posted
That's reassuring. Thanks for the responses.
My CD57 at my last LLMD visit a couple of weeks ago was a 57, so I'm definitely in full-on Lyme relapse mode.
Is it weird that transient muscle pain actually makes me happy? Dizziness, vertigo, headaches, brain fog, leg and hand weakness - all my neuro symptoms just freak me out. No matter how many years and positive Lyme tests and symptoms and signs I get between me and my erroneous MS diagnosis, I carry the trauma of it around with me where ever I go. Muscle and joint pain just seem "so Lyme" that they are a welcome diversion from the neuro-stuff, which is the bulk of the BS I deal with.
Somewhere on this forum someone posted "Never believe you have something that cannot be cured." I tell myself that everyday.
Posts: 8 | From Wisconsin | Registered: Oct 2011
| IP: Logged |
Catgirl
Frequent Contributor (5K+ posts)
Member # 31149
posted
It's so hard to tell. Sounds like herxing, but I was on meds for babs and slid backwards after 2 mos. I think the meds brought out bart and company. I know they helped with babs though.
Doc put me on different meds and I feel better (for bart/myco).
-------------------- --Keep an open mind about everything. Also, remember to visit ACTIVISM (we can change things together). Posts: 5418 | From earth | Registered: Mar 2011
| 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/