Recurring facial pain

Posted by on Sep 16 2012 | Facial Pain/Trigeminal Neuralgia , MS

Over the past month or so, I had pain on my nose, then on my upper lip. These sites were associated with cold sores. Over the past 10 days, the pain has moved and is being triggered again in my mouth, especially when I eat. The painful spots are on the gumline on both sides of my upper teeth. When the pain breaks through, it throbs and includes my lower right tooth where I had gum graft surgery in January, 2011.

I saw an oral medicine specialist last week who diagnosed me with atypical odontalgia, or ‘phantom tooth pain.’ He told me that he didn’t think that the MS was related to the pain. I wrote an e-mail to him on September 15:

I am inclined to think that my pain is from the MS — however; you are the expert! I would be ecstatic to find that it was not connected to the MS but nothing else makes sense to me, unless a herpes simples virus attack can induce this pain.

I had been hopeful that it was another sinus infection. I saw Dr. Javer briefly yesterday. Unfortunately, there was no infection. Funny that I had hoped for an infection — at least it would be treatable! He said all of my sinuses look good and healthy.

I started taking nerve pain drugs last week again. I am also using a topical ointment that the oral medicine specialist prescribed for me to numb the sensitive spots in my mouth. The drugs constipate me and the sensitive spots in my mouth are worse. The pain must be originating in my trigeminal nerve at the pons, the part of the brainstem where the trigeminal nerve originates.

I can’t stop crying. I am sinking into a deep depression. I am very lonely.

1 comment for now

One Response to “Recurring facial pain”

  1. […] I felt it was important for future patients at the hospital I was in (Dec 27, 2011 – Jan 6, 2012) to continue educating the doctor who was in charge of my care — the one who almost pulled my feeding tube out because I was being ‘non-compliant’ with the treatment plan that was developed without any input from me. At the time I wrote the first e-mail, I knew I had MS but I was unable to identify a lesion in the pons. I was holding onto hope that the facial pain had been resolved, although when it worsened a couple of weeks later, I was pretty sure I had MS-related trigeminal neuralgia. […]

    16 Oct 2013 at 10:50 pm

Trackback URI | Comments RSS

Leave a Reply