Too much saliva

Discussion in 'Fibromyalgia Main Forum' started by simple, Apr 2, 2003.

  1. simple

    simple New Member

    I've read some people on this forum have dry mouth. I have the opposite problem... too much saliva. I'm not sure it's related to my CFS but the too much saliva started few months prior to onset of CFS. It's really getting in the way when I speak to people. It's affecting my life at work because speaking to people is very uncomfortable for me because of it. Can anyone comment on this or anything I can do to help myself. Thanks.
  2. kellbear

    kellbear New Member

    But I have the opposite problem. Like you said, a lot of CFIDS patients have dry mouth. Mine was so bad for about 6 months, went away somewhat now. It was horrible. I still would like a little more saliva but anything is better than what it was.. yuck