posted
Hi all, I recently from San Francisco to Minneapolis. I need to build a new health support network here in the Twin Cities for chronic tick related complications. Flying back out to San Francisco to see providers is too costly and also logistically messy with COVID.
To deal with lyme related issues I usually have navigated by trying to find supportive Doctors I can see within my network provider for standard care and pay cash or use out-of-network benefits for visits at lyme clinics. (usually end up totally out of pocket)
I am looking for recommendations of excellent Dr's and offices in Twin Cities areas both lyme literate and conventional that may be helpful to have in the rolodex. I can use ILADS website as start point but always best to hear from people first hand as to their experience. I am a little shocked to see how MN has not been very receptive to Drs treating lyme patients with abx therapies.
Also, I can choose new insurance provider so I wish to hear experiences getting coverage with the big 3 providers here in MN.
Please PM me with any information you may be willing to share. Thank you so much!
Posts: 65 | From minneapolis, san francisco | Registered: Nov 2004
| IP: Logged |
Bartenderbonnie
Frequent Contributor (1K+ posts)
Member # 49177
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/