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

MICHIGAN

Christy Banfant
- My husband was diagnosed with Lyme in Feb 2008. About 3-4 years ago his feet swelled up and turned purple. Doc gave him steroids and within a few weeks it went away. His hearing was bad, dry cough. In March and Feb. of 2007 he experienced a few days of burry vision it would come and go. Eye doctor and PCP could not find anything. In July 2007 it never left. He is off balance, he has nystagmus (jerky eyes) and foggy head. He said it feels like his head is full of water. His LLMD did a clinical diagnosis based on his symptoms. My husband is a big hunter and works outside. He is now on Malarone, Zithromax and one other antibiotic. He has some good days but for the most part we know this will be a long road.

* * * * * * * *

Tammie Hayley - I have been experiencing strange symptoms for years such as my body locking getting lost emotional breakdowns which I thought or I was told I was bipolar until about five years ago I was diagnosed with endometriosis after five laparoscopys I was told the only thing that would help was a hysterectomy after that next year I started having stabbing burning pains in my lower back I went to a orthopedic surgeon he thought I was crazy and sent me to a psychologist after three different orthopedic surgeons I had cortisone injections had a bladder suspension numerous trips to the ER exhaustion confusion then neurologic symptoms like ms went to a neurologist and was told i had fibromyalgia went online to look it up and came across Lyme disease decided to get tested and came back positive in horrific pain in my back numbness anything you can think of I've had it so now after years of symptoms I am going to a LLMD and I start a picc line this week.

* * * * * * * *

Susan King - Lyme took over my life in 6 months. It began one winter morning with a sore throat that never left. I went to 9 doctors and 7 dentists because my mouth symptoms increased. Sore tongue, sore teeth, even after extractions, sore gums, burning TMJ, neck creaks and cracks and I couldn't turn my head. I had 2 negative Western Blots at the local hospital. Since they were both negative no one would treat me when I said I thought I might have Lyme. It began one winter morning in early December, 2005. One Sunday night, at the end of deer hunting season I flew on a plane with a group of deer hunters who had been in Northern Wisconsin. They were still in their hunting clothes and were filthy. The next morning I woke up with a large bite on my hand - thought it was a spider bite. I got sick one month later. I ended up having a very positive Western Blot test through IGeneX in May. After 2-1/2 months of antibiotics - according to my wonderful LLMD (Lyme Literate Medical Doctor) the infection is under control. Good news - right! Problem is now I still have lots of pain in my TMJ, neck, back, legs, hands - basically all over. Looks like I may have post Lyme fibromyalgia. I am exhausted all the time and barely am able to work. If I had been given 4-6 weeks of antibiotics in January - like I asked for - this would never have progressed like it did. The medical community needs to WAKE UP!!! People are suffering out there and need to be heard!!!! As far as catching it on an airplane - guess I was in the wrong place at the wrong time!! Talk about bad luck...

* * * * * * * *

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)