Hi Everyone:
I am new to this forum and have been recently diagnosed with Lyme with a co-infection of enchriolos (sp?). I've been through a long road to finally get my dx though. I've been to UCSF for the last year thinking I had MS. The doctors found 20 lesions on my brain but not typical of MS and ALL other tests were negative. Interesting though, after my UCSF MS doc looked at my brain MRI first thing he asked was "have you had lyme disease".
Anyway, fast forward to now, I finally have my dx and am on antibiotics. After just 4 doses of my meds, I was unloading groceries and suddenly became very weak, felt like I was going to pass out, starting sweating like crazy (I'm usually cold...and not sweaty) and my hands were shaking so bad I thought I wasn't going to be able to drive myself home. I was very fatigued the rest of the day and had to take a two hour nap and then woke up feeling a little better.
Then, seven days later, I had another spell of really bad fatigue and my symptoms were going nuts (my symptoms are vibrating in my left leg mostly, foot issues, slight tremor in right hand). Anyway, is it normal to get herxes seven days apart? I'm just not sure if it was a herx or not.
By the way, my symptoms started shortly after gallbladder surgery I had on 11/19/10. My doctor said that most likely my immune system was keeping it "in check" but with the trauma/stress of the surgery, the lyme was activated. My symptoms have been SUPER BAD ANXIETY, twitching everywhere, vibrating feeling in left leg, foot pain that comes and goes, numbness/tingling under left eye (went away after about a month), numbness in arch of left foot that was with me for about two months, top of big toe on left foot goes numb off and on...to this day, and my neck is constantly stiff and hurts and creaks. I have more symptoms, but that's all I can think of now.
Anyway, thanks for listening and any input on these herx's would be appreciated. I have another appt with my LLMD in March and will find out the results of the rest of my bloodwork (hoping I don't have additional co-infections). I had a brain spect image scan done a week ago and I'll get the results of that too.
As far as cognitive issues, I really have noticed any problems with that fortunately.
Carrie (Northern California)