https://www.mefoggydog.org/2015/12/14/post-exertion-malaise-shown-in-a-picture/ Raising awareness of M.E. with every paw-step Wed, 07 Nov 2018 12:12:26 +0000 hourly 1 https://wordpress.org/?v=6.9.4 https://www.mefoggydog.org/2015/12/14/post-exertion-malaise-shown-in-a-picture/#comment-47 Mon, 30 Apr 2018 09:08:00 +0000 https://foggy.asra.co.uk/post-exertion-malaise-shown-in-a-picture/#comment-47 Absolutely agree, this need to validate our illness isn't helping.

]]> https://www.mefoggydog.org/2015/12/14/post-exertion-malaise-shown-in-a-picture/#comment-49 Mon, 30 Apr 2018 09:05:28 +0000 https://foggy.asra.co.uk/post-exertion-malaise-shown-in-a-picture/#comment-49 I have M.E. or Chronic Fatigue Syndrome. It is now with me every second of every day. I have to push myself to do stuff, like take my furry friend for his walk, & I always feel worse after doing this & sitting down. I consider my level to be moderate, people that have it sever must be in a very dark place. Just because you can't X-ray it, doesn't mean it doesn't exist.

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