I am a nursing student in nebraska. Each student was diagnosed with a disease and had to research the disease and write an empathy paper. The following are a few questions?

1.When were you first diagnosed?
2.What were your signs and symptoms?
3.What types of diagnostic tests did they perform to diagnose you?
4.What types of medications and treatments have you tried for your disease?
5.Hows has this disease affected your life?
6.How have you learned to live with your disease?

IF their is any other information that would be helpful to me please write those too... IT IS GREATTLY APPRECIATED !!!!!!

list your question outline.

People might feel more comfortable being interviewed if they had more contact than via an anonymous internet connection. There are support groups in Iowa and Kansas that might be able to hook you up.

Just go to the support group link at the top left.

In the meantime, I'm sure you could learn a lot by browsing posts. One thing you'll find is that many have the illness for years before being diagnosed, and that treatment can be very difficult.

It is also a very politically controversial illness, so some may hesitate to answer your questions if they don't know who you are.

Try reading Camp A and Camp B.

Or watching California Senate Hearing on Lyme Disease
Scroll down to February 25, select Health and Human Services Committee, Lyme Disease. Scroll past the first ten minutes or so, it is blank. Amy Tan (author and patient), Ron Keith (Marin/Sonoma Vector Control and patient), Dr. Steven Harris LLMD, Dr. Raphael Stricker, LLMD, and others testify.

Good luck with your project.

Also printing off Treepatrol's NEWBIE LINKS.
Testing: read the WESTERN BLOT!
Good luck on your interviews.
Betty G., Iowa

WELCOME To LYMENET

Here's more goodys! A typical response to newcomers.

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Post for a LLMD in Seeking a Doctor. Ps remember I am not a Dr, just a fellow sufferer.
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Amy Tan's presentation will just about answer all your questions for your report.

I know you most likely need a one on one with someone but listen to what she has to say and then see if you can't work something out.

Although the presentation is in CA, the information is good anywhere and the stories are the same.

I don't think you will find such a wealth of information in one place.

I dont think she is saying she has Lyme.

I feel that emailing would be easier.

I think it is great that other nursing students can hear what lyme disease is all about. It will give them knowledge and empathy for their future patients.