Myofascial Pain Syndrome Support Group
Myofascial Pain Syndrome (or MPS) is a term used to describe one of the conditions characterized by chronic pain. It is associated with and caused by "trigger points" (TrPs), sensitive and painful areas between the muscle and fascia. The symptoms can range from referred pain through myofascial trigger points to specific pains in other areas of the body. It may be related...
Do you ever have fits of exhaustion?
chimerical
That is how I feel right now. I have been so over-extending myself for the last week +. I have moved back to Manhattan and am moving to my second rental today, because my first one did not work out. Then there was Hurricane Irene. I had to evacuate and lug all my valuables and trek up and down subway steps with them. Then last night I took a farewell hike around Tribeca, where I have been staying.
Today I am moving to this room in this fabulous apartment uptown near Central Park. The car service is coming at 3 PM. I have to pack and go to my bank (the nearest one is quite a hike away). It is past 11:30 AM and all of a sudden I feel like I cannot move. My legs fell shaky and tingly and I started sweating all of a sudden.
I took a codeine pill and my thyroid medication around 2 hours ago, and did eat breakfast. What is wrong with me? I really have to get busy, and I swear I feel like I cannot move another inch.
Today I am moving to this room in this fabulous apartment uptown near Central Park. The car service is coming at 3 PM. I have to pack and go to my bank (the nearest one is quite a hike away). It is past 11:30 AM and all of a sudden I feel like I cannot move. My legs fell shaky and tingly and I started sweating all of a sudden.
I took a codeine pill and my thyroid medication around 2 hours ago, and did eat breakfast. What is wrong with me? I really have to get busy, and I swear I feel like I cannot move another inch.
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Hope this helps.
So there is a branch of my bank right down the street where I am moving. But I don't know how that will impress my new landlord. "Oh, wait just a minute while I run to the corner to get some money."
I swear, if I live through today, I am going to spend the whole Labor Day weekend flat on my back reading novels and goofing off. I think of myself as a lazy person, not someone who pushes herself too hard. But my living situation has been so haphazard for so long. I have been living out of a suitcase--sometimes bigger suitcases, sometimes fewer--for so long, more than a year really.
The water tip is a good one, I've noticed when I'm knackered I really forget to hydrate and then end up worse. Vicious circle.
This should be short term exhaustion, hopefully, as long as you make good on your promise to rest over labor day weekend! And it's not goofing off, it's as important as a prescribed treatment. Well done for getting through so far, and good luck with the last step.
hugs, Pxx
I have been so sick for several days now, can hardly leave the couch, it sucks!
I can relate on a few levels. Stress and anxiety will do it to you. I just moved (so did Pumpkin) and it feeds the stress. Hurricane Irene is causing me a problem with the closing of my house . . . darn storm.
Living with uncertainty is hard enough for people without pain let alone people like us. You struck a cord in me that you think of yourself as a lazy person. So do I and that kind of self recrimination isn't healthy for one's self image. We should make a pack to change that . . .
Getting back to your exhaustion, that happens to me. I get to the point where I'm shaky and my brain stops working along with my body. I think it's the central nervous system being overwhelmed by pain signals. I've also been recently diagnosed with fibro. Have you ruled that out?
You've got the right idea to relax over the weekend. The Central Park area is vibrant and beautiful. When you feel better, you'll have a wonderful place to explore.
Hugs to you. Tink
I looked around on the internet, and found that the flushed sweaty feeling I have sometimes comes from the codeine pills. It is brief, just when they first kick in. The Cymbalta makes me prone to sweat anyway.
But this trembly leg thing is different I think. I remember now I had it years ago once right after swimming. This was before I knew I had MPS, even before I was diagnosed with fibromyalgia. It freaked me out, but the doctor seemed to think it was nothing.
Boy you have had so much on your plate!! Moving, lots of packing /unpacking, evacuating and lugging all your stuff. Im worn out just reading what youve been thru.
i hope this weekend you can rest and enjoy your new place, I take codiene also, i get flushed at times.
Hang in there.
(((((((GENTLE HUGS)))))))