A short CFS documentary | The Myalgic Encephalomyelitis / Fibromyalgia Society of Alberta

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A short CFS documentary

Fri, Aug 15, 2008

Tags: CFS, CFS video

1 Comments For This Post

Miriam POtter Says:
August 16th, 2008 at 6:52 am
Hello

Thank you for this insight into your world.
I fully understand, what being bedbound is like.
I spend most of my time in bed, although am grateful that now I am now just housebound!

Like you, I am a prisoner in my own body, and yes it is tough.
You are blessed to have people looking after you.

I hope you do get better than you are soon.

Miriam

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Disclaimer: The ME/FM Society of Alberta does not endorse any products or forms of treatments. Anyone with an illness or change in current health conditions should consult with a Medical Practitioner. Always seek medical advice prior to changing or considering any type of treatment, traditional or alternative. All stories are personal and express personal opinions only. We do not endorse or support any medical, nutrional or alternative treatments.