-------------------- We really know so little about the body and the microbiome. Posts: 261 | From Southern California | Registered: Jan 2011
| IP: Logged |
posted
You could also check in with your area support group, listed with Support Groups at the left of the screen - click on United States and then California.
Posts: 13128 | From San Francisco | Registered: May 2006
| IP: Logged |
posted
I see Dr. Y and her PA. She's Burrascano trained and an ILADS doctor who uses aggressive treatment. I've improved significantly, but still have a ways to go.
I actually see her PA more than the doctor, and like her because she is methodical, and stays with treatment. Dr. Y. switches up the protocol more. They work together, and everything is passed by Dr. Y.
Posts: 964 | From san diego | Registered: Oct 2009
| IP: Logged |
Haley
Frequent Contributor (1K+ posts)
Member # 22008
posted
I see Dr. Y but she is not my primary doctor.
She has been doing this for a long time and she knows what she is doing. Something that patients have mentioned is you leave with LOTS of information. That could be a good thing but can also be overwhelming for a Lyme brain.
They have everything digital now which organizes the information a bit better.
Posts: 2232 | From USA | Registered: Aug 2009
| 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/