Thanks Sally.

Jumping to conclusions is the furthest thing from my mind. I simply can't find any explanations for this extreme temperAture reaction and, whilst researching last night, came across the spasticity that MS sufferers are said to experience and that is exactly how it feels. My Doctors have no suggestions so they don't try - perhaps I need more symptoms before they get concerned but for me, it's so extreme and violent that I really fear it happening. It is now the next morning here and .i still feel as though I have pushed my body to its physical limit - just by getting cold!

Best wishes, Clare