Hi all, Meme and Tina thank you isn’t it freaky and amazing what our brains do!!! What complex things we are, thank you for responding as that does make sense I guess it’s fingers crossed any lesions we have are on useless areas hey! Helebon your symptoms sound very much like a nasty attack I had around my diagnosis, I now know as well that further relapses cause all the old ones to flare up and say “hello don’t forget I’m still here” so my lower back pain will be buzzing away again and the ants in my head sensation even though those two go away in between. I’ve been told I’m frequently relapsing 4 a year on average and I’m on copaxone. I have mostly sensory relapses but my feet and infer tips have never regained feeling. I blame that for the iPad not recognising my typing fingers haha. My ms nurse told me something I find quite useful/intriguing tat a relapse is around 6 weeks it can either reach it pinnacle at that point or filter away. My experience was It started as a pain in my armpit and moved around your body, weak arms, numb fingers pain in legs and at 6 weeks found finger tips and stayed there. The relapse could carry on or leave you with that residual damage or ease away slowly…is tat right? That’s what happens to me. I feel like its a game of spin the wheel, where’s it going to find its resting place! Lol! What a freaky disease this is, the label of frequently relapsing scares me I wish there was more reassurance for us and our fears! Thanks I’m glad I can come here when I’m feeling a bit scared and tlk to people who understand. Xxx