The cold had been making my spasticity much worse. The hug is getting tighter and tighter. I did not find baclofen to help me when I was at 60 mg per day. So now the only think I take for ms pain is clonazepam at bedtime. When I see new neuro (not supposed to have an appointment until June) I plan on seeing if he has any ideas on what might help. My old (now retired) neuro seemed to think that if 60 mg did not help then I was not responsive to baclofen.