Fibromyalgia Support Group
You're not alone in your pain. Fibromyalgia is a condition that can be difficult to diagnose and manage. If you're trying to cope with pain throughout your body, sleep problems, general fatigue, or other common fibromyalgia symptoms, you're in the right place. The community is here for you to talk about therapies and share your challenges.

I'm so tired and burned out this week. Period still hasn't freaking started, work has been busy, and I feel like I could sleep for a week. I'm dreading the brewery thing on Sunday-already my brain is just done. Yesterday by like 4 pm, I literally could have gone to bed (if I wasn't driving). Tomorrow is also supposed to be busy. I was so in my own way this morning that I didn't have time to start this, so I'm doing it now while I'm on lunch. Next week we start doing surgery on Thursdays here, and I'll be the surgery tech, so the change in the routine I've gotten used to in the past 3 months is stressful too.
Today's cute photo is Skadi in her food coma pose. Every night she does this, always on the bed. Often with chirps.

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Today (August 8) is INternational Cat Day. Don't click away! International DOG day is August 26! Both were created to raise aweareness and funds for the well-being of critters. We have many such dayts, to the pint that every day is like an old Catholic saints' day calendar: Take your pick!I'm home, obvs, and still ill. Left calf and foot not great after a tangle-fall, but i'll live. Just can't...
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I'nm exhausted. This doxycycline thing has ripped me apart and I'm eating crackers and water. I can't take (anything) or eat (anything) except saltines and toast and maybe unbuttered watery mashed potatoes. Are we sure the cure isn't worse than the possible disease?!?!And a week to go. ***Fun cures that WERE worse than the disease:ARsenic. Popular against STDs, which just compounded misery...

Thanks for doing the check-ins Miki while Leo is gone. I have been enjoying the pics of your fur babies.
I had PT today and my neck freaking hurts bad. I am sleepy and will probably take a flexeril and crash out for a while at least I hope so. I saw my provider via video yesterday and she ordered XRays of my neck (it has been 3 1/2 years since last one). and and my thoracic spine ( never had ). Its disheartening to tell your provider how much pain you are in and how little of a tolerance for PT because of the increase pain and you just get a shrug. Drs are so afraid of ordering pain meds , even one a day. The Hospital that owns the office probably forbids it. I have been having numbness and tingling in my hands and fingers which is new the last few weeks. .
We are suppose to have super gross weather this weekend so I will be hiding in the a/c
milily i hope your pain eases up! Neck pain is pure misery for me if i get neck pain i get a migraine along with it, my dr just did a medrol dose pack for my whip lash in my neck and its helped a lot, still have pain but much better. I wish they would do something for your pain. Flexeril to me is like candy it does nothing. I am on 8mg of zanaflex and even that does not make me tired at all plus other meds for pain. zanaflex only goes up to 6mg so they have me take 2 of the 4 mg 3x a day. My mom knocks out from 4mg. But most sleep meds make me hyper so does benedryl (suspected adhd)
I do have mild heart failure bsed off my echo last week
I need a third carpel tunnel surgery on my left wrist, yes third. My fingers are numb at all times now the pinky and ring finger, and at times both other fingers and thumb. My thumb locks up where i have to move it with my right hand, and the 2 tumors they said are not cacner are getting more painful. Ive know about the carpel tunnel being back since 2011 but back then was caring for my late husband. My Dr said now i have to do surgery if i want to have feeling in the part of my hand and fingers again. She doesnt wnat permement damage done. Shes setting up the eeg and i hate those they are so painful..
My physical therapistsaid today with my pain so far out of control we need to pause PT until the lupus tests can be redone. My Drs sure they will be positive again in September and she said then we will finally have answers for how much pain im in and its rapidly gettign worse, and so is my fatigue. She said theres so much more to do for lupus pain than for fibro etc.