Chronic Pain Support Group
Physicians and professionalsdefine pain as chronic if it lasts longer than three to six months and is persistent. It's distinct from acute pain that is a direct result of injury or trauma. This support group is dedicated to those suffering from chronic pain. Discuss treatments that have worked for you, find advice for your specific experience, and find support. You're not...
Stubborn T
ralop
Thanks for the post
Maybe this link will work??
I think criminals who steal controlled substances and sell them on the streets which make our life so difficult should go to jail longer, I just wish there was a way that the tax payers did not have to foot the bill and make us go in debt more as a country.
The problem with funding groups to learn how to get rid of certain diseases or finding cures in CP is that the country as a whole has so limited funds and it seems that they fund more of the big ones HIV, Cancer, Etc and CP seems so little compared to people dying from the other ones so I can understand that is why funding goes to them, not fair but I understand.
Stubborn TerrieAnn
Here's a story for your reading pleasure.........
http://www.pnhp.org/news/2004/october/break_the_insurance_.php
First our ins gets to control what meds we are allowed to take, now the DEA gets to control who is allowed to use pain meds.
I am really tired of fighting this disease already. I am tired of the constant fear,. This is no way to live.
Quote for the article........"To support grassroots groups, Dority said that Americas Agenda: Healthcare for All will utilize TV, radio, print media and the Internet to mount creative and coordinated truth campaigns. Business leaders, physicians, elected officials, labor leaders and universal health care campaign activists will be effective messengers of truth about the costs and benefits of specific health reform proposals. We will counter the insurance lobbyists by taking the truth to the American people, said Dority."
Now that is fantastic:):)........Only see one MAJOR problem:(:(
The article was written Oct 10, 2004.....................2004..............Wonder what happened:(:(:(:(
Doctors already have a national network but I've found many don't use it. It's an online system that only healthcare professionals can use to monitor patients that do doctor shop or are also getting scripts from more than one doctor going to different pharmacies to fill them. These people harm us greatly however if only the good doctors out there would use this site more to take the time to ensure they are treating true CP patients, they wouldn't have to worry so much so I feel that check & balance system is already in place through the DEA at a cheap cost. If a doctor doesn't feel it's worth the time to use it, they are putting both their patients and license at risk as they could have a staff member do this work.
I do know one pain doctor I had a very long time ago had in my chart what day I got my script, when it was due, and even had the records of when I picked them up all in my chart. I'm sure he felt comfortable seeing that I wasn't running out to the pharmacy the same day my meds were due and sometimes would be 2 to 3 days beyond that date. For some, they have to follow this date schedule as some states have changed laws for any prescription that if you don't fill it on the date due, you can't get it filled at all along with getting only the needed amount or less than if the pain is worse and they might run one day short bc of it before they have a chance to speak to their doctor about it if at all.
These pill mills should be closed by now. I know FL is touted to be the worst state & laws have been changed however watching a couple of very recent documentaries, I found these places are still in business & even have signs on their doors stating; "Walk ins Welcome" which is something I've never seen before.
I am blessed to have gone back to my 1st pm doctor ever who is involved locally in training doctors and police to spot drug seekers yet hasn't gone as far to think or feel he has any problems with the DEA because he is one of the good ones.
I was trapped in a horrible pm place that wasn't like that at all when I started going there & it took me 2yrs to get out of it bc I couldn't find a doctor to accept Medicare until I found my 1st pm doctor again.
I started seeing what I knew were drug seekers at this horrible place feeling like I was going to look bad for even having to go there. I explained it all to my good doctor who informed me after over 11yrs then, I no longer belonged in pm & found a wonderful Internal Medicine Doctor who does have the training to treat CP patients even tho that is not her largest group of patients.
When I read this bill stating how doctors must be educated, I feel like it truly a statement from the DEA of "We must put more fear into you as a doctor" vs just going after the bad ones.
I know there are hopefully more and more better treatment options coming or that exist to help with CP but there is a safe and acceptable need for the use of opiates to treat CP in a humane way without being looked at as guilty until proven innocent.
Tipper is also right as it is Big Pharma and the lobbyist who are putting money in the pockets of politicians for what their agendas are. They want the ability to keep making these pain meds that generate a lot of money for their companies yet with both the FDA and the DEA getting more & more control of running their businesses, it will be good doctors and the people in CP that don't need further discrimination that will pay for it all in the worst possible ways.