Many post CCSVI treatment MS'ers have mention improvements in bladder and bowel function - even Dr Code.  Has anyone experienced the opposite?  After Jim's treatment last Nov. we have seen some improvements in bladder function, but the changes in bowel function are not for the best. There is more constipation and infrequent times. This seems to lead to 'not so good days' and once we clear the constipation, he bounces back to 'good days'. Any Comments?