Learn how to use Mayo Clinic Connect
Request an Appointment
Wanting to see if anyone knows of this an who to see for it primary has no idea
Burning mouth and sensation of puffyness constantly ive had this for 7 years
Jump to this post
Hi @teaspoon. You'll notice that I moved your post to the discussion you started earlier. I did this so that you can share your question with the members you've connected with about burning mouth syndrome. Click VIEW& REPLY in the email to see @mamajomclane's helpful messages describing the process of coping with burning mouth syndrome. @jshdma and @cyntiamom also added supportive information.
Teaspoon, you mention that you've had burning mouth and puffiness for seven years. Can you describe the mouth puffiness and how it affects you? What do you do to reduce the puffiness or relieve it?
I have had burning mouth for a year now. Lots of blood work Mri's accupunture, no help yet. I think it started after a dentist had to pull a tooth root out of the front top part of my mouth. I had novacaine on the third injection I felt a wierd sensation up through my nose maybe he hit a nerve? I have told doctors, etc. they shrugg thier shoulders. My tongue also feels swollen and i have the constant urge to stick out my tongue. This is very depressing that there is not a solution for it.
Burning Mouth Syndrome is a real diagnosis. I have been fighting for 3 years – even spent 3 days at Mayo (Jax) where all their tests indicate normal. They recommended 10mg+ amitriptyline to try, increasing 10mg weekly till symptoms improve. After a couple months I settled at 30 mg and my symptoms virtually disappeared for around 10 months. After that, a stressful situation at home likely caused symptoms to return. Since then I tried gabapentin 100 mg at night which did nothing, then 100 mg 3X day did nothing to help symptoms but DID seem to cause immediate heartburn/reflux so I stopped that and heartburn/reflux symptoms disappeared but burning mouth remained. After a few weeks with no meds, I restarted amitriptyline and am now at 40 mg in split dose (am, pm and bedtime)….burning mouth has reduced greatly but not gone….stress brings it right back so trying to monitor the stress. I am also using 600mg r-alpha-llpoic acid, frankincense oil, 25mg. iron supplements, occasional 5,000mcg. B-12. I also have had herpes simplex-1 issues since the burning mouth began so I supplement with valtrex in various strengths, depending on the mouth ulcers. I am currently doing 1 gm. 3X day to see if this higher strength knocks the burning down. As you research "burning mouth syndrome" many will indicate that it is hormone related which is another area that I have struggled with and I am now mostly off the bio-identical hormones that I have been on for numerous years. Many doctors also end up pointing their diagnose at reflux related issues but none of their drugs brought any relief to me. .This BMS issue seems to be a process of elemination of standard diagnosis which indicate "all normal" but we do not feel "all normal". In my case, stress seems to be a huge factor but we all know that stress is VERY difficult to eliminate and/or control. I recently visited a neurologist that ordered a brain MRI and more blood work which were also normal – more tests in search of an answer but yet more dead ends. This is a very long process – stay strong and diligent all. What works for some does not work for all is mostly what I have learned in 3 years of testing, diagnosing, trials and errors. Most of me is healthy and prior to 3 years ago, I took no prescription drugs, just supplements and hormones….now I have a long list of drugs I tried. Hoping for medical research and these blogs to find an answer to our burning mouth/throat quests.
I've travelled much the same path in finding relief for my BMS. I now have to go off Clonazepam and am researching CBD oil, dose and compatibility with withdrawal from Clonazepam. If you happen to have any info on this, I'd appreciate it.
I have had Burning Mouth Syndrome for 20 years. I was diagnosed by an oral surgeon whom, at that time, was one of the few who had a clue about this problem. It is incurable and usually strikes women but men have reported it too. I have tried everything and anything but nothing takes it away but some things have helped me to sleep. I just started taking hemp oil. It is 250 mg full spectrum. I think it is helping. I probably need another month to be sure but am hopeful. I have dreamed that one day I can find the miracle drug or a remission but still not sure that it will ever happen. It is a difficult task to get through the day without focusing on the pain that BMS causes…but maybe soon I will have an answer.
Have you considered estrogen oral troches
@mamajomclane What are estrogen oral troches?
Create an account to connect with other patients and caregivers like you.Ask questions, get answers, and give and get support.Also follow blogs from Mayo Clinic experts.
Already have an account? Sign In