International ME/CFS and FM Awareness Day Is On May 12, 2018
Thomas Hennessy, Jr., selected May 12th to be our international awareness day back in 1992. He knew that May 12th had also been the birthday of Florence Nightingale. She was the English army nurse who helped to found the Red Cross as well as the first school of nursing in the world.
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weather change

Discussion in 'General ME/CFS Discussion' started by notmyself, Oct 7, 2017.

  1. notmyself

    notmyself Senior Member

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    does anyone have any ideea why the change in weather make me feel much worse?! My POTS is much worse,not just the feeling,also the numbers in heart rate, my joints ache much more than in the summer,muscle weakness is more profund,,basicly everything is worse...adn it happen suddenly after a big change in the weather,from summer ,sunny and warm to rainy,cloudy and cold..
     
    CedarHome, Orla, erin and 2 others like this.
  2. belize44

    belize44 Senior Member

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    I don't know why, but I feel the same. We had a cold front go through here and I am thoroughly crashed for the past two days I did nothing but sleep. The only good thing about it is that I didn't have to take anything for sleep.:rolleyes:
     
    erin and Invisible Woman like this.
  3. Kenshin

    Kenshin Senior Member

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    Your profile pics look so similar I thought it was the same one in the corner of my eye.
    But yes, I'm worst in hot humid weather, but crappy winterry weather isn't great either.
    I'm probably best on those cool, blue sky days.
     
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  4. erin

    erin Senior Member

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    I'm better on sunny days with no humidity and still. Slight breeze is OK too.
    I'm really terrible with wind and humid. Clouds and cold is not good, makes me even more fatigued. Wind makes me very dizzy.
     
    belize44 likes this.
  5. TigerLilea

    TigerLilea Senior Member

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    Vancouver, British Columbia
    People with arthritis often complain that their arthritis pain is much worse when the weather becomes colder and wetter.
     
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  6. belize44

    belize44 Senior Member

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    I changed my profile pic for the Fall season.:)
     
    Last edited: Oct 7, 2017
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  7. notmyself

    notmyself Senior Member

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    yep, it really feels like arthritis sometimes ,but the tests and doctors say i don t have arthritis...
     
  8. lnester7

    lnester7 Seven

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    Weather change does not affect me as bad as the Fall, Brutalll for me.
    I've heard that autoimmune plp get worst on fall ( not sure if it is truth).
     
  9. Hanna

    Hanna Senior Member

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    Jerusalem, Israel
    Cold and damp is the worst combination for me. The very first days when the weather is changing (from summer to fall) I am also experimenting major emotional stress - on top of the physical pain increase. Just now in fact !
     

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