Does anyone suffer with mouth ulcers,... - Hughes Syndrome A...

Hughes Syndrome APS Forum

10,356 members10,544 posts

Does anyone suffer with mouth ulcers, have had some for 3 weeks now

NBtired profile image
6 Replies
Written by
NBtired profile image
NBtired
To view profiles and participate in discussions please or .
6 Replies
Jade profile image
Jade

I had almost permanent ulcers until I was placed on warfarin. I was a symptom I never associated with APS and used to get a steroid gel from my dentist.

It was ages before I noticed they had quietly gone.

Professor Hughes was intrigued to hear mine have gone on warfarin.

Wenz15 profile image
Wenz15

I have just stated to get them.... kind of always had them on and of over the years, just never really made the connection to APS. I see the doctor again in a couple of weeks, so will add that to my list of things to ask!

Manofmendip profile image
Manofmendip

I used to get them, too, until I was put on Warfarin.

best wishes.

Dave

CountryGirl profile image
CountryGirl

I have had mouth ulcers for as long as I can remember. About 10 years ago I heard about taking Vitamin B50. I started taking it and have almost no ulcers since then. When I bite my mouth it used to take 10 - 15 days to heal, now it is gone in a week at the most. Can't rave about it enough. I have been taking warfarin for about 30 years. I did not notice any change as a result of the warfarin on my mouth ulcers.

Yes, I was plagued with mouth ulcers prior to being put on Warfarin. Now that I think of it they have gone but they were painful at the time.

InSpain profile image
InSpain

Both mouth and nasal ulcers are also a classic symptom of Lupus (SLE), as are dry eyes. I too always have some ulcers which can be painful. I can sympathise with you as they make me feel really run down. Usually they are a sign that I am in a Lupus flare up. But it has been interesting reading how many people with APS are affected too. xxx

You may also like...