Guest guest Posted April 20, 2008 Report Share Posted April 20, 2008 Hi Wow you discribed some things that I put down to my diabetes. The burning feet especially. The Doc told me to start wearing shoes more. I'm in my bare feet all year long as much as possible. I stopped wearing socks because they made my feet hurt. I swear I can feel every fiber pushed in to the skin. I've been that way for a long time. I'm sorry to hear about all the meds your on. But hey if it works... At least you got yourself up and out. That's a great thing. I think I'm going to see if my doc will get me some of the Lyrica stuff. I'm so frustrated right now with this stupid pain. I know this is a dumb thing to say, and I don't really mean it the way it sounds but... I almost wish it were cancer or just something that can be touched. Something that can be yanked out!!! I'm used to being fast and contrary to my size I'm very active. This not being able to move thing just makes me want to scream. Everything is falling apart and all I can do is watch. I'm being left behind. I'm sorry I'm just so frustrated right now. I need to cry. But it makes my chest hurt. Jan > > I have been reading your messages (lurking) for awhile, but by the > time I'm finished, I'm in too much pain to reply. So, unfortunately, > I have to delete a lot. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 22, 2008 Report Share Posted April 22, 2008 Welcome Chris. Nice to have you with us. Jeanne in WI I have been reading your messages (lurking) for awhile, but by the time I'm finished, I'm in too much pain to reply. So, unfortunately, I have to delete a lot. I was diagnosed with fibro in 1993, but had first symptoms in 1987. I was on active duty Navy at the time, and retired with 20 years in 1991. I am so grateful that my medical care costs me less than $20 per month, and I found great drs. at the Pain Clinic at Walter in D.C. This disease, disorder, syndrome, or whatever, is progressive and I am living proof. I spent 75% of my time in bed, until I lost 145 lbs. I got out of bed because I was dying emotionally and spiritually, and I wanted to die. I prayed for help and got it. I am a recovering alcoholic with over 29 yrs. sober, and used the 12 steps to lose the weight. What baffled the doctors, and me, was that I was in more pain after I lost the weight. I told them it was because I lost the cushion of fat that protected my muscles and bones. Seriously. I've been on various meds, some narcotics, but I have a high tolerance and they quit working in a couple of months, so they switch to something else. I am now taking 45 mg. morphine, 300 mg. Lyrica, and 200-300 mg. Tramadol. The Lyrica was just increased from 150, which worked great for about 2 months. I want to get off the morphine, but if I need it to function, I'll take it. No one has mentioned using a TENS unit, maybe because they're so expensive (another reason I'm glad my medical care is basically free). The unit really helps me on certain areas, especially my neck and shoulders, sometimes my lower back and butt. My gluteus muscles are always swollen, inflamed and painful, I have to sit on an ice pack all the time. My feet get very hot and burning if the temp is above 60. Anyone else have this problem? Also, I can't bend my knees without a lot of pain, so I have to prop my legs up. Anyway, poor me will stop whining now and remember to be grateful that this is not terminal, though there are days I think I wish it was. I identify with the guilt, frustration, anger, etc. I try to be gentle, kind, understanding, and loving to myself, even if no one else is. Take care of yourselves, everyone. Chris Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 22, 2008 Report Share Posted April 22, 2008 Hi I can relate. I have had increased pain with the more weight I lose from My Gastric Bypass. My doctors are actually telling me the same thing about the less cushion around my nerves and bones. I do use a TENS unit for my back and my knees. I feel it helps " numb " the area at least for a little while. I am also trying Aqua Therapy where I excersize in a heated pool. It helps keep my muscles moving. I am still working with my doctors on the rght medications and dosages so I am not sure what advice to give in that area. I hope now that you have found this group we can lift your spirits. Saundra > > Welcome Chris. Nice to have you with us. > Jeanne in WI > > > I have been reading your messages (lurking) for awhile, but by the time I'm finished, I'm in too much pain to reply. So, unfortunately, I have to delete a lot. > I was diagnosed with fibro in 1993, but had first symptoms in 1987. I was on active duty Navy at the time, and retired with 20 years in 1991. I am so grateful that my medical care costs me less > than $20 per month, and I found great drs. at the Pain Clinic at Walter in D.C. This disease, disorder, syndrome, or whatever, is progressive and I am living proof. > I spent 75% of my time in bed, until I lost 145 lbs. I got out of bed because I was dying emotionally and spiritually, and I wanted to die. I prayed for help and got it. I am a recovering alcoholic with over 29 yrs. sober, and used the 12 steps to lose the weight. > What baffled the doctors, and me, was that I was in more pain after I lost the weight. I told them it was because I lost the cushion of fat that protected my muscles and bones. Seriously. > I've been on various meds, some narcotics, but I have a high tolerance and they quit working in a couple of months, so they switch to something else. I am now taking 45 mg. morphine, 300 mg. Lyrica, > and 200-300 mg. Tramadol. The Lyrica was just increased from 150, which worked great for about 2 months. I want to get off the morphine, but if I need it to function, I'll take it. > No one has mentioned using a TENS unit, maybe because they're so expensive (another reason I'm glad my medical care is basically free). The unit really helps me on certain areas, especially my neck and shoulders, sometimes my lower back and butt. My gluteus muscles are always swollen, inflamed and painful, I have to sit on an ice pack all the time. > My feet get very hot and burning if the temp is above 60. Anyone else have this problem? > Also, I can't bend my knees without a lot of pain, so I have to prop my legs up. > Anyway, poor me will stop whining now and remember to be grateful that this is not terminal, though there are days I think I wish it was. > I identify with the guilt, frustration, anger, etc. I try to be gentle, kind, understanding, and loving to myself, even if no one else is. > Take care of yourselves, everyone. > > Chris > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 13, 2008 Report Share Posted May 13, 2008 Hi Donna! Nice to meet you. I think you will really enjoy this group. Everyone is so nice! I've only belonged for a short time, but I've learned so much. I look forward to getting to know you. Take care. Gentle Hugs, Kristi > > Hi everyone, > > I joined the group a few days ago and figured it's time to introduced > my self. My name is Donna. I live in Massachusetts. I, like you all > suffer with Fibro. I also suffer with depression & anxiety (which, of > course, is a part of it). I've done some reading on it, but I wanted > people to relate to about it. Sometimes I feel so alone and that > people think I'm some kind of hypochondriac. I do have a group of good > friends and family who are sympathetic, but they don't really > understand. I've been reading some of your messages and relate. > I see a therapist and am on so many pills it's ridiculous! My > therapist just died from a brief battle with cancer. So now I have to > get used to someone new, it's nice to talk to them but even they don't > truly understand. So I'm hoping this group will be a kind of therapy > for me. > > I look forward to getting to know all of you! > Donna > Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.