Guest guest Posted August 17, 2001 Report Share Posted August 17, 2001 I can tell you that my Son who has Lyme as well besides Hubby and Myself at times has the skin on his fingers peel if he's gotten them wet for a period of time. The skin on his hands is very papery. As my Aunt said...it's like he's got an old man's hands...and this was said when he was 10! Sal > hi everyone- > has anyone else experienced peeling skin? the skin on ,my legs is > continually peeling recently and i just wanted to share. > denise Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 17, 2001 Report Share Posted August 17, 2001 Hi , I have skin problems with lyme, my doctor gave me Metrocream, it is like tinidizole (sp) in cream form. It really works, My problem is mostly on my face, it get is hard, scaly, peely layer and that is the only thing that works. When I first got lyme I had a ring of this entirely around my neck. As the antibiotics worked it went away, but still get it occasionally on my face. It is super dry and sometimes burns. I do find the Metrocream is less irritating than the Metrogel, Good luck, Hugs, Connie, MI Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 21, 2001 Report Share Posted August 21, 2001 The skin on my nose occasionally gets really dry and flaky. After a couple/few weeks, it all peels off and leaves new smooth skin underneath. I also get flaky skin in one of my ears, and sometimes scabs on my scalp. My skin is also just real dry. > hi everyone- > has anyone else experienced peeling skin? the skin on ,my legs is > continually peeling recently and i just wanted to share. > den Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 25, 2008 Report Share Posted June 25, 2008 Hi everyone, I have some very dry skin problem and I had been doing real well with petroleum jelly-e & aloe. then I went to Eucerin, changed to Aquaphor and I tried Calendula cream. I also have put on lotion and then wore rubber gloves or cotton gloves. It seems nothing is working well right now. I have RA and DM and have been on the AP program now for 5 months. I do feel better, I just wonder if this is some herx or just nothing else will help. Thank you for any help. Eva Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 22, 2009 Report Share Posted September 22, 2009 > > From my reading, it is pretty much a given that adrenal issues go along with the Lyme and needs to be addressed separately. This would seem so in my case. Also Candida is a possible cause of the sores/skin issues as well, so another avenue to look at. And then underlying all of that is the heavy metals.....it just goes on. thanks for the reply - yes, adrenal issues is a possible factor. I think Candida is less likely, I tried a lot of anti-yeast treatments without any result and the problem is localised (with systemic candida problem I don't think just face/scalp and shoulders would be affected). Some kind of toxins could be a factor too. Not just heavy metals, there are thousands of dangerous chemicals like all kinds of PCB's, phtalates and dioxins piling up in our body. Especially the rashes at the hairline seem to be related to bad liver function (problem with processing/removing toxins?). > As for the collagen, I am now trying the Life Extension Fast Acting Joint Support, Biosil and a few of what Buhner had in his protocol. It is a desperate attempt to save and hopefully rebuild whatever collagen is left. I tried all the stuff Buhner recommends, for several months, no result. Over the last weeks I added pregnenolone and high dose vitamin C (like 5 grams a day), which I didn't try before. But connective tissue just keeps disappearing, it looks extremely unhealthy. On the other side, I'm wondering if maybe there is a good side to this: the bugs are hiding mostly in the connective tissue, if this disappears maybe our bodies do this to get rid of the Bb?? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 22, 2009 Report Share Posted September 22, 2009 > I'm just tossing things out here, so if they sound off base, it's because I'm not a doctor and I'm just being a sounding board... thanks, a sounding board is what I'm looking for. everything gets messed up in Lyme and the MD's often act as if I'm telling them fairy tales ... that doesn't lead to any help. > Spelt is just another wheat. Sometimes, just having bulk rice flour be in a bin next to the bulk wheat flour in the natural foods store is enough for cross-contamination to occur - especially if someone puts the wrong scoop in the wrong bin. Unfortunately for those of us who have to avoid it, that usually means total wheat abstention. OK, at least I now know the english word for spelt they tell me that the gluten from spelt is a lot less allergenic than the one from wheat; so it should help (and indeed with spelt bread I don't get serious gut problems, but maybe minor issues remain). For some reason the health food store is selling loads of spelt bread; I guess there are more customers with food problems... I'm not 'allergic' to gluten, just 'gluten-intolerant'. I don't get any immediate reaction from eating gluten (or whatever), but after eating normal bread etc. for a prolonged time I get serious gut problems (and probably other related issues). I haven't tested for other 'food allergies', I guess there may be similar problems with other stuff. > As a child, did your skin break easily, splitting between the toes after a hot bath? Are you able to touch your thumb to your wrist in one direction or another? Have you been tested for type 4 (vascular) ehlers danlos? It's a genetic condition, and type 4 has been genotyped, so it can be easily diagnosed. I never had such problems as a child, and as another reference: I have a twin brother (who was not bitten by a tick) who has none of the problems I have. However, he seems to be sensitive to some kinds of foods as well (but never as serious as in my case). > You could be manifesting a chemical sensitivity brought on by a combination of genetic predisposition and duration and intensity of exposure to a similar pesticide. yes, I remember the Vapona ... and it could be a special chemical issue that was somehow 'reactivated' by the Lyme disease. When I was 19, I was exposed to a huge dose of CS-gas during squatting riots in Amsterdam. CS is a nerve gas that was used as a riot control agent in the Netherlands at the time; it is very dangerous but was used anyway for a long time. The cops thought I was taking pictures of secret police officers who were molesting civilians (they did that on a massive scale to scare civilians and keep them away from the scenes). They fired five full CS grenades on me, I was dragged away partly unconscious by some bystanders. The few years after that I had very serious 'unexplained' skin problems (mostly severe 'peeling') in the exposed areas: face, neck, hands. Later I learned that other people had similar problems after exposure to CS gas. After 5-10 years the problem gradually disappeared. My neurologist for Lyme told me that this special gas damages the nerve endings and can cause all kinds of trouble. The current problems started quickly after the tick byte (5 years ago) and are in roughly the same area. Could be coincidence of course ... But maybe the Lyme has caused the 'toxin' problem to reappear? With all the strange things that are going on in Lyme nothing surprises me. > If you live in an apartment complex or near a restaurant, do you know what they are using as pesticides? It might be worth investigation. I suspect pesticides are even more appropriately regulated in Europe than they are in the US, so it may not be problematic for you. I'm pretty sure this is not an issue for me; also I moved to a new home this year, no difference. I know for sure (from my environmental chemistry studies long ago) that pesticides etc. are everywhere, even if you buy just the biological/eko food. So it is impossible to completely avoid them. > I get nattokinase from vitacost, the nsi brand. I've worked up to 6000 FU per day, 3 caps @ 2000FU daily. It's great stuff. I think of it as a cornerstone supplement for me. Your mileage may vary. Surely there are distributors for something similar in Europe? probably, but most supplements are FAR more expensive in Europe (even though it seems most of this stuff is produced in Europe). Even with the shipping cost from the US added, many products are cheaper than in Europe. Only some very common stuff like VitC, Glucosamine is about the same price over here if you shop around. thanks ago, I think I will try the natto first. Should I start slowly with this? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 22, 2009 Report Share Posted September 22, 2009 Not that I know what they are but I have the same type of bumps on my face that sometimes open up an ooze the clear or yellowish liquid that gets a bit crusty. I also have the bumps mostly on my forhead but also some on my chin and back of neck with the hard yellow thing that comes out of it--sort of like a blackhead. And I also have kind of like pimple things in my hair mosty along the hairline. I think these all started appearing after I started taking the Buhner herbs about 7 months ago. If you find out what they are or how to get rid of them let me know the blackhead type ones are driving me crazy. - In , " knot_weed " <tek0nik@...> wrote: > > looking for some advice/experience from others: > > After more than a year on antibiotics, and 1.5 years of Buhner protocol, I still have a lot of skin problems that seem related to Lyme (started right after tick byte or during treatment). I'm from Europe where skin problems seem to be far more prevalent with Lyme. > > Most of my connective tissue has disappeared over the last few years, especially in the face and the pads of hand/feet/shins etc. I have tried Buhners collagen support protocol, but to no avail. > > A new problem that developed over the last year is a few sores in the skin of my face. It looks a bit like a +/- 5 mm bump (infection) under the skin. From time to time it opens and some clear or slightly yellow, very sticky fluid comes out. The sores are not painful or itchy. The problem is that they don't heal, the small wound closes for a few days and than it starts all over again. There is no blood or 'pus', maybe that is why it doesn't heal. Really depressing ... > > I also have smaller sores on my scalp, mostly near the neckline and on top. The pores, sebacious glands or hair follicles in the scalp seem to produce a toothpaste-like substance on a daily basis. It is nearly dry, slightly greasy material with grey or a bit yellowish color. This itches because the hard material 'clogs' the pores. > > Reading on internet there are too many options to choose from ;( > Seems it can be related to infection or gut / circulation problems (I have those, so ...). > > I have visited a dermatologist who was not interested in the problem. He prescribed acne cream (funny - he first lectured me that 1 year of antibiotics for Lyme was way too much, and than writes down an ABX prescription for three months for a skin problem ...). This acne cream does not seem to work at all. > > I also have an eye infection that has been treated with chloramphenicol ABX cream two times, which doesn't help (so is the infection spirochetal? this eye also has persistent floaters). > > Does anyone recognize these issues, know what it is or how to treat it? I'm thinking of trying a topical Smilax preparation for my skin, as this is used to treat many skin problems. No idea how to use it, maybe prepare a decoction or mix it with Aloe Vera cream? > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 25, 2009 Report Share Posted September 25, 2009 Here is a link to doctors that have either trained with him or have been to his seminars: http://www.klinghardtneurobiology.com/referrals.pdf Jane > > > > > > Jane, > > > > > > knot_weed is very underweight. The homeopathic remedy Unda #243 is billed as being used " For the relief of symptoms associated with overindulgence in food and alcohol " . Are you sure this would really help him? > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 26, 2009 Report Share Posted September 26, 2009 Doug, Jane, Thanks for these very sensible responses. > I am only throwing suggestions out there. I definitely think everyone needs to do their own research and choose for themselves. I took the Unda 243 on a recommendation from several people that use it for their kids as well as themselves. Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.