@Jem_Carter 

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Jem_Carter

Seizures and MS

Hi all, hope everyone is doing well. I just have a question...I've had MS for a few years now, rapidly evolving severe, I've had 2 courses of lemtrada but after 1 year of my last course I had new activity so my neurologist put me on copaxone injections. I wasn't eligible for ocrevus as my immune system still was at 0.5 a year and a half later. Anyhoo recently I have been have very bad seizures, which I have never had before. The hospital said it was most likely a flare of my MS but the MS nurse said it's not something they usually see in connection with MS...any one have any thoughts/experiences?
@Stumbler

@jem_carter , don't get me wrong, MS Nurses are excellent sources of support. But, although specialists and with the best will in the world, we can'e expect them to know everything. The following may help:- https://www.nationalmssociety.org/Symptoms-Diagnosis/MS-Symptoms/Seizures