Michigan cfs Dr taking insurance?

[Lipac]

I'm in MI, having to live with relatives, after exhausting my money on West Coast private Drs. The climate was good but I'm out of money. I practiced medicine, so I'm easily frustrated by Drs who've not educated themselves, and just don't care.. The local Drs are a throwback to 18 years ago when I was " chastised" by multiple Drs for wanting to live this way. My nerves can't take this again.. A GOOD primary care Dr is all I can afford. If I could get to a West or east coast clinic, I wouldn't be in MI.
ANY IDEAS?
I'm in West Central Michigan, ( Grand Rapids closest)

 

[Eve18]

There is NO even single one CFS doctor in Michigan. I believe that there are some good primary doctors but hard to find. I have one but she is clueless about CFS and she admits it and she asked me to find a CFS specialist. Just don't try Born Clinic at Grand Rapids!

 

[*GG*]

A task for someone who has the time and energy, seems like with a Population of about 10 Million in Michigan, some resources could be put together for people to find a DR. A database that would share the info?

For reference of something similar.

https://www.masscfids.org/provider-recommendation-form

GG