Lichen Sclerosus: Any other women dealing with this disease?
Is anyone out there dealing with this disease? I am currently using a compound ointment that my oncologist prescribed but I'm looking for possible lazer treatments or anything else that might now be available.
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@eileen1022, I am anxious to hear what you find. I do have LS and burn every day. I have tried various remedies for this including three different compounded creams, lidocaine/prilocaine, and lidocaine. I am on lidocaine now, but it is not helping numb me. I have no idea what is next. I wish you the best as you search for some help. With all good wishes, @joybringer1
Hi Joy
I will let you know. I wish it was sooner than next Wed but I have so many appointments that's the soonest. Honestly I have no idea I didn't have burning, itching or pain till the started giving me steroid ointment and estrogen cream add in recurrent utis for almost a year. Not fun. But looking forward to seeing this specialist.
Hi, my name is David,
I was diagnosed with Limbic Autoimmune encephalitis 3 years ago. I had multiple seizures and spent over 7 months in the hospital. I have lost almost all of my memory. Is there anyone out there that has been diagnosed with limbic AE that I could help support each other. I am also on 16 pills per day and have 5 specialists that I see. Loosing hope.
Hi David, I don’t think there is a connection to lichen sclerosis since the latter is a women’s disease. Hope you can find answers to your dilemma though. Good luck.
Welcome David, I know it has to be difficult when you are diagnosed with a rare condition and not finding any answers. There is an older discussion that you may want to read through to learn what others have shared.
-- What type of encephalitis? Autoimmune, limbic, or encephalopathy?
https://connect.mayoclinic.org/discussion/is-it-autoimmune-encephalitis-or-encephalitis/
You mentioned you have seen 5 specialists. Have you thought about seeking help at a teaching hospital or major health facility like Mayo Clinic?
It’s been nine months now on methotrexate. I’m now at 20mg/week. It seems to have calmed down all the extragenital inflammation and stopped any new plaques from forming. I’ve lab work done every three months. My body seems to be tolerating the dosage.
Now, to see a GYN for my vulvar region. More fusing going on. I had trouble finding my urethra!
The dr was wonderful. Completely informed on LS. She took a biopsy to confirm diagnosis. Offered estrogen cream that will relieve symptoms. My past breast cancers have not been estrogen driven so I am willing to take that risk. She even called my oncologist to get their blessing. The Mona Lisa fraxel laser is a 3 step , 6 weeks apart . No pain and likely ( u know they never promise) to stop progress of LS and all symptoms. They check 1x per year to see if a 1x reboot is needed . I’ll be trying the estrogen for a month since covered by insurance. Fraxel is not covered. Fraxel also works on incontinence so I’ll be letting my leaking friends know . To Be continued….
I was put on Vagifem 10 mcg Tablet
Generic name: estradioL
INSERT 1 TABLET(10 MCG) VAGINALLY 2 TIMES A WEEK
(I prefer this over the cream inserted in the tube.
and
Triamcinolone acetonide 0.1 % Ointment
Commonly known as: KENALOG
Apply to the affected area(s) two times a week.
Then use an over the counter product like Vagisil other days if needed.
Negative Stress tends to make it worse. Wash the area daily without soap.
To clean vaginal area I soap up my hand with coconut soap and gently rub the area and use hand held wand in shower (mild temperature water) to gently rinse. My vulvar dermatologist has me alternate estradoil (use liberally) and Clobetasol (tiny bit on just painful areas). These are applied once a day at bedtime. This has controlled my LP the best in the 20+ years of painful suffering. So good to finally find a doctor who knows what to do.
Ty, great advice .