http://www.mdjunction.com/forums/lyme-fibromyalgia-discussions/feed http://www.mdjunction.com/forums/lyme-fibromyalgia-discussions/feed en-us Copyright (C) MDJunction.com. All rights reserved. Tue, 21 May 2013 20:17:50 -0700 http://www.mdjunction.com/forums/lyme-fibromyalgia-discussions/general-support/10674672-for-those-of-us-who-cannot-afford-a-llmd#10694507 P.S. Go to that Facebook page I mentioned above, and click on Webinars and you can sign up for the next one. Here is what it says when you click on that. Conversations with Marty Ross MD Bring your questions, insights, and a computer with a good internet connection. In this live forum, I will respond to any comments or questions you have about Lyme Disease. We will explore diagnosis, treatment, and pharmaceutical and natural medicine approaches to this complex illness. ... Mon, 20 May 2013 05:37:34 -0700 http://www.mdjunction.com/forums/lyme-fibromyalgia-discussions/general-support/10526648-ever-tried-biomat#10669001 I ordered mine today. Will report.... Wed, 08 May 2013 13:08:08 -0700 http://www.mdjunction.com/forums/lyme-fibromyalgia-discussions/general-support/10626674-hello-new-here-hoping-for-insight#10666445 I've had Lyme, Fibro, CFIDS for 35 years and over that time have been misdiagnosed over and over and over with various ailments, some true some not. At the time I contracted Lyme I was living in Northern California at a boarding school and was 17 years old. It was near a wooded area. No one ever suspected Lyme was already in CA. After I got very sick, my doctor couldn't identify what was going on and thought I had Mono. The treatment was antibiotics, which I took and got better but then go... Tue, 07 May 2013 10:36:13 -0700 http://www.mdjunction.com/forums/lyme-fibromyalgia-discussions/general-support/10657270-llmd-in-naples-florida#10657823 Crazy! But from what I understand they are very controversial and have been sued because the mainstream medical world does not accept their treatments and many have been sued. So not fair to us who really need them!!! I was diagnosed 3 years (after 6 months of seeing numerous doctors down here) ago with fibromyalgia, but I know now that it was LD. Trying hard to find a doctor who can treat me down here and doesn't charge that much!... Fri, 03 May 2013 06:05:28 -0700 http://www.mdjunction.com/forums/lyme-fibromyalgia-discussions/general-support/10430030-possible-lymes#10610046 Im not sure about anaplasma, but I know mycoplasma is a co-infection that they often find in Lyme patients. I was diagnosed with Rh arthritis, fibro and other auto immune diseases for my muscle and joint pain but all the symptoms and inflammation was being caused by Lymes disease. With lifestyle change , and treatment for the Lymes i only have the muscle and joint pain maybe 2 days a month instead of Every day of the month . Hope this helps, God speed :)... Wed, 10 Apr 2013 15:39:17 -0700 http://www.mdjunction.com/forums/lyme-fibromyalgia-discussions/medicine-treatments/10470230-questions-about-tindamax#10560842 I am just starting Tindamax as of today. We'll see how it goes. I am also on IV ceftriaxone so I am a little worried about it. How are you doing now?... Tue, 19 Mar 2013 14:01:49 -0700 http://www.mdjunction.com/forums/lyme-fibromyalgia-discussions/general-support/2960402-tindamax-for-lyme/limitstart/10#10532447 Anyone else on tidamax and IV ceftriaxone? I will be starting the tindamax in about a month. I have severe neuro sxs including dystonic storms, generalized dystonia, cognitive dysfunction etc and dont' want to lose what little functioning I have. I am still struggling with a herx that increased my convulsions and then they increased more after a week off my meds, even with a detox. I am getting afraid to be alone with my small children (3,5) as I can barely care for myself some days. I cant... Thu, 07 Mar 2013 13:12:03 -0800 http://www.mdjunction.com/forums/lyme-fibromyalgia-discussions/general-support/10532237-sorry-for-not-being-on#10532237 Hi All: Sorry I have not been on much...I was told last week that I had a slient heart attack so I have a lot going on at the moment. They think radiation from my BC caused my heart to weaken they are not sure until I have an Angiorgam next week... I hope everyone is ok and doing as well as can be. Hugs to all Julie... Thu, 07 Mar 2013 11:37:27 -0800 http://www.mdjunction.com/forums/lyme-fibromyalgia-discussions/general-support/10459136-need-help-with-treatment-for-lyme-fms#10527712 I live in TN and don't have a referral for you, but just wanted to offer my support. I am from NY and have been in TN for 17 years. I was diagnosed with fibro after I had my second child and ended up closing my psychotherapy practice for the same reasons you have problems. I have now since learned that lyme can be triggered by childbirth so it makes me wonder if I have had fibro or if I have had lyme all these years. It is something I will never know. I did get very sick rapidly with lyme, p... Tue, 05 Mar 2013 11:25:03 -0800 http://www.mdjunction.com/forums/lyme-fibromyalgia-discussions/general-support/10397552-new-to-this-support-group-need-help-with-lyme-and-fibro#10454937 I definitely feel for all of us...I can not believe that I went back to work 40 hours a week and my job is so stressful....I just wasn't ready to be disabled but I am. I have been getting a recurring rash on my left arm and hand, vertigo and nausea and now my hair is falling out in clumps literally, when I take a shower, heart palps and muscle twitching/spasms. At first, I thought it was stress but this is crazy. I left my hair on the side of the tub to ask my husband to look at how m... Sun, 03 Feb 2013 19:57:15 -0800 http://www.mdjunction.com/forums/lyme-fibromyalgia-discussions/general-support/10431447-llmd-in-mobile#10431447 Dose anyone know if there is a llmd in mobile al, I'm searching for a new one thanks everyone shelia... Sat, 26 Jan 2013 07:02:52 -0800 http://www.mdjunction.com/forums/lyme-fibromyalgia-discussions/general-support/10302134-advice#10431439 I haven't went to my llmd yet but thinking of making appointment soon to get my cd 57 level checked out last time it was really low .. But I did get some results back my vitimin d is very low and I know that could be a big problem in my pain as well .. I don't know much about it but have read a little on it . Kinda has symptoms of Lyme and fibro .. Huh lucky me like I don't already have those pain symptoms from Lyme and fibro .. Guess I need more sun I was trying to avoid the sun as much as ... Sat, 26 Jan 2013 06:59:25 -0800 http://www.mdjunction.com/forums/lyme-fibromyalgia-discussions/general-support/10422786-looking-for-llmd#10422786 I think that I could benefit from a LLMD as i've been suffering endlessly from neuropathic pain and would appreciate a referral someone in my area if possible. I live near Toronto,Ontario Canada.Post edited by: crpslymer, at: 01/28/2013 04:00 PM... Wed, 23 Jan 2013 12:47:49 -0800 http://www.mdjunction.com/forums/lyme-fibromyalgia-discussions/general-support/10393054-flu-shot#10398198 Thanks cmany I didn't think it would be a good idea ,,,,, my mom keeps telling me I need to because of my condition she has fibro and says she's fine when she takes them . But I'm afraid it will back fire on me ... So I have never got one and most likely won't... Mon, 14 Jan 2013 16:00:11 -0800 http://www.mdjunction.com/forums/lyme-fibromyalgia-discussions/general-support/10345206-what-can-i-take-to-help-my-chronic-fatigue-along-with-my-morphine#10368334 Thank You Raven, I a definitely will look into that. My mom said to get Magnesium and I got some B complex and WOW what a difference they made. I have done more today with all this energy than I have in months. I will definitely check out what you suggested because I do not eat properly for sure. Thank you so much.... Wed, 02 Jan 2013 11:37:30 -0800 http://www.mdjunction.com/forums/lyme-fibromyalgia-discussions/general-support/10364052-fibromyalgia#10364052 I have it. I don't know how long I have had it though. It flared up while teaching 14/15 yr olds, a new course being developed and streamed stress. I developed excruciating headaches ( not actual migraines) , but burning ones. I lived with that for several years. Not fun. I then found to have multiple chemical sens and Fibro. Didn't realize that it was the Fibro is a syndrome at the time and that the MCS is actually a symptom of it. I found that avoiding a lot of chemicals , has all but taken aw... Mon, 31 Dec 2012 18:11:35 -0800 http://www.mdjunction.com/forums/lyme-fibromyalgia-discussions/general-support/10153432-could-use-some-advice#10351276 well.hmmmmmmm okay then. lol... Wed, 26 Dec 2012 09:43:24 -0800 http://www.mdjunction.com/forums/lyme-fibromyalgia-discussions/lyme-facts/1222379-lyme-neuro-toxins-do-we-have-to-herx#10302361 I would highly recommend using Dr Jernigan's remedies or going to the clinic if you can. He brought me back from barely able to walk to full health in very short period of time. He is my first choice for anything health related. Brilliant man and a very big heart. Hope this helps.... Tue, 04 Dec 2012 07:39:25 -0800 http://www.mdjunction.com/forums/lyme-fibromyalgia-discussions/general-support/3690174-lyme-doctor-in-georgia#10277779 Please send me a pm and I will get to sending you a list first thing Monday morning Christine... Fri, 23 Nov 2012 12:30:22 -0800 http://www.mdjunction.com/forums/lyme-fibromyalgia-discussions/general-support/10258011-llmd-in-delaware#10277778 I can get you a list...I haven't been on much lately...been very busy with many things... I can get to it on Monday...just have a couple of minutes now... Please send me a pm - the link for that is under my pic...this way I will remember to do it Monday after I take the kids to school Christine... Fri, 23 Nov 2012 12:29:23 -0800