Yes, it is totally permissible to post the names of medications or supplements that people are taking. The only thing that we don't allow on this forum is direct outside links to other places on the internet. But if you ever want to direct people to something on the internet, you can do so by telling people how to search for it, such as: "Search for XXX on YouTube" or "Search for Pain Study at Harvard Med", or something of the kind.I can totally relate.....and it's a really awful that you wake up in the night covered in sweat. My thoughts are perimenopause, or a medication, or a combination of meds. Even some supplements can cause hotflashes/night sweats. My physician gave me a very low dose of a blood pressure medication and it was fantastic. I now have substantially fewer night sweats and hot flashes and they are less intense. Not sure if I'm allowed to post the name but it's clonidine and this is considered an 'off label' use.
You might want to review any medication that you are taking, because sometimes meds will cause this. And even if you have been taking them for a while, it's still good to take a look at their side effects and/or talk with your doctor about it because as time goes by our bodies can change and our reactions to medications can also change.Yes me too !! Been having a flare up since 22.02.25 . New symptoms to me are night sweats,nausea,loss of balance, no appetite ?
Can't keep awake during the day ?
I got sick of my H saying I don’t look like I am in pain .I have a slightly different feeling about that. While at times it feels ironic to me when someone says I look fine, and it is most definitely annoying if I tell someone I am in a lot of pain and they say, with a dismissive attitude, "but you don't LOOK sick!", most of the time if I leave my house I try very hard not to look as if anything is wrong with me.
Sorry if the images upset youGod @Harpy that actually made me cry. Its so true, how we present ourselves to others as how we really are.
I have been struggling with personal hygiene as well , without to much info , the D.I.S.H in my thoracic spine makes it impossible for me to twist and make it extremely painful for me to wipe,Great timing, I have just got off the phone to adult social care services, after a pain clinic referred me as they were shocked at, not so much what I can do, but the things I just cant do - even some basic self care to a point. I am struggling a bit with the 'obvious signs' of how bad my health has deteriorated.