Hi all, I’ve been on Kesimpta for exactly one year (I was previously on Tecfidera for a long time which worked well until a yearly scan showed new lesions so I was taken off and put on Kesimpta). I consider myself very lucky as I don’t really have any MS symptoms, any relapse I have had I’m made a full recovery from apart from one which has left tingling around my face when I’m stressed. Anyway, I have numbness and tingling around my right foot and lower leg, I have my yearly neurology appointment soon as well as my yearly MRI scan so I guess that will show if there are new lesions. So I’m wondering, please can anyone share their experiences with Kesimpta and mild MS activity. I’m worried when I tell my neurologist that she will want to take me off Kesimpta but that will feel like a knee jerk reaction to me! What would other drug options be at this point? Has anyone had experience of how much activity they allow before being pulled from one medication? I feel like I need to do some research on my options so that I can go into my appointment with some knowledge! Thank you in advance for any thoughts and guidance