Hi madisongrrl. Glad to see you had some improvement, although we all know it is a long road.
Do you pay all your IV antibiotics yourself? No insurance will cover it?
I too think I need to see a Lyme literate doctor here in France. There seems to have less than in the US.
In my case, as I was treated 2 times with antibiotics (3 weeks amox, 3 weeks doxy) early after my infection, I really don't know if I have persistent infection. I think that the infection triggered the auto immune reaction, and so I think I would benefit fro IVIG. But it seems like it is hard to get.

I hate feeling that I have to wait to worsen to have a better treatment.

It is very great to see that some people have healed. I had no clue about HBOT and had to search. Looks like an interesting alternative treatment, but I have no idea how I could have access to that ! Do you plan to try?
Wishing you the best