new site nightmare

im finding it very hard to use the new site and fel like im being denyed the help and support ive always gained from the seems to me that its all bout raising money withe the message boards shoved into a corner and hard to find.the old site worked fine was easy to use and welcoming this new one seems to do everything it can to disuade use
the only help ive ever had from any medical person or the ms society have been my monthly ms matters magazine and the message boards and now im starting to feel that the mesage boards are too much hastle to bother with