Just wanted to know of your experience. Also about the PA.
Posted by 365SunnyDays (Member # 29969) on :
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Posted by Robin123 (Member # 9197) on :
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.
Posted by nspiker (Member # 22824) on :
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.
Posted by Haley (Member # 22008) on :
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.