Hi KathyP!!
Welcome to our spot!! The next test you were speaking of is likely the CD57. Lots of LLMD's use this test. There is a good article written by a well known Nurse-Practitioner that treats Lyme, Ginger Savely titled, "Everything You Ever Wanted to Know about
CD57". Here is a link:
www.researchednutritionals.com/information.cfm?id=200 Basically researchers don't know for certain why, but the CD57 count is suppressed in some who have chronic Lyme disease, but not all. Chronic Lyme is the only thing that has been found so far that can suppress the CD57, and researchers have found that with treatment, the count will rise. It's just another 'tool' for a LLMD to use to help determine where you are in the disease.
Please do watch for a bull's eye rash, or any other rash - both at the site and elsewhere on your body. A bull's eye rash all by itself is diagnostic of Lyme. If you find any kind of rash though, please take a picture of it - be sure to put something like a coin in the picture as well so that whoever looks at it will get an idea of the size of the rash.
You can also start a symptoms list. If you have read through our "New to Lyme?...Start here!" thread, you will have seen a Master symptom list to help you get started. If you haven't yet read through that thread, I would highly encourage you to do so, as it's packed full of really good info and links!!
We also have a really great search function here that you can use to help you find threads of interest. Please do be aware of 2 things though - 1)This is a large forum, so to narrow your search down when using the search function, it's best to always include the word Lyme so that you don't get posts from the Depression forum or the Fibro forum.
2) You may very well bring up old posts from days, months, or even years ago - please be aware while these threads may be useful for you to read, the posters may or may not still be with us.
Hang in there! You are not alone in this! You just inherited a larger family!! LOL!!