Sunday, February 16, 2014

What does the moon havta' do with it?


For the last, at least 5 years I have been noticing a pattern between the moon, and my own body sensitivity/pain levels. In the last year, I have been secretly, half fast keeping track of the full moon and how I am feeling on the day and night of the rise and set of the moon.

The Moon's gravitational influence produces the ocean tides and the minute lengthening of the day. So what makes you think it wouldn't effect the way your body feels? I seem to experience a number of symptoms and sensitivities, that I'm pretty sure I can associate directly with the lunar cycle or seemed to be worsened by it.
  1. headaches
  2. restless legs and body
  3. pain intensity
  4. moods
  5. increased sensitivity to environmental annoyances (smells, light, sound, stress etc.)
I have read that the full moon can be responsible for mood changes and can affect stress levels. Since stress in one of the leading causes of fibromyalgia flare-ups, my theory of the moon affecting fibromyalgia sufferers can assume to be true. 

I would love to hear from others who experience pain and/or have FMS or Arthritis. Please comment and tell me your own experience with the Lunar Cycle. ~Thanks :-)



Helpful LInks:

Full Moon Ion Effect








http://www.moonconnection.com/moon_cycle.phtmlhttp://www.moonconnection.com/moon_cycle.phtml

Do people REALLY go crazy during a full moon? New study analyzes links between everything from lunacy to labor pains

Study confirms myth of lunar cycle driving us mad is false... but doctors claim more mental health patients come in at full moon

Pain Levels 1-10 being the worst
(note full moon)
  • The last two days I've had really high pain levels all over and slept most of today. 
  • Head, neck shoulders pain levels 7
  • Lower back, butt, hips, legs/thighs pain levels 8 but was at 10 earlier and I was very irritable (my poor poor husband)
  • arms, wrists, and hands pain levels 6
  • knees, ankles and feet pain levels 5 but was higher earlier today before i took a nap.

Wednesday, February 12, 2014

Meteorologist Kiki here

It feels like there is some more snow on the way. I've read a lot about experts saying they've proved that FMS is not impacted by weather changes, however, I disagree. I'm not an expert, but I have had FMS symptoms as long as I can remember, and finally diagnosed in 2007... That's a lot of pain and weather predicting.      

In my own experience, whenever the temperature and/or barometer changes drastically, I feel increased pain in numerous areas of my body. Usually I tend to develop a migraine that will intensify as the weather change moves closer, and after it has passed my head starts feeling better right away. All my joints are also sensitive to the weather changes and the all over body aches that are associated with Fibromyalgia always intensify during these changes too. Even the slightest weather system of any sort of precipitation at all will affect my body in negative ways.

When I was a kid I use to love storms, but by my early 20's I started noticing the increased pain before and during, so I've grown to not so much care for them. I do still love a beautiful lightning storm. Michigan is not a "Fibro weather friendly state". 

Currently smack dab in the middle of a FLARE-UP. . . but on the bright side I am making leaps and bounds of progress where doctors and treatment are concerned. So there is a light at the end of the tunnel...along with a ton of really hard work to get there.

I will be starting pain management next week and physical therapy, along with aquatic therapy. YAY!!! Pool Time! We love that! Don't we? :-)

I have also been eating very well and using myfitnesspal app on my phone religiously. Yay me! I lost 2 lbs. so far and I'm hoping I lost more this week but I do not weigh up until Friday. So I shall keep ya posted.

I'm trying to exercise the best I can through the pain also. I have been doing short 5 min walks on my treadmill. I did 7 and 1/2 yesterday and I think I angered my knees and lower back. That could be a little part of my flare-up today... it just seems like 7 mins walking is nothing, and how could it make me feel this bad today? I've been being so careful not to over-do-it. I feel like a very delicate bubble... don't touch me, ... i'll break. Ridiculous. I must get stronger.

Helpful links: