I live with Lyme in CT and I know what your husband is going thru. Lyme is very very debilitating in mid-later stages. He needs to rest as much as possible along with light exercise, good diet and good sleep. You guys should watch the movie "under our skin". If you goto youtube.com and type in under our skin you will find a preview of the movie. I might even be able to shoot you over a DVD. I go thru the same things with my non LLMDs. The Elsa and the WB are NOT accurate tests and most Drs still do not even know it! That is what they are trained to use to diagnose lyme. In fact most lyme literate Dr's can and will diagnose based on overwhelming clinical symptoms alone after ruling out other causes. You need to find lyme literate Dr's. I think I can help you guys, I am going to include strong evidence that your Dr will have a hard time refuting. Be careful though, they are not usually too happy to get educated by a patient even if they are correct but in some cases that is what it is going to take. You need to be your own advocate and sometimes even your own Dr. Please feel free to get in touch with me if you would like more help, I will do whatever I can. My email is
[email protected] I have been in the battle for 6 years and counting. I have been researching this for quite some time and when I get 100% better I would like to goto medical school to be a Dr. I have seen too many good people being swept aside by the system and I am out on a mission to put a stop to it!!
Please watch this news clip on inaccurate testing.
http://www.youtube.com/watch?v=gTSXQfPI19c
Here are some good solid sources on how inaccurate lyme tests are and the great controversy. The first link is from the FDA, the second is from the Attorney General!!
http://www.fda.gov/medbull/summer99/lyme.html
http://www.ct.gov/AG/cwp/view.asp?a=2795&q=414284
http://general-medicine.jwatch.org/cgi/content/full/1989/1226/1