This is a tough one. I referee soccer and am out in the sun for a few hours on Saturday mornings in Vegas. I try to be done by noon. I am not sure if I am sun sensitive or not. I went two years after diagnosis of lupus without covering up. I never had any pain, nausea, fatigue etc. from the sun exposure but I got a sunburn at the beach in Cali and three months later I was urinating every 2 hours and three months after that I was diagnosed with lupus nephritis. I dont know if there was a connection or not. But after that, I am like a vampire for the most part
. Not willing to take a chance.
What I do for the sun when I referee - I sunscreen first. Whole body. SPF 50. Then I wear a long sleeve shirt. The referee shirt I wear isnt SPF rated which is why I sunscreen first. Normally I wear Coolibar long sleeve SPF 50 shirts but they dont make a referee shirt. The Coolibar shirts are nice but honestly, they cook you.
I wear a big brimmed hat too. Looks silly but it is what it is. One of my hats has the neck protector thing that hangs down.
I wear long pants but not jeans. I wear runners "wind pants". They are comfortable without being too hot. But they are not SPF rated either which is why I sunscreen under them.
After that - it is about
being in the shade when I can be and drinking a lot of water. I also use one of those towel things that you can get wet and wrap around your neck. Not sure if you have seen them on TV or not. They really help keep me cool. You "snap" them to restart the cooling. I have about
five of them. Love them.
One of my issues is I am 6'7" (thus "Talldoode"). So they dont really make SPF clothing for me.
Finally, I know that after being in the sun for a few hours I may be tired. I think a lot of that is just heat exhaustion since I am not used to the heat anymore. So I dont plan anything for after my referee stint. I go home and rest if needed.
So that is what I do. Hope it helps. I wish there was a test for sun sensitivity. Not everyone with lupus is sun sensitive. But it would be nice if there was a way to know for sure if we were. I miss the sun. It sucks. That is what I hate the most about
lupus - it has taken everything I loved to do away from me. Golf, flying R/C helicopters and planes, playing in the pool with my kids, gardening, vacations at the beach. It simply isn't the same when you have to dress like a mummy to go in the sun.
Good luck and have a great time! We still have to live our lives as much as possible.
Cheers,
/Tall