Linchen Schlerosis / Biopsies

Posted , 10 users are following.

I know I’m a little late here, but ANY help would be appreciated! I’m 24 and just had a biopsy (holy cow, OUCH) and will get the results back within 2 weeks. I’m nervous and upset after researching this disease, and am worried about what problems this will cause for the rest of my life 😢 the biopsy I had is still bleeding 5 hours later, and the doctor recommended using soap and water and using Vaseline to clean it. Any tips on treating the biopsy spot or tips about how to go about this disease in the future? I’m so sorry you all have to deal with LS 😢

0 likes, 11 replies

11 Replies

  • Posted

    I'm so sorry dear Tori, I had a biopsy too and it hurt like hell.  I guess we can hope that it was helpful.  Try the soda soak baths and maybe the borax soak too.  It will heal.  All of the info on this forum is helpful.  LS is manageable.  I am old...;.75 (but young at heart tho) and feel like my life is just starting,,,so read what you can and try things.  There are so many other maladies that are so much worse.  You can do this.  Take care and let us know how you get on.

    • Posted

      Hi Jer what lovely comforting words . I am four days in in this and so so scared , feel like it’s sll going to fuse together and I can’t stop it happening . Trying to be positive but just can’t find it xxx
    • Posted

      Thank you so much for the kind words ❤️❤️❤️ Very true many are much worse and it does seem manageable, so glad I found this thread THANK YOU!!!
  • Posted

    No stitches? It hurts something fierce! I remember screaming and that was a long time ago. Just do what you were told as it sounds open and would be very sore.

    I had stitches so don’t understand there being none for yours.

  • Posted

    The first thing I would do is TOTALLY IGNORE THOSE INSTRUCTIONS !!! NEVER use soap OR Vasaline with LS. Soap will irritate and Vasaline is a petrochemical and not good for ANY skin. I'd be inclined to use just plenty of clean water or maybe add some salt or baking soda. You need to use a barrier cream to protect from urine and to moisturise. I use HYDROMOL OINTMENT which is hypoallergenic and moisturising. What symptoms to you have hon ? I understand your panic and upset on reading about LS. The pictures alone had me freaking out but trust me, the best thing you did was find this forum. There is a wealth of experience here and wonderful, caring people . LS cannot be cured but it can be managed. It's an autoimmune disease so firstly look up anti inflammatory diet . Sugar is a major cause of flare-ups. Basically if it is confirmed you do have LS you will have to use a steroid - don't panic over long use of that LS makes skin thicken so it does not have a major thinning effect on MOST women ( though everyone is different) You will use that as prescribed , essential you rub it in for 90 seconds and ask for OINTMENT NOT CREAM as this is absorbed better into the deep layers of the skin where the inflammation is. You will also need to use the barrier ointment to protect and moisturiser the skin. It's really importable that you check your vulva regularly in a mirror. Get to know what it looks like then you can see any changes quickly. When rubbing in your creams gently stretch the skin to prevent any fusing. Stress is also a big enemy of LS though inevitable in this day and age. If you do the basics for a while till you get your head around everything then investigate and experiment as you wish after that. Loads of info on this site but it can be overwhelming at first hence my suggesting you just do the basic steroid and barrier first. Good luck and keep us informed on results and how you're doing. YOU'RE NOT ALONE. We all care about you sands will help in any way we can x

    • Posted

      Hi Caroline, 

      THANK YOU for such a comforting and through message!!! ❤️ It made me feel LOADS better.  I was able to hop in the shower and used nothing (didn’t wash my hair or body) and the bleeding stopped, so I will go get that cream ASAP! I had read that it’s autoimmune so it’s interesting to hear about the sugar and stress flare ups - of which I have BOTH. So kind of a wake up call. She prescribed a small tube of steroid for temporary itching while the biopsy is being looked at but I would like my sore to heal for a few more days before I use it. Thanks so much for all the encouragement and information, what a wonderful forum ❤️❤️❤️

    • Posted

      So happy I could be of help Tori, that's made my day 😊. It's kind of a pay it forward scenario I think. I felt terrified and desperate when I found this forum and people comforted and encouraged me so I always try to do the same for other newbies.

      I think its wise not to use steroid on open wounds. The barrier cream will sooth and protect it. Any problems or just want reassurance, you know where we are 😉 xxx

  • Posted

    Who is this doctor. Let him put soap on it. Warm water and Neosporin on cut. Had 2 of them. Good luck. Stay in touch. Will pray for you
  • Posted

    Hi Tori,

    Really sorry to hear you have LS , mine took ages to diagnose, as it came out on my back, quite unusual. I have my LS under control by using the clob steroid cream. I also got a specialist nurse at my local hospital and she was great as she know all about LS. Through this site i heard about dialiators which help stop fusing or the vagina tightening ( Amielle comfort is the name)., this was provided by the hospital. You can find them on the  internet too. I am sure that stress is one of the factors which make LS worse, so try and stay calm and look after yourself. If you look after yourself you will be able to get the LS under control and this site has been so helpful. I amazed by how little doctors know about LS. Take Care x

     

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