Hi everyone! Hope you’re all doing well.
I’ve just had my follow up appointment following my Lemtrada treatment last month. Mainly positive as I have recovered from the treatment well and have had hardly any side affects!
Anyway, scary part was once again it was mentioned that both my Neurologist and MS nurses are worried about the amount of lesions my MRI scan showed. So now I’m just frustrated again that I literally have no bloody control over this awful disease and I’m worried about what could happen to me before I have my next round of treatement next year, as I am already experiencing a new symptom which I didn’t have before or during my treatment.
So, I’m wondering if anyone has any tips/advice of any ways I can keep myself as healthy as possible to give myself the best chance of not letting things deteriorate. I’m going to start making smoothies to ensure I get my 5a day etc etc.
Sorry for the rant 😂 any tips welcomed thank you ! X