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HELP! I Have Lichen Sclerosus! Hope for remission of LS symptoms via natural healing methods including Sodium tetraborate (borax) therapies: Collated wisdom from fellow sufferers
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About HELP! I Have Lichen Sclerosus! Hope For Remission
You don’t have to buy this book – there is lots of information out there on the internet – but finding it (if it is still there) and sifting it out of the tangle of threads that come and go on a daily basis – that is hard! We have written what we would have liked to find when we first heard that we had Lichen Sclerosus (LS) Allicia and Ann are well-known in the LS community for sharing their loving support and collated information on the many aspects of how this condition affects our lives and what works for them and others – with all the hope that this offers. Here, all this wisdom is gathered in one place, easily accessible for all. Maybe you’ve been told you have Lichen Sclerosus (Sclerosis) and you want information and to know that you are not alone in your suffering – that’s here – or you’ve had it for a while, and things aren’t going so well, you’re still uncomfortable and you want to explore other, or complementary, ways to help control the symptoms – that’s here. What you won’t find here is a medical opinion – we are not doctors – but there is a lot of detail to enable people to make their own informed choices. This slim book is packed with information and explanations, tips on coping with many of the problems LS throws at us, as well as protocols and good practice - from people who know this from the inside. For both Ann and Allicia, borax therapies have been key to their finding remission – so these are dealt with in great detail, including safety issues and protocols.Other aspects covered include; other natural methods to ease the symptoms, triggers and flares, fusing, atrophy, bruising, foods and supplements that support skin health, what to wear or use for comfort, sex and pregnancy, notes on LS in men and in children, problems concerning urination or defecation, lists of useful information and where to find support groups. Finally, we wrote this book because, though this information is, currently, out there on the internet, not least in Allicia's support group 'sharing is caring about LS et al', we know from bitter experience, that this can suddenly vanish, at the whim of a faceless FB bot, with no warnings, no reasons given and no recourse to appeal - and over 4,000 people left bereft of this information, support and help. This is, ultimately, why this book was written.
