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GED

Sativex advice

Hey, my MS team have referred me to start Sativex as nothing else has helped ease the spasms or muscle pain. Have you been on this? What’s your thoughts, did it help, did you have any side effects? It’s a new one for me so it would be great to hear your experiences. Thanks so much, Diagnosed 2021 RR, in the UK
First posted on the Shift.ms app
2
@Lowlander
@Lowlander
 

Hi I've been using it for 3 years, works great

@Woody68
@Woody68
 

The pain clinic trialed me on the later part of last year. I have to say it really helps my spasticity, just a shame it doesn’t help my Trigeminal neuralgia as well. I hope it helps you.