Going for my next treatment today. I will admit with the bad weather we have been having, and the stress of Jack not feeling his best, and my grouchy husband, I have not felt my best for the last two days.

Saw the neuro yesterday who said I look better to him. MUCH better. He was very pleased. He said I am still "hyper reactive" which means the MS is still not behaving its best, but he said its calmer than it was. he left me defer seeing him till november. We can then tell after being thru the treatments, out the other end and time to recover how well I am doing. He said he likes what he sees so far, keep it up.

She is just going to poke a metal pen into my finger tips for a few minutes, then tip a buzzy box on my tummy for about 30 minutes. I will spend the rest of the day wiped out, and want to sleep. Last time I got this burst of energy and starting feeling much better. lets see what this time brings.