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 Jennifer Munn Islip Terrace, NY
In 1996 I was unable to function. Doctors tested me for things and decided that I had Chronic Fatigue Syndrome. Doctors were dismissive and annoyed by me asking for help to live my life. I became totally disabled in 1997. In January 2001, I was finally correctly diagnosed with Lyme Disease and several co-infections. The testing is poor although I had had a positive test back in 1996 which was ignored because I didn't have "swollen joints." (I now do get swollen joints at times.) My disease is severe and disabling and now I will be treated aggressively for years to get better. I will be lucky if I am ever well. No one understands how a 27 year old woman can be so ill and how doctors can be so clueless. I've found that I'm not alone suffering with Chronic Lyme Disease.
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YOUR STORIES
Karin M. Amour, Fibromyalgia
Lyssa Bode, Chronic Fatigue Immune Disfunction Syndrome
Frankie Campling, Chronic Fatigue Syndrome
Laura Cerasuolo, Fibromyalgia/Myofacialsyndrome
Karen Cerio, Fibromyalgia
Rhonda Dewinter, Various Immune Diseases
Jennifer Embree, Fibromyalgia/Raynaud's Syndrome
Lynne Enman, Turner Syndrome/Various
Fibromyalgia Patient, Covington, KY
John Kennedy, Chronic Fatigue Immune Disfunction Syndrome
Susan Larick, Fibromyalgia
Melissa Lawler, Fibromyalgia
Irene Leeder, Fibromyalgia/Various
Cait Lommel, Pseudotumor Cerebri
Jennifer Munn, Chronic Lyme Disease
Robin Poole, Fibromyalgia/Lupus
Pam Schmidt, Phenylketonuria
Lynn Tonoli, Various
Various Patient, Haughton, LA
Suzanne Witt, Muscular Dystrophy/Fibromyalgia
ARCHIVED STORIES
WHAT WOULD YOU DO?
Jose Pedro Greer, Physician
W.F. Nagle, Physician
Ronda Riebman, Exercise
Cathleen Schilling, Case Manager
Jim Sykes
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