CHRONIC ILLNESS AND THE FINE ART OF SAYING "NO"
They say "sorry" is the hardest word for many of us, but for me the word "no" has been my downfall. After a lifetime of being a "yes" person it would take years for me to actively accept that saying no isn't necessarily a bad thing or one that should wreak emotional havoc in one's life. While most are well educated in this word and use it with relative ease, it would take the emergence of two illnesses in my life to encourage its use in my vocabulary. This was done not only for my health, but also for my survival in my daily life. In many ways, saying "No" has offered me a path towards freedom, as much as it has helped me to define my own limits and boundaries, fearlessly and confidently, and despite any repercussions.
Throughout most of my life one could best describe me as a "yes" person, a good girl, a nice girl, and a "proper" girl, one expertly skilled in social etiquette by her mother and father. By the time I was 6 I knew that I had to call or write my grandparents, aunts and uncles and my parents friends to thank them for a gift they sent me. At first, and even when so young, I thought this was a chore, but I understood my parents' message: it was important to be nice and proper and to make people feel good about the efforts they made on my behalf. Through their example, I watched my parents bring gifts and goodies each time we, as a family, were invited to attend a function, just as I observed my mother sitting at her desk writing the hosts a thank you card immediately after we returned home from the event. By the time I was 9, I was the Junior Princess of Yes, properly schooled in all aspects of social etiquette and "ladylike" behavior, of being a "nice girl".
At home, despite the fact that my family was prone to lively discussions about almost everything, there were unspoken rules that my siblings and I had to follow. Beyond the obvious ones of not interrupting anyone while they spoke or chewing our food with our mouths open, certain areas were "No No's" in the book of our family life and dynamics. Talking about difficult subjects, expressing anger or hurt, or confronting another member of our family in an argument was a no-no and one of my parents' forbidden zones. If my older siblings and I made an error in judgment or acted out in anyway deemed inappropriate by our parents, especially our father, we were forced to sit in silence while he lectured us about the errors of our ways for hours at a time. My mother sat beside him, quietly nodding her head in agreement, while we sat there numbed by his endless refrain. In short haste I would learn that expressing my feelings, whether good or bad, was wrong and I would stuff my feelings inside. Little did I know that doing so would contribute to my illness years down the road.
I was a shy kid when I was young, so shy in fact that I was almost paralyzed with fear each time I had to speak in class and express my thoughts. This fear would last throughout my scholastic years, including through college and the beginning phases of my long career when I had to speak publicly at a meeting. Ironically, outside the classroom, with friends and especially at home, I was articulate, lively, funny and silly, but in the hallowed halls of the schools I attended, I was quiet, fearful that I would say something wrong as to incur public humiliation.
Though I had few friends as a little girl, I would go on to have lot of friends in high school, college and in my "real" life after I graduated from school. With them, I was my lively self most of the time, but I kept a part of myself on reserve and on the sidelines, hidden from view. This was the part of me that was unable to express anger or say no, nor able to set boundaries and limits in my life. If people insulted me, put me down, or laughed at me, I swallowed my rage, stuffing it deep inside the cavernous, echoing halls of my pride for a lifetime, never to forget, never to speak to what I felt. This would apply to my friends also, especially because I needed them to like and approve of me in the best light. Too often I let things go and avoided confrontation at all costs, so paralyzed with the fear that if I did speak to my feelings and truths I would be lost to the abyss and abandoned, alone. In short, the Queen of Yes was born, with no one actually knowing the real person I was, one with real feelings and needs that didn't always match my image.
As an adult, and even during treacherous, painful times in my life, I was the friend that always said yes, even if I really wanted to say no. Because my parents died when I was young, I was gripped by an utter terror of being abandoned by my friends, left alone to disintegrate into the dust, forgotten for an eternity. To prevent that from happening, I would agree to help anyone and everyone at nearly a moment's notice, more often than not dropping my own needs in favor of helping them with their own. Like a white Knight on a valiant steed, I was the Queen of Selflessness, rescuing everyone all the time, despite my own needs, my fears and my issues. Naturally and through no fault but my own, everyone expected me to be this way all of time as if it were part of the natural course in life, the plan. If I declined to assist someone, anger and guilt were hurled in my direction as if I had no choice in the matter. But I did, didn't I? For most people, "yes" would be the correct answer, but because I didn't place myself first on my hit parade, everyone else assumed that I didn't need to make a choice, when in fact I did. When I got sick everything changed and for the first time in my life I would learn the fine art of saying no and speaking to my feelings.
Being chronically ill is very hard, but it is made harder when one has spent a lifetime being nice and agreeing to everything. When my fibromyalgia first emerged I tried to maintain the image I had created until I realized I no longer had any energy stores left in my body. In short haste I would finally acknowledge that I no longer had the energy to give my all to everyone, just as I no longer had the strength to be the proverbial rescuer in life. As my energy stores fell and my fatigue, stiffness and soreness grew greater, I realized that I had to start saying "no" to things I once did and ways I once lived my life. I became more aware of the people and circumstances that were too toxic for me and made steps to change them. I learned to set limits, say no, define boundaries, and in some cases, close the door on several lengthy friendships of 25-30 years duration because they sapped me of my energy, made me tired and drained, worn down. Though this was sad for me, relief was found at the end of the tunnel because I no longer had to deal with the toxicity of others in life.
Saying no has most certainly changed my life, as much as it has changed my familial dynamics, business relationships, social interactions with friends, and how I live my life. Though I am, at times, lonely and in need of some hearty partying, the truth remains that I can no longer do most things anymore. I have limitations and if I am to recover and function at my best, even I have to heed the boundaries I have set with others. As hard as this is, at least I know I have placed myself first on my list of priorities.


Comments: 19
I'm glad you're learning how to set healthy boundaries and how to take care of your needs first ... but I wish a chronic illness weren't involved in any sense. It's odd, though, how sometimes these types of chronic inflammatory illnesses can mirror emotional states. I'm not saying that's the case here, but your description of stifling your anger and rage for all these years gave me a mental image of some hidden inner fire consuming you. It's interesting how we misunderstand or misinterpret the connections that can exist between emotional health and physical health ... our emotional states create chemical and hormone reactions in the body that can be very challenging over the long term.
I remember as a teenager, being very offended when it was suggested to me that my chronic stomach troubles were "psychosomatic." And yet, they were ... in the sense that my continual stress and fear were causing my body to malfunction. I wasn't imagining the pain I was in ... a few years later, the doctors finally found the hiatal hernia that had been distressing me for so long. But without the emotional component, I probably wouldn't have had the illness.
Adrenaline and cortisol are hard as hell on the body. I do wonder whether you may find, over time, that putting yourself first helps to heal you. I do hope so. I hope, I hope.
I wish you peace and painless days.
Thank you as always for your support, honey!
As my health deteriorated over the years, and more and more issues were revealed (e.g. major "female" problems since I was 12 that got worse, irritable bowel syndrome, hormonal problems throughout my life that got so bad in my 40's I developed panic attacks while driving), I began to wonder if all of my symptoms were interconnected, with each one playing a part in creating the conditions I have now. In effect I intuited what my regular doctors didn't want to focus upon because they merely concentrated on their specialty. What did I learn when I saw holistic doctors instead? They DID have a correlationship to one another! Funny how we intuitively "know" what's going on with us.
Now that I am working with holistic doctors, improvement is coming. While I take a multitude of supplements that make me queasy at times, I am feeling better. It's why I have returned to Gather after a long absence!
Thank you for your support and for being there!
Thank you for the support!
I have experienced the same thing in my life. Most of my friends are supportive of me and know that winter is not the time for me to engage in social activities. They know I can't so invitations are few and far between. Most know that I have to decline them anyway, just as they know I emerge somewhat victoriously in spring when the weather is warm and my body stops hurting. I am grateful to them in ways I cannot even describe.
I do have one friend that regularly pisses me off, however. She is and always has been an "all about me" kind of person, convinced that her traumas, tragedies are far worse than anyone else's even if they are identical. The sad thing for me is that she should know better. She is extremely smart and well-educated but for some reason she suffers from a kind of emotional disconnect when it comes to her issues versus someone else's. I am very patient with her and try to encourage her to understand that you cannot draw comparisons in life; that a similar tragedy another person experience is no less important than one's own...that they are equal and should be respected accordingly. Even with that, she still doesn't get it.
I am glad you have your cousin in your corner, hon!
Bless you for the healing thoughts for my sister.
Hi. This is a powerful and insightful article. I wish for you pain-free days and high spirits. You sound like a terrific person with a lot of courage.
Peace.
You are a gift!
Blessings and healing light to you and your sister! How is she?
Peace and blessings to you!
(We have good news. It wasn't a heart attack. My sister's blood pressure was crazy, the pain and other things showed up but it turned out to be issues with nerves in her neck!)