ME/CFS and the Change of Seasons: How Does This Affect You?
The advent of autumn can hit Jody Smith pretty hard. She's learned a few ways to lessen the damage every year. How do you handle the change of seasons?
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Discussion in 'General Symptoms' started by helen41, Sep 12, 2010.

  1. helen41

    helen41 Senior Member

    Sleepy Hollow Canada
    I am starting to suspect I am a person who had a lengthy remission from ME/CFS. I suddenly became ill 12 years ago. When I went back and re-read the neuro consults, my previously solid sleep became broken, my thoughts were slowed and confused, I had poor balance, I was light sensitive, and extremely fatigued with no stamina. My MRI showed a few tiny lesions, but not MS. I was housebound for 3 months, then managed to return to my part time work, but I remember despite telling everyone I was feeling fine, I used to go to my car 2 or 3 times a day for months to nap just so I could manage. The diagnosis at that time was probable viral encephalitis.

    I never completely regained what I lost in that episode, either intellectually or physically. I stopped doing the NY Times puzzle because I suddenly couldn't do it anymore. I did manage to take courses and did well, but it took more work than in the past. I always paced myself and avoided exercise, simply because it was the best way to manage. I believed it was related to damage from encephalitis. It wasn't obvious (I cover well) but I knew there were impairments.

    In 2009 I had a series of illnesses (anemia, shingles, cellulitis, and abdominal surgery). Throughout all that time my primary complaint was fatigue. I suspect those illnesses made me susceptible to a resurgence of a latent virus, or maybe the virus exploded and made me susceptible to the illnesses- (any thoughts?). Each of those illnesses were treated and resolved but I didn't get better. I stayed exhausted, had broken sleep again, developed myalgia and figured out that I have PEM, not just weakness. (I have no idea if I've had it for years or not, but it certainly was not a huge barrier in my life). My MRI now shows numerous tiny lesions but again not indicative of MS. I have all the classic signs of ME/CFS now and I'm spending a lot of time trying to learn the best way to manage it.

    I haven't read histories like this. Does this seem like a reasonable theory or does it seem more likely I simply had 2 illnesses? I wish I could go back a few years and compare blood samples! Thankyou in advance for any thoughts on this.

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