♂️

Best,

Danny

Yes it is, Trace!

Thank you Danny. This has got to be one of the most misunderstood illnesses.