Keep on Blogging for Invisible Illness


Invisible Illness 2009 comes to a close today. It does not mean that if you suffer from an invisible illness or love someone who does you should stop blogging and stop talking about those invisible conditions. It estimated that 25% of the population from some kind of invisible disease. More than half of those people suffer from more than one condition. Only 7% of persons with an invisible condition will use a wheelchair, cane or crutches. The rest suffer in silence. Because of this, we encounter sociocultural indifference and support is limited. Moreover, many invisible diseases even remain controversial even by the standards of the medical community.

There are more than 80 autoimmune diseases that are known to the medical community, and the majority of those invisible conditions. Because of that, there is much indifference when it comes to cultural and social views of such conditions. For example, diabetes, heart disease and cancer are considered invisible diseases, but no one would ever question the limitations of those who suffer from those conditions. Yet, that happens for individuals who suffer from Fibromyalgia, Chronic Fatigue Syndrome, Lupus or Rheumatoid Arthritis.

I know there will not be cures for many of the autoimmune diseases that exist, including RA, not in my lifetime at least. I know that Fibromyalgia, RA, and CFS are a part of my life and I have been for quite some time, and a cure is something that is currently out of reach, but I can lower my expectations. I can deal without a cure and I can live my life. However, I want more understanding for myself and for others who suffer from invisible conditions such as these. I don’t want to always explain to others how these conditions affect me, and how taking a vitamin or two, eating better, or even exercising isn’t going to make these diseases go away. These conditions are on their own schedule, and not mine.

So I ask of my fellow bloggers who suffer from an invisible illness or who have a loved one suffering from an invisible condition to keep blogging and keep making their voices heard. Awareness is the next thing to a cure.

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This entry was posted in Chronic Fatigue Syndrome, Fibromyaloga, Invisible Illness, rheumatoid arthritis. Bookmark the permalink.

2 Responses to Keep on Blogging for Invisible Illness

  1. Helene says:

    What a great way to spread the word about these types of illnesses!! And you have an amazing attitude!!

  2. Sonia says:

    Thank you for continuing to encourage awareness and education regarding these invisible illenesses. My mother struggles with Fibromyalgia and RA everyday. Some days worse than others but as you know, on those bad days, it sure doesn’t seem invinsible. She is in so much pain at times that the most menial of tasks is almost impossible. I do what I can for her, but I wish there was more. If I could take her pain from her I would. It’s not fair and it’s even worse when you have to explain it to people who just don’t get it. Woud using a wheelchair or a cane make it more visible? Would people be more understanding then?

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