LymeNet Home LymeNet Home Page LymeNet Flash Discussion LymeNet Support Group Database LymeNet Literature Library LymeNet Legal Resources LymeNet Medical & Scientific Abstract Database LymeNet Newsletter Home Page LymeNet Recommended Books LymeNet Tick Pictures Search The LymeNet Site LymeNet Links LymeNet Frequently Asked Questions About The Lyme Disease Network LymeNet Menu

LymeNet on Facebook

LymeNet on Twitter




The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

LymeNet Flash Discussion
Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive


The Lyme Disease Network is a non-profit organization funded by individual donations.

LymeNet Flash Post New Topic  New Poll  Post A Reply
my profile | directory login | register | search | faq | forum home

  next oldest topic   next newest topic
» LymeNet Flash » Questions and Discussion » Medical Questions » Where can I get tested?

 - UBBFriend: Email this page to someone!    
Author Topic: Where can I get tested?
Jeni MF
Junior Member
Member # 38477

Icon 5 posted      Profile for Jeni MF     Send New Private Message       Edit/Delete Post   Reply With Quote 
To start with, I have a family that doesn't believe in going to doctors. You'll see why this is a problem.

When I was a child, I would go to summer camp in Southern Illinois. One year, I came back with a tick embedded in my shoulder. My dad removed it but didn't think anything of it (this would be in the late 80's) In 1988, I had an attack of Bell's Palsy, one whole side of my face quit working! I was taken to my doctor but I don't recall any treatment. It went away on its own, but to this day (I'm 37) my face still is uneven a touch and I get muscle twitches around my eyes when I'm tired or stressed.
I also remember a time I had a very strange outbreak of fluid filled lesions on my legs (again, no doctor and they went away) In my high school years, I struggled with depression and fatigue, many many ear infections and headaches that lasted forever. One particular one lasted over a month, my doctor suspected the flu (?!) and prescribed antibiotics and lo, it went away. In the past 5 years, I've developed psoriasis. At least, I think it's psoriasis, it responds to treatments for it (no insurance - can't afford a dermatologist) Emotionally, I'm very anxious and depressed, prone to outbursts of intense anger. From 8th grade through high school, I became very overweight and remained so and it's very difficult to lose weight even with diet and exercise. I constantly get a stiff back and neck, I have very poor sleeping habits.

I stumbled on the symptoms of lyme disease and I started to wonder. I perused some of the threads of late-diagnosed people and I started to worry. I want to get tested but I have a huge problem. I have no insurance. I live just outside Chicago. Are there any places or resources you could suggest to help me out?

Posts: 1 | From Chicago, IL | Registered: Aug 2012  |  IP: Logged | Report this post to a Moderator
sixgoofykids
Moderator
Member # 11141

Icon 1 posted      Profile for sixgoofykids   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Most Lyme doctors aren't covered by insurance anyway and the lab they use for tested generally isn't either.

What kind of treatment are you thinking about? Will you pay for a Lyme doctor out of pocket? And the meds?

If you're going to go a self-treat, herbal route, why bother with testing? Maybe just try some herbs and see if they make you feel better.

--------------------
sixgoofykids.blogspot.com

Posts: 13449 | From Ohio | Registered: Feb 2007  |  IP: Logged | Report this post to a Moderator
   

Quick Reply
Message:

HTML is not enabled.
UBB Code� is enabled.

Instant Graemlins
   


Post New Topic  New Poll  Post A Reply Close Topic   Feature Topic   Move Topic   Delete Topic next oldest topic   next newest topic
 - Printer-friendly view of this topic
Hop To:


Contact Us | LymeNet home page | Privacy Statement

Powered by UBB.classic™ 6.7.3


The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:

The Lyme Disease Network of New Jersey
907 Pebble Creek Court, Pennington, NJ 08534 USA


| Flash Discussion | Support Groups | On-Line Library
Legal Resources | Medical Abstracts | Newsletter | Books
Pictures | Site Search | Links | Help/Questions
About LymeNet | Contact Us

© 1993-2020 The Lyme Disease Network of New Jersey, Inc.
All Rights Reserved.
Use of the LymeNet Site is subject to Terms and Conditions.