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When really, it is Lyme Disease

Post a new topicby livingwith on Fri Aug 17, 2007 10:35 pm


Many people are diagnosed as having Chronic Fatigue Syndrome (CFS), ALS Parkinson’s, Multiple Sclerosis, Fibromyalgia and more diagnoses when really it is Lyme. Sometimes these ‘misdiagnoses’ aren’t really misdiagnoses because you do have CFS, fibromyalgia, demylenation….when you are infected with Lyme (which usually also includes co-infections. Lyme is very sneaky, so to speak and can evade current testing. The current tests often only include a few species of ...Read the full article

livingwith
 
Posts: 5703 | Joined: Thu Aug 09, 2007 2:36 pm

Re: When really, it is Lyme Disease

Post a new topicby writer on Wed Sep 05, 2007 3:47 pm

Do you have lyme disease? I do and I am writing a book about it. The book is designed to help those who are sick and those who know they have lyme disease. It focuses on the consumer needs.

Please help us help you by taking a 20 to 30 minute survey - click the "Online Survey" link in the top navigation bar – [moderator note: website address has been removed]

Data will be included regarding lyme victims source of exposure (ticks, other insects, lyme vaccines ( the failed one that was purchased by millions), organs or blood purchased in the marketplace, breast milk, intercourse, diseased animals and in-utero), percentages of lyme victims misdiagnosed with Multiple Sclerosis, Amyotrophic Lateral Sclerosis, Fibromyalgia, Chronic Fatigue, Behavior Problems, Alzheimer's Disease, Lupus, Parkinson's disease, Mental Illness,Trigeminal Neuralgia, Attention Deficit Disorder, Autism, Asthma and Blame the Patient/All in Your Head), the financial cost of lyme disease to lyme victims and society, success rates of numerous diagnostic tools used to evaluate the sick and the best treatment plan to use for lyme disease and its co-infections and much more.

writer
 
Posts: 2 | Joined: Wed Sep 05, 2007 3:45 pm

Re: When really, it is Lyme Disease

Post a new topicby jlk on Wed Mar 19, 2008 11:35 pm


I just turned 30 and it took about 10 years until I got diagnosed. I haven't been able to work for 2 years now. Can you tell me what I can do to maybe help get back to a semi normal life if there is anything. As of right now I go to pain management and take 20 mg of oxycontin twice a day but that really doesn't help much. I have been on cymbalta for a few months which works better then the oxycontin and I take vitamins to try and help with my tiredness and weakness but I'm still tired all the time. If you can suggest anything that might help it would be greatly appriciated.

jlk
 
Posts: 3 | Joined: Sat Mar 15, 2008 8:05 pm

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