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Oct 16, 2018 · Erosive oral lichen planus in Autoimmune Diseases

I have some information I would like to share.
My husband came down with lichen planus many years ago.He was treated at Tufts dental clinic.in Boston.They treated with a cream he had to put on a cotton ball and place it on the ulcer.
He did it for maybe 10 days or more.
It has been years that hes been free of lichen planus. I don't remember the name as it has been maybe 10 yrs or more.
There is a cream treatment for lichen planus.Once he used the cream ,he has been free of it.
Believe me there is hope for you.
It's just a matter of getting that cream.
I'm going to try and find the name for you.
Remember stress makes the condition much worse.
My husbands lichen planus was brought on by stress.
Please consult a medical school of dentistry.
They saved my husband from the awful feeling in your mouth.God bless

Jul 30, 2018 · Erosive oral lichen planus in Autoimmune Diseases

So sorry to hear such awful news.
My husband had lichen planus on the inside of his cheek.
It will stay dormer in his body forever.However if he's badly stresses there's a chance it will come back.Only once since his flair up did it come back. I thought I may have given you the wrong name.Ill.look for it and send the name off to you.
My suggestion to you would be Tufts school od dentistry.
The Dr he saw has since retired.I would highly recommend you to at least call there clinic.
My husband on his first visit was well taken care of.
I'll check for the cream. Good luck..

Jul 30, 2018 · Erosive oral lichen planus in Autoimmune Diseases

My husband suffered many years with lichen planus.He received care from Tufts medical center in Boston ,Ma.
It's a dental school.
They put him on a cream called ,I'm pretty sure it was bethamethasone.You can google it
He put it on twice a day with a cotton ball.
He's been pain free.
If by chance,which is few and far between.
He just puts cream on ot,and within a day or so it's completely gone.You can be free of it.Good luck in your research.
Please let me know how it worked for you..

May 4, 2018 · burning mouth syndrome very severe in Just Want to Talk

If you are having your teeth pulled because of b.m.s don't do it.
Unless your doing it for some other reason.people think that it's going to stop the burn.It has nothing to do with it.
It's a nerve that comes from the brain.
I've had 18yrs plus with this horrible condition.
Google botox for b.m.s.
Also for laser for b.ms.
Good luck.
Do not pull your teeth out for this condition.
Good luck

May 4, 2018 · burning mouth syndrome very severe in Just Want to Talk

Please read my comments.I've been suffering for 18yrs plus
I'm currently receiving botox shots.Going to try laser.please Google ,botox for b.m.s.
and Google laser treatment.
Boston would be the best place to receive the treatment..
Good luck.
Dr's in Boston ,definitely know all about b.m.s.feel free to contact me anytime..

May 4, 2018 · burning mouth syndrome very severe in Just Want to Talk

I had taken gabbapentine many years ago.
I've had this condition for many years.I have taken amatriptoline,currently on cymbalta,clonazapan,and a mild dose of oxycodone.
I have been receiving botox shots,which I read had been helping with this horrible condition. It really doesn't help.
My next move is to check out laser.I have been to a hospital in Boston.A oral maxofacial surgeon has been giving me the shots.He recommend laser.I'm going to find a Boston hospital who gives laser.
If you have some time,please Google ,botox for b.m.s.
Also Google, laser for same.
This is a horrible condition.
I've been to most Boston hospitals, and so many meds.it over 18yrs.
I'm mentally drained.
As a psychologist, referred to it as ,the devil in the mouth.
If you need any additional info.please feel free to ask.
I wish you luck with the gabbapentine, but sadly nothing has helped me..
God bless..

Mar 22, 2018 · burning mouth syndrome very severe in Just Want to Talk

Would like to know how you are doing???
I to have bms for many many years.Tried everything.
Maybe you have some news to share.I would greatly appreciate it.

Feb 18, 2018 · burning mouth syndrome very severe in Just Want to Talk

I have trigeminal neuralgia as well as b.m.s.
I have been receiving nerve block shots for a year now.I get 25 per month.that's one day if shots.
It has helped my nerve,but not the tounge.I'm quite surprised they would do that in your mouth.
If you do have trigeminal neuralgia, seek out a good neurologist. Discuss the nerve blocks.I wish you luck.
God bless.
I feel your pain.