Went to see my neuro today, got a checkup and I'm doing well as in my MS is stable and my reflexes are good. Hopefully shouldn't need meds till 2024, Cladribine worked 🎉! Now the bad news, I've got to start thinking of my future, I've got a really good chance of being ok well into my 60s. I know they don't have a crystal ball but I guess monitoring progression is a thing. I've been so tired lately, really tired. I can take meds but I think she is reluctant to give them me because part of my problem is that I'm doing loads. I'm balancing working, teaching, studying as well as being a mum and doing it myself. Something has got to give and it's that which has upset me, I've worked so hard since I was diagnosed to do and achieve what I have but I'm going to burn out if I don't pull back. It's hard for me to hear but there has got to be a way of doing it all 🤔😭?!