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Real members of MyMSTeam have posted questions and answers that support our community guidelines, and should not be taken as medical advice. Looking for the latest medically reviewed content by doctors and experts? Visit our resource section.

Has anyone experience burning mouth syndrome (BMS) from their MS?

A MyMSTeam Member asked a question 💭
Casper, WY
October 2, 2024
 · 
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A MyMSTeam Member

It feels like my tongue is recovering from being burned; kind of like when you burn your tongue on pizza cheese. It's been constant for 5 years now. I didn't know I had MS these 5 years, but since being diagnosed, so many things such as BMS make sense now. The only med that seems to help is ClonazPam which I HATE knowing I'll take it my whole life since it's a narcotic. Chewing minty gum helps too.

October 3, 2024
A MyMSTeam Member

interesting. what happens ?

October 3, 2024
MyMSTeam

Yes, some people with multiple sclerosis (MS) do experience burning mouth syndrome (BMS). This can be due to several factors related to MS:

- Medications: Certain disease-modifying therapies (DMTs) and other medications used to manage MS symptoms can have oral side effects, including a burning sensation on the tongue
- Show Full Answer

Yes, some people with multiple sclerosis (MS) do experience burning mouth syndrome (BMS). This can be due to several factors related to MS:

- Medications: Certain disease-modifying therapies (DMTs) and other medications used to manage MS symptoms can have oral side effects, including a burning sensation on the tongue.
- Nerve Damage: MS-related nerve damage can affect the mouth and face, leading to sensory changes and pain.
- Inflammation: Systemic inflammation associated with MS can impact the nerves and tissues in the mouth, contributing to symptoms like burning mouth.

If you are experiencing these symptoms, it's important to discuss them with your healthcare provider for appropriate management.

October 2, 2024

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