Seasonal associations?

Has anyone been able to link a fluctuation in their symptoms based on the weather, namely, how hot or cold it is outdoors?

I'm working on a theory that while I dislike the hot months here in NC, apparently the heat likes me. My symptoms decrease a good bit!

I haven't heard about that type of sauna before. Interesting.

I'm worse in the heat, it just really sinks me, in part because I don't sweat much. I'm worse in the dead of winter and best in late spring, summer and the first part of fall. I know of someone who was in a long battle with Lyme and just couldn't get past a certain point in her healing. She decided to move back to CA since she felt better whenever she went to visit there and she improved a lot.

My daughter is worse in the winter and better in the spring, summer and early fall. She's impacted by light a lot. She will perk up in the winter if it snows, because it brightens up our typical rainy winter. She can't use a light box, because it's too bright for her, so I need to get her a full spectrum lamp to see if that helps her. She likes the heat in summer and has less pain when its sunny and warm.

The longer I'm infected, the worse I can tolerate heat (I could very well tolerate high temperatures when I was younger). But heat is better than cold damp weather, cause that makes my joints hurt more...
And like GardenPeace's daughter I'm experiencing more problems because of the bright spring/summer weather: more migraine auras, and more bothered by blurry vision and floaters, just overwhelmed by the brightness.