What resources are available to find an ME/CFS provider?

[Friend]

Where can I find a treating MECFS provider?

 

[SarahTee]

Facebook support groups can be good for local knowledge. And some support organisations keep a list of providers.

Which country do you live in?

 

[Friend]

Facebook support groups can be good for local knowledge. And some support organisations keep a list of providers.

Which country do you live in?

Hi Sarah,
I live in the USA, PA.

 

[tlh111]

Hi Friend,
Any luck with your search for physicians that treat ME in PA? I have been looking this past year in PA and basically have come up blank. Many searches have listed doctors that "have experience with ME/CFS", but I am having a great deal of trouble finding one with actual ME sufferers as patients.

 

[AnnaLamothe]

Where can I find a treating MECFS provider?

I have - after a 10 year duration of undiagnosed illness - been lucky to find and be under the care of an exceptional Infectious Disease Immunology in NY who diagnosed me with ME/CFS as well as reactivated EBV and HHV-6 as well as MCAS and treated me from a Bell's score of 20 to presently 80. He's very busy as one would imagine however is extremely proactive with regiments and readily available - I know the above posts are somewhat old however am happy to recommend as does offer telemedicine.