← Return to Chronic Pain members - Welcome, please introduce yourself

Discussion

Chronic Pain members - Welcome, please introduce yourself

Chronic Pain | Last Active: Mar 16 11:12am | Replies (7172)

Comment receiving replies
@hazelblumberg

I developed earaches in September 2016. My primary care found no ear or sinus infection and sent me to an ENT, who diagnosed TMJ pain. I went to my dentist for help. He gave me weekly anesthesia shots into trigger points (OUCH!) and exercises to do, including massaging the trigger points and opening my mouth as wide as I could numerous times in the shower while my face was warm and wet. (I have been wearing a night guard made by my dentist for over 20 years; he replaces them as they wear out.) The pain continued and only got worse; it was at the top of my head, in my ears, in my jaw, above my palate (as though I'd eaten hot food). My dentist sent me to an oral surgeon, who did 360-degree x-rays and found no joint damage. He told me I was therefore not a candidate for surgery (YAY!) and prescribed Flexeril, a muscle relaxer. The pain only got worse, and I continued to wake up in the night with horrific pain. Ibuprofen didn't even touch it.

My dentist then sent me to a physical therapist, who didn't listen to a word I said. I came in on a "good" pain day: my pain level was about a 5 out of 10 (10 being the worst). After his examination and showing me how to do various exercises, he triumphantly told me that my pain level was now reduced. I said "No. My pain level is now about 7.5." He said he didn't believe me. He attempted to push me to go to his outside clinic to get "magnet therapy," and he tried to push me to see a friend of his who is a naturopath. Two days after this session, I was still in excruciating pain and doubt I'd ever return to this physical therapist, although he had me schedule 4 more 1-hour sessions with him.

I called my dentist again, and he called in a prescription for Tylenol plus codeine, which I can take every 4 to 6 hours. My dentist seems to have no further solutions for me.

My primary care is currently out of town, but I will see her when she gets back (in August); she may be referring me to a pain management specialist, which my dentist recommended--however, my dentist refuses to give me a referral to such a specialist, even though the specialist will take referrals from dentists or doctors.

I have been treated for many years for clinical depression and panic/anxiety disorder by my psychiatrist, and the meds have helped me immensely. On Monday I see my psychiatrist for my usual 6-month med check, and I'm going to ask him for help with the terrible TMJ pain. I have also had fibromyalgia and chronic fatigue syndrome for a long time. The fibro pain has greatly lessened over time and hardly bothers me, but the CFS continues.

The TMJ pain makes it difficult to concentrate. I'm self-employed, and I enjoy my work. But pain gets in the way, as it does in every single situation: work or pastimes. My dentist mentioned massage therapy, but I'm in too much pain right now to try it. Another friend mentioned using a TENS unit. I feel as though I'm not living; to be in constant pain is hardly living, at least to me.

Any other suggestions? Would a TENS unit help? I'm more than willing to purchase one. I'll try just about anything to be pain free. Sometimes I am pain free. But I spend about 2 weeks out of every month in serious pain. I am feeling very discouraged.

Jump to this post


Replies to "I developed earaches in September 2016. My primary care found no ear or sinus infection and..."

Thank you for the complement but I am really close to you in age....74 but who's counting. ☺

I just looked it up in the iPhone App Store, it's there called Round Health-Medication Reminder. I just looked it up under the word round and it comes up. It's got a picture of a circle. I don't know it works really well if you can find it.

@jenapower

I have an account at MediGuard.com. It keeps my list of meds, and gives me the interactions with the other meds. I just check it whenever I change a med.

Jim

Thank you Jim, that sounds like a great resource. I'll look into it. Jennifer

Hey @JustinMcClanahan, have you had pharmacogenomic (PGx) testing done?

Pain meds don't work for me because I'm a slower metabolizer (genotype status level Poor for the enzyme CYP2D6, which the body uses to fully- or partially-metabolize most pain meds).

Here are the metabolizer statuses for each enzyme:
Poor < Intermediate < Normal (Extensive) > Rapid > Ultra Rapid

I'm willing to bet you're a fast metabolizer by genotype (rapid or ultra rapid) for at least one of the enzymes that metabolizes Dilaudid. (Dilaudid is metabolized by five enzymes, three of which (CYP3A4, CYP2C9, and CYP2D6) are included in the standard PGx test sets like the ones provided by Mayo and Oneome.)

When doctors prescribe meds, they will assume that a patient is a Normal metabolizer unless they are provided with info like I have (and then they usually just become confused and somewhat scared, except for my Mayo doctors).

I haven't actually. But, maybe I should. I will have to have my right ankle fused within the next 3-5 years, so I know for certain I will need pain medications again. Maybe this time around it would be better to go in with a little more knowledge about how I process medications so I don't bottom out so quickly and get behind the pain. Luckily, I have always been able to ween myself of pain medications with my physicians and have not had any hints of addictions, but this information could be helpful for certain.