Chapelle,
It does seem like we're on a similar path. I've got a few months more of being sick, and you're a week ahead of me on treatment, but our symptoms sound similar. I've got the sharp pains too...especially in my finger joints which really is bad since all the jobs I'm qualified for require me to use my hands. I've also got some muscle twitching, some vision issues and the headaches and foggy feeling I mentioned in my earlier post. I have done better with the doxy when I eat enough, but I feel like I'm eating all the time which isn't very good for my weight loss goals, but I guess it's better than feeling nauseous all the time.
I am like you, I try to stay positive, but have bouts of anxiety and fear about
whether I'm on the right track with this. I had the option to choose between two lyme docs and am hoping that I made the correct choice. I mainly picked because the insurance I had with my last job was accepted by one and not the other. I feel pretty good about
my choice though. From what I understand she and her husband work as a team and they are more aggressive in their approach than the other doc. She is hopeful that we caught it early enough that we can beat it without long term treatment and without any other antibiotics. She mentioned co-infections at my last visit, but didn't really go into much since it was the first appt. I'm expecting her to talk more about
that this time. Do they usually test for them or just go by symptoms...or do you know?
Is there a book or something outlining the Lyme diet? I try to eat healthy, but I'm not sure if my version of healthy matches with what I should be eating.
I think we should keep in touch too. It would be good to have someone else to "talk" to who is on a similar path.
hang in there