posted
Is it possibke to get a sense of what percentage of Lyme sufferers were initially diagnosed with Depression/Anxiety and/or Chronic Fatigue Syndrome?
Thanks in advance.
[ 07. December 2007, 02:22 PM: Message edited by: BunkerHill ]
Posts: 21 | From Upstate New York | Registered: Oct 2007
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Geneal
Frequent Contributor (5K+ posts)
Member # 10375
posted
My initial diagnosis (after refusing to test me for Lyme)
Was Post Traumatic Stress Disorder.
Then came the Generalized Anxiety disorder.
Count me in.
Hugs,
Geneal
Posts: 6250 | From Louisiana | Registered: Oct 2006
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joalo
Frequent Contributor (1K+ posts)
Member # 12752
posted
Count me in. I was misdiagnosed with CFS for 21 years.
-------------------- Sick since January 1985. Misdiagnosed for 20 years. Tested CDC positive October 2005. Treating since April 2006. Posts: 3228 | From Somewhere west of the Mississippi | Registered: Aug 2007
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heiwalove
Frequent Contributor (1K+ posts)
Member # 6467
posted
That's exactly what my doctor thought it was, today I had a neurologist appointment and he wants to do MRIs of my spine and a lumbar puncture. 2 Negative ELISA tests, but now the neurologist wants to do a WB just in case.... I feel so bad, with tingling hands and feet from the knee down, fogginess, headaches, no fever however. I don't have a diagnosis of why I feel this way, so I'm kinda hoping it's LD, even if treatment will be difficult.
Posts: 25 | From US | Registered: Nov 2007
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