http://lymecommunity.com/forums/ubbthreads.php RSS Feed for General Discussion Lyme Community Forums - UBB.threads(tm) http://lymecommunity.com/forums/ubbthreads.php?ubb=showflat&Number=4903#Post4903 He has had symptoms for about 5 weeks and started Doxy for two and Amoxicilin for 2 more. What should we expect? No one is absolutely sure he has it as there was no rash. Thanks for your feedback. Wed, 10 Mar 2010 01:20:38 GMT http://lymecommunity.com/forums/ubbthreads.php?ubb=showflat&Number=4902#Post4902 I have heard about taking MMS but have been a little afraid to take it do to the fact that it kills both the good and bad bacteria. I have been treating my lyme naturally without any antibiotics or anything that will kill my good and bad bacteria. So I guess I don't know for sure if the MMS kills both. Tue, 09 Mar 2010 18:03:53 GMT http://lymecommunity.com/forums/ubbthreads.php?ubb=showflat&Number=4899#Post4899 My wife was diagnosed in October of 09 with chronic lyme. She went to Reno, spent 5 weeks and over $15,000. Had some major Herx reactions to the "Shake and Bake" IV therapy that Fong uses. We learned alot. Mostly that Lyme can't be beat in 5 weeks. Fong sent my wife home and said she needs to work on physocological issues before he could treat further. I believe he is a good doctor, just not a great Lyme Dr. He mentioned in passing during a followup callup that we may consider using a rife machine. He was only familiar with the F-scanner. Like I said, I think he is a good Dr, just not what we needed for the Lyme. Hope that helps. Sun, 07 Mar 2010 18:28:50 GMT http://lymecommunity.com/forums/ubbthreads.php?ubb=showflat&Number=4896#Post4896 Hi Rachel, I have to look in my medical supply at home (I'm at work right now). Right now I take "Iodox", which is in pill form. Mainly it is different types of iodine in one pill. I just finished a bottle labeled "Cortex" (I bought it from my ND). I'm now taking something labeled "Adernal Support". I'm sure this does you no good without knowing who makes it. Hopefully I'll remember and post back with more detailed information. It may take me a few days to remember to look it up and then post again. With supplements that come in drops and contain alcohol, I usually let it sit in water for a few minutes before drinking. This allows the some of the alcohol to evaporate. I question how much evaporates, but Dr. Lee Cowden did direct his patients to do this with his NutraMedix tinctures. I don't know of any doctors in Europe. I've heard of Dr. Andrew Wright in the UK as a good one. But you may not have to go that far. Just make sure the doctor you see believes in chronic lyme, does not pronounces "lyme" as "lymes" (that's a give-away), and you feel that he takes the fact that you have lyme seriously. Mainly you should be looking for a doctor that will not prescribe steroids that will make your lyme worse. You can try this link, but I think they only list US doctors: http://www.lymediseaseassociation.org/referral/LogIn.php?setcookie=yes I would log on and give you the information, but I think they only give you a few LLMDs in your area. This is to protect the doctors (long story). Good luck, Rich (skiweasel7) Fri, 05 Mar 2010 14:58:14 GMT http://lymecommunity.com/forums/ubbthreads.php?ubb=showflat&Number=4890#Post4890 Hello Steve, I am impressed about your thread herein, started in dec 07. Now it is Feb 10, more than two years and you are still using MMS/DMSO and other stuff, hope as well you are eating a lot of antioxidants in the break of MMS. And the real great thing I want to thank you for is your good encouraging story, you now feel some 80 to 90% better. If this is not a real good outcome of your experiment with MMS and Lyme, what else will be. I am just in the beginning of it, so to say my first course has been finished 7 days ago, I was up to 3x15 a day for a week and then going down to nothing within a week, bad thing was I felt so good under the MMS, only a few days "big D" and nausea, but nearly no herxing, except strong headaches. But my energy level was tremendous. The first day without MMS was ok, but the second I felt horrible, all the Lyme symptoms came up again but I have to go through that. What luck I have a good natural ayurveda medicine against all this lyme pain. In about two weeks I will start with my second course ... at the moment I am seeking for an alternative way for the intake, it sounds good to take it unactivated and trink short time afterwards some lemonade made out of a fresh citron. Tue, 02 Mar 2010 11:48:05 GMT http://lymecommunity.com/forums/ubbthreads.php?ubb=showflat&Number=4888#Post4888 Hi, new to the forum which comes highly recommended by friends also suffering from lyme. After much reading I feel the EMEM type machine is worth trying. I'm looking for a reputable manufacturer to buy one from that others have used and would recommend. Pre-built with a user friendly frequency selector would be ideal. I heard of RifeLabs but it appears the website has been taken down. Any help would be greatly appreciated. - Rick Thu, 25 Feb 2010 18:10:30 GMT http://lymecommunity.com/forums/ubbthreads.php?ubb=showflat&Number=4887#Post4887 I had the target rash. I walked through a nest and was bitten by hundreds of ticks in the New Jersey Pine Barrens. I have been disabled for 9 years. My career, 401k and house have been consumed long ago. I am on medicare and need a lyme doc. Lyme docs seem to only take cash. Does anybody know of a charity that might help? Thu, 25 Feb 2010 14:54:33 GMT http://lymecommunity.com/forums/ubbthreads.php?ubb=showflat&Number=4886#Post4886 I had the target rash. I walked through a nest and was bitten by hundreds of ticks in the New Jersey Pine Barrens. I have been disabled for 9 years. My career, 401k and house have been consumed long ago. I am on medicare and need a lyme doc. Does anyone know where to find one anywhere in the US? Thu, 25 Feb 2010 14:52:06 GMT http://lymecommunity.com/forums/ubbthreads.php?ubb=showflat&Number=4885#Post4885 Hello my name is Katy and I have had lyme disease for nine years. I'm currently on the East Coast getting treatment while my fiancee is in San Diego where we live. We have entered a contest to win our dream wedding since our medical expenses have depleted our finances. Please vote for us! [url=http://www.ultimateweddingcontest.com/entries/23109]Vote for Ultimate Dream Wedding[/url] Also, Fox News ran a 'Dealing with Lyme Disease' story based around this competition. I looked for the clip on their website, but no luck Thank you so much for your help, we just hope to make the top 50 and it means so much to us!! Thu, 25 Feb 2010 11:30:39 GMT http://lymecommunity.com/forums/ubbthreads.php?ubb=showflat&Number=4884#Post4884 Geeze! Do they accept any kind of insurance? Thu, 25 Feb 2010 09:09:13 GMT