posted
I know there is a link about why lyme docs need to charge a substantial amount and often do not accept insurance. can anyone locate that for me?thanks so much. I was misdiagnosed for 6 years, and returned to a forum of people with my prior diagnosis. I am explaining lyme to them as I suspect MANY have it and am being hit with much, expected, resistance. including the question of why lyme docs charge so much. I can answer them but I recall this link explains it much better than I ever could. they are also disputing existence of chronic lyme which enrages me. but, I don't want to jump back in defending chronic lyme without supplying an appropriate response. it's so hard to think of the words sometimes. if there's any links supporting chronic lyme that would be much appreciated as well. thanks
Posts: 138 | From Connecticut | Registered: Dec 2012
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You should read, "Cure Unknown", the book by Pamela Weintraub and view the DVD, "Under Our Skin", for free on www.hulu.com. Check to see if your local library carries them or you can buy the book used on Amazon.
Btw - please break up your posts into 2-3 sentence paragraphs, as there are people on Lymenet who cannot read large blocks of text due to neurological problems from Lyme. Thanks.
Posts: 8981 | From Illinois | Registered: May 2006
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poppy
Frequent Contributor (1K+ posts)
Member # 5355
posted
Other people have also tried to go back to forums for diseases that they had been misdiagnosed as having....mostly unsuccessfully. Minds are hard to change. But still worthwhile, if you have the energy.
Posts: 2888 | From USA | Registered: Mar 2004
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