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Now this was during the time that society was compassionate for people who suffered from chronic pain and doctors were nudged to prescribe the pain medication available for these patients.
My family doctor took over my pain managment since it was a Workers Compensation case and the insurance company paid generously for any claims associated with that injury.
So, a few years ago, after tinkering for the kind and quantity of medication for my particular body makeup, I was prescribed 360 tablets of Roxycodone 30 mgs each month and 180 tablets of Opana 30 mgs each month. That prescription every month for several years saved my life because before that, I had no life. Then, of course, the Opana ingredients were changed. However, by this time, society now nudged the doctors and the public to be AGAINST prescribing pain medicine and my medicine and the amount was "WAY TO MUCH" according to these "pain clinics" that cropped up overnight. These pain clinics have gone along with our society's thought of not prescribing pain medicine and/or immediately reduce the amount and type. HOWEVER, THEY'RE PROCEDURES, INJECTIONS, ETC. IS FINE EVEN THOUGH THOSE RISKS ASSOCIATED WITH THOSE PROCEDURES ARE EXTREMELY HIGH.
Cutting to the chase, my nice primary doctor will not do long term pain management any longer so my only alternative is 3 ways. Look around for street drugs, go to Mexico or Canada which my insurance company will NOT pay for, or kill myself.View Thread
Try reading this below, see link. Also the more you go without sleep the worse it gets! You have to sleep to help compensate. So try chammomile or other relaxing tea just before bed you have to try to rest I only take during flareups as keeping everything moderate to little is best. Never get addicted to any one thing. Keep it natural as possible and treating yourself is good but be careful. I crave coffee, chocolate, ice cream, fast food for my splurges--small splurges. Especially during stress but try only to have on my splurge days I choose.
And change your diet, please read:
http://www.fibromyalgia-support.net/articles/whatdoctors.htm Also start reading your food labels google preservative listings both for foods and products. They are all chemicals your body cannot tolerate anything that's foreign to it and will think it's under attack even more so than it already acts. Reduce them as much as possible. It can take weeks to months depending on how long it's been since your body has seen goodness. Even natural or organic foods should be watched, they are not perfect either so my best advice is read, read, read and get educated. I ate a bag of GMO corn chips and was sick as could be so add GMO to your list as well. Unfortunately not everything is 100% labeled like we can understand it or stands out blatantly. Take care and God Bless You.View Thread
A hot bath every morning (wish it was a whirlpool) but still works, a heated mattress pad (to help with the bursitis in the hips since I sleep on my side) just feels good to the ole body, I keep a heating pad in the living room for my mid back when it flares up, and also a heated throw to put on the leather furniture (it's cold).
Skin sensivitivy is also an issue, so the bra comes off as soon as I get home, the tops of my feet bother me so I wear my work shoes so loosely tied they almost flop on my feet
Can't wear anything constrictive. The hair has to be kept low on my head as it can drive my scalp nuts with the weight of my hair (mid back length). The Vitamin D is truly a miracle. Short story-had mine checked it was 25, which is normal according to the lab standards. The bone physicians I work with keep their patients in the mid 40's. I was put on the vit D 50,000 for 8 weeks with addl 1000mg daily, rechecked when that was done and I was up to 47. Maintained the 1000mg vit D daily and rechecked in 3 months and still at 45. Had all this done during the summer, so didn't realize until halfway through winter that the light bulb came on that my pain was dramatically reduced that winter.
I got off the Ambien, I was doing weird things at night. Started melatonin 6mg about an hour and half before bed-and that has helped with my sleep throughout the night. Able to go back to sleep when woken up for a bathroom break.
I'll update more later.
Have a good day!View Thread
"Master Your Pain" by Jill B. Fancher, PhD
It is about Comprehensive Science-based
Method to Help You Live Well With Chronic Pain
I found this book to be quite helpful Living with Fibromyalgia and Chronic Pain is not easy though I have learned that if you find something that works don't quit doing it. Share with others that have a similar problem.View Thread
"Master Your Pain" by Jill B. Fancher, PhD
It is about Comprehensive Science-based
Method to Help You Live Well With Chronic Pain
I found this book to be quite helpful Living with Fibromyalgia and Chronic Pain is not easy though I have learned that if you find something that works don't quit doing it. Share with others that have a similar problem.View Thread
View Thread
ME ON OVER 7 MEDS,- DXS, SCOLISOS- PINCHED NERVES,
SI JOINTS RESTLESS LEG SYNDRROME,, DID 2 INJECTIONS
OF DEPO MEDROL UNDER FLOUROSCOPY. -
NO HELP, I CHANGED TO AN HMO. SHE HAD ME ON VICODIN,
CLONOPIN, AND A HOST OF TRYING TO GIVE ME NEUROTIN,
RECUIP, FLEXERIL, REPODIMOLE,TRAMODOL, AND FINALLY,
SAID WELL ILL JUST ADD 1/2 MG TO YOUR CLONOPIN WITH
NO HELP, CRYED ALLNIGHTS, AND FINALLY ,
I BROKE THE CODE OF ETHICS, EVEN BEING A DRS. WIDOW,
WITH 2 CHILDREN IN AS DRS, AND COME FROM A HOST OF
FAMILY OF DRS, AT CORNELL, AND COLUMBIA,
DR. WHEN YOUR IN PAIN, AND CRYING TOALL NIGHT,
YES I WAS WRONG, SO THEY DISCHARGED ME AS
A PATIENT AND I HAVE BEEN WITHDRAWING FROM THE
VICODIN, AND CRYNG WITH PAIN, AND UTILIZING 800.00MG
MOTRIN,
THE DR. HAD ME ALSO ON GABAPITIN,
THERE OFFICE ONLY SENT 60 PAGES OF MEDICAL RECORDS
WHICH I PERSONALLY HAVE , AND 5 DR, WITHOUT SEEING
ME, HAVE SAID NO I DO NOT WANT THIS PERSON IN MY
PRACTICE.
THIS DR. 1YR AGO PUT ME ON METHATDONE
AFTER 1YR 1/2 IT SAID GO HOME ITS NOT WORKING
FOR YOUR DETOX, NO TITRATTION, AND IT WAS
HELL,
PEARLS OF SWEAT HIGH BLOOD PRESSURE,
DID THERE OFFICE CALL TO CK ON ME
NO.
WERE THOSE MEDICAL RECORDS SENT TO
THE NEXT DR.
NO.
PUPOSSELY, THAT DR. DID NOT WANT TO LOOK BAD
IN THE SOCIAL EYES OF THE NEXT DR.
I HAVE 2 COLLEGE DEGREES, IM NOT STUPID
ALTHOUGH, IM DISABLED BY THE SOCIAL SECURITY
I CAN WALK WITH A CANE,
YES I BROKE THE CODE OF ETHICS,
ALLTHESE YRS AS A PATIENT, THIS DR.
WOULD TELL ME
YOU ARE NOT AN ADDICT!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!
EVERY 3 MOMTHS DID SHE APPLY THAT IN THE CHART
WHO KNOWS,
DID SHE TELL ME ABOUT -
THIS DRS PERSONALL LIFE
YESS OH!!!! YESS CHILDRESS DYFUNCTIONAL DRUGS,
DIVORCE I COULD GO ON AND ON.
HENCE THE END, I WAS A HIGH MAINTENANCE PATIENT
NOW ON A HMO PLAN, - PREVISOULY, I HAD
MEDICAAREE, WHEN ME HUSBAND DIED I COULD
PAY MY BILL
BUT THAT MONEY DOES NOT LAST FOR EVER,
IVE DONE SOMETHING RIGHT TO RAISE DRS, AS
IN THE FUTURE TO TAKE THAT HIPOCRATIC OATH
THEY SEE WHAT I HAVE BEEN THRU,
I FEEL SUICIDAL, SOMEDAYS THE PAIN
IREAALY FEEL LIKE GOINT TO THE DEA AND SHARE
MY STORY???
THANKING YOU IN ANDVANCE
AND I REMAIN,
SPIRITUAL AND HOPEFUL
GOD BLESSView Thread
My personal exchanges are Vitamin D and Pain and Wrath of the Dragon....if you care to visit..
My personal exchanges are Vitamin D and Pain and Wrath of the Dragon....if you care to visit..
i just rejoined this group. i have fms since 93 when noone knew much about it. I was recently hospitalized with cardiac arrythmias and High BP.Being controlled on meds But this last 4 days I have been in severe pain. MD put me back on celexa 10mg. I have been on Klonapin and neurotin for years but have come up with this severe flare. Unable to sleep more than 2-3 hours. Also was prescribed ambien which has has a reverse effect on me. All this anixety is bringing the BP up.Anyone have any thoughts about this. Thanks FranView Thread
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