The Faces Of Lyme

These Stories are REAL people
with Lyme disease & coinfections

LEARN  -  SHARE  -  GROW

"Together We Grow Stronger"


For the non-lyme literate: Common Lyme abbreviations: abx=antibiotics  dx=diagnosed/diagnosis

SOUTH DAKOTA

Kathy Rick -
I woke up on April 16, 1986 with what I thought was the worst flu I'd ever had.  I went to the emergency room and was told I had the flu.  When I didn't get better I went from doctor to doctor and was told I had everything from the flu, to viral meningitis, to post viral syndrome. I was only 26 years old, married, with three small kids. Before getting sick I was very healthy and active.  I did have a bulls-eye rash that appeared two weeks after getting sick.  I went to the Mayo Clinic six months after being sick and they did a Lyme test which came back negative. I was bed-ridden the first two years and in a wheelchair for the last 19 years. In 1988 I was diagnosed with Chronic Fatigue Syndrome.  I have been on Social Security Disability since 1988. This has affect my whole family.  My kids do not remember me any other way then being really sick. I feel like I've been a burden to my husband. No one should have to go through this!!  I have been so sick, and lost such a huge part of my life. I had a IGeneX Western IGG, and IGM for lyme in the spring of 2005.  They came back very positive. I went to so many doctor's who could not or would not help me. I've been treated for Lyme for the last 2 years with some improvement.  My goal is to be able to get out of my wheelchair.

* * * * * * * *

In the interest of making the stories palatable for everyone, please spell-check your submissions, and substitute a word like "antibiotic(s)" or abx for drug names. This site is foremost about telling the story of our disease and problems with diagnosis, treatment, etc. Please refrain from listing every drug and/or dosage you have been on. We have all been through a unique experience and that is the focus of this page. Thanks for your understanding and cooperation.
NOTE: If you ask for help when writing, please provide your email address so that we can respond!

MAKE YOUR VOICE COUNT

Please limit to approximately 500 words or less. E-mail us if your story is longer & I will happily edit it for you.

© Copyright 2006 by Lyme League of America, All Rights Reserved.

Contact Us  |  Home  |  Find your Representative  | 
ILADS web site | Sewill (SE WI/IL Lyme Site)