stemm cell therapy completed

Posted , 10 users are following.

I had the stemm cell therapy 2 months ago now in Italy from Dr.Casabone. I have heard that 2 Docters are now offering it in England. It may not be a cure and I really don't know how long it will work but it works for me now which is the important thing.

Since the operation I only use emu oil. I had a check last week with a gynocologist and she confirmed that there are no symptoms of LS. It could well be that I need a second treatment in autumn but Dr.Casabone thought I had a very mild form and one treatment would be enough.

I did a lot of research on the subject and its more like taking fat from one part of the body and inserting it into another part plus the enriched plasma which stimulates growth.

It is expensive but if other docters can start offering this treatment then maybe it will become a standard therapy one day. I really really hope so for everyone that has this condition.

I will try to do an update at least once a year and keep people aware that there are options with which they can argue for in their own country.

5 likes, 25 replies

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  • Posted

    Thank you for sharing about the stemm cell therapy.  I've read a lot about it.  I hope one day my dermatologist who specialized in vuvlar diseases will learn to do the therapy.  Even though she has done a excellent job at getting all my LS gone.  I just hate having to use the temovate ointment for the rest of my life with the possible side effects of it.  Best wishes to you and I do hope other doctors begain to preform the stemm cell therapy because it would be so needed.
    • Posted

      Yes I did but it's all clear on the vuvlar area.  Thanks to my g reat dermatologist.  I happen to be 1 in 30 women who has LS on my upper body too. 
    • Posted

      well thats wonderful news rebecca!

      are you also clear on the upper body ...or still working towards recovery there?

  • Posted

    Thank you Marie, so I understand that the LS is totally gone? 

    Did the doctors explain how this came to be - what is their theory?  What are their thoughts?  Would you be able to explain? 

    • Posted

      Hello Hanny,

      the gynocologist I saw was new to me and had very little idea of LS other than I have a healthy vagina and no signs of LS and added if I really did have LS it would come back as there is no cure for it - such wonderful words of comfort. Needless to say I shan't be going back to her again-

      I had a biopsy that was positive for LS early this year but Dr.C felt my symptoms were very mild and partly due to being post menopausal. He said atrophy is part of the aging process along with the shrinkage of the vagina-

      How it works I don't really know and that it doesn't work for everyone is also true for that reason we need more doctors to take the plunge and offer it on the health service in which ever country someone lives in. The more women who have a positive experience and the more who cannot get this treatment have to put pressure on their Doctors and ask why its not available.

      The

  • Posted

    Thank you Marie,

    I understand that your LS was caught in its early stages.  I myself would have to go back many years.  Even though it was officially detected about a small year ago.  The fusing is enormous.  I totally agree that successful treatments should soon become available to all.  (My Gyno just told me that he couldn't help me any further, after he diagnosed that the Glob had made matters worse.  Luckily I already was in contact with a good nature path.  But I still feel that I'm mostly left to my own initiative and devises.  This web connection is so helpful therefore.

    Thanks again. 

  • Posted

    marie....thank you so much for your pioneering attitude and your positive and assertive mindset!

    exactly so...what your last consultant was saying is that SHE and the conservative members of her profession don't know how to cure LS ...that does not mean its incurable! 

    I know a woman who has cured herself....and I'm slowly introducing myself to her protocol and the preparations towards following it....plus there are a number of women now from this site who have cured themselves using alternative methods and yet another who slowly cut out the steroids after a remission and she remains clear. So it can be done.

    And you are another wonderful example.

    In addition to maintaining your healthy mind ....I hope you'll join us in taking care of your bodily self too.  In my case I'm striving for a nutrient dense diet, balancing of my hormones, supplementation with all the vitamins and minerals that my body now seems to need - missing elements of which may have just contributed to a slip in health; together with avoiding chemicals and doing lovely de-toxing....for example by enjoying epsom salt baths!! (I tell myself...but have yet to actually buy this magnesium rich bath joy!!! another woman is making her own magnesium rich  body cream....so we're all very inventive!)

    I am sure you will stay healthy....you've tipped your body back into good health...and sort of tricked it out of LS....its brilliant I love it. I see no reason why you shouldn't stay that way especially if you can think of the toxins or other causative factors in your case to avoid, if that was it. Actually may I ask what in your case you think might have been the cause of LS for you? I know you mention the menopause  and having been a mild case anyway. Had you been on a low fat diet or anything like that or got run down or stressed? Pleased don't feel obliged to answer if I'm being intrusive!!! Its just so exciting to hear about your success!!

    Loads of love 

    marey x

  • Posted

    Tell you what marie...

    I'll start a new thread posing the above question....yours will remain open. I would like to invite you to submit your thoughts in the new thread if you would possibly be so kind xxxxxxxx

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