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...
Speaking of...your profile is set to private and, therefore; I am unable to view your photo.
Thanks for the share though...I think it helps others really understand illnesses and issues that they are not personally familiar with when they can see what the other is talking about.
HUGS to you
Thanks for sharing as I am sure for those who dont know like me it helps understand what you are going through.
Thanks Manny. I think for some people it's different, but when I get a BAD flare, it is all about the TOP of my foot being colored and/or sweaty. It's not that the hell doesn't get bluish b/c it does and sometimes the entire foot! But when it starts, it starts on top, and is always darker there. The pain is also worse on top- it's a strange thing. I can walk on my foot and do so carefully, but have anyone touch the TOP of it and I freak out. And it makes buying shoes an even bigger pain.
But the icy/burning is worse now than it was when that photo was taken, and the coloring can go bad all the way up toward my knee. I always had & still have terrible muscle spasms there but the RSD pain going there, is, unfortunately, a fairly new event. :(
Maybe after almost 15 years as I approach the anniversary of the accident, the RSD has decided I've gone too long just having it in my foot.
Not oddly, that is where the last injury was the worst. I tripped over a dog kennel and a bookshelf fell on my foot, but went back to bed b/c we all have our priorities & mine was sleep for work. I awoke to see something similar to the photo but much worse as I'd done so much damage (but no broken bone THIS time.)
They were SO certain it was vascular damage and had a vascular surgeon in b/c of the way it looked. But then they couldn't figure it out as the damage cleared but the foot would LOOK fine 1 minute and oddly colored the next. Mottled IS a good word for it and I think it's in the RSD description.
Well, as long as we keep the MI winter mild as it has been, I might make it through w/o too much trouble, if I can find a handicapped parking sticker and if I just don't overdo it.
Anyway, THAT's my RSD flare-up, although lately they've been much worse and reach a lot further up the leg. I'm really hoping the knee isn't involved!
take care massive hugs xxx
I know when the Dr. Mentioned RSD in my medical records that I recently just got and was able to read was because of the red area over by my big toe. and spreading across my foot. That's at least what the records say. I know for me the burning gets so intense that Ice is the only thing to calm mine down and the Gabapentin makes it bearable the rest of the time.
Cathy
Cathy- that always makes me cringe- the idea of ICE on RSD! Proves how different we all are! That pic was from last year- today my RSD flare ups are more spacious, as in moving up the leg. I once saw an RSD patient with blue and purple splotches like a Walt Disney movie. Scary disease.
Hugs...