My LLMD advised me to see a neurologist also. Has anyone done this and had any luck. I suffer from intense back and rib/chest pain. Western Blot was positive. I'm on Lyrica and narcotic pain meds now. What another alternative to the narcotics and I'm not even sure the Lyrica is helping. Need all the input I can use. Thank You. Suffering in Connecticut. Sal
Posted by Allie (Member # 10778) on :
Do I have the best LLMD neurologist for you? Yes I do!!! And he's in CT. I owe him and my LLMD EVERYTHING! I'll pm you his name and number.
Allie
Posted by Lymetoo (Member # 743) on :
Not just "any" neuro will do. Take Allie up on her offer!!!!
Posted by tdtid (Member # 10276) on :
Very true, Lymetoo. Too many Neurologists totally dismiss Lyme to be a cause for so many of our neurological symptoms. If Allie knows one that is lyme friendly, I'd definitely take her up on that offer.
Good luck!
Cathy
Posted by Aniek (Member # 5374) on :
If you are looking for pain relief, I'd suggest finding a physiatrist rather than a neurologist. Physiatrist are a type of doctor who usually are pain specialists. They look at the body in its entirety and often combine physical modalities, like physical therapy and myofascial release, along with medications.
However, sometimes it is important to see a neurologist to rule out other disorders or to make sure there is not degeneration or other neurological injury occurring. My LLMD had me see a neurologist when my muscle tics increased to make sure there wasn't something besides the Lyme going on.
Posted by canbravelyme (Member # 9785) on :
Allie,
Can you describe further your experience with this Neurologist? I'm looking for one as well.