Since being diagnosed I've become aware how little people know what MS is or anything about it. It's such a pot luck kind of deal, I've been lucky so far but who is to say if I will be this time next year. Someone could of had it the exact amount of time as me and be in a completely different state of ability or disability. It is definitely something that needs more attention and more awareness raised. I've lost count of the amount of times I've had to say "no it's not just being tired, I'm not tired" and in regards to MS no I'm not tired. Sometimes my thighs feel full of concrete or like today my entire right leg feels like it's full of jelly but I'm not tired. Not tired from this anyway.












