Profil de MARCIA CARSONMARCIA'S SPACEPhotosBlogListesPlus ![]() | Aide |
|
17 novembre DESCRIPTION OF A FIBRO FLAREDESCRIPTION OF A FIBRO FLARE
Below you will find one of the best descriptions of a Fibromyalgia Flare that I've ever come across. This was written by a fellow Fibro sufferer, Caroline White, who belongs to one of my Yahoo Groups. http://health.groups.yahoo.com/group/Fibromyalgia_Support_Group/ Everyone experiences Fibro a bit differently. I am rarely not in a Flare up. The meds really do not touch my pain which stays pretty constant at about an 8 or more. They do help me to rest a bit however. Thank you Caroline for helping others understand. If you've never had a flare, then you are one of the few lucky ones. It's really hard to describe it, and it's a bit different for everyone, but for me, it is the pain "blowing up" so to speak, it's much worse, and none of my pain meds will even begin to take the edge off of it, and I'm on some heavy-duty meds. When I'm not in a flare, the meds will bring my pain level down to a 4 or 5 (not even the heaviest pain meds work right on fibromites) but it is down to a place where I can pretty much ignore it and do things without it intruding. When I have a flare, my pain level stays at nearly a 10, and nothing helps for more than a few minutes, not meds, nor hot baths, not a massage, in fact a massage almost KILLS when you're in a flare. None of the usual things that help when you're not flaring help now. Also, in a flare, every symptom that you occasionally have will be there at once...in my case, IBS, migraine, insomnia, muscle cramping (charley horse) arthritis symptoms, muscle symptoms (body wide), tender point inflammation, and worst of all, the brain fog becomes overwhelming. I just had to look up 3 words while writing this, including insomnia, as I kept wanting to write...?? Now I can't remember that either. I also have to keep back-spacing, and I will have to spell check this (if I remember to) before I send it off. Also, due to the brain fog, I'm sure I've forgotten to list a few things, even though I can feel them. It's nuts. I'd say we all know what it would feel like to have Alzheimer's, although at least this isn't terminal. Just incredibly annoying. No, much worse than annoying. As I said, consider yourself very lucky if you've never had a flare. If you have one, you will know it beyond a shadow of a doubt. CommentairesPour ajouter un commentaire, connectez-vous avec votre identifiant Windows Live ID (si vous utilisez Messenger ou Xbox LIVE, vous avez un identifiant Windows Live ID). Connectez-vous Vous n'avez pas d'identifiant Windows Live ID ? Inscrivez-vous RétroliensL'URL de rétrolien de ce billet est : http://marciacarson.spaces.live.com/blog/cns!CFDF79294097A9AF!437.trak Blogs Web qui font référence à ce billet
|
|
|