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Triginimal Neuralgia

  • 12-01-2014 4:48am
    #1
    Registered Users, Registered Users 2 Posts: 194 ✭✭


    Need help
    I've recently found out that I've this disease its horrible.I've been to see a few different doctors and neurologist, but not finding their not really helping me as they keep changing the medication I was first given to treat the pain. As the tablets wear off which only lasts about an hour of pain relief. All of the tablets I'm on at the moment impair my ability to do simple tasks around the house. Has anyone got this disease that could share experiences triggers and how you are coping because I'm not coping very well

    Thanks in advance


Comments

  • Registered Users, Registered Users 2 Posts: 194 ✭✭vanessamee


    Have had two MRI scans done.


  • Moderators, Education Moderators, Regional South East Moderators Posts: 12,514 Mod ✭✭✭✭byhookorbycrook


    I get it as part of my MS, what meds have you been on and for how long? Many of these meds need to be built up slowly so maybe you hadn't reached a high enough dose?


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