This is topic Moved from CA to MN..Need new Dr in area in forum Seeking a Doctor at LymeNet Flash.


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Posted by electric (Member # 6572) on :
 
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!
 
Posted by Bartenderbonnie (Member # 49177) on :
 
Welcome back electric

You can contact the Minnesoda Lyme Association for LLMD referrals here;
https://mnlyme.org/contact-us/

You can contact Global Lyme Alliance for LLMD referrals here;
https://globallymealliance.org/education-awareness/find-medical-professional/

I will send you a pm.
 
Posted by hopingandpraying (Member # 9256) on :
 
PM sent for MN.

Check the MN Lyme Support Groups - maybe they can help. They would know better about MN.

http://whatislyme.com/lyme-in-minnesota/

http://mnlyme.com

http://www.lymenet.org/SupportGroups/UnitedStates/Minnesota/
 


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