I was only sat outside for a short time under a gazebo which was not in full sun yesterday. Today all my joints are aching. I know I have some uv sensitivity but it normally aches.
Has anyone with sjorgrens started having aches in... - LUPUS UK
Has anyone with sjorgrens started having aches in their joints in this nice weather?
Hi nikki , i have found that in the past that a change in the weather causes increased pain. Im sore and fatigued at the moment but im months over due rituximab as having surgery on disc soon . My wrists and hands are particularly sore.
Thank you for replying. I hope your surgery goes well and that the you feel better when you can get back on medication. I am not a lover of sitting in the sun as I get burnt easily. I think I am going to have to get some prescription sunglasses and a very big floppy hat. Take care x
I have Sjögren’s and just seem to be a generally much happier, healthier person during the summer months full stop. But I do have Raynauds, live in Scotland, put on Factor 50 first thing each day and don’t sit in direct sunlight or expose much flesh at all - long sleeves, leggings, prescription shades and a wide brimmed hat. My very fair skin is erratic but wind and cold seem to be the worst thing for mine. It would be different if I lived somewhere hot with air conditioning I’m guessing. I don’t think I’d tolerate real heat well now.
I love to see the sun shining as long as I'm not in it. I think it generally lifts everyone's mood. Going out in it is a different thing. I totally agree that the cold, wind etc are horrible and cause so many problems. As I said above I think I need prescription sunglasses and a large hat. Thanks for replying and please take care x
Good prescription sunglasses have changed my relationship with sunlight and also bright lighting for the better by far! 😎
Hi - change in weather always affected my joints, even before diagnosis. Staying indoors doesn’t help. It will happen again after the summer but it is usually only for a day or so. I love the warm weather and sunshine so I feel much better ! Sjogrens just keeps on giving doesn’t it !!
YES YES YES but I have to ask myself do I want to stay in forever? I went outside and did a bit like sprayed the car, covered in mud from winter. We live in rural Devon in the middle of farmland so mud is a way of life. Today I'm paying for it, but it was soooo worth it! I was outside The House!
So absolutely I'm right with you it does hurt, but for me mentally it was worth it.
But you most definitely have to pay for it. I'm sorry you have to go through it at all, be well 💕
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It's a shame we have to pay the price but it's all about priorities. Is it worth the price?
I lived in N Wales for 2 yrs when my husband and I first married. In Llithfaen Pwllheli on the side of a mountain just beautiful!
Enjoy your day whatever it may be doing. I'm paying for enjoying yesterday but it was so so worth it.
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Weather changes do bring my symptoms out! Cover up with cotton clothing, floppy Sun hat, wrap around sunglasses, oh, I look a sight! Also use factor 50 suncream on face and hands..
Yes! My joints aching badly, eyes blurred vision, throat itching, stinging, ankle itching, sunrash, but then again, I get horrible symptoms cold weather too! Lol
I have diagnosis Sjogrens/?lupus..oh, joy...