Experiences with

Facial pain

I have severe facial pain and have to take daily painkillers anyone have any tips, I am still waiting to see someone at the Bell’s palsy clinic

has anyone ever dealt with facial pain? They at one point said I had Ms and mg, then said no to mg, but I have facial, jaw pain. Went to dentist he said teeth looked good. Hummm

anyone else got this ??

For me this means constant facial pain (migraine earache and toothache all at the same time ) I am told this is a very rare health condition . Are there any other members on the forum that have this condition ?

Also, is chronic facial and neck pain and tmj a potential cause of tinnitus? My dentist feels that a night guard would help alleviate my tinnitus.

Although I have experienced facial pain, headaches and slurred speech as this is how my condition presents itself. However, this year, I have had four episodes with my slurred speech going on from 1 week to 2 or 3 weeks.

Since the brain surgery I have been getting really bad facial pain on and off but they said it shouldn’t be happening because they have removed the trigeminal nerve in my head. Has anyone else had these symptoms ?

I am gradually learning how to walk again The stroke has affected the nerves in the left side of my face and eye Is there anything I can do or treatment I can seek to reduce this facial pain? Many thanks Andykilburn

it got bad after a very stressful emotional period of a year or so - constant fight or flight status, bad sleep etc - and facial pain .

I have been taking shot of Prolia and shot of methotrexate every Tuesday.i have no pain but have tender spots on my head and if does not hurt to touch. I only seem to have it in my temple are and top and back of head.. I had a mri of my head a few years ago. I have had a couple of bad concussions 2

I've had daily chest pain since 2020, unexplained (excruciating) atypical facial pain since 2021 and now unexplained throat pain since June 2023. I've had multiple MRIs, cameras, x-rays and no explanation for any of it.

Has anyone in our group tried the antispasmodic Spasfon? Generic name is Phloroglucinol. It is approved and is an over the counter medication in France, Spain and I believe in a few other countries but not in the U.S. The research studies that I reviewed shows promise for IBS-D related pain and

Source: https://www.youtube.com/watch?v=L6CtKeOAzGE BUT the likelihood of patients to respond to these treatments is lower if treated for 5+ years with dopaminergics. The reason being the upregulation of D1 receptor responsible for sensitivity to pain and abnormal sensations.

I’m from Ireland so very little knowledge of RLS by doctors here!! I weaned off premipexole as I mentioned here in my last post. I cannot take gabapentin as it really upsets my stomach. I am now taking 1 codipar tablet before bed. I find it helps quite a bit but am worried that I will become dependent

Acetyl-DL-leucine in two individuals with REM sleep behavior disorder improves symptoms, reverses loss of striatal dopamine-transporter binding and stabilizes pathological metabolic brain pattern—case reports: https://www.nature.com/articles/s41467-024-51502-7#:~:text=In%202020%2C%20we%20treated%20a

phone update with GP early December suggested I taper to 12.5 which I did on 11th dec About 4 days after started to feel fatigued and headaches now constant , 20th December shoulder pain , feeling of facial pain more like sinus pain earache/tooth pain (no jaw pain) fatigue worse Struggles on with

hello all My question is about the Pneumovax-23 and Prevnar 13. I got the Prevnar 13 in 2015 The Pneumovax-23 in 2015 as well. Is it time to get these again? I live in the US. On W/W for over 20 years. Having immune globulin infusions for the last 5 years or so. Thank you for any insight.

the Vimpat stopped working to completely resolve my RLS. Recent MRIs showed multiple Tarlov cysts on my spine, which is possibly causing the left leg pain and movement. It is positional and separate from the RLS in both legs in my arms and body. I see a new neurosurgeon next week. I’ve had multiple

I took one dulcolax last night at about 10pm. I had 3 bowel movements in the space of an hour, 11am-12pm today. No pain or discomfort. I felt amazing after but it’s now 3:30pm and i feel like i’m constipated again and that there is still more to be released. Shall I take another one tonight to clear

Hello friends, has anyone with a diagnosis of GA or another type of ataxia been diagnosed with cluster headaches or a facial pain type headache if so how do you get on with it while having typical ataxia symptoms. Thank you NO SURRENDER