Category Archives: Support

They just don’t get it – How to explain FMS/CFS

They just don’t get it How to explain chronic fatigue syndrome & Fibromyalgia to friends and family By Kelli Ellis Not having support from your family and friends will put a strain on these relationships impacting your stress level which can affect greatly both negative and positive on your health. Explanations need to be ...

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How to Give a Killer Massage

20 massage techniques to help relieve back pain and stress, for your special someone. By Katy Dreyfus http://www.lhj.com/health/stress/relaxation-techniques/how-to-give-a-killer-massage/ Share this with someone special, so you can GET the killer massage.. *g* Posted via email from Kelli's Posterous

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20 Things to Say… (Invisible Illness)

Tweets! 20 Things to Say to an Ill Person Oftentimes people are told what not to say. This is a great help in giving them an idea of what to say! Feel free to add your own ideas in the comments below. ...

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20 Things NOT to say… (Invisible Illness)

20 Things NOT to say to a Chronically Ill Person These lists are compliments of National Invisible Chronic Illness Awareness Weekat www.invisbleillness.com.Get involved in Invisible Illness Week this year during the week of September 14-20, 2009, including the 5-day ...

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How to Act Right When Your Spouse Acts Wrong

$13.50

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Understand before you judge..

There are the things I would like you to understand before you judge me... Please know that being sick doesn't mean I'm not human. I may spend most of my day flat on my back and I might not seem like great company, but I'm still me stuck inside this body. I ...

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Surprise!

I was pleasantly surprised today. Today was one of those days where I needed a cane for support, or at least I felt I would before I got home. I went to the post office, then the grocery store next door. They didn't have what I wanted so I crossed the street & ...

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Five Simple Words….

Five Simple Words to Keep Chronic Illness at Bay by Madeleine Parish When I was diagnosed with Chronic Fatigue Syndrome seven years ago, my illness began to consume my thoughts and time. Questions taunted me like unrelenting harpies: What will I do? How will I manage? Who will take care of me? To try ...

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It’s not real.. Not for me apparently. :(

What would you do? How would you react? If you got told by the person that has been your primary support person for the last 3 + years.. That he/she doesn't believe you're sick? Doesn't believe you're really *that* tired? Doesn't believe you're in *that* much pain? And thinks it's all ...

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What support looks like

What support looks like: 1) Ask someone how they are 2) Ask what they are doing to cope 3) Ask them what you can do Source: Andrea Martell aka @killandra

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