JenniferEvelynn
01-27-2005, 01:13 PM
Hi all,
Can someone explain this in detail?
God bless, Jen
Can someone explain this in detail?
God bless, Jen
Sponsor
bluelakelady
01-27-2005, 02:54 PM
hi jen,
myofacial pain is inflamation of the facia in your body. facia, pronounced like fashion, is a slimey coating of tissue that surrounds every fiber of your body. down to the smallest cell. have you ever removed the skin from chicken and had to wash off that slimey clear stuff between the skin and the meat? well, that's facia. i know, yuck!
cmp is when the facia becomes inflamed, swells and causes pain. alot of pain. as you have facia thruout your body it can flare up any place. i have had it flare up in my eyes causing temporary blindness until the swelling went down. for no reason a place on my body will swell up with a lump that causes pain, especially when touched. but touch it i do. i gently massage the swelling, sometimes it takes days, until the tissue relaxes and the swelling goes down. it affects my entire body. one day my bladder, another my armpit, another my eyes, another, well, you get the idea. often the pain lasts for weeks without easing.
check it out online in your search engine. there are quite a few good sites. so far i do not use steroids or injections. those scare me. i do warm water therapy and myofacial release therapy. i swim laps and tread water for strength.
peace,
bluelakelady
myofacial pain is inflamation of the facia in your body. facia, pronounced like fashion, is a slimey coating of tissue that surrounds every fiber of your body. down to the smallest cell. have you ever removed the skin from chicken and had to wash off that slimey clear stuff between the skin and the meat? well, that's facia. i know, yuck!
cmp is when the facia becomes inflamed, swells and causes pain. alot of pain. as you have facia thruout your body it can flare up any place. i have had it flare up in my eyes causing temporary blindness until the swelling went down. for no reason a place on my body will swell up with a lump that causes pain, especially when touched. but touch it i do. i gently massage the swelling, sometimes it takes days, until the tissue relaxes and the swelling goes down. it affects my entire body. one day my bladder, another my armpit, another my eyes, another, well, you get the idea. often the pain lasts for weeks without easing.
check it out online in your search engine. there are quite a few good sites. so far i do not use steroids or injections. those scare me. i do warm water therapy and myofacial release therapy. i swim laps and tread water for strength.
peace,
bluelakelady
twisten
01-27-2005, 04:23 PM
BBL, you're one of the lucky ones to have had responses to things you've tried for cmp. I've had it so long (over 11 years) and have tried everything but the treatments either don't work at all or don't last for long. My neurologist says that all that can be done for mine now is pain meds. My family doctor though is researching some new guy. His practice is 3 hours from me but if he can help I'm more than willing to travel there. My family doc isn't sure what all treatments he does. She just referred another patient of hers to him but he can't get in for 4 more months. She is going to find out what all he offers and if it isn't something we've already tried then she will see if he will take me on as a client. She warned me though that he is selective on who he will treat and because I've had it so long he might say he can't offer me anything. I've got my fingers (and toes) crossed though!!
LFCA
01-28-2005, 06:53 AM
My wife is a Big Fan of Clair Davies' "Trigger Point Therapy Workbook", which she happened to run across when she was having throbbing knee pain for no known reason a few years ago. After massaging a trigger point in her upper thigh for short periods over only a few hours per the book's instructions, her knee pain was almost totally gone (this was a month into the condition), & after a day or two more of the massage, totally gone & has never returned. She just ordered a "Theracane" to use in addition to the tennis ball. I'll probably try it myself.
Although we're well into our sixth (her) & seventh decades (me), we're amazingly not bothered by chronic pain so far, but acute pain can & does occasionally pop up.
Although we're well into our sixth (her) & seventh decades (me), we're amazingly not bothered by chronic pain so far, but acute pain can & does occasionally pop up.
bluelakelady
01-28-2005, 09:17 AM
hi lisa and all,
i forgot about the restriction aspect. thanks. i too have the book. it is on loan to my physical thearpist at the moment. i will get the other one by claire davies.
it rained hard all night. i heard tree branches crashing in the wind. for the moment it is quiet out.
peace,
bluelakelady
i forgot about the restriction aspect. thanks. i too have the book. it is on loan to my physical thearpist at the moment. i will get the other one by claire davies.
it rained hard all night. i heard tree branches crashing in the wind. for the moment it is quiet out.
peace,
bluelakelady
JenniferEvelynn
01-28-2005, 05:44 PM
HI everyone,
Thank you all so much for your responses. CMP sounds far worse than FM. I'm in enough pain now, I couldn't imagine how I would feel having CMP. Is it possible for someone to have both? Bluelakelady: thanks ever so much for your eloquent analogy of the chicken skin. Makes me wonder if I want to de-skin a piece of chicken ever again!! LOL
God bless, Jen
Thank you all so much for your responses. CMP sounds far worse than FM. I'm in enough pain now, I couldn't imagine how I would feel having CMP. Is it possible for someone to have both? Bluelakelady: thanks ever so much for your eloquent analogy of the chicken skin. Makes me wonder if I want to de-skin a piece of chicken ever again!! LOL
God bless, Jen
bluelakelady
01-28-2005, 07:25 PM
hi jen,
yes, i have both. you are right. cmp is more difficult to live with than fms. at least from where i sit. if i could choose between the two (dreamer) i would choose fms.
makes you want chicken for dinner, right? yuck! ever since reading that analogy i buy my chicken already peeled, so to speak.
peace,
bluelakelady
i am glad you don't have cmp!!!!!!!!!!
yes, i have both. you are right. cmp is more difficult to live with than fms. at least from where i sit. if i could choose between the two (dreamer) i would choose fms.
makes you want chicken for dinner, right? yuck! ever since reading that analogy i buy my chicken already peeled, so to speak.
peace,
bluelakelady
i am glad you don't have cmp!!!!!!!!!!

