posted
hey everyone, I came to this support group before on a different screen name, i couldn't remember mine for crap.. CRS syndrome. Well, im 21 now and all of a sudden i got bursitis in my hip.. now i didnt think anything of it until my chriopractor said something to me about it possibly being my lyme again. basically a lightbulb appeared. So anyway, i've been off IV treatment for almost a year now. i went to my GP today and hes testing me.. if im positive i go back to my lyme doc. Im not happy. I find myself with a short temper again, and its getting worse, i don't really want to talk to my boyfriend on the phone cause he can tell when im not happy and im getting ****ed off at the dumbest things. I'm sure this has happened to others before. I just think i need not talk to anyone right now until i get myself back on treatment. This is so hard for me cause i was thinking it was gone. Just need some support.
korinne
-------------------- Koryn Posts: 13 | From Pocono's, PA | Registered: Jan 2007
| IP: Logged |
-------------------- --Lymetutu-- Opinions, not medical advice! Posts: 96239 | From Texas | Registered: Feb 2001
| IP: Logged |
clairenotes
Frequent Contributor (1K+ posts)
Member # 10392
posted
That must be very dissappointing to have to face the possibility of more LD treatment.
At least you have some experience to draw from, as well as this support group. I have learned a lot since I have been participating here.
Take care,
Claire Posts: 1111 | From Colorado | Registered: Oct 2006
| IP: Logged |
5dana8
Frequent Contributor (1K+ posts)
Member # 7935
posted
Hi (((( Koryn))))
Just wanted to say hang in there
When you hurting & feeling frustrated it is difficult to see any hope or light at the end of the tunnel, but you will get better & it will be gone again. Here's some more hugs Good people here so stay in touch. They really help me alot!! take care Dana
-------------------- 5dana8 Posts: 4432 | From some where over the rainbow | Registered: Sep 2005
| IP: Logged |
trueblue
Frequent Contributor (1K+ posts)
Member # 7348
posted
Hey Kori! Is that you? I've been thinking about you and wondering how you were. Good to see you, sorry you're here. If you know what I mean.
I hope you're back on and have this taken care of soon. trueblue
Could you have been Korinne21 before?
-------------------- more light, more love more truth and more innovation Posts: 3783 | From somewhere other than here | Registered: May 2005
| IP: Logged |
quote: Well, im 21 now and all of a sudden i got bursitis in my hip..
Hummmmm 21 and bursitis? Suspicious. CRS? Sounds like me! But I call it my lyme brain.
Please go back to your lyme doc. Positive or negitive tests..... 'cause it sure sounds like lyme.
Posts: 258 | From Washington State | Registered: Nov 2005
| IP: Logged |
-------------------- Koryn Posts: 13 | From Pocono's, PA | Registered: Jan 2007
| IP: Logged |
Michelle M
Frequent Contributor (1K+ posts)
Member # 7200
posted
Get OUTTA here! Hey Kori!!! I remember you! I also remember you NOT getting enough treatment, and after you stopped your IV your doc recommended NO orals.
I also remember you charging back to work, prolly long before you shoulda!
Anway - what others said: Don't wait for a test to be positive. Just get treated. Find an LLMD. Other docs will say "post lyme syndrome" - RIGHT.
Anyway, welcome back!
Michelle
Posts: 3193 | From Northern California | Registered: Apr 2005
| IP: Logged |
posted
hey michelle.. yep your right, doc didnt follow me up with orals at all. Yep im back to work now after getting outa drug rehab, i also wonder if drug dependency has anything to do with lyme. Considering the fact that i have real bad anxiety from lyme.. hmmm.
-------------------- Koryn Posts: 13 | From Pocono's, PA | Registered: Jan 2007
| IP: Logged |
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,
NJ08534USA http://www.lymenet.org/