LS seven years

I'm sorry for anyone with LS.  No one knows it's there. No one sees it but LS is extremely painful.  I was diagnosed 5 years ago.  For two years I was misdiagnosed with yeast infection.  After a biopsy it was confirmed LS.  I also have Vitamin D defiency, depression and some times anxiety.  As others have admitted, I too have been molested, for years by my father, then by a dentist while having my wisdom teeth pulled and again by a gynocologist. No sense in dwelling in the past.  Move forward, think positive for a cure for this disease.  I've tried, coco butter, A & D ointment, and because I live in Washington state, I've even tried ointments with cannabinoids, CBDs they are called.  Yes, I've tried the Clobetasol ointment.  Anything to stop this pain that will wake up in night.  Anybody get those shooting pains like you're being stabbed?  Clobetasol works for a while.  For me, only a few months of treatment lead me to two bacterial infections under the hood of the clitoris.  Be careful not to use too much as it does thin out your skin.  Yes, I've also tried Estrace. Estrace set my bottom on fire. Seriously felt like a sat on a bee hive hence I don't recommend it.

Luckily I have an understanding family.  They know when I'm in pain, even if try and hide it. What I reccomend is getting a shower head that attaches like a hose.  Rince with water, saline solutions anything that releaves that pain.

A&D ointment and Desitine has helped with urinating because it coats your skin. Although bowel movements for me can be excruciating when LS reaches your rectum area, warm or cool warm while going helps.

I think I will try the Manuka honey and actually the H202 mix with saline makes perfect sense to me.  I'll try that too.

Thank you all for your messages.  Maybe together we'll figure this LS thing out.

der

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