When I was diagnosed with fibromyalgia, the rheumatologist (who I never saw again) told me that fibromyalgia was related to being a perfectionist, and that I needed to exercise. And that was it. That was all that his many years of training and experience could bring him to say.
When I told a family member (who shall remain unnamed) that I was diagnosed with fibromyalgia (just like his sister had), my unnamed family member replied with, “She’s crazy!” (meaning, the sister, of course, but implying that those with this diagnosis are crazy). Again, he was a healthcare professional.
Now, before I go any further, I should tell you that I am also a healthcare professional, a bachelor-prepared registered nurse of twenty-five years. I was taught that nurses are healthcare advocates for their patients. I took a Florence Nightengale pledge to care for my patients compassionately and be their advocate. I take this very seriously.
I choose to believe that all healthcare professionals go into the field of medicine to help people. We all take a pledge when we graduate. Yet when I got out of nursing school, I was surprised to find that so many doctors and nurses are what I call “jaded.” They have become burnt out in patient care and become immune to people with pain or other illnesses they cannot understand. They have worked a long time (most of them), and are just trying to get through their unbelievably crazy shift.
Doctors have even longer shifts to work than nurses, but they also have something else working against them: an ego that tells them they must always know what their patient is experiencing and must also be able to fix it. When one or both of these things becomes untrue, it is extremely hard for the typical physician to say, “I don’t know, and I can’t fix it.” Those doctors willing to say this are good doctors, indeed, because they recognize their own humanity. Those that cannot say this tend to call everything that they can’t understand or fix a “psych” problem–something that the patient has made up or that their mind has created in their physical body (psychosomatic illness).
Most doctors were taught about algorithms and medicine (pills). They were not taught about the mind-body connection or the possibility that there is a definite spiritual and emotional connection to physical illness. And most of them have never experienced what their patient is going through. Most surgeons have not actually had surgery and experienced real pain, yet they are expected to treat it. Most rheumatologists do not know what lupus or fibromyalgia feels like and must, instead, rely on what research studies have told them about their patients’ pain and pain management. They were also not taught about natural health remedies and, therefore, have a general mistrust of anything labeled “natural.” All of these things combined puts them at a severe disadvantage when trying to treat pain.
I am just going to say it as I believe it to be true: pain is usually assessed and addressed by the subjective opinions of uninformed, inexperienced, and often, uncompassionate people who just don’t get it. There. I said it.
These healthcare professionals should be able to say, “I JUST DON’T KNOW, BUT I AM SO SORRY YOU ARE GOING THROUGH THIS.” But it is very hard for a doctor to not understand and admit that they don’t. And, unfortunately, the younger doctors learn from the older doctors, and so many of the younger doctors adopt the same attitudes. This is true of many nurses as well.
In their defense, I will say that many of the people we see at the hospital who are complaining of pain do often LOOK like they are drug-seeking. They come in with positive urine screens for illegal substances. They sometimes lie about their history. They hop from one hospital to the next, and back again. They tend to come in often, while missing their own appointments with their specialists. (Hear me, chronic pain and invisible illness patients when I say, please don’t do this because it truly makes a patient look “suspiscious.”) Some of the time it is hard to distinguish between the ones who want pain medicine and the ones who are truly in pain. It is hard to help someone with an invisible illness in one short hospital stay and is usually best for the patient to go to their own doctor for pain management needs.
I try to encourage anyone who is in chronic pain and who has a chronic invisible illness to get established with a good doctor that believes what their patients say. Try not to use the Emergency Room, as it is for true emergencies. Healthcare workers in the ER get frustrated with this and are less able to be compassionate to those patients who have symptoms that don’t add up with what they see. Chronic illnesses are better dealt with by a specialist, not ER personnel. That being said, I too have had to use the ER because I needed a refill of pain medicine when I left quickly to go to my dying grandmother’s bedside. In my haste, I forgot I needed a refill before I left. Thankfully the ER doctor had a close family member with fibromyalgia. He saw that I was established with a specialist and on a pain regimen, and he was willing to give me a 30 day refill, even though I was only asking for enough medicine for 3-4 days until I could get home. (This was before the new healthcare regulations were established which require patients to get pain medications from only one doctor.)
Other ideas that may help you when you are frustrated with healthcare professionals are:
1. Realize your healthcare professionals are human and can make mistakes. They get tired. They get frustrated when they can’t help a patient, because most of them truly do want to help their patients.
2. Always bring all your medications to every doctor appointment and ER visit. Bring your own hospital records when you go to a new doctor or make an ER visit. Physicians need to see your history, and when you are able to give it freely and openly, they are usually more able to help you, and more importantly, believe you. Be as transparent as you can be, and always let them know what you are doing to better your own health, for instance, participating in therapy or medical education.
3. When you go to the ER or hospital for surgery or a short stay, please expect that there will be long waits. There are a lot of people who need help, and most hospitals and ER’s are overloaded with patients. Always bring someone with you who is able to be your advocate, track down the nurse when you need something, and provide for your immediate comfort needs (such as help to the bathroom or a drink of cold water).
4. Try to be as unemotional as you can when giving your history, and just give the facts. That is how doctors are taught to receive information. They need the black and white details and get frustrated without them. When you do this, they are then more prone to believing you when you are emotional for pain-related reasons. Think back to the childhood story, The Boy Who Cried Wolf. If you cry “wolf” all the time, your healthcare professionals won’t know when to believe you.
5. Don’t expect your nurses and/or doctors to be able to meet all your needs. In medicine today, there are case managers, social workers, discharge planners, therapists, and educators who all have different roles in providing for your needs. Find out who the right people are to arrange for medical equipment, give insurance information/assistance, teach and provide patient education, and provide for various therapies.
6. Always get a second opinion and find specialists for your medical needs, even if it means looking outside your current location. Don’t keep going to a doctor who is truly not helping you or isn’t complying with standards of care. Research your diagnosis so you will know what appropriate standards of care are and what treatment options to discuss with your doctor. Be careful about appearing “cocky” with the information you have researched because many physicians don’t know how to respond well to a patient who may know more than they do about a particular illness.
7. Find support for your own needs, including encouragement groups online (such as God-Living Girls for women with chronic illness), support groups with others who share your diagnosis, and friends who truly understand your pain. Don’t always expect your immediate family to be able to understand and help you with your medical needs. If they don’t have a chronic illness, they probably won’t get it. They don’t understand, and they probably need their own support system as the caregiver of someone who has a chronic illness. (For more information about God-Living Girls, contact Laurie at firstname.lastname@example.org)
8. It may be helpful for you to know that new healthcare regulations have changed the way doctors can administer pain medications and when pharmacies can dispense them. The new laws require that patients sign a pain contract, which usually states that you will only get your pain medications from the doctor with whom you have signed the pain contract. Physicians take this very seriously and will discharge you from their care if you get pain medications from any other doctor. The new laws also require a urine drug screen once per year. This is not only to check for illegal substances, but also to make sure you are being compliant with their current therapy (taking their ordered pain medications). The new laws also have specific time frames for how soon you can refill your medication and how early the pharmacy can dispense it. They also require you to go to only one pharmacy for your pain medications. Hopefully, knowing this information will prevent unneeded frustration with your doctors who cannot dispense pain medications in a way that is outside these legal boundaries.
As a nurse with fibromyalgia, I get it. I understand what you are going through as a patient who is frustrated with healthcare professionals that don’t always adequately meet your needs. It is so very hard on both sides of this healthcare continuum. I hope that the above suggestions will provide you with resources you need to have better relationships with your doctors, nurses, and other healthcare professionals.
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Disclaimer: The author and God-Living with Chronic Illness do not receive any compensation for references to specific products, ideas, people, or websites. The ideas posted are not intended as medical advice and should not be taken as such in place of your physician’s recommendations.
Hi! My Name is Laurie, and I am a wife, mom, nurse, and patient living with fibromyalgia. I understand first-hand what life is like with chronic pain and illness. My passion is to help provide others with the spiritual encouragement and resources that I so desperately needed when I was first diagnosed. Please join us on the blog (god-livingwithchronicillness.com) and Facebook page (www.facebook.com/godlivingwithchronicillness) for regular encouragement and hope. Welcome!