Mona Lisa touch reviews
Posted , 63 users are following.
I had my third treatment 10 days ago. No uti since I started like 3 months ago. BUT now pain n stinging. Thought uti but tested not. Uncomfortable for a week. Even used prep h to try to stop painted it actually work for a while I'm also doing the ice cubes… So anybody out there can share their experience with me I sure would appreciate it
1 like, 331 replies
peg30370 nancyo
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lisa48333 peg30370
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In about 2 weeks I will be having my 3rd treatment. I've had very little change for the better. More change in not a good way, not sure if I made the wright choice on doing this. You spoke about (I'm about 90% improved with the Estrace 3x a week, supplemented with coconut oil ) what is this and how does it help?
nancyo peg30370
Posted
Hi
Called to schedule my treatment one year after tongibd the quote doctor gave me a year ago doubled from 500 to 1000. They know we have no alternative. Have to do it as it worked for me but need theconecyear later treatment. Will let you know how it goes
Hope you're feeling relief soon
dancin peg30370
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donna18720 lisa48333
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peg30370 lisa48333
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I was using Estrace cream 3x a week which was when I finally started to feel some relief. Had been on it 2x a week for months and no improvement. The coconut oil is sold with the cooking oils in every grocery store. It's a solid like Crisco, but liquefies when warm. I just used it all over the outside areas (can also be inserted vaginally), as it's really soothing, and also has anti bacterial properties which help as well. I would have been comfortable with this routine before the Mona Lisa, but it has to be constantly maintained...skip one time, and symptoms flair😩!
beverly52803 nancyo
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nancyo beverly52803
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beverly52803 nancyo
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Did you get to speak with the doctor today? Maybe he could prescribe a small amount of pain meds till you heal.
I have been off this site for a while. has anyone else reported problems with it? When I google it now there is a whole lot of info that wasn't there last summer. Guess it has hit the US big time. Not surprised. That's why I think there's a chance insurance will be forced to cover it sooner than later.
nancyo beverly52803
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beverly52803 nancyo
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If they will be conducting actual studies, maybe some of us can volunteer to be part of the studies and have it done at no cost (?)
nancyo beverly52803
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Stanford is doing a study now. check the teaching hospitals in your area
marilyn090257 beverly52803
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Hi Ladies
I had a total of four treatments - all six weeks apart -and not successful yet.
The third treatment was definitely stronger, I felt the "pinch" if I can call it that...
I never had any swelling, but always felt a tiny bit of burn, especially after the third treatment. However, I continued to have the itching burning vaginally and in the vulvar area even after the third treatment.
My gynocologist has given me the fourth treatment on Aug. 16th, 2019, and it was much stronger than the third treatment, it hurt a bit each time he applied the laser on the vulvar area. I did have swelling and burning in the vulvar area immediately afterward.
I still have itching/picking from time to time but I guess it's too soon to see results, since I'm a difficult case anyhow.
I was told to give it time, maybe another 2 to 3 months to see if the collagen starts to regenerate again.
I heard so many ladies have excellent results, some right from the first treatment, but I wasn't so lucky so far....I'm praying that this fourth treatment does the trick for me.
I wonder why my body is slower to react to the laser treatment and others have immediate results???
I don't want to take estrogen and will have to resort back to natural supplements if this treatment don't work.
Desperate too....
beverly52803 marilyn090257
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marilyn, I had to look back to try to remind myself of your situation, but couldn't find but 2 posts.
Were you getting the ML for atrophy or LS (or both)? You certainly have hung there with repeated treatments.
I assume your dr is examining you before each treatment. Has he proceeded with the treatments hoping to see improvement or because he has actually seen some? It sounds as though you have felt none.
Do you not want to use hormone cream because you have had cancer in the past? I also was avoiding the cream due to my sister's estrogen dependent breast cancer, but now I have no other option. The cream has really been quite effective. My more serious problem is the LS.
Thank you for posting. It's really important that we share our experiences with each other. There's a lot some doctors seem reluctant to discuss.
Hope you do start to feel an improvement after all you've been through with the ML.
pam31747 marilyn090257
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I'm so glad i found this site. I was ready to take money and get this procedure done. From the majority of the reviews, it's not helping most women. I would hate to feel worse than I do now. To everyone having difficulties I hope you feel better soon.