It really is trial and error. Sometimes you can eat and enjoy someone and the next day realise it has affected the OLP. My best advice is to clean your teeth with Sqigle toothpaste from The mouth ulcer shop online. The only one that doesn't burn your mouth.
I'm 57 and like you had precancer cells about 15 years ago, I was diagnosed by my dentist with the whitish patches inside my mouth around the same time but didn't realise I had LP then it is really these last couple of years it troubles me, can't eat anything spicy or anything full of sugar also dairy even a glass of wine sometimes, it is a bit trial and error also I have itchiness that drives me mad on my arms and scalp I got some shampoo from the doctor and sweating to, good to speak to you Annie xx
The biggest triggers for me are alcohol of any type, vegetables from the nightshade family (tomatoes, peppers, potatoes (except sweet potatoes), & eggplant), too much sugar (I can tolerate a little)....just can't go overboard. The jury is out yet on grains and dairy for me. I seem to be able to tolerate some of both...but many say to only indulge in non-gluten grains...and they avoid flares.
Renee that's my food gone although I try and stay of wheat if I it's avoidable just as well I love chicken & fish I don't suppose I can keep my tartare sauce. On a serious note. Do you know if any research is being done on the possible connection
I find that I can eat good quality meats, fish and poultry without issue. Just have to watch what I put on it. The tartar sauce may be fine...I seem to be able to eat it...but make my own. Mayo, pickle relish and some onion...powdered or finely chopped.
I did not have any pre-cancerous condition...although some on here believe there may be a connection with abnormal smears and developing LP, oral LP or lichen sclerosis. I've not looked into if there is any research going on. It's somewhat rare...although being on these forums you certainly wouldn't think so. I would be more likely to believe there is some connection in all the chemical additives in our foods may have some impact on developing this disease.
Hi just wanted to answer you ,,I don't think it's anything to do with cancer cells ,,,it would not affect you 15yrs on olp & skin Lp comes on so quick iv had it for years also my sister has it ,the profeser who I was seeing had delt with it for years ,he blamed the medication I was on anti inflamertry tabs that I was on ,,,but to be honest ,they don't know much about it ,me I think it's a lot to do with nerves ,if I get stressed ,it is worse ,iv got it in the mouth and skin ,at the mo men it's on palm of my hands an feet an mouth ,but you have to get on with it ,more you worry worse it gets ,,,,,
I have had abnormal cells which is caused by a virus a virus doesn't go away and does take years to become cancerous it causes cells to change in different parts of the body
Hi Annie, I have had LP for about 3 years now and it was horrible! I got to where I could not eat or talk because my mouth was totally covered in white lesions and my tongue was swollen. It eventually got into my esophagus and I couldn;t even swallow my medications. The esophagus was dilated 3 times and seems ok now. My mouth has cleared up except one spot on my tongue which is raw, but no ulcers. I am hoping this will clear up eventually.
My history: My dentist noticed the ulcers when I went to have a cleaning. He didn't do the cleaning. I was referred to an oral surgeon who said it was LP but there was nothing that could be done for it and there was no cure. I was so depressed, and even more after the lesions got worse. I searched the internet to find help and discovered LP also affects the skin, so I finally went to my dermatologist who did a biopsy to confirm the diagnosis and he prescribed medication. It was a trial and error situation to find the medication that would work. I was eventually given Mycophenolate Mofetil in capsule form. I take 500mg twice daily. Ask your doctor to let you try this medication. Maybe it will work for you also.