New CDC Guidelines Effects on the Pain Community

By: Traci Patterson, CH, CI – Owner and Founder, Advanced Pathways Hypnosis

 

In the last month the Centers for Disease Control (CDC) handed down new guidelines pertaining to opioid prescribing and the National Pain Strategy (NPS) was implemented. These guidelines and strategies have left the chronic pain community reeling, discouraged and feeling left behind. This is the time for advocacy for all evidence and outcome based treatments to be available to patients.

At this time the majority of chronic pain patients are receiving inadequate care and are not receiving information on all treatment options. With the new guidelines that have been set in place doctors and insurance companies are now limiting access to medications that can keep patients functional. If these limitations are going to be put in place then pain patients need access to all evidence and outcome based, non-invasive, drug-free treatment options.

I am proud to be the owner and founder of Advanced Pathways Hypnosis. I was diagnosed with Complex Regional Pain Syndrome (CRPS) myself in 2007 and was fortunate enough to get into remission in 2013. I take what I learned through my journey with chronic pain and utilize that to help others regain their lives.

To make this situation even more horrifying, is the realization that the majority of patients do not have access to the appropriate treatments. It is a disgrace to know that medical professionals are being forced to follow the oath they took to do what is best for their patients, or to follow new guidelines provided to them by the government due to fear of losing their medical license. These same clinicians’ feel that their hands are tied because other treatments that hold much potential to bringing relief – such as integrative and complementary therapies – are not covered or paid for by health insurance companies. Therefore, these treatment options for the most part are not even discussed with the patients.

I understand the feeling like no one cares or is listening. There should not be so many roadblocks for people to have access to information on all viable treatment options and to receive adequate care. Society needs to stop minimizing the pain of which they do not understand or cannot see on display.

However, lashing out against rhetoric and society is not going to solve these problems. The community needs to come together to advocate for access to all viable treatment options. A message that is honest and real needs to be pushed forward to the doctors, universities, insurance companies and elected officials. Now is the time to push for more than medications. We need to push for access to treatment options that will create a real difference in the lives of those living with pain. Become empowered and unify.