Chronic Pain Support Group
Physicians and professionalsdefine pain as chronic if it lasts longer than three to six months and is persistent. It's distinct from acute pain that is a direct result of injury or trauma. This support group is dedicated to those suffering from chronic pain. Discuss treatments that have worked for you, find advice for your specific experience, and find support. You're not...
s*es" to perimenopause. Could it per*aps be t*e morp*ine? I take Oxy IR for breakt*rou** pain.
The more I think of it, that has me taking more meds such as sudafed and motrin, and I have my muscle relaxants for my legs (diazepam) so I used to wonder if I was just taking too much medicine.
But what was the other possibility? If I don't take the sudafed, my face feels like it is being hit with a rock. If I don't take the diazepam, my RSD leg spasms will go nuts. I HATE taking so many different meds and am so glad the stone passed. Now maybe I'll get some sleep? Well, it IS a possibility. Not a good one, but still...
Oh boy, it feels like another of those nights.
Are you on antibiotics? I ask because antibiotics can *ive me t*e *ot face.
I started menopause at 35 when I was trying to get pregnant. I was on so many hormones and had PCOD, so cyst after cyst. I got pg thru IVF but miscarried, exactly a year after I buried my baby boy. Menopause at 35 was a nightmare for me. I'm married for a few years and suddenly have hot flashes, night sweats and no libido. And years later I'm still going through it!
But I do know that menopause IS different from these hot face flashes. They're calming down as my breakthrough morphine wears off. So that means I can take a breakthrough again in a half hour and get the face sweating/red face, or suffer from the pain and not sleep at all.
This is a difficult decision. I also wonder if the muscle relaxer might cause red face? My kidney stone was causing me to bend in an odd way as I lay in bed and it made my muscle spasms terrible. I'm due for another if needed, but i don't want to get the hot red face again. This is just weird. What do other people do when it's time for bed? Oh yeah, they sleep! ;) I SO wish I was normal again.
And Thalia i am another Michigander with the open window winter policy.....
And now I'm wondering, as you have also had this hot flashy thing with pain meds, if it's just that I've taken the max amount b/c of the kidney stone. I guess we'll see. I'm due for a breakthrough med but am wondering if I should skip it. I'm on that fine line with my foot where I might survive w/o it but might also be up all night w/o it.
Choices, choices.
I like the fresh air at night, though. It sometimes helps me sleep. But this MI weather lately...I don't know. I want more snow!
I am so sorry about your menopause experience. You *ave been t*rou** *ell. Your son's picture (*e's *or*eous) always makes me smile.
Well, I *uess t*e old morp*ine is t*e cause. Every symptom realized is always *elpful. I *ope you can *et some sleep.
Kinda OT but when he was an infant I took him in MARCH after a huge snowfall, all bundled up (both of us) and pulled him around our pool (which you couldn't see b/c the cover was covered in snow) and I took pictures. I stopped at one of our pine trees and posed the sled there, took a few steps back and bamm! I felt myself tripping/twisting on the stake that held the pool cover in place and the rope that attached.
I went down hard, right on the pool cover! I heard the pop, and felt intense pain in my ankle (not my RSD foot, thank God!) and knew something was wrong. But priorities first. I took a cute photo of my son under the tree in his sled and snowsuit, and then had to limp ALL the way around the pool, pulling the sled in the heaviest snowfall we'd had all year. I could barely walk but Motherhood gives you superpowers! To this day, my hubby doesn't get how I pulled our 10 month old all the way around the pool with a fractured ankle and RSD in my other foot.
I remember refusing the ER b/c I don't do them unless it really IS an emergency, and making an appt with my family doctor. He took 1 look and put his head in his hands, telling me I should prepare b/c RSD spreads and this was a huge possibility. I had fractured my ankle in a few places but got away with a splint/cast for a few days with crutches, then a permanent type cast thingy. (I don't know the medical terms.) They didn't put it the way they wanted to b/c they were scared of swelling and of RSD developing.
After all of that, I don't know that my son would appreciate a sled ride, LOL, but I still want him to enjoy the snow as I did as a kid. It makes my RSD worse and I swear, I can most often tell you when snow is coming! It sounds like I'm nuts but my RSD foot sweats and turns a grey color whilst my knee throbs. That is better than my hubby's Master's Degree in Meteorology!
Thanks for the sweet words about my son- I have to agree, he's cute. I can say that b/c he's adopted and I had nothing to do with his genes. He and I have Playgroup tomorrow so now that my questions about the hot face are done, I can either take another pill soon (actually both are due at same time) and possibly get a few hours of sleep, or I can just choose to stay awake. I have to get up by 9:30am and it is already 12:35am. It'll take at least 2 hours to fall asleep and my son could wake at anytime as he went to bed early tonight. Again, decisions, decisions.
Oh well, at least I passed the stone. That's huge. I couldn't do a darned thing if I still had that.
Thanks all for the input, and hoping you're all getting some sleep, and that maybe I do too. ;)
I am just the opposite; if anything I am cold all the time but don't keep my heat set very high either to keep the cost down as I can always bundle up but even in the summer, I'm cold in my house; not warm.
I have had RSD for almost 13yrs now & RA for about 5yrs. My hands stay ice cold & the R side of my body is cold too.
When I have my temp taken at the doc office, it's usually lower than average; about 95.4
If my temp does get up to normal, I feel like I have a low grade fever.
RSD does weird things to us all & no 2 are alike is what I've found & I do believe meds play a role as they affect us all differently too.
Rhonda, IN