Husband told me he’d read this thought may be of interest. I get them most nights 😏never made the connection .
Definitely worth adding to your list of symptoms if you have night or daymares . Take care x
Husband told me he’d read this thought may be of interest. I get them most nights 😏never made the connection .
Definitely worth adding to your list of symptoms if you have night or daymares . Take care x
Morning Tiggywoos
A very interesting article. Thank you for posting it.
I have nightmares and strange dreams which don't make any sense so found this article very interesting.
I've had lupus sle for 4 years and am still finding things out. Every day is a challenge.
I don't think I normally remember my dreams, but when I do it's usually because they're bad (I've been taking melatonin for a few years, so not sure if that has any impact). I'm not convinced that outside of the top specialists in autoimmune diseases and people doing these research papers that the neuropsychiatric symptoms are understood or taken very seriously, unfortunately. I don't know whether the constraints of the NHS and lack of funding mean they limit the range of symptoms they look at or if it's just generally not that well understood yet.
I had a dream last night where I was shot in the head, but I did have a *very* stressful day yesterday. I hope it's not a sign that things are about to get worse!
This is very interesting Tiggy 🤗I'm glad to know I'm not alone. Nightmares is one of the first signs that I'm gonna flare. Please thank Mr Tiggywoos for bringing it to our attention🙏Three cheers for Melanie hip hip....👏👏👏 💜🌈🦋Xx
It's a fascinating study - I too had never connected the screaming night terrors with lupus, but now I have started thinking about it . . .
Wow!!