Hpv and Lichen Planus
Posted , 8 users are following.
Anybody have hpv and lichen planus
0 likes, 28 replies
Posted , 8 users are following.
Anybody have hpv and lichen planus
0 likes, 28 replies
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Lainimac karen41728
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Lainimac karen41728
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karen41728 Lainimac
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samantha1970 karen41728
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Chrisy karen41728
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karen41728 Chrisy
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Yes my lichen planus was found by my dentist at the same time I had some abnormal cells removed from cervix, that was about 12 years ago I didn't have any problems with the lichens until about -
18 month ago when it started burning and ulcers can't eat certain things and now noticed my body hair is sparce because it's autoimmune but when I ask the doctor he won't say they are connected but I'm certain they are he put me on pills for anxiety so I don't think about it but I still constantly worry about this thing becoming cancerous, so that's why I'm asking the questions Chrisy and I know a few ladies with the same problem Xx
Chrisy karen41728
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karen41728 Chrisy
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I thought the use of steroids and hydrocortisone reactivate hpv
Just with things Iv read, would be great if we could get a group together over a coffee but think we all live in different directions!!! Typical Xx
dani2590 karen41728
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When you say worried about it becoming cancerous do you mean the LP or the LS, or both? I find having a good doctor helps in lowering that anxiety.
karen41728 dani2590
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Both really, after having precancerous cells about 15 years ago I then discovered the LP which in done cases is caused by the hpv virus, my doctor has given me anti depressants and just takes my mind off it if I confront him about it he just moves off in another direction Xx
karen41728 Chrisy
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Just wondered how your doing hope you are keeping well, I am a bit up and down with one thing and another Xx
Chrisy karen41728
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Just got back from Gloucestershire late on Sunday. Have been helping daughter move house. I let my vigilance with the Ls slip as I didn't have my bag nearby all the time and have a little flare that I am dealing with. I have to see my GP next week to see if the Clobetasol has helped with the urethra closing. I don't think it has. At present I am a little down about it all. Sorry you are in the same boat. Having a chat with someone might help. x
karen41728 Chrisy
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Sorry you havnt been to good it's just a nightmare, your doctors do seem understanding but mine don't seem to want to discuss it, I get checked from my dentist regular but my doctor, well just won't talk about it anything I go with he will say it's age things like this happen after the menopause, drives me mad.
Don't know about you Chrisy but my vulva hair is really sparse now that worries me but again doctor says it's age he goes on as if I'm about 70, would be nice for us ladies to meet up sometime Xx
Chrisy karen41728
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Sorry. I am ok chatting about this on this site but I am not comfortable about meeting anyone. I have two friends already who have this condition and talking with them in person can sometimes be hard. It is somehow more emotional.
karen41728 Chrisy
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Chrisy karen41728
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Take care......