Wednesday, August 03, 2005



Fibro Fog

I have been in the midst of "fibro fog" since Sunday - and believe me, it's not fun. I have a condition called fibromyalgia, and I get episodes on a sporadic basis. They seem to coincide with either really cold weather, or humid weather. Well, it seems like all of us have been in the midst of a tropical heat wave - and thus, I've had a few episodes over the past two months. They usually last a day or two, and sometimes longer. This one hasn't really lasted all that long, but it's a pretty ferocious attack.

It begins with neck pain, then it becomes a tension headache, then my shoulder gets stabbing pains. I do take some medicine (makes me really tired) and ibuprofen or acetominophen - but there are times even that doesn't touch the pain. This is one of those times.

I do exercise and walk to help keep myself flexible, and I get massages to help my muscles from hardening. I went to one support group when I was first diagnosed, and saw some ladies in wheelchairs. I decided then and there that I would do all I could to not allow that to happen to me. I mentioned it to my doctor, and he bluntly told me that if I didn't exercise and walk, then I would become incapacitated. That scared me!

This episode shall pass. But for now, I am laying low until it subsides.

3 Comments:

At 2:41 PM, Blogger Valerie said...

Thanks for your comment, Paul. I was diagnosed right away, but it had bothered me for quite awhile before going to the doctor. I was just relieved that it wasn't a "terminal" illness. I would much rather have the medical profession find a cure for Lupus, which is afflicting my oldest daughter. I hate the thought of her having to deal with it the rest of her life!

 
At 5:00 PM, Blogger Valerie said...

Thank you, Barbara and Paula! Today has been a better day - I am about halfway back to normal. By tomorrow, I should be much better. Barbara - if you read this, can you tell me where your blog is? Are you the same Barbara I am thinking about who lives in England? Blessings to both of you!

 
At 8:25 PM, Blogger Valerie said...

Thanks, Paul - I appreciate your kindness! Two of my daughter's specialists are actually leading researchers for lupus nephritis, so we are blessed to be right on the edge of all the new treatments! Thirty years ago, her prognosis would have been very, very bleak.

 

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