I have Lupus, and I'm newly diagnosed, as well. My first trip as a Lupie was June 2008. I was also there for a quick trip for Labor Day weekend and just two weeks ago for a
very last minute one night trip. I had to do things a bit differently than previous trips, but still had a great time. I am sun sensitive, and get fatigued easily as well, especially in the heat. In addition, as part of my treatment, I am on blood thinners, and therefore it is recommended that I not spend too much time in the heat.
For me, an
ECV really makes my life easier, it helps me not to get fatigued so quickly, and helps with my joint pain and leg pain (I have post-thrombotic syndrome due to a DVT... the DVT was the catalyst that helped the docs discover the Lupus). I wear hats, SPF 80 sunblock (Neutrogena makes some and it's about $10 for a small tube, but soooo worth it for sun-sensitive folks), and I carry a Misty Mate and a fan. All of those things help keep me cool, keep fatigue at bay, and help me deal with sun sensitivity (FYI - the sun also gives me a rash, but also makes my joints hurt and brings on fatigue like nobody's business!).
Another way to deal with it is to leave for the parks later in the day. So, I may hang out around my resort, sleep in (that fatigue again), etc. Then I head out for the parks around 1pm or 2pm. That way, I'm spending less time out during the periods when the sun is most intense. I've looked into sun-protective clothing, but honestly (for me) it is quite expensive, and also the idea of wearing long sleeves in the heat makes me hot just thinking about it!
Anyway, feel free to PM me if you like. Happy travels!
