Skip to content
My WebMD Sign In, Sign Up
Newbie
avatar
fibromomof4 posted:
Hi. I have been suffering from fibro for years I just didn't know it. I finally have been diagnosed correctly and WOW. I am overwhelmed both in a good way and a bad way (if you know what I mean). I feel helpless. The meds. I am one are not helping and the new med. the dr. put me on has sooo many side effects I am scared to start it. People around me don't understand the severity of my symptoms. I cannot be the person I want to be because of fibro. My family deserves better than what I can give them. I am so depressed. Does anyone else know how I feel?
Reply
 
avatar
alv4n responded:
Absolutely understand how you feel. I was diagnosed almost 7 years ago, and it has waxed and waned. I have tried this and that medication and stopped as many as I've started.

The most interesting thing happened to me yesterday, though, when I was out to lunch with my husband. We were sitting at the table, waiting for our food, and I looked over at him and it occurred to me that, he was just sitting. Just sitting and feeling fine. I asked him, "Are you feeling fine, just sitting here right now, just waiting for our food?" and of course, he was terrified this was some sort of trick question. But once he saw it was safe, he said "yes". I said, "So, you do not have any aches or pains while you're just sitting there" And he said "no". And I told him, that while we were sitting there, doing such a normal everyday thing, I was in agony. I told him my upper back/ shoulders were like on fire, or sort of crampy, but really just painful, hard to describe. And I said to him "you know, I always feel like this when I'm just sitting." And he was completely surprised. He said he thought I was only hurting when I actually complained about it. I said that if I complained every time I was aching, it would be all that came out of my mouth. Even after 7 years with this syndrome and my husband being with me all the way, he still didn't really get it. I don't think anybody can, except for other fibro sufferers.
The single most important factor that has helped me, however, is PACING MYSELF. I don't care how much I thought I had been pacing myself in the past, I absolutely WAS NOT. And fibro sufferers are the people who want to do it all, so pacing is counterintuitive. But believe me, let your family know how you are feeling, tell them it is a fact of your and their lives that you will need to lie down to rest often, that you will need help with heavy to moderate lifting: sometimes even washing large pots in the sink nearly brings tears of pain to my eyes.

You are not alone. :Let yourself be depressed, let yourself be angry, and let yourself be loved.


Spotlight: Member Stories

I was diagnosed with Post Traumatic Fibromyalgia after being rear ended twice in a three week period in 2008. It's been an awful and frustrating 2...More

Helpful Tips

Does this disease last forever?
I have had fibermyalgia since an auto accident in 99. Its like labor pains with no break, no epiderals, and no baby. I have gotten ... More
Was this Helpful?
4 of 11 found this helpful

Related News

There was an error with this newsfeed

Related Drug Reviews

  • Drug Name User Reviews

Report Problems With Your Medications to the FDA

FDAYou are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.