If you are taking all those meds at the same time, you may be a pill popper. Are you taking magnesiem atleast 4 hrs from taking anything else? If you take it along with other meds-the other meds will not be aborbed correctely into your system, like you won't get the true effects. Have you tried positive feedback or hypnosis for the pain. Try positive thinking and speaking. Yoga breathing exercises. Physical therapy, swim less in a heated pool. Stationary bike slowly for five minutes to restart a new ecercise program. You won't be happy with harder drugs, most pain killers don't even work on fibro type pain believe it or not. I've tried morphine and I've tried oxycontin (doctors choices not mine) and they did nothing but make me tired. Watch how you stop your meds too, get doctors help on how to do that or else it could kill you. Good Luck and God Bless
just tell your doc that what you are taking is not working and in my opinion nothing does that i have ever had,so i stopped takng the lot and i dont seem to be any worse off cos the pain remains the same ,and and i clear each med out of my system before i try something new.hope this has been of some help to you,and ask him how long you shold wait before you try something new.
I agree with kitty 51 just tell the doc that what you are taking right now is not helping at all with the pain. Ask if there is something else. I was taking percecet one 3 times a day. Which did nothing. I was afraid to overdose so I just suffered. Then a friend of mine told me that his wife is also on them and she takes two at a time which helps. So that is what I did. It did help. I told my doc & he said no that is to much and then switched me to morphine. Just tell the doc what you are taking is not doing a thing. See what he says.
I have been wondering the same thing! I am scared to ask too, I am on lyrica and ambien and I am still having a really hard time! I am not on any pain medications which I have taken before and they do help some, I hope you find out, good luck! Also if you do find out let me know, I want to ask too but am scared!
I wrote this post when I was in dying pain. I do alternate between Rx meds and homeopathic treatments/remedies. I also do water exercises and emotional therapy. AND I take a break about every 5-6 months from Rx meds, so that I do build a tolerance or harm my other organs more than I do. I have Post Traumatic Syndrome with Panic Disorder on top of FMA, TMJ, and likely MS.
I do not like that I have to take any meds at all and since posting this I have quit Lyrica because I thought it might be a culprit to my involuntary jerking and shaking. Also, I do not take pain meds daily, only when needed. And I am not going to apologize that sometimes I NEED something to take away this pain!!!
I encourage everyone when reading someone's post/question to really understand that they are being honest, open and putting theirselves out there. Also take in mind every one of us hurts but none of us know to what extent the other persons pain may be or what their threshold for pain may be. What you may not be able to tolerate, maybe I can or vice versa.
Let's all remember why we are here and that this is the one place we should all feel free to be open, honest and ask whatever is bothering us. Non-suffering people in our every day lives do not have a clue so this is the only place we can come to.
I've rec'vd some private messages regarding this and so I had to come back and post this comment. Everyone is free to express their opinions and suggestions- just keep in mind real people in real pain are behind each post!!
I do not know how it is for others, but for me I have never been able to get a Docter to give me more meds for my pain. I only take my cymbolta and busepar and balacet. And sometimes I feel as if im going mad. But my doc wont help me. So i go to the emergency room and they always help me.
A supplement.. well actually it is a type of sugar, has been shown in research studies that it can improve pain and quality of life in many CFS & fibro patients. It is called "D-Ribose"... you may want to check it out. Here is a link to the article;
HERE'S INFO ABOUT ME THAT'S ON MY PROFILE SHOWING ALL.... MY MANY AILMENTS. I'M POSTING THIS 2 SHARE MY STORY & MAYBE U'LL UNDERSTAND WHY I TAKE (HAVE TAKEN) SO MANY DRUGS ETC.!!
MANY, many health problems!!
*L4-5 FUSION 11/2006 **but be4 that i had a botched "clean up" & obtained an infection of pus & fluid in my spine 9/2005. Had 2 have a pic line put in for IV antibiotics & weekly nurse visits for 8 + wks.
*C5-6 FUSION 3/01
*STILL have 2 hern disc's in lumbar, 2 in thorasic, 1 in neck
*Degenerative Disc Disease
*Arn. Chiari DAILY headache/migraines for 13 yrs. now
*DAILY chronic pain
I take 11 perscriptions for my ailments: Some include; lyrica, cymbalta, etolac, percocet, ms contin, zanaflex! They HAD me on MAJOR strong stuff 3-5 yrs. ago including: Dilata's, Methadone, Soma & Clonopin. Couldn't handle ALL the side effects & was house bound & became severely depressed & OVERSLEPT constantly.
In the PAST my dr. has tried EVERYTHING........... w/ my chronic pain: tramadol, darvocet, vicodin, loratab, celexa, bextra, MANY diff. anti-depressants ETC.
~~ I go 2 the dr. EVERY month for pain management. I LOVE my dr.! I've been seeing her for quite a few yrs.! And she's VERY conservative about giving pain meds. SEE................................ the thing is MOST dr's WON'T give pain meds for fibro. INCLUDING my dr.!! She prescribes my pain meds for my torn up spine, neck & head. The herniated disc i have ARE pinching nerves etc.! So, she is compassionate that i HAVE 2 have SOME quality of life. She's SEEN me NOT be able to hardly walk & or stand up straight. I'm DEFINITELY not a pill seeker. Since i've refused pain meds MANY times. JUST because one is on a lot of scripts doesn't make them one.
**I've TRIED ALL kinds of natural herbs & alternate relief. Phy. Therapy/Chiro (made it WAY worse) biofeedback, injections, hypnosis, weekly massages, acupuncture, low impact aerobics. YOU name it i've tried it. And SOME of these made my pain MUCH worse.
AS far as ASKING 4 something stronger............. if u have a good relationship w/ u'r dr. they should be willing to try something stronger on you if what u'r taking ISN"T working. If they give u the run around FIND a dr. that's compassionate & maybe even SPECIALIZES in u'r ailments.
Meditation/Yoga, positive thinking is THE BEST DRUG there is. BUT w/ out my reg. meds I'd be in bed........ praying for god to take me & end my pain!! I've been there be4 & it's NO place for our minds to go.
GOD BLESS YOU ALL
PEACE, LOVE & HAPPINESS TO YOU ALL =)
I'm new on here, and I understand I'm in alot of pain too. They are not sure if I have Fibromyalgia or neuropathy but I take Darvocet now and was on Percocet. They do nothing for the nerve and body pain. I only take them for the Migraines, and that pain doesn't compare to the pain in my legs. As far as meditation I've studied Martial Arts for 17 years, and as it is helpful - I am still having trouble copeing.
Has u'r regular dr. ordered any specific labs; like SED RATE, Growth Hormone etc.?? If they did & then sent u 2 a fibro clinic u could find out EXACTLY what's going on w/ ya.
I'm sorry u'r having a hard time coping. :( I feel for ya sista. We all have bad days & some good. Hopefully, today is a good day for u. I TRY to FOCUS on the fact that @ least i'm NOT wheelchair bound. Or that i could be legless or have 1 arm or something. I guess i'm just trying to say.... "i have to say in my head.......IT COULD always BE WORSE"! It might sound kinda silly. But, it works for me. Try 2 find something that works for you. Remind u'rself of that & focus on u'r blessings. ;)
Like most of the others here, the meds don't do much for my pain. I've found that how I feel on any given day depends on the quality of sleep I got the night before. I sleep on an air bed (Wal-Mart, $10.00) on my floor.
I keep a chair close to help me get up in the morning. You have no idea how much difference that little change made! Any inner-spring mattress feels like I'm sleeping on a sack full of doorknobs. I also take .5 mg Clonazepam at bedtime. I hope this helps
I have had all kinds of physical therapy and all kinds of drugs. I have found nothing to relieve the pain. As well I have been on many meds and am allergic to most pain meds and come monday I have no choice but to go back on morphine. Last time I was on morphine it almost caused a divorce. My new husband said it made me very mean and it was him or the morphine. Well my doctor at my last appt. told me that no matter what I had to get back on the morphine for my sanity and for the pain. It is all I can do now to get out of bed. I have had 3 false heart attacks in 2 weeks time. Because of over doing on my good days. The muscles around my heart were the weakest in my body so that is were the fibromyligia attacked. May God Bless you and ask your doctor for something that is going to work because you feel like you are going in saine with the pain you are in. I have had firbomyligia for 11 years now and was just diagnosed 5 years ago. I have been stuck in bed for more than 6 mth and confined to a wheelchair for over a year. I am now back up slowly and gingerly and can't make a full day of things but I am atleast out of the house. Believe in yourself enough to not let this disease take you over. No matter how bad it hurts at least step outside and check the mail or walk down your side walk.