People often do not understand just what I deal with every day as an individual who is currently dealying with Lyme Disease.
Often people think I am being lazy or just making excuses--especially when they see me on a good day and two hours or a day later, I can't even get out of bed.
It is very difficult for me to explain concisely what it is like dealing with Lyme. However, I found two things that help somewhat. The first is a documentary called, "Under Our Skin."
The second is an article written by Christine Miserandino and can be found on a website for Lupus, which incidentally is very similar in symptoms to Lyme Disease. I cannot reprint the article here but I can put up the link. I hope you will check out the article. It is only two pages, but it explains a lot.
To Your Greatness,
KC-B
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