Hi everyone, hoping some of you can help me out here.
I was wondering where I can get or find research on the link between Lyme and MS?
I’m working with two dr’s who are VERY open and willing to listen about the potential links to other illnesses and lyme.
The two dr’s have quite a lot of influence and I would love to get them “on board” with this lyme cause but need some good info to knock their socks off.
Can anyone here help me or send me any info they have with regards to the Lyme /MS connections or even just to share your stories if you were dx with MS and Lyme
You can email me if you wish