Blood blisters in the mouth and more. - Fibromyalgia Acti...

Fibromyalgia Action UK

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Blood blisters in the mouth and more.

Dodo71 profile image
11 Replies

Hi everyone.

Hope you are all as well as possible. Does anyone ever get blood blisters in the mouth? I've had a lot of them over the last few months. I'm a little bit worried as I'm getting short of breath at times and I had a leg cramp that was so painful I couldn't weight bear on it for several days last week. I've had 2 negative covid tests, so I know it's not that. My Dr. is treating me for restless leg syndrome, and I'm taking Pramipexol at night, which has helped. I'm going to see my Dr again next week about my other symptoms.

I'm just wondering if anyone else has come across this.

Thanks.

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Dodo71 profile image
Dodo71
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11 Replies
Dizzytwo profile image
DizzytwoModerator

Hello Dodo, I see this is your first post welcome to the group 😊

I'm not aware mouth blisters are fibro related. There could be many reasons. Medication, lacking in some kind of vitamin or even mouth hygiene. I'm not saying any of these are related to your problem. But if you was wondering about it been fibro related I personally would say no. Glad your going to speak to your GP hopefully they will be able to get it cleared up for you xx

I see you've left your post unlocked to this community only for privacy reasons you may want to lock your post. If you wish to lock your post this link will show you how.

healthunlocked.com/fibromya...

Dodo71 profile image
Dodo71 in reply to Dizzytwo

Thank you for your reply and your welcome, and for telling me about locking my posts.

I'm going to try to get an appointment tomorrow with my Dr as my breathing has not been great today. I have mild asthma, so it may be that I need a different inhaler.

Thanks again. Keep safe and as well as possible.

Spanner46 profile image
Spanner46

Hi Dodo71,

I do get them. Its usually upon either eating or drinking upon the first bite or sip one will appear, then they seem to just disappear or i can go a few days/week without any . I have FND and Fibromyalgia and i too wondered if it was related.

Dodo71 profile image
Dodo71 in reply to Spanner46

Hello. Thank you for your reply. It's nice to know I'm not alone. I hadn't heard of FND, I've just looked it up, and I'm sorry you suffer from this. I too am noticing that they appear upon either eating or drinking. I feel as if my illness has changed for the worse over the last year. I think I'm due a MOT.😁

Spanner46 profile image
Spanner46 in reply to Dodo71

Hi Dodo71,

I have oftened wondered if anyone else got these too. Like all the symptoms to these Disorders mine have always added, and usually got worse. I do have days where i just lie in bed till 2pm, and instead of feeling guilty as i once did, it is just nice to put no demands on your Body which you do if you get up. Take Care

Kitten-whiskers profile image
Kitten-whiskers

Good afternoon, Yes I am prone to them under occasions of stress - it would appear. Gathering from the response of a endocrinologist I once saw, mouth Ulsers etc are a sign og a weakened immune system. I do take Buffered Vitamin C, which seems to help

Dodo71 profile image
Dodo71 in reply to Kitten-whiskers

Hello. Thank you for your reply. The stress angle is interesting to me based on everything that the world is going through. I seem to be always worrying about some member of my family. I do take daily vitamins, but it is worth keeping in mind. Everyone on this site has been really helpful, I feel my mind have been eased. Thank you.

Kitten-whiskers profile image
Kitten-whiskers in reply to Dodo71

Your welcome, we are always here to help x

Hi yes i get them with fibromyalgia they are a symtom my rheumatologist asked me if i had ulcers in my mouth canker sores x

Dodo71 profile image
Dodo71 in reply to

Hello. Thank you for your reply. It's really helpful to know this. It has never been mentioned to me, and I've been ill for years.

MaggieSylvie profile image
MaggieSylvie

I get them on the roof of my mouth occasionally. I was tested for lack of B15 (I think) but that was before I was diagnosed with MDS/MPN. So it's probably due to high platelets that can cause bleeding. They are not the same as ulcers, which are probably caused by something more obvious.

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