LS diet that is working for me

Posted , 12 users are following.

I have suffered from LS for over 3 years. Took 4 specialists to finally diagnose me. Was prescribed clobetasol, hydrocortisone suppositories and told to continue my HRT. I read forums and visited other websites trying to find answers. Cutting back on sugar helped a little. I was so frustrated and ready to give up on ever feeling better. This past January my husband had watched a few documentaries on going plant based eating. I thought why not try it. So we cut out all meat, dairy and eggs. My husband lasted a week but I continued to follow the lifestyle of plant based eating because I noticed my LS symptoms were improving. But after 4 months of no meat, I felt sluggish and tired. I chose to add meat back to my diet, but only turkey and chicken that is antibiotic and hormone free. I chose to still not eat or drink any dairy and eggs. I am 6 months into it and I have not had any LS symptoms return! I stopped the clobetasol and suppositories to see if symptoms would return and so far they have not. I believe staying away from all dairy and eggs helped . I also believe eating poultry that is antibiotic and hormone free are really important to help symptoms. As long as it is cleared up I am going to continue to do what I am doing. I go back to my specialist next week and look forward to hear what she thinks and I am curious how test results will show my ph levels and white blood count to be. I can't guarantee that my symptoms won't return, but as long as it is working for me at this time, I will continue to eat this way. I wanted to share my experience in case anyone else wants to try. You have to read all ingredients on foods to watch for dairy and eggs. I am not a doctor, just a patient wanting to share my results.

1 like, 22 replies

22 Replies

Prev
  • Posted

    So glad to hear this diet worked for you! How many weeks/ months did it take for you to start seeing improvements? i just started eating plant based this week in hopes that it will help!

    • Posted

      It took about 6-8 weeks when I noticed I was not having any flare ups. At first I did not connect it was how I was eating, but then I realized it was the only change I had done. I see my OB/Gyne specialist this Tuesday. I am not sure what she will think of it being my diet that seems to have helped. I have been guilty of eating a ton of sugar lately which usually triggers a flare up, but it has not happened. Only time will tell if my plant based eating is truly helping. I buy mostly organic foods. Good luck, I hope it works for you. Please keep us posted on your results.

    • Posted

      I think it's nearly impossible to tell if dietary changes are curing anything unless it's a very radical change. There are so many variables. I do think most are in agreement nowadays that sugar and processed food offer little nutrition and actually encourage diabetes. Other than that I guess it leaves gluten and unless you have celiac I guess it's debatable....unless as I say the elimination causes an obvious remission.

      My LS seemed to go away for months then returned despite my diet getting healthier if anything. same is true re supplements. I am breaking the bank with those.

      I would be happy to see an FM doctor if I could see one who accepted insurance. Good luck with that!

  • Posted

    Lindajoy, That is great news! I am so happy for you that the plant diet is working. May I ask what symptoms you suffered from? And, what bearing did the white count have on the LS? Was your WBC count high? I know I have eliminated Monosodium Glutamate (MSG) and nitrates but I also learned that carageenan, an additive in many types of foods is a cause of inflammation and so have avoided that too. I stopped all alcohol but that did not seem to make a difference. biscuit

    • Posted

      Eggbicuit- Yes my WBC was high. I believe the white blood cell count elevates when your body is trying to fight what it thinks is invading, which can happen with autoimmune. I will have to question this at my next appointment so I know I am sharing correct information.

      My symptoms started with a thick yellow/green discharge that hardened like cement. My undergarments were stuck to me like brick and mortar. This then caused irritation. This mostly affected the vagina area. At the same time I started to notice clusters of 2-4 small bumps on different areas of my body, wrist, lower arm, calves, chest, neck. Dermatologist said probably bug bites, but I know they were not from bugs. They did nit itch. I think it was part of the LS. Then the skin on my vulva area tore easily and itched horribly. Intercourse became horribly painful. About a year later it affected my anal area, itching, tenderness, hurt to sit. That was when I found that caster oil helped relieve some of the irritation, but the clob helped more. I am not 100% free of LS, but the worst of my symptoms have subsided. Maybe I am in a honeymoon stage, only time will tell. But after going plant based for the few months and now cutting out all dairy, eggs and cheese I do have major improvement in my symptoms. My doctor appointment is tomorrow, I will post an update afterwards to let all know if she sees any significant changes.

  • Posted

    So I had my doctor visit yesterday. She was very pleased at how well my LS is under control. She felt I was 90% improved on the outside from 1 year ago. I still have a lot of tightness and tenderness inside the vaginal area but outside looks great. She is requesting I keep up maintenance by applying clobetasol once a week and insert vagifem once a week. She worries about developing cancer, which can happen from LS. So I will begin the maintenance routine again

    . I plan to continue to eat plant based with antibiotic and hormone free poultry since it seems to be working for me. She suggested I use dilators to help with the tightness. I still remember when I was first diagnosed and the doctor had to use the child size speculum because I had closed up so much. Who knows what tomorrow will bring, so I will count each day a blessing . I know for now we have no cure, but lets never give up hope. I am so happy to have found this community after feeling so alone on the LS island for so long. Having others to share with helps both physically and mentally.

Report or request deletion

Thanks for your help!

We want the community to be a useful resource for our users but it is important to remember that the community are not moderated or reviewed by doctors and so you should not rely on opinions or advice given by other users in respect of any healthcare matters. Always speak to your doctor before acting and in cases of emergency seek appropriate medical assistance immediately. Use of the community is subject to our Terms of Use and Privacy Policy and steps will be taken to remove posts identified as being in breach of those terms.