Cancer: Doctors, Chemotherapy to Prescriptions – Knowing Your Options

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

 

According to statistics from the American Cancer Society and NIH there are 14 million new cases of cancer each year. Diagnoses of cancer are expected to increase by 70% in the next 20 years. Fortunately, only 5-10% of these cases are attributed to hereditary genetics. This means that 90% of cancers are preventable! Thus it is tied back to environmental toxins, poor nutrition and other stressors that are incredibly toxic to our health.

When a patient initially receives that diagnosis and hears the hollow word of “cancer” it is more than devastating. Our society has made this word, “cancer”, to be the equivalent of death, but it should not be this way. Cancer does not have to be a death sentence. It does not have to mean months or years of treatments that will suck the life from you. It is a wake-up call to the person diagnosed and to their family members and a message that needs to be taken very seriously.

What I have seen and learned from walking down this path with a loved one is that cancer is scary, cancer can be emotional and jeering, but ultimately we have control. Control over the doctors we choose to entrust with the care, the road we choose to go down, the treatments we choose to accept or decline, and the medications that we choose to take or not take. Ultimately it is about being as knowledgeable as possible, being your own advocate, not being afraid to speak up for yourself and trusting your gut instinct.

I cringe every time we walk into the oncology office with the bowl of candy on the counter and the cancer patients helping themselves. Hello, sugar feeds cancer and causes it to grow! So, why in the heck would you put a bowl of candy out for your cancer patients?

Remember, knowledge is power.

Do your research, look online, read some books and make yourself an expert in your diagnosis. Know that if you change your nutrition and add in specific supplements that it can alter your course for the better.

After several bouts with cancer and working with many different protocols my husband made the decision to move forward with chemotherapy. The combination and dosages were going to be grueling to say the least. We were told that he would have nausea, vomiting, mouth sores, diarrhea, etc. It wasn’t if, it was when. Needless to say we were given all of the typical medications that are dispensed for the side effects and sent home to get ready for the big day. I could not just sit back and watch someone that I cared for go through that knowing that something could be done to help decrease the side effects. It was time to reach out to colleagues and friends. I found a protocol and case study from Harvard that showed utilizing a photon bed within 24 hours of chemotherapy would increase healthy cells and decrease the noxious side effects of chemotherapy. More research showed using probiotics would increase the good flora in the stomach and intestines. This is key because chemotherapy kills off the good flora and this is what leads to vomiting and diarrhea. Rinsing with warm salt water can help prevent mouth sores. Add in some hypnosis specific to chemotherapy and giving an anchor to control any symptoms gives the patient the ultimate control. Of course diet, nutrition, juicing, sleep, decreased stress, etc. also play a big part in the body being able to recover and heal.

The addition of the protocols and resources that were researched has kept my husband from having to go through the nausea, vomiting, mouth sores and major side effects of the chemotherapy. It is amazing to see the difference between what he is doing and the other patients that I see on a weekly basis that are weak, beaten down, and going through hell due to a treatment that is supposed to help them. It breaks my heart watching and listening to the other patients that are dealing with unneeded side effects because physicians are unwilling to do more than dispense medications. Medications that may not be needed if protocols could or would be put in place to keep their patients from suffering needlessly.

Life is a journey. Cancer is its own journey and one that cannot be taken lightly. But, with proper tools, protocols, knowledge and treatment options it is survivable. Don’t be afraid to be your own advocate or to be your love one’s advocate. Ask questions, speak from your heart and listen to your gut.

Be well.

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.

It All Starts in the Waiting Room, and It’s a Wrap with Your Doctor

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

 

If you or a loved one has ever been diagnosed with a chronic pain condition, CRPS, cancer, PTSD or any other debilitating condition, this will hit home as you’ve been there. Where is ‘there’, you ask? The doctor’s office to obtain verification of a diagnosis, to gather information, and hopefully gain the answers you are seeking. What most people don’t realize is that initial time in the waiting room is starting to set the stage for what is to come. The thoughts that are whirling and twirling through your head all while sitting there in those uncomfortable chairs. The body language of those sitting around you is dreary, gloomy, and everything but uplifting. Starting to sound familiar? And these are just the uncomfortable feelings even before you get to see the doctor. What most people don’t realize is all of these uncomfortable feelings and emotions are setting the stage and putting us in a place where we are more vulnerable. We are in a place physically and mentally where anything that is said to us is taken very literally, and can either help us or hinder us.

You’re finally called back to ‘the room’, or the examination room. It is cold, sterile and very unwelcoming. After a few questions and the typical vital signs, the wait continues. Stress levels are increasing, anxiety is starting to settle in, and you are on the edge of your seat not knowing what to expect.

The doctor finally arrives. You get a quick handshake, if you’re lucky, and then it is down to business. During this time, what the doctor says, how they treat you, their mannerisms, whether they actually examine you or dismiss you, and their words, set the stage for how well you will fare. Patients that are dismissed, not examined, and/or are talked down to, tend to walk away feeling degraded and hopeless. The words that are spoken to a patient at a vulnerable time are key to their success or failure in their future.

Many patients with chronic pain, CRPS, cancer, PTSD, and other debilitating illnesses end up hearing negative statistics during their doctor’s visits. They are told things like, “This is probably the worst case I have seen,” or “You are one of my most complicated patients,” or “I’m sorry, but I don’t think we have anything else to offer you.” All of these negative comments set the stage and start the patient(s) down the path to future failures.

I am not here to bash physicians or Traditional Medicine. What I am here to state is how the information, the way it is presented to a patient, and the tone in how it is said, affects their outcome. As a whole, the healthcare industry needs to do a better job teaching practitioners to communicate effectively with their patients, to make sure that all of their options are on the table, and to keep an open mind about alternative solutions.

Patients and their loved ones are searching for answers. They are holding onto hope that they will find a way to get better. They are trying to find a doctor or practitioner that will provide solid answers and solutions to help them get better. I understand there are times that traditional therapies and treatments may not be enough to help heal someone or get them into remission, but that is the time for the treating physician to be open to looking outside of the box in order to help find a solution, or perhaps encourage the patient to do so. No one treatment will work for everyone. Thus, it is very important that patients have access to information on all treatment options available.

I think I can talk about this as I have been there as a patient diagnosed with CRPS and now as a loved one of someone diagnosed with cancer. I have learned through all of these experiences that the power of suggestion at the times when we are most vulnerable can determine our outcome if we allow it. Just know there are always options out there.

Never give up hope!