Guest guest Posted February 16, 2008 Report Share Posted February 16, 2008 I just wanted to say it looks like alot of us here are trying to explain why, when, and how we take our pain meds. I feel that somehow some of us have got caught up in feeling guilty for having to use a pain med no matter which one we are on. There are so many people out there who DO abuse these meds, and take them for the high not for the pain management, but I think all or most will agree that the pain that comes with this disease and others like it are unbearable and at times we would rather be put out to pasture like an injured horse then go thru 1 more min, let alone day of pain. This is when these meds help. Think of it, people who have been diagnoised with cancer, tumors, and other terminal illnesses, are using pain meds and much more than we are given and I don't blame them, NO ONE should be in pain. Now if we were put on Hospice the thought and theary is treat with comfort and care, and use whatever it takes to make the person comfortable, not anxious, and without as much pain as possible. So just because we are not on Hospice does not mean we do not need to take meds to alleveate our pain, anxiety, and help to just function thru a day. And to those of you who have small childeren and face these trials daily I have been you only I was not diagnoised back then and had no medication to help. Don't feel guilty when you have to lay down and rest when they want to run you around in all different directions, I lived with so much guilt because I looked back for so long and said I was a bad mom as I could not do anything much with my kids, oh we did disneyland, I got sick, 10.mins into it and hospitalized, and that seemed to be the pattern, anytime I made a day trip deal I ended up sick, and with some bizzare thing that put me in the hosp. We ended up joking when traveling check out where the Hosp is here for mom! To all I wish the best Sharon ddean228 wrote: You know, before I was dx'd with FM, I would have low back pain and spasms that I attributed to gaining weight, doing too much, etc. etc. Flexeril worked on those times and a few times, when the spasm was big enough for the doctor to see, a shot of cortisone (yeah, taking chances there, but what isn't a chance anymore?). Anyhow, when I went to the doctor's just prior to being dx'd by rheum, I mentioned I was having to take 2 flexeril to take the edge off the spasms; that's when I was switched to Robaxin, given Naproxen for the inflammation for my pleurisy (due to bronchitis) and if it was really bad, Darvocet. Since being dx'd, I take the Lyrica and ONLY if I am having some breakthrough pain do I take any of the other 3 pills. Like the night my knees were flaring (I could have cheerfully found DH's chainsaw and cut my legs off...lol), then I grabbed a darvocet, only it didn't really help. I try to " read " my body and determine if the breakthrough pain is due to inflammation (I am holding fluids due to some lower extremity blockages that are getting checked out) so I can take a Naproxen, if they it is due to spasms so I can take a Robaxin or if it is due to pain, in which case I will take a darvocet. The challenge for me is I have a set of 8 yr old twins who are special needs. They do not need to always see mommy sleeping and unfortunately, are not as adept at watching out for themselves as my bio sons were at that age (they could be counted on to do what they were told, these two? well, its a crapshoot a lot of days...lol). Anyhow, I don't feel I am abusing the meds in any way shape or form. I am not getting the scripts filled monthly, just using them as needed, just like the bottle says! My 2 cents here in Georgia, where the left hip woke me up this morning! Yippee.... Darlene Quote Link to comment Share on other sites More sharing options...
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