NATURAL REMEDY STARTS WORKING WITHIN A FEW DAYS

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Hi to all you LS sufferers out there, I'm 63 and had it so servere that my life was a living hell, l was competent horse rider and a very active person all that changed. I have had LS for about 10 years and it got to the stage where l ended up with multiple ulcers six or seven at a time that would NEVER go away because as some were healing new ones would appear and it was a never ending cycle, then l was hospitalised for three days as l had 11 ulcers at the one time and could not pee as the pain was so excruciating l had tried everything , nothing worked then l though enough is enough. None of the cortisone or steroid creams were helping at all in fact l think that they were making it worse. Out of sheer desperation l threw everything out and started to apply olive oil to the LS just the cheap plain home brand olive oil that l had in the pantry. Within three days the ulcers started to heal but the the best thing was that NO more were appearing they were finally clearing up and the burning and itching was also disappearing as well and the only thing l was using was the olive oil. Within two weeks l had absolutely no itching or burning and NO more ulcers, the skin that had suffered from the LS was now soft again. That was eight months ago. l now enjoy a normal pain free sex life again the skin stretches without burning or tearing (just use plenty of lube) and l had an excessive amount of white patches which has now mostly disappeared all thanks to the olive oil. My gyno was amazed at the improvement, there is no swelling, no dryness, NO inflammation and almost all of the white patches have disappeared even the scaring and lesions have completely healed, he was so impressed that he has documented my success and is monitoring my continual improvement he has even now started several other patients on the same treatment that were having little or no positive results on the steroids and cortisone creams. Ok this is all l do l have an egg cup full of olive oil that l leave in the toilet and when l go to the toilet l pat the area dry, liberally apply the olive oil in around and between my labia lips ,clit and up inside my vagina as far as possible soaking everything in the oil then gently pat with toilet paper the area ALMOST dry but leaving the area still moist. That is it, that is all l do nothing more, l have a small container that l fill with oil and pop in my purse if I'm going out for the day . I use the oil EVERY time l go to the bathroom. You will notice a distinct improvement within about three days and 100% Within a couple of weeks. Good luck to all those who try this l hope it works for you as well as it has worked for me, l now ride my horses everyday and can were tight jeans without any issues at all which was a thing of the past. It's natural it's cheap and everyone one of us has olive oil in our pantry . 😀😀😀

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  • Posted

    Hi there, thanks so much for sharing what great success you've had using good old olive oil, so pleased for you. Since my diagnosis 4 months ago, I've been using many different things, prescribed and natural, and seem to be symptom-free, my issues were white skin/fusing around perineum area. But think maybe the olive oil used regularly could help with the pliability of all the skin around that area in general. Many thanks x

  • Edited

    Well I must let you know how pleased I am to have read your post Hot2trot! I myself started using the olive oil only last weekend. Already my white bits have almost disappeared and everything feels so nice down there again! I have used it after most (not all) wee stops then again before bed. It’s unbelievable the change in such a short time. My LS is not too bad compared with most people but I have recommended it to a couple of friends who are now trying it too. Thank you so much for sharing this. 
    • Edited

      No problem Jill, l am just so happy that this has helped you too, hopefully more ladies will try it as the results are absolutely amazing. 😁

  • Edited

    Thank you so much for sharing your experiences.  It is so useful.  I was diagnosed with LS 4 months ago and am still finding my way through how best to cope with this condition.  I have steroid ointment from the doctor but don't want to rely upon it too much.  I am definitely going to try olive oil.  Hope I have as much success as you have achieved.

    • Edited

      Hi Gill, give the olive oil a go l think.you will be really happy with the results. I stopped using the steroid cream altogether after starting the olive oil as l was worried about using the huge amounts of cream that l was using that made absolutely no difference what so ever and l found that the oil had made such a HUGE different, you will really pleased with the results, Barb
    • Posted

      Thanks Barb, I have a little tub of olive oil in the bathroom ready to use and will let you know how I get on. Fingers crossed. Love Gill

       

    • Edited

      Hi Gill, I just used normal cheap home brand cooking olive oil but what you have should still work good luck, keep me updated as several people have used it so far with 100 % improvement and it's always good to get feedback as others read it and it give them hope too. l feel really confident that it will work you as well, you will notice a big improvement within about 3 days 😁

    • Posted

      Has anyone used the Ozonated Olive Oil? It's starting to come to peoples attention and gettin good results. Just type in Ozonated Olive Oil and LS . I'm convinced that these harsh steroids aren't the answer to use as often as our doctors tell us. They also do a lot of harm. The doctors tell us that's all they have and that is the PROTOCOL. (I hate that word).

    • Posted

      Svenska, who has told you they have had good results with it for LS? I found a site (Global Healing Center). Doesn't actually mention LS. Suppose it can't hurt, but all these stabs in the dark add up. They do say they ship free and you can return if not satisfied. Would love to hear from someone who has actually tried it though.

      Life essentials also has an oil product made by an LS sufferer. I could not tolerate it as it burned me terribly. But she has had success and says has customers who have. She has been kind enough to offer me a refund.

      We all react so differently to things.

    • Posted

      As a LS sufferer, I have been to 4 doctors and have been prescribed 5 different, very expensive hormonal salves and NONE gave me the relief that plain, any brand olive oil has. Don't know why it works, but it does.

    • Posted

      HI Nancy

      IT's extraordinary. I wonder if through some alternative medicine we can deal with the underlying causes while using the oil for relief. Yes I have been to a couple of doctors and figured they weren't going to be able to help. One gynacologist advised me to try wearing white cotton undies. My friends and I had a laugh about that. One of them suggested I try different coloured undies on different days of the week and see which colour works best!

      Good talking. Thanks.

  • Posted

    Oh my lord I hope your advice works for me. The sun is shining and I lay in bed trying to decide how part with my horse, trailer tack etc etc. I have given up!! Am dealing with multiple autoimmune diseases as well as LS and it gets a little overwhelming at times. Am so very excited and desperate for some relief so here goes!!! Am also a gramma, age 70 and nowhere near ready to give up my riding. Our routine daily ride is the country square which is 6 miles as well as horsemanship work. So.... Here's to olive oil and success!!!

  • Edited

    Ok I am going to give this a try I tried castor oil with lavender and lemon grass seed oil it stops the itching but it not clearing up the lesion is getting bigger.i am scared of getting another biopsy done and the doctor said I need  ti I feel like the last biopsy never healed up and that is where the lesion is and like I said it is getting bigger and worse".........

    .as I said I really need support here thanks

    • Posted

      So sorry to hear that Dorotha. I'm also very concerned about biopsy especially after reading your experience . I haven't yet had one and am increasingly worried. Is it truly  a necessity do others think? 

    • Posted

      Dorotha67

      I believe the only way to determine the presence of cancerous cells is by doing a biopsy

    • Edited

      Hi Annie, no a biopsy is nearly always not necessary.  Most doctors that know their stuff can give a visual diagnosis.  The problem we all face is that most doctors are clueless when it comes to LS and so as soon as they see the white plaques of skin (which is classic LS) they want to do a biopsy...because they dont know what it is?   

      When a biopsy is necessary in my view is when you have a sore/lesion that hasn't healed for months.  The white plaques of skin are 'normal' for Lichen Sclerousis and I just wish some of the 'specialists' would take the time to do their job and do some research.

    • Posted

      These comments definitely have me wondering two things: how people perceive what is being read and how much medical background commentors have ? We can't guess what's on any doctors' mind. Yes some doctors recognize this "rare" condition immediately especially in locales where there are hundreds of women riding horses daily or frequently. And definitely a biopsy is required to confirm presence of cancerous cells if and when a doctor feels the individual is in a higher risk category. TALK to your doctors ladies, ask questions, no question is silly when you're the one living with LS. and remember, as with every condition, we are all individual and our experiences will have commonalities but also individual levels of pain, healing, and response to various treatments. Respect what your body is telling you and work with your doctor to find the combination that gives you the best results. smile

    • Posted

      Guppy 007 I agree with you for the most part to me I thought that people became doctor because they cared and I mean really cared about their patients and what they are going and do every research they could to try to help their patents..I feel they lost or misplaced that because now it seems to be about money nothing more nothing less
    • Posted

      And honestly that hurts my heart to know that
    • Posted

      Hi dorotha, I dont think its about money with regard to LS, it's about ignorance. A LOT of women post on here with terrible stories.  How they were misdiagnosed for years, how they were diagnosed with a STD, how they were advised to take thrush treatments and so on, when in fact it would only take a doctor five minutes of research to discover that someone has LS.

    • Edited

      Hi, no one on here has said that they are a doctor, we are all just sharing tips and advice.  Once you have been on here longer and have read some of the stories that get posted every day then you will realise that doctors are constantly messing up, which is why you would be foolish to trust everything they tell you or rather don't tell you..you have to be your own advocate for Lichen Sclerosus.

       

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